Список из самых популярных хештегов по теме #AUTOIMMUNEDISEASEAWARENESS

#Repost @asecretspoonielife ・・・ While some people been standing in front of Wednesdays and salads some of us have been standing in front of dismissive doctors. Shoutout to everyone whose heard “it’s all in your head” from a doctor while desperately searching for a diagnosis. Keep trying, there are still good doctors out there, and you are not alone . . #livingwithchronicillnesses #chronicillness #chronicillnesswarrior #autoimmunediseaseawareness #chronicpain #chronicpainwarrior #spoonie #spoonielife #spoonieproblems #spooniesupport #spoonies #invisibleillness #butyoudontlooksick

So much this. @spoonie_village #chronicallyfatigued #autoimmunediseaseawareness #mentalhealthjourney #mentalhealthrecovery #mentalhealthisimportant #endthestigmaofmentalhealth

As many of my clients know, working with autoimmune disease is an area I’m very interested in. I know first hand how troubling it can feel to be diagnosed but I also know how much control you hold by altering how you nourish your body. ☯️ It’s one of the main reasons I decided to study gut health and healing. This is an area I’m going to post more on soon. Feel free at any time to drop me questions you may have or if you would like to know more about improving your gut health or managing an autoimmune condition. ☯️☎️07786-333-699

Something that I don't often talk about with my Ankylosing Spondylitis is the cognitive side effects it can have. Anyone living with a chronic illness most likely has some sort of cognitive side effects from their illness as well. "Brain fog" is just lightened term for something so heavy. Sometimes I have trouble finding my words, I have trouble speaking correctly, I mess up and jumble up my words, I have trouble with short term memory, I have trouble focusing on the task I am doing, I forget very easily, I may even have trouble focusing on what someone is saying to me and I may have to ask them to repeat themselves more than once, and the list goes on. I can deal with and accept the pain. I can deal with and accept the limited mobility. I can deal with and accept many of the side effects that Ankylosing Spondylitis causes. I can not, however, fully deal with or accept the cognitive problems it causes for me. I don't know why. Maybe it is because it is the one side effect that can not be somewhat countered with ANYTHING! Pain can be addressed with pain relievers or pain relieving methods; not that those help all that much. Rest helps too. Mobility issues can possibly be addresses with physical therapy and there is always a cane, walker, or wheelchair to aid in mobility. What do I do to address the cognitive issues? Sure, there are activities available to help keep your brain active and functioning healthily, but those seem to be for an already well functioning brain, to keep it that way; not for one that has been disrupted by an illness. I say this for awareness and understanding of this complex illness. Ankylosing Spondylitis does not solely affect our spines. It affects so much more than that! #Ankylosingspondylitis #ankylosingspondylitisawareness #ankylosingspondylitiswarrior #chronicillness #chronicillnessawareness #chronicillnesswarrior #chronicpain #chronicpainawareness #chronicpainwarrior #spoonie #spooniewarrior #brainfog #iamdoingthebestican #autoimmunediseaseawareness #autoimmunedisease #autoimmunedisorderawareness #autoimmunedisorderwarrior #autoimmunediseasewarrior #autoimmunedisorder

August 2017. The month my life got flipped on its head. The month I went from “normal 21-year-old” to “sick 21-year-old.” The month I was told I had a disease that would never go away. A month of confusion, and fear and newness. August 2017. Also the month I got the answers I was so desperate for. Also the month I was able to start taking steps forward. Also the month where the healing began. A month full of strength and courage and hope. This past Sunday was #WorldIBDDay and it brought me back to everything that has happened since August 2017. The flares, the pain, the hospital stay. The fear, the anxiety, the seemingly never ending blood draws and medications. But also the personal growth, the incredible leaps and bounds in my mental strength and grit, the friendships I’ve formed, the voice I’ve developed and the purpose IBD has given me in life. You see, I’ve found through this all is that life with IBD is all about the “also’s.” It‘s incredibly difficult, but I’m ALSO grateful for how I’ve grown. I feel weak some days, but I ALSO know I’m stronger than I could have ever imagined. I feel alone at times, but I ALSO know there are so many of you who know exactly what I’ve gone through. Forever looking for the “also’s,” the silver linings and the GOOD in it all. Never fake, never forced, but simply how I’ve learned to work with all I’ve been handed So, on that note, happy belated #worldibdday to my fellow fighters. I’m inspired by you daily and humbled to be able to share in your journeys

