Liste des hashtags les plus populaires par sujet #RHEUMATOIDARTHRITISAWARENESS

Just a little humor today lol #fibromyalgia #lupus #rheumatoidarthritis #psoriaticarthritis #sickeveryday #fibromyalgia #arthritisawareness #arthritis #chronicillness #autoimmunediseases #warriors #fibromyalgiawarrior #fibromyalgiaawareness #rheumatoidarthritis #psoriaticarthritisawareness #lupusawareness #rheumatoidarthritisawareness #chronicillnesswarrior #autoimmunestrong #connectivetissuedisease #connectivetissuedisorder

Never thought I would be able to do this. I was diagnosed with rheumatoid arthritis and was under the misconception that I would continue to get weaker. There are days where the pain is terrible. There are days when I can't even get out of bed. But I still believe you need to build your body and don't give up! You're stronger than you think you are. You can build your muscles to help support your body. This is only the beginning, but I feel like I have some semblance of power over my own body again. It's empowering and gives me hope . . . #rawarrior #buildyourbody #strongwomen #staystrong #fitnessmotivation #motivation #weekendmotivation #fitness #fit #fitlifestyle #lifestyle #mindbodysoul #bestrong #rheumatoidarthritiswarrior #rheumatoidarthritisawareness #rheumatoidarthritis #empowerment #motivationalmoments #fitspo #livelifetothefullest #fitforlife #healthyhabits #healthylifestyle #challengeyourself #weighttraining #strong #buildyourself #believeinyourself #inspiration #empowered #strong

. . . . .. . . . . . . . . . . . . #shoutout #invisibleillness #lupus #lupusawareness #lupuswarrior #lupusproblems #yougotthis #sjogrenssyndrome #sjogrens #raynaudsdisease #raynauds #sle #rheumatoidarthritis #rheumatoidarthritiswarrior #rheumatoidarthritisawareness #warrior #fighter #hughessyndrome #autoimmunedisease #autoimmunewarrior

#arthritisawarenessmonth What is the hardest part about having Rheumatoid Arthritis? That is a tough one. It attacks the body and threatens the mind. The pain and swelling in my joints is often unbearable. The rash and blisters are terribly uncomfortable. The fatigue can be overwhelming. My immune system is compromised so I’m sick all the time. I’m faced with a string of other autoimmune diseases. Sooooo many meds. I could go on. But you know what is really hard? Being strong all the time. I am tough for me but I’m even tougher for my family. I don’t ever want to be an inconvenience to my husband. I don’t want my kids to grow up with memories of their mom sick and in pain all the time. The last thing I want is sympathy from anyone. And so I’m strong. I suck it up. I put on a smile and I don’t show my pain. And sometimes that load gets really heavy and hard to carry. It is survival for me. It helps me cope with my disease, and it’s the right thing to do for my family, but sometimes it’s really, really hard. And I know I’m not alone. We each have our own load to bear. So remember whatever load you are carrying - you are not alone!! Being an athlete, and having goals, has given me a way to lighten my load. You don’t have to be an ultra runner or an Ironman or run any races. But I do believe that physical activity/exercise is the most under prescribed and yet most effective medicine there is. And this goes for both physical and mental health. So even when it’s bad and you feel awful, do what you CAN. I know I can’t say simply go for a walk because it’s not always so simple. But even if it’s just walking to the mailbox - do whatever you can. I promise it will help. And remember you’re not alone! We are all carrying a load!

. . Brace yourself for long post! . Do I look unwell in any of the picture? . None ! . This is why #ankylosingspondylitis is also called #invisibleillness ! Those who were around me while these pictures were taken might have noticed my struggle to keep myself together because of lack of sleep or intense pain in spine , knees, pelvic joints ,chest,ribs and #sciaticapain as well. If you didn’t notice , I might not have mentioned it then because it’s a daily thing for me besides I have been judged plenty of times when I have tried explaining it in the past so I gave up. . . I usually don’t write or share about my health issues because I am definitely not looking for sympathy, self pity or sorry feelings but past few days have been so stressful and exhausting that I am having emotional breakdowns at least twice a day ! . . Nobody in my circle is aware of this condition and I don’t know any support group that I can talk to about it. Most of you are as unaware about it as my friends and family and that doesn’t help either. I am sharing this to reach out to other human beings battling with this chronic illness on daily basis to tell them they are not alone ♥️ . . It took doctors good 9 years now that I am counting before they could diagnose my condition. . . In 2003 one evening I had tormenting pain in my leg which was not something I had experienced ever . Everyone at home panicked . My mother thought its a muscle pull or some strain so she tried massaging it but that aggravated it so much that I was unable to breathe and I kept crying. They took me to the hospital , I was given some painkillers and in a day or two it went away . Only to come back again after every few days and now I could tell that the pain was starting from my lower back and travelling all the way to my foot. Pain was excruciating and restricted me to bed. Breathing , coughing , sneezing , turning from one side to another .. everything seemed an uphill task when I had that pain in the leg. Doctors kept giving me painkillers and some vitamins but never told me what is it. I got my MRI done , xrays done.. nothing would come in that so nothing was diagnosed either. . Continued in comments..

