#sjogrens

I just recently got these forearm crutches. They sat in a box for a week after they came. I still have only used them once despite the pain that I’ve been having in my hip since like 2014. I was diagnosed around 2015 with a labrum tear on my right hip after I had my knee surgery on my right. I have chronic subluxations of that hip as well. I’ve been told by 3 different surgeons I would eventually need surgery on it. I’ve had multiple injections and have capped off at 3 due to my risk factors. I’ve pushed through long enough. -
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I have pretty intense surgical PTSD from the complications with my knee surgeries that have made me continue to push this surgery for my hips back over and over again. I still push through and work mostly 48 hours a week, night shift, in a busy ER with this. It’s now gotten to the point that I’m having pain and coming home in tears after almost every shift and even sitting I can’t get comfortable anymore. I see the top hip specialist at Duke on Tuesday. Fingers crossed 🤞🏼he can come up with a better plan than surgery. I’ve done it all, PT, injections, acupuncture, taping, bracing, etc. The idea of surgery has made my anxiety go through the roof. -
So, I gave in and got a mobility aid (my first since my knee surgeries) to help with my mobility and pain until we can figure out a plan. I’m struggling with accepting the use of a mobility aid. How did those that use them chose which type and accept being able to use them intermittently (if you do)? -
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#posturalorthostatictachycardiasyndrome #forearmcrutches #mcas #pots #hyperpots #eds #ehlersdanlossyndrome #hypermobility #lupus #sjogrens #labraltear #hippain #hiparthroscopy #mobilityaids
I just recently got these forearm crutches. They sat in a box for a week after they came. I still have only used them once despite the pain that I’ve been having in my hip since like 2014. I was diagnosed around 2015 with a labrum tear on my right hip after I had my knee surgery on my right. I have chronic subluxations of that hip as well. I’ve been told by 3 different surgeons I would eventually need surgery on it. I’ve had multiple injections and have capped off at 3 due to my risk factors. I’ve pushed through long enough. -
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I have pretty intense surgical PTSD from the complications with my knee surgeries that have made me continue to push this surgery for my hips back over and over again. I still push through and work mostly 48 hours a week, night shift, in a busy ER with this. It’s now gotten to the point that I’m having pain and coming home in tears after almost every shift and even sitting I can’t get comfortable anymore. I see the top hip specialist at Duke on Tuesday. Fingers crossed 🤞🏼he can come up with a better plan than surgery. I’ve done it all, PT, injections, acupuncture, taping, bracing, etc. The idea of surgery has made my anxiety go through the roof. -
So, I gave in and got a mobility aid (my first since my knee surgeries) to help with my mobility and pain until we can figure out a plan. I’m struggling with accepting the use of a mobility aid. How did those that use them chose which type and accept being able to use them intermittently (if you do)? -
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#posturalorthostatictachycardiasyndrome #forearmcrutches #mcas #pots #hyperpots #eds #ehlersdanlossyndrome #hypermobility #lupus #sjogrens #labraltear #hippain #hiparthroscopy #mobilityaids
It takes a tough person to constantly go through the things that us spoonies do.
spooniestrong #spoonie #spoonielife #invisibleillness #invisibledisability #lupus #lupusflare #sle #lupuswarrior #sjogrenssyndrome #sjogrens #sjogrenswarrior #potssyndrome #posturalorthostatictachycardiasyndrome #fibromyalgia #fibro #dontgiveup #survivor #interstitialcystitis #hashimotosdisease #hashimotosthyroiditis #arthritis #inflammation #autoimmunedisease #chronicillness #chronicpain #fatigue #cfs #fatigue
😂😂 truth 💕
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#shoutout #invisibleillness #lupus #lupusawareness #lupuswarrior #lupusproblems #yougotthis #sjogrenssyndrome #sjogrens #raynaudsdisease #raynauds #sle #rheumatoidarthritis #rheumatoidarthritiswarrior #rheumatoidarthritisawareness #warrior #fighter #hughessyndrome #autoimmunedisease #autoimmunewarrior #spicegirls #spicegirlwarrior #ifyouwannabemylover #spoonie #lupusawareness #lupusproblems #truth #relatable
⏸ I hope you've done that this weekend- or will when the time is right for ➰you➰, dear sisters 💙💐 @morganharpernichols 👩‍🎨 READS: "May you never overlook how powerful it can be to slow down for a moment and take a little time to breathe." ✨ - {morgan harper nichols}
⏸ I hope you've done that this weekend- or will when the time is right for ➰you➰, dear sisters 💙💐 @morganharpernichols 👩‍🎨 READS: "May you never overlook how powerful it can be to slow down for a moment and take a little time to breathe." ✨ - {morgan harper nichols}
As a #disabledauthor I have to be pretty good at holding things like schedules with loose hands. If it works, awesome. If it doesn't, it's okay, I'll just consider my options and try again. Healthy Avery was an overachieving perfectionist - and ten years in to my autoimmune condition making decisions for me it still rankles that I can't have a set schedule. So I still have goals, but my deadlines are flexible. It sucks. But the alternative (not writing) sucks even more. 
TLDR: I write when I write and I don't focus in time of day.
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#augustauthorwipchallenge #augustauthorchallenge #autoimmunedisease #disabledauthor #disabledwriter #chronicpain #chronicfatigue #sjogrens #rheumatoidarthritis #notlupus #notcancer #iih #ideopathicintracranialhypertension #vpshunt #immunesystem #spoonlife #spoonielife #spoontheory #authorloop #authorsofinsta #authorsofinstagram #writerscommunity #hustlingwriterscommunity #WriteDreamBelieve
As a #disabledauthor I have to be pretty good at holding things like schedules with loose hands. If it works, awesome. If it doesn't, it's okay, I'll just consider my options and try again. Healthy Avery was an overachieving perfectionist - and ten years in to my autoimmune condition making decisions for me it still rankles that I can't have a set schedule. So I still have goals, but my deadlines are flexible. It sucks. But the alternative (not writing) sucks even more.
TLDR: I write when I write and I don't focus in time of day.
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#augustauthorwipchallenge #augustauthorchallenge #autoimmunedisease #disabledauthor #disabledwriter #chronicpain #chronicfatigue #sjogrens #rheumatoidarthritis #notlupus #notcancer #iih #ideopathicintracranialhypertension #vpshunt #immunesystem #spoonlife #spoonielife #spoontheory #authorloop #authorsofinsta #authorsofinstagram #writerscommunity #hustlingwriterscommunity #WriteDreamBelieve
Cleared a few downed trees on the trails at Oak Mountain then got in a little road ride for myself. #loveyourtrails #oakmountainstatepark #discovershelbyal #challengeyourlimits #celiac #sjogrens #onekidney #bump_mtb_official #getoutsideandride #bethebestversionofyourself #sawyer #treebeast #volunteer
Cleared a few downed trees on the trails at Oak Mountain then got in a little road ride for myself. #loveyourtrails #oakmountainstatepark #discovershelbyal #challengeyourlimits #celiac #sjogrens #onekidney #bump_mtb_official #getoutsideandride #bethebestversionofyourself #sawyer #treebeast #volunteer
Guess who was able to stand up long enough to take a shower? I was in so much pain today; I didn’t think I could do it. However, I have come out of the holy waters of my shower renewed, or at least cleaner than before I took a shower. 🤷🏽‍♀️ #sjogrens #sjogrenssyndrome #sjogrensawareness #sjogrenslife #autoimmunedisease #autoimmune #autoimmuneawareness #autoimmunity #autoimmunewellness #autoimmunedisorder #chronicillness #chronicpain #pain #shshshakin #shaking #tremors
Guess who was able to stand up long enough to take a shower? I was in so much pain today; I didn’t think I could do it. However, I have come out of the holy waters of my shower renewed, or at least cleaner than before I took a shower. 🤷🏽‍♀️ #sjogrens #sjogrenssyndrome #sjogrensawareness #sjogrenslife #autoimmunedisease #autoimmune #autoimmuneawareness #autoimmunity #autoimmunewellness #autoimmunedisorder #chronicillness #chronicpain #pain #shshshakin #shaking #tremors
It's our mission here at CDMDA to INNOVATE by taking what was meant to break us and turn it around to help not only ourselves but those who were/ are on the brink of giving up. We are here to INSPIRE every person that stops by our page, whether you're chronically ill or not! It is our duty to INFORM the masses that yes chronically ill models are more than capable of slaying the runway! We are here to make a profound IMPACT on every person that stops by to view our page & content! We are CHRONICALLY DOPE!
#determination #inspiration #strength #power #progress #motivation #strong #invisibleillness #mylife #mystory #spoons #fighter #illness #warrior #chronicillness #medicine #arthritis #cannabis #autoimmunedisease #anxiety #icandoit #sjogrens #marijuana #dontgiveup #model #CDMDA #chronicallydope
It's our mission here at CDMDA to INNOVATE by taking what was meant to break us and turn it around to help not only ourselves but those who were/ are on the brink of giving up. We are here to INSPIRE every person that stops by our page, whether you're chronically ill or not! It is our duty to INFORM the masses that yes chronically ill models are more than capable of slaying the runway! We are here to make a profound IMPACT on every person that stops by to view our page & content! We are CHRONICALLY DOPE!
#determination #inspiration #strength #power #progress #motivation #strong #invisibleillness #mylife #mystory #spoons #fighter #illness #warrior #chronicillness #medicine #arthritis #cannabis #autoimmunedisease #anxiety #icandoit #sjogrens #marijuana #dontgiveup #model #CDMDA #chronicallydope
If I ever feel trapped or down or mad at my circumstances I just need to get somewhere beautiful that reminds me how beautiful the world can be. #chronicillness #invisibleillness #beach #fun #sjogrens #waves #family #autoimmunedisease #freedom #life #play
If I ever feel trapped or down or mad at my circumstances I just need to get somewhere beautiful that reminds me how beautiful the world can be. #chronicillness #invisibleillness #beach #fun #sjogrens #waves #family #autoimmunedisease #freedom #life #play
Warning: this is content about my own experience with #autoimmunediseases ... My own symptoms started as young as elementary school. I never had as much energy as other kids. Even if I kept up for a few days or even a week then I would have setbacks for days or weeks when I didn’t have enough energy. My actual pain started in my right hip at age 21. Suddenly getting up from sitting on the floor was painful and I limped until the stiffness wore off. My range of motion in my hips was compromised. Doctors diagnosed me with arthritis. Progressively it got worse until I was finally diagnosed with autoimmune disorder at age 32. Eventually I found the right doctors who could decide which disease I had but overlaps are not uncommon so eventually and currently I have dx of #psoriaticarthritis and #rheumatoiddisease with overlaps of #lupus and #sjogrens which have all caused #fibromyalgia and #degenerativediscdisease .. There are no cures only treatments and changes in lifestyle. Some days I can walk, dance and balance...some days I can only crawl or stay stuck in bed. This will never change my outlook on life... I try to never complain to friends and coworkers. I have even tried not complaining to significant others but I do sometimes try to hide it from new relationships because in #Colorado everyone is active and looking for partners who can keep up... I will never stop #smiling and #laughing and being #happy . I love my life and #blessings I love #thelord #jesuschrist because everyone has a #crosstobear so #bekind #chronicpain #chronicpainawareness #chronicfatigue #love #loveyourself #loveiseverything #shine #behappy #happygirl
Warning: this is content about my own experience with #autoimmunediseases ... My own symptoms started as young as elementary school. I never had as much energy as other kids. Even if I kept up for a few days or even a week then I would have setbacks for days or weeks when I didn’t have enough energy. My actual pain started in my right hip at age 21. Suddenly getting up from sitting on the floor was painful and I limped until the stiffness wore off. My range of motion in my hips was compromised. Doctors diagnosed me with arthritis. Progressively it got worse until I was finally diagnosed with autoimmune disorder at age 32. Eventually I found the right doctors who could decide which disease I had but overlaps are not uncommon so eventually and currently I have dx of #psoriaticarthritis and #rheumatoiddisease with overlaps of #lupus and #sjogrens which have all caused #fibromyalgia and #degenerativediscdisease .. There are no cures only treatments and changes in lifestyle. Some days I can walk, dance and balance...some days I can only crawl or stay stuck in bed. This will never change my outlook on life... I try to never complain to friends and coworkers. I have even tried not complaining to significant others but I do sometimes try to hide it from new relationships because in #Colorado everyone is active and looking for partners who can keep up... I will never stop #smiling and #laughing and being #happy . I love my life and #blessings I love #thelord #jesuschrist because everyone has a #crosstobear so #bekind #chronicpain #chronicpainawareness #chronicfatigue #love #loveyourself #loveiseverything #shine #behappy #happygirl
Cienna: Having a chronic illness isn’t easy. Having multiple chronic illnesses isn’t easy. Trying to navigate life and friendships as a disabled young woman isn’t easy. As chronically ill individuals, we use so much of our daily energy taking care of our bodies. Any extra energy leftover after that is extremely valuable. Any time spent socializing with friends is very intentional and means that I deeply value our friendship, whether that is texting to say hi, calling to check in , enjoying a meal together, or spending an afternoon with one another. Many of my friends I know from daily life, but a growing special number I have met through chronic illness and the communities we have online. We may not have ever had the opportunity to spend time with each other in person or maybe we see each other rarely. These friendships are built on a deep bond of understanding and are some of the most kind and passionate people you will ever meet. This past June out at @mayoclinic I had the opportunity to finally meet my chronic illness twin: @cece_getyoursicktogether ! From the way we view our conditions, our attitude towards life, our adventurous spirit, and even a good amount of our conditions themselves, we had so much in common! I will forever cherish the hours spent talking, eating, and enjoying each other’s company. We have big dreams for future projects together and while I can’t tell you about them just yet, I can tell you that I am so excited to share them with you sometime soon! Tomorrow Cece has a huge surgery for one of her vascular conditions. I hope you will join me in sending her all the love, good thoughts, strength, spoons, good vibes, and prayers to help her kick this surgery’s butt! I love you so much Cece! Thank you for being an extraordinary friend! Sick chicks stick together! #servicepuppiper #pots #chronicillness #disabled #chronicallyawesome #sickchickssticktogether #servicedog #catahoulaleoparddog #friendsforever
Cienna: Having a chronic illness isn’t easy. Having multiple chronic illnesses isn’t easy. Trying to navigate life and friendships as a disabled young woman isn’t easy. As chronically ill individuals, we use so much of our daily energy taking care of our bodies. Any extra energy leftover after that is extremely valuable. Any time spent socializing with friends is very intentional and means that I deeply value our friendship, whether that is texting to say hi, calling to check in , enjoying a meal together, or spending an afternoon with one another. Many of my friends I know from daily life, but a growing special number I have met through chronic illness and the communities we have online. We may not have ever had the opportunity to spend time with each other in person or maybe we see each other rarely. These friendships are built on a deep bond of understanding and are some of the most kind and passionate people you will ever meet. This past June out at @mayoclinic I had the opportunity to finally meet my chronic illness twin: @cece_getyoursicktogether ! From the way we view our conditions, our attitude towards life, our adventurous spirit, and even a good amount of our conditions themselves, we had so much in common! I will forever cherish the hours spent talking, eating, and enjoying each other’s company. We have big dreams for future projects together and while I can’t tell you about them just yet, I can tell you that I am so excited to share them with you sometime soon! Tomorrow Cece has a huge surgery for one of her vascular conditions. I hope you will join me in sending her all the love, good thoughts, strength, spoons, good vibes, and prayers to help her kick this surgery’s butt! I love you so much Cece! Thank you for being an extraordinary friend! Sick chicks stick together! #servicepuppiper #pots #chronicillness #disabled #chronicallyawesome #sickchickssticktogether #servicedog #catahoulaleoparddog #friendsforever
Guys my body has started to respond.... When i started my new position i weight myself n i was 118 kg. I remember converting that n thinking "wow" i let the excuse of my diseases beat me. I remanber posting. I feel Defeated.. N i started to think n eat as if i was never diagnosed. Heard advice of a few very knowledgeable people n tarrrrraaaa -15 pounds

