#mctd

MCTD Is a rare autoimmune condition that’s kind of like a mash-up of several others. Think lupus, scleroderma, and myositis —MCTD shows features of all three. That means symptoms can range from joint pain and fatigue to muscle weakness, rashes, or even Raynaud’s—where fingers turn white or blue in the cold. 🩺 If you need help managing your autoimmune disease, don’t hesitate to reach out to The Healing Rheum. 📞 (818)696-8767 📧 [email protected] 📍Glendale, CA The information provided should not be used for diagnosing or treating a health problem or disease, and those seeking personal medical advice should consult with a licensed physician. #integrativerheumatology #integrativerheumatologist #inflammation #mixedconnectivetissuedisease #mixedconnectivetissuedisorder

Sometimes your body sends quiet signals long before a diagnosis appears. Mixed Connective Tissue Disease (MCTD) is one of those complex autoimmune conditions that often hides behind everyday symptoms, making it easy to overlook. But the sooner we learn to recognize these patterns, the sooner we can take control of our health. MCTD is known as an “overlap disease,” combining features of several autoimmune disorders. It affects the body’s connective tissues — the framework that supports your skin, joints, muscles, and organs. Understanding it isn’t just about knowing the symptoms; it’s about tuning in to what your body is trying to communicate. Your body’s signals are never random — they’re messages asking for attention and care. Learn how to recognize and respond to them in my full video on YouTube! #MCTD #MixedConnectiveTissueDisease #AutoimmuneDisease #ChronicIllness #AutoimmuneSupport #HealthAwareness

I recently got diagnosed with an autoimmune disease called Mixed Connective Tissue Disease. I wasn’t sure if I should share this video. It’s not normally the content I post but I felt like maybe this could help someone dealing with the same thing or something similar. It also felt weird for me to keep posting as usual when I have been dealing with such a major life change. I am now feeling so much better and have been taking steps to keep this in remission and under control. Thank you if you listened and stayed till the end! 🤍🙏🏽 #mixedconnectivetissuedisease #mctd #autoimmunedisease #nycmodel

Hey, I’m @alexandrawildeson 👋 I’m chronically sick AF! I battle MCTD / lupus, PAN vasculitis, endometriosis, small fiber neuropathy and CRPS. So my life is basically a mix of doctor visits, naps, and making bad jokes about my joints. 😅 If you’re into chronic illness humor, keeping it real, and *occasional* chaos, come stay awhile! And if you simply cannot get enough… give my podcast, Calling in Sick, a follow. Glad to have you here — I can’t wait to get to know you ❤️ #callinginsickpod #callinginsick #chronicillnesscommunity #autoimmunewarrior #butyoudontlooksick #chronicillnessmemes #chronicillnesslife

A Doença Mista do Tecido Conjuntivo (DMTC) — também chamada de Mixed Connective Tissue Disease (MCTD) — é uma doença autoimune sistêmica caracterizada por apresentar manifestações clínicas de várias colagenoses, principalmente: • Lúpus eritematoso sistêmico (LES) • Esclerodermia sistêmica • Polimiosite/dermatopolimiosite • Artrite reumatoide (AR) E, sobretudo, pela presença de altos títulos de anticorpo anti RNP, que é seu marcador mais específico.

There were days I felt slightly better. There were days everything felt worse. I couldn't even lift my child. Even simple daily work became difficult. I became dependent on my husband, parents, in-laws… even my kids. After many tests doctors diagnosed Lupus + MCTD. This was my lowest phase. Part 4 coming next. #TransformationJourney #RealStoriesMatter #ComebackStory #HealingJourney #myhealthjourney

Even though I’ve been sick my entire life, each new diagnosis was a life-flipping moment. One day I was finally settled into navigating MCTD/lupus… and the next I was swiping my hospital membership card constantly because of vasculitis. I’ve always tried to find a why, but most of the time I’m left scratching my head. Chronic illness rarely has one cause… it’s a perfect sh!t storm. And you didn’t cause this. You can’t control it. You can’t just take one magic pill and feel better… that’s healthy-person magical thinking. Instead, you spend years piecing together your formula to feel better. Trying different meds and supplements, sitting through endless infusions, changing your diet, calming your nervous system, getting sunlight and movement, meeting enough doctors to field an entire football game… and realizing you can do all of that and still not get “back to where you were.” On that note, people love to say “you’ll get back to normal”… and it’s far too earth shattering to tell them that there isn’t a normal to go back to. There’s only this new version of you, this new reality you never asked for. And that you are both grieving your old normal life and focusing on building a new beautiful life that honors this new body. And look at you, you’re literally doing that right now!! By getting through IV drips that last longer than a long-haul flight, using mobility aids with your invisible illness bravely, laughing on FaceTimes while curled up with your heating pads and emotional support water bottles, recognizing that rest is mandatory and leaning into duvet days, taking hot girl walks even with your port showing. Because healing isn’t about going back, it’s about building forward, honoring the hard and being grateful for the good, feeling the grief and finding glimmers. So in case nobody has told you this recently… I’m really proud of you ❤️ #ChronicIllness #AutoimmuneDisease #SpoonieLife #InvisibleIllness #grief #glimmers

