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Public Support Group 256 total results
Discussions (18)
Puritus with MCTD
Does anyone experience itching prior to a flare or at the beginning of a flare?
MCTD and Angular Cheilitis
I was recently diagnosed with MCTD. I frequently get angular cheilitis. It seems to happen when I don’t feel well. The rheumatologist doesn’t think it...
Possible MCTD and Vasculitis
I'm a 34 yr old female mother of two. I started experiencing a hive like rash in 2014. It took three years before one of...
Low WBC and MCTD
I have been following this group for some time just to listen and try to get some insight and some answers from others with autoimmune...
MCTD, Fibromyalgia, Reynauds
Hello, I'm new here. I was just diagnosed with MCTD, Fibromyalgia, and Reynauds. Just wanted to connect with others dealing with similar things. I have...
MCTD (Mixed Connective Tissue Disease)
Ok, here goes my story....4 Weeks ago I was diagnosed with Mixed Connective Tissue disease...I am normally a busy busy person, I work full time...
Carob Seed flour question related to MCTD
My daughter suffers from MCTD and I am looking at getting Organic unsweetened Almond milk for her but one of the products has Carob seed...
Severe brain fog with possible MCTD
I finally found a rheumatologist after 4 years of issues who ask the right questions and took the time to go through my test history....
If you suspect Lupus or MCTD, be sure
And see an ear nose and throat doctor. My ENT is the one that discovered my lupus. I was having trouble breathing while laying down....
MCTD, Fibromyalgia, and Hot Weather - Oh My!
Hello all,I am writing at the end of both summer and my wits! I have been diagnosed with MCTD, fibro, celiac, reynauds, neuropathy.... the list...
MCTD: Preparing for evaluation appointment at Mayo Clinic
Recently diagnosed with MCTD (Lupus & PA/OA, tested positive for RA, but no symptoms yet) Prescribed Plaquenil & just started Tremfya (1st injection was last...
Process for getting Mixed Connective Tissue Disease (MCTD) diagnosis
Hello, I just found this group online and I’m hoping there’s someone who can give me some encouragement. I have lived with chronic pain and...
Botox for chronic migraines: is it safe(ish) for MCTD person?
https://connect.mayoclinic.org/discussion/botox-for-chronic-migraines-is-it-safeish-for-mctd-person/
My wife has battled with autoimmune disease(s) for several years, and tried dozens of medications. She is facing Botox injections to counter her chronic migraines....
Does MCTD (mixed connective tissue disease) ever go into remission?
I was diagnosed a year ago with mctd. I am a very active busy person. But have lost muscle tone and strength. Which makes me...
MCTD flares and hip/thigh pain that is limiting mobility and activity.
Has anyone with MCTD experienced a flare up that has lasted for months? My hips and thighs get so tight I can barely walk, stairs...
Diagnosed with MCTD recently. RNP 1.5, Reynauds and swollen fingers.
Hi, I am new to this group and in general to support groups. This is my first. I am a 37 old female. All was...
How do you cope with Mixed Connective Tissue Disease (MCTD)?
Would someone else please join this discussion and let me know how you cope with Mixed Connective Tissue Disease? How can you explain it to...
Looking for the best lifestyle changes to reduce symptoms
https://connect.mayoclinic.org/discussion/looking-for-the-best-lifestyle-changes-to-reduce-symptoms/
Hi, everyone! My name is Secoyia and I am a 27 year old female. I was diagnosed 2 years ago with Fibromyalgia and MCTD after...
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