Today I woke up & I can’t move my right shoulder or my left wrist. When I have flare ups, it honestly bums me out. I’m a very active person and, well, a perfectionist. I think when people think of arthritis, they think of joint pain, but what you don’t see is how ridiculously severe it can be. I wake up in the middle of the night screaming, my boyfriend has to give me shots once a week, and some days I just can't move at all. Living with rheumatoid arthritis has taught me to be patient and kind to myself. My body can't handle what it used to; I understand that, but it doesn't mean I have to lie down and give up. Products like @myriadcbd and other natural remedies like turmeric, hot showers, and visits to the chiropractor have seriously improved my life and I am grateful to have at least some bit of control back. As it’s Autoimmune Disease Awareness month, it is important to recognize that not every disease, mental or physical, is visible. If you suffer from anxiety, depression, chronic pain, etc, I highly recommend finding a CBD oil that can help! If you'd like to try @myriadcbd, use code JASMINE15 at checkout to save yourself some $$$. The website is in my bio! Thank you for your love & support! -Jaz . . . . . . . . . . #cbd #cbdoil #chronicpain #chronicpainwarrior #rheumatoidarthritis #rheumatoidarthritiswarrior #rheumatoidarthritisawareness #autoimmunedisease #autoimmunediet #autoimmunewarrior #autoimmunedisease #cbdheals #chronicpainawareness #anxietyrelief #depressionhelp #anxiety #naturalmedicine #naturalpainrelief #painrelief

Humor when it comes to my physical pain in the mornings. ‍♀️ #chronicillness #chronicpain #migraine #migrainerelief #rheumatoidarthritis #rheumatoidarthritiswarrior #rheumatoidarthritisawareness #supportsystemstrong #arthritisawareness #arthritisrelief

At the research level ... mycoplasma is something that interest me with the upmost fascination. Why? Aside from it having been one of my coinfections of Lyme disease... it’s also the most common cause of bovine mastitis in agriculture (one of the biggest challenges faced in dairy management and a condition which often does not respond to antibiotics). Mycoplasma, however... is also... get this... strongly correlated in the autoimmune manifestation known as rheumatoid arthritis...with over 90% of the RA population testing highly positive for it ! Mind blown yet . . How exactly does this all go down? The encapsulated version essentially is ... that mycoplasma overstimulates synovial tissues in the pursuit of invading and liquidating nutrients within those structures; nutrients which mycoplasma happens to necessitate for its survival. As would be expected , inflammation ensues and synovial tissues begin the process of structural degradation, drawing in the surrounding protein rich fluids into the joints and consequentially causing edema and severe swelling as a result. As would be expected , the longer this pathology continues ... the more damage and structural disfiguration one is forced to suffer with... and if you’ve ever personally known someone with RA... You’ll concur that the verb “to suffer” is hardly sufficient in conveying the degree of torment these individuals know as daily life. . . While I never suffered with RA, upon testing at the beginning of my Lyme journey, my RF (rheumatoid factor) coming back above range was perhaps one of the most shocking discoveries of my entire Lyme journey. It also served as the ultimate motivation to seriously address this pathogen and so I did ...Using a botanical approach. . . Some of my favorites were : Sida Acuta Red Root- unbelievable for any condition where clearing of dead cellular tissue is on overdrive. This made my stabbing spleen pain and spasms disappear in days ! Houttuynia- shown to produce comparable clearance results to conventional antibiotics in the treatment of bovine mastitis. Olive Oil, Isatis , Biden’s, Chinese Skulkcap, Kudzu, Celandine, and Cryptolepsis. . Out of space

I wish everyone just knew how I feel pretty much every day of my life so I didn’t have to keep explaining. Literally everything is a struggle, just finding the energy to sit up and ignore the fatigue, to then ignore my stomach pains/nausea/ vomiting and get out of bed, to then ignore the pains in my joints to clamber down 3 floors to start the day. Just leaving the house is a struggle for me but I’m so determined to function and come across as ‘normal’ that I just pretend all the time. Today I couldn’t manage it for all of the above reasons so instead of forcing myself up to go to work I am going to stay home and rest and I will not feel guilty or embarrassed. I am doing my absolute best each day. I just wish everyone knew because I hate feeling like I’m complaining all the time so 9 times out of 10 I’ll just say ‘yeah I’m alright’ while my body implodes from the inside . . . . #rest #crohnsdisease #crohns #crohnie #ibd #ibdawareness #spoonie #inflammatoryboweldisease #chronicillness #chronicpain #rheumatoidarthritis #rheumatoidarthritiswarrior #rheumatoidarthritisawareness #autoimmunedisease #youdontlooksick