350 total results
Comments (313)
Just an idea - I have post exercise malaise and tremendous amounts of painful inflammation from...
https://connect.mayoclinic.org/comment/1409602/
Welcome, @regeanna. Thank you for re-initiating this discussion. Let me introduce you to a few active...
https://connect.mayoclinic.org/comment/56449/
My daughter has been diagnosed with Mctd and ILD. She also has Reynolds and is now...
https://connect.mayoclinic.org/comment/795584/
I was diagnosed with MCTD in Feb 2021. It started with me feeling like my hands...
https://connect.mayoclinic.org/comment/701070/
I've tested negative once for RA even though my grandmother had it. I think I probably...
https://connect.mayoclinic.org/comment/1263480/
Hi all! Thanks for all the great info shared here! While awaiting diagnosis on what I...
https://connect.mayoclinic.org/comment/1494791/
It started many years ago with an enlarged parotid gland. Then aching in my hands and...
https://connect.mayoclinic.org/comment/658074/
I have had fibromyaglia and questionable Lupus or MCTD. The summers are brutal with the high...
https://connect.mayoclinic.org/comment/931765/
Hi @charlottet, I don't have any experience with Mixed Connective Tissue Disease but there are quite...
https://connect.mayoclinic.org/comment/1133508/
I was only able to find a Scleraderma group when I started with this and learned...
https://connect.mayoclinic.org/comment/840543/
I presented with Raynauds (Hands and feet), swollen hands/feet, general malaise in addition to being very...
https://connect.mayoclinic.org/comment/963744/
@loross You are right- most doctors don’t understand brain fog. The last few years I have...
https://connect.mayoclinic.org/comment/807302/
@elisabeth007 Thanks for your continued support. I believe you are correct about the "red tape" and...
https://connect.mayoclinic.org/comment/1092573/
I had a positive ANA, and followup ENA showed Mixed Connective Tissue Disease which contains Lupus...
https://connect.mayoclinic.org/comment/959244/
@dkelban Good afternoon and welcome to Mayo Clinic Connect! We’re glad you found us. I, too,...
https://connect.mayoclinic.org/comment/1125028/
When I was first diagnosed with MCTD the Raynaud’s was severe in my hands, feet and...
https://connect.mayoclinic.org/comment/715269/
Just because you have MCTD doesn’t mean you can’t get sick, actually you are more likely...
https://connect.mayoclinic.org/comment/1229614/
@reagan1mc It must have been really frightening to find yourself paralyzed. How fortunate that you have...
https://connect.mayoclinic.org/comment/170422/
Hello @krcc I’m so sorry that you’re still having a difficult time. Are you seeing specialists...
https://connect.mayoclinic.org/comment/737117/
I have mctd my Rhumatologist put me on Simponi Aria It seems to be working most...
https://connect.mayoclinic.org/comment/56496/
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