Its all in the mind guys.. Fight for what you want.

I am coming back stronger the never 😊😊😊😊🙏❤ #fitfam
#sjogrens
#pcos 
#fitmotivation 
#fitforlife 
#motivationforwoman 
#fitig 
#gymrat
Guys my body has started to respond.... When i started my new position i weight myself n i was 118 kg. I remember converting that n thinking "wow" i let the excuse of my diseases beat me. I remanber posting. I feel Defeated.. N i started to think n eat as if i was never diagnosed. Heard advice of a few very knowledgeable people n tarrrrraaaa -15 pounds

Its all in the mind guys.. Fight for what you want.

I am coming back stronger the never 😊😊😊😊🙏❤ #fitfam
#sjogrens
#pcos
#fitmotivation
#fitforlife
#motivationforwoman
#fitig
#gymrat
You never know what’s going to happen in life.🤷🏼‍♀️
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A lesson I’ve learned so many times over the past few years, in both welcome & unwelcome ways.😅
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It’s a truth that can easily be viewed as scary - change is hard, especially when you don’t see it coming.👁
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But it can also be reframed as exciting! The opportunities in this life are endless. You don’t know what life will bring, so what if it’s the best thing to ever happen to you?✨
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You can’t plan for everything because life will always throw you curveballs.⚾️
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All you can do is just keep riding the train wherever it takes you🛤and making the best of things along the way!
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#SundayNightSendoff
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#embracethejourney #joyinthejourney #selfcaresunday #wellnessblogger #wellnessjourney #mindbodygram #iamwellandgood #liveinspired #livingwell #healthyhappylife #sjogrens #autoimmunedisease #invisibleillness #holisticliving #balancedlifestyle #makeitblissful #wellpreneur #holisticwellness #mindsetiseverything #mindsetmatters #changeyourmindsetchangeyourlife #womaninprogress #thejoysquad #longrunpresets #lifeunscripted #authenticliving #lifeisgood
You never know what’s going to happen in life.🤷🏼‍♀️

A lesson I’ve learned so many times over the past few years, in both welcome & unwelcome ways.😅

It’s a truth that can easily be viewed as scary - change is hard, especially when you don’t see it coming.👁

But it can also be reframed as exciting! The opportunities in this life are endless. You don’t know what life will bring, so what if it’s the best thing to ever happen to you?✨

You can’t plan for everything because life will always throw you curveballs.⚾️

All you can do is just keep riding the train wherever it takes you🛤and making the best of things along the way!