March is National Autoimmune Disease Month. Living with Chronic Lyme Disease and Sjögren’s Syndrome, most days feel just like this☝although most of the time, I’m posting otherwise. Even though I “look fine”, I’m suffering from a disease you cannot see. My body betrays me every day. I have no energy no matter what I do or what supplements I take, my joints throb constantly, my immune system is non-existent, people and events exhaust me, and some days I can hardly get out of bed without feeling like I haven’t slept in days. I am overwhelmed. I am foggy. I am hurting. But the most shocking part of this is that no one seems to talk about or know much about Autoimmune diseases at all. Shoot. My doctors don’t even know! Similar to mental illness, it can consume a person and make them feel so isolated, and most of the time, both diseases go hand in hand. So check on your “strongest friends” and never assume you know what they’re going through or what they’re feeling. Choose your words carefully and be aware of the fact that even though you cannot see anything wrong in front of you, it does not mean the symptoms don’t exist. So let’s do it. Let’s talk about it. Let’s bring these mystery diseases into the light and stand by those fighting every day. @thespooniesisterhood @thechrillness • • • #AutoimmuneDisease #ChronicIllness #ChronicIllnessWarrior #Spoonie #SpoonieSisters #LymeDisease #Sjögrens #SjögrensSyndrome #ChronicIllnessAwareness #AutoimmuneDiseaseAwareness #Warrior #Fighter #StrongWoman #SickOnTheDaily

REST is BEST... . . . This week I was off from the pharmacy for my son’s Spring Break. We wound up not going away for the week and I stayed home and all I really did was rest. I can’t tell you how much I feel relaxed and renewed. . . . My husband and I were talking about this last night. We are not Type A personalities, we are Type A +++. The words rest, relax, renew were not in our vocabulary for many years. . . . What I have learned is that rest really can be best. We have both come to listen to our bodies and when it is time to rest that’s what we do without feelings of guilt, laziness or shame. . . . I can’t tell you how instrumental this was to me after a recent unexpected Interstitial Cystitis flare several months ago. I rested, sent healing energy to my body and also sent thoughts of healing. My recovery time was shortened to about two weeks versus months or years. . . . So if you need to rest this weekend, then rest! Rest is an essential part of any wellness plan. This may include healing from chronic illness or just the need to renew your energy. . . . Do you allow time for rest in your healthy living journey?

Unfortunately, this is true. It is such a fine line. #Ankylosingspondylitis #ankylosingspondylitiswarrior #chronicillness #chronicillnesswarrior #chronicpain #chronicpainwarrior #spoonie #spooniewarrior #chronicillnessawareness #autoimmunediseaseawareness #autoimmunedisorderawareness #chronicillnessawareness #chronicpainawareness

“I really feel like people with disabilities are invisible to a lot of people. Because they’re uncomfortable, or don’t have the energy to dress up, don’t want to be seen.… - @selmablair - Vanity Fair . I can relate to this statement so much. There are many days that I’d rather lay in bed or wear pajamas everywhere. Is that frowned upon? . Not complaining just helping to bring awareness to an #invisabledisease that affects so many. Last year I got a handicap placard. It took me a long time to be ok with using it. The silent stares and judgements as I slide out the car, still able to walk but at a much slower pace. . Illnesses comes in all shapes and sizes. Next time you look over at someone in a handicap parking, stop, don’t judge. You have no idea what they are going through. . On another note, I’m on the hunt for a rockstar cane!! . #soapbox #multiplesclerosisfoundation #multiplesclerosisawareness #overcomingms #overcomingmultiplesclerosis #mswarrior #msfighter #autoimmunedisease #autoimmunediseaseawareness #selmablair #strongwomenrock #takingitslow #notafastwalker #handicapable #walkwithacane #unapologetic #godsgotme #looktotheson #lookupchild #thisisms #msstruggles