Living with chronic illness doesn't mean we have to stop enjoying life. Despite the daily challenges, pain, and limitations we face, we still crave the same joy, connection, and experiences as our healthy friends. When we manage to push through the pain and fatigue to attend a gathering, go for a walk, or participate in any activity, it’s not because we don’t feel the impact of our conditions. It’s because we’re choosing to embrace life in every way we can, even if it comes with painful consequences later. . Our presence in social settings is a testament to our resilience and determination to live fully despite the chronic health battles we fight. We strive to enjoy the moment, to laugh, to connect, and to experience the world around us, just like anyone else. When you see us out there, please remember that we're making a conscious effort to be part of the world and to savour these precious moments of normalcy. . So, join us in these moments of joy. Celebrate with us, laugh with us, and understand that behind our smiles may be layers of pain and struggle. Your support, empathy, and willingness to share in our happiness make a significant difference. Together, we can create memories that transcend the limitations of illness, showing that joy and connection are possible, no matter the circumstances. Tap ❤️ if you agree with this post. ➕️ Follow for more awareness & encouragement content. 😃 Help others by sharing this post. ✅️ Save this post for future reference. #chronicillness #autoimmunedisease #invisibleillness #chronicallyill #lupus #fibromyalgia #rheumatoidarthritis #stiffpersonsyndrome #chronicillnesshumor #mentalhealth #mixedconnectivetissuedisease #spoonie #mctd #antiphospholipidsyndrome #polymyositis #spoonielife #depression #raredisease #migraine #invisibledisability #dynamicdisability #disabled #lupuswarrior #fibrowarrior #chronicillnesswarrior #chronicpainwarrior #butyoudontlooksick #mystory #healthjourney #fightingwhilesmiling😁

Mixed Connective Tissue Disease (MCTD) - 📸 Source: @ coachyvette2 on TikTok All credit are reserved for their respective Owners - 💥Want credit or removal?👉 DM @ fixposts - - - - #livingwithlupus#lupuswarriors#lupuswalk#lupuschick#lupuscommunity#lupusawarness#walkforlupus#cruelmystery#lupusuk#lupusdiet#lupusfl#lupuswithstyle

Even after almost 15 years of knowing I have a mixed bag of autoimmune diseases, I didn’t realize March is Autoimmune Awareness month. I’ve seen so many people post pics of their struggles with autoimmune issues, and for years I’ve kept it very low key. When you “look” healthy, it’s hard to explain how you’re feeling on the inside. For example: these two pics (which are pretty mild, but didn’t want to scare you🤣) are moments that a flare up happened randomly during the day with no warning sign and one sent me to the ER… twice. But after years of trial and error, lots of tests, medications and holistic treatments, etc… I still don’t REALLY have an answer but I do have things that lower my risks of a flare up. This isn’t a pity post but a post to shed light on those of us who deal with these types of things on a day to day basis and don’t say anything. Those who are in similar situations and feel alone, or clueless on what to do… just know you aren’t alone and I’m here if you need to talk to someone. Prior to my fashion week gigs, I had a ton of flare ups and wanted to just call it off… I’m glad I didn’t, but I know the struggle that so many of us have. So, happy(?) auto immune awareness month? 🤣 be kind to those who have it, and just be kind to people in general… you never know the battles they’re dealing with inside. 🙏❤️

For those living with chronic illness, feeling as if life has only ever been half-lived… While other kids were just learning who they were, I was learning medical terms, test results, and how to live in a body that felt like it aged decades too soon. Growing up with chronic illness means grieving the life you imagined before you even had a chance to live it and I wouldn’t wish it on anyone 🫶🏻✨ . #tooyoung #heartbroken #youdontlooksick #invisibleillness #disability #disabilityadvocate #hiddendisability #rheumatoidarthritis #mctd

I started viewing my “sickness” as an initiation. I was diagnosed with Mixed Connective tissue disease about 10 years ago. MCTD is a combination of disorders like lupus, scleroderma and polymyositis. I’ve had symptoms such as massive hair loss, alopecia, raynauds, severe inflammation, acne, and thrombocytopenia (dangerously low platelets). From the very beginning, I have been an avid researcher. I read every article I could find on this issue, and when those failed me on finding a solution, I went to social media. I found every person talking about natural healing I could and ran with it. I stopped taking any pharmaceuticals I was on and rejected the many doctors suggestions to take certain meds (unless necessary for survival. I had many rounds of prednisone which led to a host of of other issues🙄). I’ve been through tremendous trial and error, many dark nights of the soul, and extreme pain and suffering. HOWEVER, I deepened my relationship with myself and the world so much. I’ve realized that healing can be a rollercoaster chile, but in that process I’ve learned that keeping it simple is what works the best. My priorities are: 🍓 Whole foods no matter what diet you choose, and better quality water💦 😄 Joy through Hobbies 🫂 Cultivating loving relationships focused on growth and grace 🏋🏽‍♀️ Mindful Movement - dance, walks, jump rope, strength training, yoga and stretching (If you fall off, just get back on) 🎙️🎶 Listening to high vibe music and wellness leaders through podcasts 🪷 Deepening my spiritual practice and essence 🧘🏽‍♀️ Trusting my intuition If you are someone who is experiencing autoimmune dis-ease, cancer, or any other ailment, it is incredibly important for you to make the decision to become more in tune with your lifestyle habits. Keep going, find what works best for you and grow your belief in yourself to feel better than ever‼️ You are so worth it💓✨ #autoimmune #autoimmunedisease #lupus #cancer #findyourjoy #findyourpeace #mixedconnectivetissuedisease #liveyourtruth #healingjourney #feeltoheal #raynauds #mentalwellness #dailyhabits #trustyourintuition #trustthejourney #healingisnotlinear