#SundayNightSendoff




#embracethejourney #joyinthejourney #selfcaresunday #wellnessblogger #wellnessjourney #mindbodygram #iamwellandgood #liveinspired #livingwell #healthyhappylife #sjogrens #autoimmunedisease #invisibleillness #holisticliving #balancedlifestyle #makeitblissful #wellpreneur #holisticwellness #mindsetiseverything #mindsetmatters #changeyourmindsetchangeyourlife #womaninprogress #thejoysquad #longrunpresets #lifeunscripted #authenticliving #lifeisgood
Out Living Sjogren’s Strong.... enjoying a day of road closures for cyclist at #Cyclavia! 🚴🏻‍♀️❤️🚴🏻‍♂️.
... Good weather feeling Ok... making the most of it on my bike today! 🚴🏻‍♀️❤️🚴🏻‍♂️.
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#SjogrensStrong
#SjogrensSyndrome 
#ShiningALightOnSjogrens 
#StrongerTogether
#ThisIsSjogrens
#MotivatinalQuotes
#Autoimmune #ChronicIllness 
#InvisibleIllness #SjogrenSyndrom
#sjogrensWarrior
#SpoonieSupport #Sjogren #SpoonieProblems #Sjogrens
#SpoonieLove #SpoonieLife
#ChronicFatigue #Podcast #Sjögren #Sjögrens #Spooni
Out Living Sjogren’s Strong.... enjoying a day of road closures for cyclist at #Cyclavia! 🚴🏻‍♀️❤️🚴🏻‍♂️.
... Good weather feeling Ok... making the most of it on my bike today! 🚴🏻‍♀️❤️🚴🏻‍♂️.
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#SjogrensStrong
#SjogrensSyndrome
#ShiningALightOnSjogrens
#StrongerTogether
#ThisIsSjogrens
#MotivatinalQuotes
#Autoimmune #ChronicIllness
#InvisibleIllness #SjogrenSyndrom
#sjogrensWarrior
#SpoonieSupport #Sjogren #SpoonieProblems #Sjogrens
#SpoonieLove #SpoonieLife
#ChronicFatigue #Podcast #Sjögren #Sjögrens #Spooni
#sundayreflection #faith #hope #love #prayer #thankyoujesus ➖➖➖➖➖➖➖➖➖➖➖➖➖➖➖ #positivityispretty #letyoursparkleshine 💖 #chroniclesofthechronicallyill #beautifullybroken 🎭 #autoimmunedisease #bronchiolitisobliterans #butyoudontlooksick #chronicillness #chronicpain #fibromyalgia #lupus #migraine #sjogrens #tryingtosparklethroughit ✨
👩🏼👦🏻: Like we always say, if you don’t have a chronic illness, then you will never understand what it’s actually like living with one.

Follow our page 👉 @how.u.feeling 👈 for more!
👩🏼👦🏻: Like we always say, if you don’t have a chronic illness, then you will never understand what it’s actually like living with one.

Follow our page 👉 @how.u.feeling 👈 for more!
Let me share something about those of us with chronic illnesses. Chronic, for those who are forgetful or unaware, means what we’re battling doesn’t go away. You might be tired of your friend or family member’s condition and just wish they’d “get over it” or “feel better,” but, as my mom would say, “dollars to donuts” they feel the same. The problem is that you can walk away from our pain, but we cannot. We have our upswings and our downturns, but just because we are having a good day doesn’t mean we found a magic cure. It doesn’t mean, after you see us that day, that we won’t be crying at 1:30 in the morning because the phantom pain throttles our every nerve, making sleep elusive. We become exceptional chameleons who can blend in without your even realizing we’re sick, and when we are too sick to function, we can choose to hide quite effectively. No quote over the years has ever spoken to me more than the one that says everyone is fighting a battle you know nothing about, so be kind. Be kind. Be gentle. Give others the grace you wish for yourself, and then actually give some of it to yourself.
Let me share something about those of us with chronic illnesses. Chronic, for those who are forgetful or unaware, means what we’re battling doesn’t go away. You might be tired of your friend or family member’s condition and just wish they’d “get over it” or “feel better,” but, as my mom would say, “dollars to donuts” they feel the same. The problem is that you can walk away from our pain, but we cannot. We have our upswings and our downturns, but just because we are having a good day doesn’t mean we found a magic cure. It doesn’t mean, after you see us that day, that we won’t be crying at 1:30 in the morning because the phantom pain throttles our every nerve, making sleep elusive. We become exceptional chameleons who can blend in without your even realizing we’re sick, and when we are too sick to function, we can choose to hide quite effectively. No quote over the years has ever spoken to me more than the one that says everyone is fighting a battle you know nothing about, so be kind. Be kind. Be gentle. Give others the grace you wish for yourself, and then actually give some of it to yourself.
True story. #AmericanLovinMom #Truth #JustSaying #TrueStory #Sjogrens #Lupus #AutoImmuneAwareness  #GetBehindMeSatan #AintNobodyGotTimeForThat
I don’t know what I’d do without pills and injections. I hope your weekend is going okay and I hope you have an easy week ahead. Just for fun, put the number of pills you take each day in the comments. I’m gong to have to stop and count mine and then I’ll comment too. Sending hugs and spoons! ✨💛💊🥄💊💛✨ _ #TeamPajamas #Spoonie #SpoonieLife #SpooniesUnite #MCTD #AutoimmuneDisease #MixedConnectiveTissueDisease #MCTDsupport #MCTDsucks #UCTD #Lupus #Sjogrens #RheumatoidArthritis #Scleroderma #Polymyositis #Fibromyalgia #MS #AnkylosingSpondylitis #ChronicIllness #ChronicFatigue #ChronicPain #PatientsNotAddicts #Opioids #OpioidHysteria •
Follow @mctd_support on Twitter & follow 'MCTD_Support - Spoonies Unite' on Facebook! 👍
I don’t know what I’d do without pills and injections. I hope your weekend is going okay and I hope you have an easy week ahead. Just for fun, put the number of pills you take each day in the comments. I’m gong to have to stop and count mine and then I’ll comment too. Sending hugs and spoons! ✨💛💊🥄💊💛✨ _ #TeamPajamas #Spoonie #SpoonieLife #SpooniesUnite #MCTD #AutoimmuneDisease #MixedConnectiveTissueDisease #MCTDsupport #MCTDsucks #UCTD #Lupus #Sjogrens #RheumatoidArthritis #Scleroderma #Polymyositis #Fibromyalgia #MS #AnkylosingSpondylitis #ChronicIllness #ChronicFatigue #ChronicPain #PatientsNotAddicts #Opioids #OpioidHysteria
Follow @mctd_support on Twitter & follow 'MCTD_Support - Spoonies Unite' on Facebook! 👍
🔸️🔹️Hoy🔸️🔹️ voy a conquistar ♡El cielo♡  Sin mirar lo alto
🔸️🔹️que queda del suelo🔸️🔹️ ☆bello y bendecido domimgo☆
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#sjogrens #sjögren 
#fibromialgia 
#fibrosis
#neumopatiainyersticial
#insuficienciarenalcronia
#chugstrauss
#vasculitis
#polineuropatias
#enfermedaddesmieralisante
#insuficienciasuprarenal
#nefropatiaporIgA
#cushing
#herniahiatal
#raynaud
#loscoladosmascolados
#jamasdejesdesonreir
#undiaalavez
#unpasoalavez
#guerreraautoinmune
#autoinmune
#yosoyfenix
Simple is the best way to stay on track for me. I find if I make myself eat simple, single ingredient foods and track everything, I am so much more likely to stay the course and not stray. #keto #simpleketo #ketoweightloss #weightloss #weightlossjourney #rollups #pickles #autoimmuneketo #sjogrenssyndrome #sjogrens #fibromyalgia
Simple is the best way to stay on track for me. I find if I make myself eat simple, single ingredient foods and track everything, I am so much more likely to stay the course and not stray. #keto #simpleketo #ketoweightloss #weightloss #weightlossjourney #rollups #pickles #autoimmuneketo #sjogrenssyndrome #sjogrens #fibromyalgia
Sjogren’s peeps, are stress balls/arm/wrist/ankle/hand/any weights helpful for the pain? I mean to strengthen joins and muscles in the long run? I find them to be more painful. 😭😩😬 #sjogrenssyndrome #sjogrens #sjogrensawareness #chronicillness #chronicpain #chronicillnessawareness #chronicpainawareness #autoimmune #autoimmunedisease #autoimmunedisorder #autoimmunediseases #autoimmunewellness
Sjogren’s peeps, are stress balls/arm/wrist/ankle/hand/any weights helpful for the pain? I mean to strengthen joins and muscles in the long run? I find them to be more painful. 😭😩😬 #sjogrenssyndrome #sjogrens #sjogrensawareness #chronicillness #chronicpain #chronicillnessawareness #chronicpainawareness #autoimmune #autoimmunedisease #autoimmunedisorder #autoimmunediseases #autoimmunewellness
For those of you who don't know my story, I started getting sick in 2016 and no one knew why. I saw doctor after doctor AFTER DOCTOR and became extremely discouraged. I was told things like you're skinny it's probably an eating disorder or it's probably just stress you should see a psychologist. For a long time I felt absolutely insane. I was so nauseous, always in pain, I was so dizzy and weak, kept losing feeling in my limbs, loss of vision...the list goes on. I had test after test AFTER TEST and they couldn't figure out what was wrong and I just felt lonely,  despondent,  depressed and I realized it was hard to find people who understood me. I had to cancel plans, I could barely get out of bed. Work became miserable. Years later, still largely undiagnosed but I have been told I have lupus, sjögrens, POTs, anemia. Hearing those things gave me a bit of hope, but what really helps me get through days is having people who get where I'm coming from and sharing how they keep going. I'm still building my own personal community but I hope to create a space for everyone else who also needs one. This is my story. What's yours?

#commonhealthapp #liveinspired #wellnessjourney #wellpreneur #mindbodysoul #mindbodygram #undiagnised #invisbleillness  #warriors #outsidethebox #chronicillness #symptoms #wellness #illness #sick #nausea #thoughts #mystory #share #sjogrens #autoimmunedisease #potssyndrome #lupus #resolution #pain #depression #coping #spoonie
For those of you who don't know my story, I started getting sick in 2016 and no one knew why. I saw doctor after doctor AFTER DOCTOR and became extremely discouraged. I was told things like you're skinny it's probably an eating disorder or it's probably just stress you should see a psychologist. For a long time I felt absolutely insane. I was so nauseous, always in pain, I was so dizzy and weak, kept losing feeling in my limbs, loss of vision...the list goes on. I had test after test AFTER TEST and they couldn't figure out what was wrong and I just felt lonely, despondent, depressed and I realized it was hard to find people who understood me. I had to cancel plans, I could barely get out of bed. Work became miserable. Years later, still largely undiagnosed but I have been told I have lupus, sjögrens, POTs, anemia. Hearing those things gave me a bit of hope, but what really helps me get through days is having people who get where I'm coming from and sharing how they keep going. I'm still building my own personal community but I hope to create a space for everyone else who also needs one. This is my story. What's yours?

#commonhealthapp #liveinspired #wellnessjourney #wellpreneur #mindbodysoul #mindbodygram #undiagnised #invisbleillness #warriors #outsidethebox #chronicillness #symptoms #wellness #illness #sick #nausea #thoughts #mystory #share #sjogrens #autoimmunedisease #potssyndrome #lupus #resolution #pain #depression #coping #spoonie
Let’s start of by saying why I started this account. I got diagnosed with sjogrens  a year an a half ago. Along the way came ibs and my anxiety hit through the roof. 
I’ve had a few surgeries as well. I Wanted  to share my journey and experiences. It’s helps to know you’re not alone. I’ll go more in detail as I start to share more with you guys. 
#autoimmune #chronicillness #autoimmunedisease #spoonie #invisibleillness #health #chronicpain #anxiety #tired #restless #pain #sjogrens #ibs #sick
Let’s start of by saying why I started this account. I got diagnosed with sjogrens a year an a half ago. Along the way came ibs and my anxiety hit through the roof.
I’ve had a few surgeries as well. I Wanted to share my journey and experiences. It’s helps to know you’re not alone. I’ll go more in detail as I start to share more with you guys.
#autoimmune #chronicillness #autoimmunedisease #spoonie #invisibleillness #health #chronicpain #anxiety #tired #restless #pain #sjogrens #ibs #sick
👦🏻: I’m not sure how many times I have to explain what a chronic illness is...Who else relates?

Follow us 👉 @how.u.feeling 👈 for more!
👦🏻: I’m not sure how many times I have to explain what a chronic illness is...Who else relates?

Follow us 👉 @how.u.feeling 👈 for more!
Isn't that the truth! Hi everyone! I started this page as a look into my own personal journery with being chronically ill but then I realized it could be so much bigger than just me. WE need a community. So that's the goal! Check out the link for more information. Sign up! Email to get involved!

#commonhealthapp #liveinspired #wellnessjourney #wellpreneur #mindbodysoul #mindbodygram #undiagnised #invisbleillness  #warriors #outsidethebox #chronicillness #symptoms #wellness #illness #sick #nausea #thoughts #mystory #share #sjogrens #autoimmunedisease #potssyndrome #lupus #resolution #pain #depression #coping #spoonie
Isn't that the truth! Hi everyone! I started this page as a look into my own personal journery with being chronically ill but then I realized it could be so much bigger than just me. WE need a community. So that's the goal! Check out the link for more information. Sign up! Email to get involved!

#commonhealthapp #liveinspired #wellnessjourney #wellpreneur #mindbodysoul #mindbodygram #undiagnised #invisbleillness #warriors #outsidethebox #chronicillness #symptoms #wellness #illness #sick #nausea #thoughts #mystory #share #sjogrens #autoimmunedisease #potssyndrome #lupus #resolution #pain #depression #coping #spoonie
When you love what you do, it shows. First work trip after being diagnosed with my Autoimmune disorders.  Had a little hiccup in the beginning but I made it thru like a champion.  #lovewhatyoudo #dowhatyoulove #lovemypotterybarn #potterybarnoutlet #pboutlet #hashimoto #sjogrens #autoimmunedisease #mylife #champion #autoimmunechampion #autoimmunestrong #visualinspiration #fall2019 #baybrooktexas #wsispirit #wsioutlet #wsispiritweek #anotheropening #theycallmestacey
When you love what you do, it shows. First work trip after being diagnosed with my Autoimmune disorders. Had a little hiccup in the beginning but I made it thru like a champion. #lovewhatyoudo #dowhatyoulove #lovemypotterybarn #potterybarnoutlet #pboutlet #hashimoto #sjogrens #autoimmunedisease #mylife #champion #autoimmunechampion #autoimmunestrong #visualinspiration #fall2019 #baybrooktexas #wsispirit #wsioutlet #wsispiritweek #anotheropening #theycallmestacey
Mood 😵 What do you guys do for an instant pick me up??
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#chronicpain #chronicpainwarrior #chronicillness #chronicillnesswarrior #autoimmunedisease #autoimmunewarrior #spoonie #arthritis #juvenilearthritis #rheumatoidarthritis #rawarrior #lupus #sjogrens #chrons #lymedisease #fibromyalgia #pots #pcos #eds #ibs #ulcerativecolitis #multiplesclerosis #invisibleillness #dysautonomia #endometriosis #endowarrior #dailymemes #motivation #weekendvibes
🌟 Enjoyed every minute of time with my parents and family last week in PA and Ohio. So thankful I felt fairly well most of the time as long as I rested a lot and paced myself every day. 
It has been such an internal struggle for me to share photos of myself over the past few years. With my autoimmune conditions, I have been on prednisone (steroids) for 3+ years. Despite eating extremely healthy, it changes your body composition and makes you gain weight, especially in the belly and face/chin. I’ve finally realized that I don’t want to look back on these years and regret not having memories of all these moments and experiences just because of the extra weight. Life is certainly way too short for that. 🌸
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#autoimmunedisease #autoimmunewarrior #sjogrens #sjogrenssyndrome #potssyndrome #relapsingpolychondritis #stiffpersonsyndrome #mastcellactivationdisorder #dysautonomia #familylife #familyvacation #liveyourbestlife
🌟 Enjoyed every minute of time with my parents and family last week in PA and Ohio. So thankful I felt fairly well most of the time as long as I rested a lot and paced myself every day.
It has been such an internal struggle for me to share photos of myself over the past few years. With my autoimmune conditions, I have been on prednisone (steroids) for 3+ years. Despite eating extremely healthy, it changes your body composition and makes you gain weight, especially in the belly and face/chin. I’ve finally realized that I don’t want to look back on these years and regret not having memories of all these moments and experiences just because of the extra weight. Life is certainly way too short for that. 🌸
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#autoimmunedisease #autoimmunewarrior #sjogrens #sjogrenssyndrome #potssyndrome #relapsingpolychondritis #stiffpersonsyndrome #mastcellactivationdisorder #dysautonomia #familylife #familyvacation #liveyourbestlife
Surprise dinner before I move to Charleston SC tomorrow to be closer to Scleroderma Center at MUSC, lovely plant as a house warming. #scleroderma #sclerodermawarrior #stage3ckd #autoimmune #autoimmunesucks #raynauds #sjogrens
Surprise dinner before I move to Charleston SC tomorrow to be closer to Scleroderma Center at MUSC, lovely plant as a house warming. #scleroderma #sclerodermawarrior #stage3ckd #autoimmune #autoimmunesucks #raynauds #sjogrens
🙌❤👉 @are_you_better_yet :""Wow this place must be crawling with germs!” said a man within clear earshot of me at a cardiologist appointment when I wore my mask last week. Another lady at a public rest area point blank intruded and said “Are you sick!?” Then when I gave her a stunned look she followed up with “It’s ok, my family is in healthcare” like that gave her permission to cross that boundary. 🤷🏻‍♀️ 🗣IT IS NONE OF THEIR BUSINESS why I choose to wear this mask! Do you really think they want my full life’s story? My pages of medical history? The 3-4 reasons I wear the mask, not including germs? 
You might be thinking, this girl shares her story every day with strangers on the internet...why wouldn’t she feel inclined to share it in public? It’s different. First of all, this is my coping mechanism. My way to connect with my hive, to chronicle my journey so I can look back on it, and it’s easier to hide behind a screen. And do it on MY terms. Not to satisfy someone’s curiosity. 
It’s not their place to ask about someone’s disability or illness in public. Especially not behind anyone’s back but loud enough for them to hear. End Rant. 📢

On a happier note... if you want to talk to me about my @awarecauses necklace and the reason I wear it, I’d be happy to talk to you about that! I’m much more approachable when you compliment my jewelry instead of ostracize me for my illness aids. 👌🏼"
🙌❤👉 @are_you_better_yet :""Wow this place must be crawling with germs!” said a man within clear earshot of me at a cardiologist appointment when I wore my mask last week. Another lady at a public rest area point blank intruded and said “Are you sick!?” Then when I gave her a stunned look she followed up with “It’s ok, my family is in healthcare” like that gave her permission to cross that boundary. 🤷🏻‍♀️ 🗣IT IS NONE OF THEIR BUSINESS why I choose to wear this mask! Do you really think they want my full life’s story? My pages of medical history? The 3-4 reasons I wear the mask, not including germs?
You might be thinking, this girl shares her story every day with strangers on the internet...why wouldn’t she feel inclined to share it in public? It’s different. First of all, this is my coping mechanism. My way to connect with my hive, to chronicle my journey so I can look back on it, and it’s easier to hide behind a screen. And do it on MY terms. Not to satisfy someone’s curiosity.
It’s not their place to ask about someone’s disability or illness in public. Especially not behind anyone’s back but loud enough for them to hear. End Rant. 📢

On a happier note... if you want to talk to me about my @awarecauses necklace and the reason I wear it, I’d be happy to talk to you about that! I’m much more approachable when you compliment my jewelry instead of ostracize me for my illness aids. 👌🏼"
Answers have finally come for my health.

#1 I am allergic to and was slowly being poisoned by a medication I was prescribed following a back injury in 2017. The seizure like spasms, constant infections, daily migraines, memory loss, inability to digest food, extreme fatigue, and severe neurological problems were my body reacting to this medication. Not one doctor I saw all this time thought of it. In desperation a month ago I called my pharmacy and they tipped me off that my symptoms were common adverse reactions to it. I am now off it, still detoxing but feeling like myself again for the first time in a very.long.time.

#2 At some point, my scleroderma flared up again, causing scarring in my left lung and all the muscles on the left side of my body. It has been a joint effort between an internist at the U of M and a physical therapist I see with experience in my disease to finally diagnose and begin treating this. The twisting, barbed wire sensations I was experiencing were from this - the scars very really spreading like barbed wire across my muscles.

#3 I had adenoids and they were chronically infected with staph the whole time. Adenoids are glands the body grows in childhood to help protect the immune system in early life, disappearing sometime around puberty. Because my scleroderma froze the growth in my face, my adenoids never left, and had a pretty severe staph infection when finally discovered. I had them removed this Spring, and have slowly recovered my singing voice as a result.

PT and a MUCH better medication regimen is finally working, giving me a functioning body to live in. I will have to deal with some effects for the long run, but it is finally achievable.
So many doctors told me this was all in my head, despite continual severe infections.
So many friends came through to help me. I wouldn't have made it without you all.
I don't know what life holds for me now. But I know I will be okay.
You bet there's some good music coming out of this and I can't wait to get working on it💗🙏🎶✨
Answers have finally come for my health.

#1 I am allergic to and was slowly being poisoned by a medication I was prescribed following a back injury in 2017. The seizure like spasms, constant infections, daily migraines, memory loss, inability to digest food, extreme fatigue, and severe neurological problems were my body reacting to this medication. Not one doctor I saw all this time thought of it. In desperation a month ago I called my pharmacy and they tipped me off that my symptoms were common adverse reactions to it. I am now off it, still detoxing but feeling like myself again for the first time in a very.long.time.

#2 At some point, my scleroderma flared up again, causing scarring in my left lung and all the muscles on the left side of my body. It has been a joint effort between an internist at the U of M and a physical therapist I see with experience in my disease to finally diagnose and begin treating this. The twisting, barbed wire sensations I was experiencing were from this - the scars very really spreading like barbed wire across my muscles.

#3 I had adenoids and they were chronically infected with staph the whole time. Adenoids are glands the body grows in childhood to help protect the immune system in early life, disappearing sometime around puberty. Because my scleroderma froze the growth in my face, my adenoids never left, and had a pretty severe staph infection when finally discovered. I had them removed this Spring, and have slowly recovered my singing voice as a result.

PT and a MUCH better medication regimen is finally working, giving me a functioning body to live in. I will have to deal with some effects for the long run, but it is finally achievable.
So many doctors told me this was all in my head, despite continual severe infections.
So many friends came through to help me. I wouldn't have made it without you all.
I don't know what life holds for me now. But I know I will be okay.
You bet there's some good music coming out of this and I can't wait to get working on it💗🙏🎶✨
Was able to get out and about with my love today... feeling thankful for days like these✨💜🥄🦋
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#lifeoverautoimmunediseases #autoimmunedisease #autoimmunediseasewarrior #lupus #kikuchifujimotodisease #sjogrens #fibromyalgia #sjogrenssyndrome #hashimotosdisease #ms #rheumatoidarthritis #chronicillness #crohns #invisibleillness #spoonie #survivor #support #faith #passion #awareness #fitness #health #inform #knowledge #life #live #strength #advocate #lupusawareness
Some exciting collaborations are in the works! DM me to join the waitlist. #yoga #yogadiversity #curvyyoga #chronicallyillyogi #chronicillness #sjogrens #fibromyalgia #neuropathy #plussizeyoga #spoonie #spoonielife #spooniesupport
Some exciting collaborations are in the works! DM me to join the waitlist. #yoga #yogadiversity #curvyyoga #chronicallyillyogi #chronicillness #sjogrens #fibromyalgia #neuropathy #plussizeyoga #spoonie #spoonielife #spooniesupport
My vegan peeps! Whole Foods Market has stepped up their Vegan Game. They now have dressings with NO OIL 😳 Soooo excited for my salad adventures this week with “Vegan Caesar”. @wholefoods #wholefoodsmarket #wholefoodplantbased #wholefoodplantbaseddiet #wholefoodplantbasedlifestyle #wfpb #nooil #healthyvegan #whatveganseat #lupus #lupusawareness #goodbyelupus #lupuswarrior #sjogrens #sjogrenswarrior #autoimmunedisease #healingthroughnutrition #foodisthymedicine #eathealthy #nutrition #veganofig #veganismo #veganiseasy #veganaf #veganlife #lovemywholefoods
My vegan peeps! Whole Foods Market has stepped up their Vegan Game. They now have dressings with NO OIL 😳 Soooo excited for my salad adventures this week with “Vegan Caesar”. @wholefoods #wholefoodsmarket #wholefoodplantbased #wholefoodplantbaseddiet #wholefoodplantbasedlifestyle #wfpb #nooil #healthyvegan #whatveganseat #lupus #lupusawareness #goodbyelupus #lupuswarrior #sjogrens #sjogrenswarrior #autoimmunedisease #healingthroughnutrition #foodisthymedicine #eathealthy #nutrition #veganofig #veganismo #veganiseasy #veganaf #veganlife #lovemywholefoods
Piper: Just before this video was taken I alerted my girl to an allergic reaction! There is a common misconception that us service pups live a life of all work and no play. I may work hard, but I play hard too! I’ve been enjoying days at the lake keeping my girl safe while we learn to kayak together, go boating, swim, play plenty of fetch, and work on our synchronized dock diving! What do you like to do during the summer? #servicepuppiper #opietheservicedog #vizsla #wirehairedvizsla #dogsofmichigan #dockdiving #summertime
Piper: Just before this video was taken I alerted my girl to an allergic reaction! There is a common misconception that us service pups live a life of all work and no play. I may work hard, but I play hard too! I’ve been enjoying days at the lake keeping my girl safe while we learn to kayak together, go boating, swim, play plenty of fetch, and work on our synchronized dock diving! What do you like to do during the summer? #servicepuppiper #opietheservicedog #vizsla #wirehairedvizsla #dogsofmichigan #dockdiving #summertime
The only things that make my back stop hurting are the heating pad and walking. Thankfully, I am blessed to live in the middle of a six mile walking trail with a water view. 🤗
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#uctd #connectivetissuedisorder #connectivetissuedisease #sjogrens #arthritis #spoonielife #warriorlife #nostoppingme
The only things that make my back stop hurting are the heating pad and walking. Thankfully, I am blessed to live in the middle of a six mile walking trail with a water view. 🤗
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#uctd #connectivetissuedisorder #connectivetissuedisease #sjogrens #arthritis #spoonielife #warriorlife #nostoppingme
We are excited to be educating & providing support on Molokai 💙💜 We would love to connect with everyone who is living with an autoimmune disease or interested in learning more about it. Rheumatologist, Kristine Uramoto will be there to help you better understand how to live healthy as well as answer your questions. We hope to meet all of you 😊 #lupus #lupusawareness #lupusflare #lupuswarrior #lupuslife #sjogrens #sjogrenssyndrome #sjogrensawareness #autoimmune #autoimmunedisease #health #healthy #wellness #healthandwellness #healthandwellbeing #education #support #takecareofyou #takecareofyourbody #takecareofyourself #alwaysbehealthyandhappy #sjogrensandlupusfoundationofhawaii
We are excited to be educating & providing support on Molokai 💙💜 We would love to connect with everyone who is living with an autoimmune disease or interested in learning more about it. Rheumatologist, Kristine Uramoto will be there to help you better understand how to live healthy as well as answer your questions. We hope to meet all of you 😊 #lupus #lupusawareness #lupusflare #lupuswarrior #lupuslife #sjogrens #sjogrenssyndrome #sjogrensawareness #autoimmune #autoimmunedisease #health #healthy #wellness #healthandwellness #healthandwellbeing #education #support #takecareofyou #takecareofyourbody #takecareofyourself #alwaysbehealthyandhappy #sjogrensandlupusfoundationofhawaii
Happy Monday Conquerors! 🌞
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I remember my mom always used to tell me when you worry you don't pray. When you pray you don't worry. I didn't quite understand what she meant then but now it makes complete sense! *
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When you pray, leave it with God, speak on the problem no more, and move on with life. It will all workout for your good even though it doesn't look like it right now. 💜 *
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#shiftthestigma #youhaveoptions #lupusconqueror #gratitude  #faith #belief #lupus #trol #kkatrice #stlucia #scleroderma #sjogrens #raynauds #stlucian #godislove #changeyourfocus
Happy Monday Conquerors! 🌞
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I remember my mom always used to tell me when you worry you don't pray. When you pray you don't worry. I didn't quite understand what she meant then but now it makes complete sense! *
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When you pray, leave it with God, speak on the problem no more, and move on with life. It will all workout for your good even though it doesn't look like it right now. 💜 *
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#shiftthestigma #youhaveoptions #lupusconqueror #gratitude #faith #belief #lupus #trol #kkatrice #stlucia #scleroderma #sjogrens #raynauds #stlucian #godislove #changeyourfocus
Heyy Conquerors! Happy Tuesday. I hope today has been beautiful to you, and if not I 🙏 it becomes so. 💜
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August has been pretty busy for me and there's no sight of it slowing down anytime soon! Thankful for my oil and my cream, as they have been soooo instrumental in helping me to be at my best. *
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Even with all that is going on I've learned from previous situations like this to pace myself and work at a speed that I can be most productive without causing a flare. This is key because it helps to keep fatigue in check.
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Conquerors, when you have a lot that needs to be done, what are somethings you do to maximize your productivity without causing a flare? *
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#shiftthestigma #youhaveoptions #lupusconqueror #sjogrens #productivityhacks #lupus #cbd #cbdtopicals #lifesaverplant #lupusflare #anxietyreliever #stlucia #trol #kkatrice #conquerors #hemp  #sclerodermawarrior #anxietytips
Heyy Conquerors! Happy Tuesday. I hope today has been beautiful to you, and if not I 🙏 it becomes so. 💜
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August has been pretty busy for me and there's no sight of it slowing down anytime soon! Thankful for my oil and my cream, as they have been soooo instrumental in helping me to be at my best. *
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Even with all that is going on I've learned from previous situations like this to pace myself and work at a speed that I can be most productive without causing a flare. This is key because it helps to keep fatigue in check.
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Conquerors, when you have a lot that needs to be done, what are somethings you do to maximize your productivity without causing a flare? *
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#shiftthestigma #youhaveoptions #lupusconqueror #sjogrens #productivityhacks #lupus #cbd #cbdtopicals #lifesaverplant #lupusflare #anxietyreliever #stlucia #trol #kkatrice #conquerors #hemp #sclerodermawarrior #anxietytips
Hey Conquerors! 💚 I hope you all had an amazingly beautiful day. *
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As I talk to more and more of you, sooo many have not tried quality hemp CBD oil, which honestly saddens me. 😞 CBD from the gas station is NOT quality and can cause more harm than good. *
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So from today until Saturday @ 11:59 I will be giving away a FREE sample of the quality hemp CBD oil I use.
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NO PURCHASE NECESSARY TO ENTER! *
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To be entered into this contest there are 2 steps. 1.Comment #freesample in the comments. 
2.Tag someone you think would benefit from the oil.
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Contest runs from today until Saturday @11:59pm EST. Good Luck! ☺
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#shiftthestigma #youhaveoptions #lupusconqueror #freecontest #entertowin #entrepreneurminds #hemp #cbd #conquers #networkmarketing #lupus #scleroderma #sjogrens #kkatrice #raynauds #cbdwellness #cbdoilbenefits #trol
Hey Conquerors! 💚 I hope you all had an amazingly beautiful day. *
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As I talk to more and more of you, sooo many have not tried quality hemp CBD oil, which honestly saddens me. 😞 CBD from the gas station is NOT quality and can cause more harm than good. *
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So from today until Saturday @ 11:59 I will be giving away a FREE sample of the quality hemp CBD oil I use.
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NO PURCHASE NECESSARY TO ENTER! *
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To be entered into this contest there are 2 steps. 1.Comment #freesample in the comments.
2.Tag someone you think would benefit from the oil.
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Contest runs from today until Saturday @11:59pm EST. Good Luck! ☺
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#shiftthestigma #youhaveoptions #lupusconqueror #freecontest #entertowin #entrepreneurminds #hemp #cbd #conquers #networkmarketing #lupus #scleroderma #sjogrens #kkatrice #raynauds #cbdwellness #cbdoilbenefits #trol
🤓Did you know that your body produces it’s own cannabinoids? It’s true! 
Just like the hemp plant 🌱produces cannabidiol (CBD), your body 🚶🏼‍♀️produces cannabinoids as well. They’re called Anandamide and 2-ag. They’re in human breastmilk, and they contribute to that milk-drunk bliss 😌 we observe in nursing babies. They are also responsible for what is often referred to as “runner’s high”. 🏃🏽‍♀️ But sometimes, our bodies just don’t make enough cannabinoids, and we need to supplement by taking CBD. 💧

When we have enough cannabinoids in our system, they activate receptors that are found on our cells throughout our bodies. This allows our cells to produce adequate amounts of signalling molecules which help maintain balance or homeostasis in our immune system and nervous system. These signalling molecules reduce swelling and calm our nervous system. 
CBD 🌱 is like the key 🔑 that unlocks 🔒 our bodies’ miraculous ability to heal itself! How cool is that?! 😎
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#shiftthestigma #youhaveoptions #lupusconqueror #cbd #hemp #homeostasis #trol #kkatrice #naturalhealtheducation #lupus #scleroderma #sjogrens #raynauds #educate #cbdoils #cbdhelps #cbdwellness #blackhealthmatters #blackwomenshealth
🤓Did you know that your body produces it’s own cannabinoids? It’s true!
Just like the hemp plant 🌱produces cannabidiol (CBD), your body 🚶🏼‍♀️produces cannabinoids as well. They’re called Anandamide and 2-ag. They’re in human breastmilk, and they contribute to that milk-drunk bliss 😌 we observe in nursing babies. They are also responsible for what is often referred to as “runner’s high”. 🏃🏽‍♀️ But sometimes, our bodies just don’t make enough cannabinoids, and we need to supplement by taking CBD. 💧

When we have enough cannabinoids in our system, they activate receptors that are found on our cells throughout our bodies. This allows our cells to produce adequate amounts of signalling molecules which help maintain balance or homeostasis in our immune system and nervous system. These signalling molecules reduce swelling and calm our nervous system.
CBD 🌱 is like the key 🔑 that unlocks 🔒 our bodies’ miraculous ability to heal itself! How cool is that?! 😎
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#shiftthestigma #youhaveoptions #lupusconqueror #cbd #hemp #homeostasis #trol #kkatrice #naturalhealtheducation #lupus #scleroderma #sjogrens #raynauds #educate #cbdoils #cbdhelps #cbdwellness #blackhealthmatters #blackwomenshealth
I AM are the most POWERFUL two words in any language. How many times have you heard this but still continue to put negative words after them? *
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I AM is a declaration of who you see yourself as not what family or friends see you as.  When you say things like I'm stupid, I'm fat, I'm dumb, ect. you are declaring those things to be. It sounds soooo cliche but it is so very true that what you call yourself is what you believe you are. *
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I declare that I AM healed. I AM healthy. I AM wealthy. I AM magical. I AM brilliant. I AM abundant. I AM the SHiFT! I AM all that God created me to be and I give my gift openly and freely to all I encounter. *
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What are you declaring about yourself and your life today? *
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#iam #shiftthestigma #gratitude #shiftyourmindset #selflovetips #youhaveoptions #scleroderma #lupusconqueror #declarations #fearfullyandwonderfullymade #iamaconqueror #lupus #sjogrens #raynauds #cbd #hemp #lupuswarrior #chronicillness #trol #kkatrice #chronicillnesswarrior #sclerodermawarrior
I AM are the most POWERFUL two words in any language. How many times have you heard this but still continue to put negative words after them? *
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I AM is a declaration of who you see yourself as not what family or friends see you as. When you say things like I'm stupid, I'm fat, I'm dumb, ect. you are declaring those things to be. It sounds soooo cliche but it is so very true that what you call yourself is what you believe you are. *
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I declare that I AM healed. I AM healthy. I AM wealthy. I AM magical. I AM brilliant. I AM abundant. I AM the SHiFT! I AM all that God created me to be and I give my gift openly and freely to all I encounter. *
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What are you declaring about yourself and your life today? *
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#iam #shiftthestigma #gratitude #shiftyourmindset #selflovetips #youhaveoptions #scleroderma #lupusconqueror #declarations #fearfullyandwonderfullymade #iamaconqueror #lupus #sjogrens #raynauds #cbd #hemp #lupuswarrior #chronicillness #trol #kkatrice #chronicillnesswarrior #sclerodermawarrior
How CBD, THC and other cannabinoids work together. 
How you can enter to win FREE product or cash.
How CBD, THC and other cannabinoids work together.
How you can enter to win FREE product or cash.
It's our mission here at CDMDA to INNOVATE by taking what was meant to break us and turn it around to help not only ourselves but those who were/ are on the brink of giving up. We are here to INSPIRE every person that stops by our page, whether you're chronically ill or not! It is our duty to INFORM the masses that yes chronically ill models are more than capable of slaying the runway! We are here to make a profound IMPACT on every person that stops by to view our page & content! We are CHRONICALLY DOPE!
#determination #inspiration #strength #power #progress #motivation #strong #invisibleillness #mylife #mystory #spoons #fighter #illness #warrior #chronicillness #medicine #arthritis #cannabis #autoimmunedisease #anxiety #icandoit #sjogrens #marijuana #dontgiveup #model #CDMDA #chronicallydope
It's our mission here at CDMDA to INNOVATE by taking what was meant to break us and turn it around to help not only ourselves but those who were/ are on the brink of giving up. We are here to INSPIRE every person that stops by our page, whether you're chronically ill or not! It is our duty to INFORM the masses that yes chronically ill models are more than capable of slaying the runway! We are here to make a profound IMPACT on every person that stops by to view our page & content! We are CHRONICALLY DOPE!
#determination #inspiration #strength #power #progress #motivation #strong #invisibleillness #mylife #mystory #spoons #fighter #illness #warrior #chronicillness #medicine #arthritis #cannabis #autoimmunedisease #anxiety #icandoit #sjogrens #marijuana #dontgiveup #model #CDMDA #chronicallydope
Smoking my Saturday away!! This #goldendelicious I got yesterday at #MUVPHX  is just that ... delicious! #AZMMJ #TheErrlCup #mymedicine #allherbal #allnatural #cleanmeds #grateful #Ckdstage3 #painmanagement #Plantsoverpills #spoonie #swishergirl #loyaltotheoil #MCTD #Lupus #Sjogrens #NeverGiveUp #DreamBig #workhard #Playhard #pakalolo #IYMD #errlcup #ErrlCamp #mytribe #includeCBD
My positives and negatives this first week of school. Starting with this double edged sword: I got so many welcome back hugs 🤗 that it bruised my port. But hugs are always worth it💗
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Positives:

Started school. My students are amazing
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My class schedule is perfect for my needs
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My coworkers have been so supportive with all my medical needy-ness .
No one made any rude comments when I used my walker/seat for the first time at school .
My kids (the ones I birthed) love their teachers and classmates
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My husband has spoiled me for my first week back and always takes care of me
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Negatives:

On day one, I had such severe back, hip and leg pain that by the evening I had to take ibuprofen, a second pain killer and third prescription pain med. In bed at 5pm .
On day two, in addition to the hip and leg pain, I had a pounding headache that wouldn’t go away with Ibuprofen so I had to take the prescription again
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I learned this week that insurance stopped covering my home visits for port access. So I owe $1600 because she comes every week and they stopped paying in June. And I have to find a new way to be accessed. Apparently it will involve going to the hospital every single week now
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I have spent every single minute of planning period and lunch breaks for the past two days on the phone with insurance, my doctor, my nurse, or the home health clinic
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.Draining
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I wish I were asleep right now since I have to wake up early but instead I’m waiting for more meds to kick in because my bladder spasms are excruciating and even a warm epsom salt bath didn’t help .
Peripheral neuropathy is spreading up my legs. I’m thinking it’s connected to the physical stress on my body
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Trying to remind myself of all the positives because, wow, there are a lot! But realistically I’m facing a whole lot of challenges too. And sometimes you just need to complain about how it’s not fair
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#spoonie #spoonielife #chronicillness #chronicillnesswarrior #dysautonomia
#autonomicneuropathy
#dysautonomiaawareness
#familialhypercholesterolemia
#sjogrens #invisibleillness
#invisibleillnessawareness #infusion  #autoimmunedisease
#hypophosphatasia #HPP
#HPPstrong #softbones #strensiq
#raredisea
My positives and negatives this first week of school. Starting with this double edged sword: I got so many welcome back hugs 🤗 that it bruised my port. But hugs are always worth it💗
.
Positives:

Started school. My students are amazing
.
My class schedule is perfect for my needs
.
My coworkers have been so supportive with all my medical needy-ness .
No one made any rude comments when I used my walker/seat for the first time at school .
My kids (the ones I birthed) love their teachers and classmates
.
My husband has spoiled me for my first week back and always takes care of me
.
Negatives:

On day one, I had such severe back, hip and leg pain that by the evening I had to take ibuprofen, a second pain killer and third prescription pain med. In bed at 5pm .
On day two, in addition to the hip and leg pain, I had a pounding headache that wouldn’t go away with Ibuprofen so I had to take the prescription again
.
I learned this week that insurance stopped covering my home visits for port access. So I owe $1600 because she comes every week and they stopped paying in June. And I have to find a new way to be accessed. Apparently it will involve going to the hospital every single week now
.
I have spent every single minute of planning period and lunch breaks for the past two days on the phone with insurance, my doctor, my nurse, or the home health clinic
.So
.Draining
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I wish I were asleep right now since I have to wake up early but instead I’m waiting for more meds to kick in because my bladder spasms are excruciating and even a warm epsom salt bath didn’t help .
Peripheral neuropathy is spreading up my legs. I’m thinking it’s connected to the physical stress on my body
.

Trying to remind myself of all the positives because, wow, there are a lot! But realistically I’m facing a whole lot of challenges too. And sometimes you just need to complain about how it’s not fair
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#spoonie #spoonielife #chronicillness #chronicillnesswarrior #dysautonomia
#autonomicneuropathy
#dysautonomiaawareness
#familialhypercholesterolemia
#sjogrens #invisibleillness
#invisibleillnessawareness #infusion #autoimmunedisease
#hypophosphatasia #HPP
#HPPstrong #softbones #strensiq
#raredisea
👦🏻: All I want is relief. It’s sometimes hard for others to understand the choices of the chronically ill. We didn’t choose this life and all we want is to feel better. I want to work full time, I want to be able to go out with friends without having to cancel all the time, and I want to be like a normal 28 year old. It’s hard to see your friends achieve success when you feel like your stuck in this constant battle everyday, but everyday I work towards getting better. Comment below if you relate. 
Follow 👉 @how.u.feeling 👈 for more!
👦🏻: All I want is relief. It’s sometimes hard for others to understand the choices of the chronically ill. We didn’t choose this life and all we want is to feel better. I want to work full time, I want to be able to go out with friends without having to cancel all the time, and I want to be like a normal 28 year old. It’s hard to see your friends achieve success when you feel like your stuck in this constant battle everyday, but everyday I work towards getting better. Comment below if you relate.
Follow 👉 @how.u.feeling 👈 for more!
👦🏻👩🏼: How’s your year going? 
Check out/follow our page 👉 @how.u.feeling 👈 for more content!
👦🏻👩🏼: How’s your year going?
Check out/follow our page 👉 @how.u.feeling 👈 for more content!
Your current state of health is the results of the thoughts and habits that you have had up until this point in your life. If you want different health, you need different habits.  Here is some coaching I did in my rapid recovery group about the habit of making excuses rather than taking action. Her excuse was that care-taking others was a getting in the way of her own self care. Here was my  coaching response to help her overcome this habit.  #goodbyelupus #goodbyeautoimmune #goodbyeautoimmunedisease #lupus #lupusawareness #lupusflare #lupuswarrior #lupusproblems #lupusnephritis #lupussucks #lupusfighter #lupusnephritis #lupusadvocate #autoimmunedisease #autoimmune #lupusnephritis #vegan #sjogrenssyndrome #sjogrens #scleroderma #multiplesclerosis #autoimmuneprotocol #autoimmunediet #mixedconnectivetissuedisease #lupusnephritis #lupusdiet #smoothieshred #thomastadlock
Your current state of health is the results of the thoughts and habits that you have had up until this point in your life. If you want different health, you need different habits. Here is some coaching I did in my rapid recovery group about the habit of making excuses rather than taking action. Her excuse was that care-taking others was a getting in the way of her own self care. Here was my coaching response to help her overcome this habit. #goodbyelupus #goodbyeautoimmune #goodbyeautoimmunedisease #lupus #lupusawareness #lupusflare #lupuswarrior #lupusproblems #lupusnephritis #lupussucks #lupusfighter #lupusnephritis #lupusadvocate #autoimmunedisease #autoimmune #lupusnephritis #vegan #sjogrenssyndrome #sjogrens #scleroderma #multiplesclerosis #autoimmuneprotocol #autoimmunediet #mixedconnectivetissuedisease #lupusnephritis #lupusdiet #smoothieshred #thomastadlock
Dollar Tree 🏃. then back to cleaning. Happy Saturday Conquerors!💪 What's on your agenda today? *
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Dollar Tree 🏃. then back to cleaning. Happy Saturday Conquerors!💪 What's on your agenda today? *
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Having a flare when you’re far from home is something else. More so when you can’t tell anyone because you don’t want them to worry 😔
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#chronicpain #chronicpainwarrior #chronicillness #chronicillnesswarrior #autoimmunedisease #autoimmunewarrior #spoonie #arthritis #juvenilearthritis #rheumatoidarthritis #rawarrior #lupus #sjogrens #chrons #lymedisease #fibromyalgia #pots #pcos #eds #ibs #ulcerativecolitis #multiplesclerosis #invisibleillness #dysautonomia #endometriosis #endowarrior #dailymemes #motivation #weekendvibes
Vlogging con Yessica. #chronicillness #chronicpain #pain #sjogrenssyndrome #sjogrens #sjogrensawareness #sjogrenslife #autoimmunedisease #autoimmunedisorder #humor #copingmechanism 🙄🤷🏽‍♀️🤦🏽‍♀️💁🏽‍♀️✌🏽🤘🏽
Vlogging con Yessica. #chronicillness #chronicpain #pain #sjogrenssyndrome #sjogrens #sjogrensawareness #sjogrenslife #autoimmunedisease #autoimmunedisorder #humor #copingmechanism 🙄🤷🏽‍♀️🤦🏽‍♀️💁🏽‍♀️✌🏽🤘🏽
First week #backtoschool had me making all the wrong food choices. I paid for it dearly in the form of a wicked stomach ache and fatigue. When I over do the sugar, my #sjogrenssyndrome tries to drag me down. I know better, but I have really bad stress #copingmechanisms 🤦🏼‍♀️ Back at it today full force and had this awesome #breakfastfordinner spinach and mushroom omelette with Swiss cheese and bacon. #bacon #keto #ketodiet #ketoweightloss #weightloss #weightlossjourney #weightlosstransformation #autoimmuneketo #sjogrens #fibromyalgia #teacher #preschoolteacher
First week #backtoschool had me making all the wrong food choices. I paid for it dearly in the form of a wicked stomach ache and fatigue. When I over do the sugar, my #sjogrenssyndrome tries to drag me down. I know better, but I have really bad stress #copingmechanisms 🤦🏼‍♀️ Back at it today full force and had this awesome #breakfastfordinner spinach and mushroom omelette with Swiss cheese and bacon. #bacon #keto #ketodiet #ketoweightloss #weightloss #weightlossjourney #weightlosstransformation #autoimmuneketo #sjogrens #fibromyalgia #teacher #preschoolteacher
I have decided to do away with most of my makeup for a little while. I have worn makeup since I was in probably the third or fourth grade. My Mom used to have to come to the school and have me wash my face. The last time she came there was no water involved in getting the makeup off. 😂 It kinda broke my habit for awhile. Sometimes I think women use makeup as a mask or a way to feel better about themselves but then become uncomfy going without makeup. Until I am comfy with bare minimum makeup then I will not totally be comfortable with me so until then I will just keep barin’n it! 😊 And no more coloring my hair for awhile either. I want to see what my natural color is. 
#barinit
#realmarshaann
#real
#flawsandall 😘
#48andfeelinggreat 😎 #nofilter #thefaceoflupus #comfy #comfyinmyskin #lupuswarrior #lupus #chronicpain #chronicillness #newme #newmarshaann #realhousewifewithLupus #realhousewifeofShelbyCounty #sjogrens #ulcerativecolitis #braidaddict
I have decided to do away with most of my makeup for a little while. I have worn makeup since I was in probably the third or fourth grade. My Mom used to have to come to the school and have me wash my face. The last time she came there was no water involved in getting the makeup off. 😂 It kinda broke my habit for awhile. Sometimes I think women use makeup as a mask or a way to feel better about themselves but then become uncomfy going without makeup. Until I am comfy with bare minimum makeup then I will not totally be comfortable with me so until then I will just keep barin’n it! 😊 And no more coloring my hair for awhile either. I want to see what my natural color is.
#barinit
#realmarshaann
#real
#flawsandall 😘
#48andfeelinggreat 😎 #nofilter #thefaceoflupus #comfy #comfyinmyskin #lupuswarrior #lupus #chronicpain #chronicillness #newme #newmarshaann #realhousewifewithLupus #realhousewifeofShelbyCounty #sjogrens #ulcerativecolitis #braidaddict
😂😂😂 But really, WHY???? Repost @msjenez 
Seriously! Who would do this voluntarily?! It's exhausting!
#glutenfreehumor #glutenfreelife #hashimotos #sjogrens
😂😂😂 But really, WHY???? Repost @msjenez
Seriously! Who would do this voluntarily?! It's exhausting!
#glutenfreehumor #glutenfreelife #hashimotos #sjogrens
PreK Meet the Teacher! #babiesgrowingup #momlife #livelaughlove #smile #sjogrens #rheumatoidarthritis #lupus #fibromyalgia #hidradenitissuppurativa #survivor
100% accurate! #chronicillness #chronicillnesswarrior #spoonie #spoonieproblems #invisibleillness #chronicpain #chronicfatigue #fibromyalgia #sjogrens #sjogrenssyndrome #autoimmunedisease #nope #crashandburn #momlife #boymom #momof4boys #disabled
[ #sjogrens #sjogrenssyndrome #sjogrensawareness #sjogrenswarrior #sjogrenslife #autoimmunedisease #autoimmune #spoonie #fibromyalgia #trigeminalneuralgia #health ]
My Sjögren’s brethren, and anyone who has weak hands, limbs, joints, muscles, etc.,- I recommend getting a water bottle with a small spout or a straw (straws sometimes leak if you put them in your bag, because they “pop” open). I noticed I was having more and more difficulty opening up my wide mouth bottle. Therefore, I got a bottle with a smaller spout. Plus, this color is too pretty. I had never seen a bottle that was a lilac shade, and I am shallow, so there’s that. 🤷🏽‍♀️💁🏽‍♀️ #california #valleygirl #818 #sjogrenssyndrome #sjogrens #sjogrensawareness #autoimmunedisease #autoimmunedisorder #chronicillness
My Sjögren’s brethren, and anyone who has weak hands, limbs, joints, muscles, etc.,- I recommend getting a water bottle with a small spout or a straw (straws sometimes leak if you put them in your bag, because they “pop” open). I noticed I was having more and more difficulty opening up my wide mouth bottle. Therefore, I got a bottle with a smaller spout. Plus, this color is too pretty. I had never seen a bottle that was a lilac shade, and I am shallow, so there’s that. 🤷🏽‍♀️💁🏽‍♀️ #california #valleygirl #818 #sjogrenssyndrome #sjogrens #sjogrensawareness #autoimmunedisease #autoimmunedisorder #chronicillness
It's Fri-Yay Conquerors! 💪 We made it through another week.🙌 *
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 In my business coaching group #rankmakers it's Celebration Friday and we celebrate our wins for the week. *
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Today I'm celebrating growth in my business, beating my cold 100% naturally and making it through the first week of school! Lol. 🎉 I'm going to get me a watermelon lemonade. ☺
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I'm learning to celebrate all wins no matter how big or small because all are needed to get you to your destination. *
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So let's 🍾 celebrate together! 🎉 Comment below what you're celebrating today?
It's Fri-Yay Conquerors! 💪 We made it through another week.🙌 *
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In my business coaching group #rankmakers it's Celebration Friday and we celebrate our wins for the week. *
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Today I'm celebrating growth in my business, beating my cold 100% naturally and making it through the first week of school! Lol. 🎉 I'm going to get me a watermelon lemonade. ☺
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I'm learning to celebrate all wins no matter how big or small because all are needed to get you to your destination. *
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So let's 🍾 celebrate together! 🎉 Comment below what you're celebrating today?
I’ve just registered to walk for Conquer Chiari’s Walk Across America. I learned of this organization a few years back through my friend Heather when her sweet daughter was diagnosed. It was the first time I’d ever heard of Chiari Malformation. 
As some of you know, I was also recently diagnosed with this debilitating condition. When my primary care physician called to review my brain MRI report with me, he had to literally Google Chiari while speaking to me over the phone. I had no idea how little doctors knew about this and because of this, am still in the process of cycling through Kaiser’s neurosurgeons to find one that’s actually knowledgeable about it. I meet the next one 8/28. 
I’m hoping to help spread awareness and help Conquer Chiari in their research and awareness efforts. Link to my donation page is in my bio if you’d like to help too. 💜💜 #chiari #chiarimalformation #zipperhead #spoonie #spoonielife #chronicillness #sjogrens #sjogrenssyndrome #awareness #chiariwarrior #chiariawareness #chiarimalformationawareness #chiarisucks #chiaristrong #chiarilife #conquerchiari #conquerchiariwalkacrossamerica #brainsurgery #fundraiser #fundraising #research #medicalresearch #findacure
I’ve just registered to walk for Conquer Chiari’s Walk Across America. I learned of this organization a few years back through my friend Heather when her sweet daughter was diagnosed. It was the first time I’d ever heard of Chiari Malformation.
As some of you know, I was also recently diagnosed with this debilitating condition. When my primary care physician called to review my brain MRI report with me, he had to literally Google Chiari while speaking to me over the phone. I had no idea how little doctors knew about this and because of this, am still in the process of cycling through Kaiser’s neurosurgeons to find one that’s actually knowledgeable about it. I meet the next one 8/28.
I’m hoping to help spread awareness and help Conquer Chiari in their research and awareness efforts. Link to my donation page is in my bio if you’d like to help too. 💜💜 #chiari #chiarimalformation #zipperhead #spoonie #spoonielife #chronicillness #sjogrens #sjogrenssyndrome #awareness #chiariwarrior #chiariawareness #chiarimalformationawareness #chiarisucks #chiaristrong #chiarilife #conquerchiari #conquerchiariwalkacrossamerica #brainsurgery #fundraiser #fundraising #research #medicalresearch #findacure
Farmor vid öppna spisen. #carlmalmsten #sjogrens #sjögrens #swedishdesign #swedishmodern #easychair #nordicdesign #vintage färgen är mellerad gröngul lin
Farmor vid öppna spisen. #carlmalmsten #sjogrens #sjögrens #swedishdesign #swedishmodern #easychair #nordicdesign #vintage färgen är mellerad gröngul lin
Hey, everyone! I just posted another video giving an update on my chronic illness journey. The link is in my bio if you’d like to check it out! 😊 #chronicillness #fibromyalgia #sjogrens #pots #dysautonomia #chronicpain #chronicfatigue #makeup #youtube #chronicillnessawareness #hydrojug
Hey, everyone! I just posted another video giving an update on my chronic illness journey. The link is in my bio if you’d like to check it out! 😊 #chronicillness #fibromyalgia #sjogrens #pots #dysautonomia #chronicpain #chronicfatigue #makeup #youtube #chronicillnessawareness #hydrojug
#dryeye has Been all over #peoplemagazine and #peoplehealth while I was on Vacay. Have you noticed more National Attention of this chronic condition affecting Millions of us?
#dryeye has Been all over #peoplemagazine and #peoplehealth while I was on Vacay. Have you noticed more National Attention of this chronic condition affecting Millions of us?
#concouringthecomplicationsofsjogrens
#autoimmunedisease 
#sjogrens 
#slowdown
#stressmessesyouup 
#Ana
#pcos
#fitfam
#fitmotivation
#yourloved
#smile
I had a pancake craving this morning. Really it was a maple syrup craving, but I needed something to dip in it 😆. These banana pancakes, made with cassava and coconut flour (and 100% AIP compliant), totally hit the spot. On a fun note, this maple syrup comes directly from the property of a firefighter my husband works with... it doesn’t get fresher or more delicious than that!
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#aippancakes #autoimmunedisease #chronicillness #autoimmuneprotocol #antiinflammatorydiet #healingfoods #foodismedicine #healthyfood #healthyeats  #rheumatoidarthritis #rheumatoidarthritiswarrior #sjogrenssyndrome #sjogrens #sjogrensawareness #healingautoimmune #spoonielife #spoonie #fightingautoimmunedisease #aiprecipes #aip #aipbreakfast
I had a pancake craving this morning. Really it was a maple syrup craving, but I needed something to dip in it 😆. These banana pancakes, made with cassava and coconut flour (and 100% AIP compliant), totally hit the spot. On a fun note, this maple syrup comes directly from the property of a firefighter my husband works with... it doesn’t get fresher or more delicious than that!





#aippancakes #autoimmunedisease #chronicillness #autoimmuneprotocol #antiinflammatorydiet #healingfoods #foodismedicine #healthyfood #healthyeats #rheumatoidarthritis #rheumatoidarthritiswarrior #sjogrenssyndrome #sjogrens #sjogrensawareness #healingautoimmune #spoonielife #spoonie #fightingautoimmunedisease #aiprecipes #aip #aipbreakfast
Si en los super mercados ya hay decoración de navidad pues nosotros ya estamos  listos para el aire frío de otoño - invierno jaja .
#lupuslife #sjogrens #autoinmune #love #mask #queremosvogmask
Si en los super mercados ya hay decoración de navidad pues nosotros ya estamos listos para el aire frío de otoño - invierno jaja .
#lupuslife #sjogrens #autoinmune #love #mask #queremosvogmask
My twin, my other half, my sister from another mister. @pass.the.salt.please thannks for not being some random creepy online stranger 😂❤️
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#bestfriends #ehlersdanlossyndrome #eds #posturalorthostatictachycardiasyndrome #pots #hyperpots #lupus #sjogrens #bechets #exhausted #meredithandchristina #youremyperson
My twin, my other half, my sister from another mister. @pass.the.salt.please thannks for not being some random creepy online stranger 😂❤️
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#bestfriends #ehlersdanlossyndrome #eds #posturalorthostatictachycardiasyndrome #pots #hyperpots #lupus #sjogrens #bechets #exhausted #meredithandchristina #youremyperson

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