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102 total results
Comments (91)
I’ve taken both AZA and LDN (but never together), for UCTD. The AZA caused my liver...
https://connect.mayoclinic.org/comment/905181/
and LDN (but never together), for UCTD
@creatiff357 ah yes, somehow relating UCTD to lupus… this can be a useful technique for explaining...
https://connect.mayoclinic.org/comment/1438973/
creatiff357 ah yes, somehow relating UCTD ... And instead of UCTD, at almost 5 years ... might add- thrown me out of my beloved UCTD
I have been diagnosed with UCTD. I like Plaquinil and it has helped in a few...
https://connect.mayoclinic.org/comment/1298104/
I have been diagnosed with UCTD.
I have UCTD. I have completely changed my diet and found it has helped a lot....
https://connect.mayoclinic.org/comment/1178652/
I have UCTD.
I have bilateral trigeminal neuropathy from the midline of my scalp down to my chin, involving...
https://connect.mayoclinic.org/comment/610866/
rheumatologist have diagnosed me with UCTD
Hello, I have UCTD recently diagnosed to add to my list of AI diseases.. I have...
https://connect.mayoclinic.org/comment/210377/
Hello, I have UCTD recently diagnosed
I am sorry people have to be so stuck with this! I feel stuck, too, and...
https://connect.mayoclinic.org/comment/633049/
pernicious anemia, celiac disease, and UCTD
I have UCTD and a couple others. My dentist comments on the precarious state of my...
https://connect.mayoclinic.org/comment/629349/
I have UCTD and a couple others.
Thank you for the words of wisdom, Christine. I have friends that were 'in the loop'...
https://connect.mayoclinic.org/comment/1025874/
never heard of" and told them UCTD
I use generic dry mouth gel from CVS, Cyclosporine eye drops (Restasis), sips of water all...
https://connect.mayoclinic.org/comment/750898/
I have UCTD and a few AI problems.
Hello Marj @mtrapp987, Welcome to Connect. Thank you for sharing your experience with what helps you...
https://connect.mayoclinic.org/comment/308771/
experience with what helps you for UCTD
Yep I have this to just got diagnosed and have no clue just as I went...
https://connect.mayoclinic.org/comment/210369/
of what I have I come out with this uctd
Welcome, @regeanna. Thank you for re-initiating this discussion. Let me introduce you to a few active...
https://connect.mayoclinic.org/comment/56449/
undifferentiated connective tissue disease (UCTD
I have a Link Loop Recorder. After 6 months it showed paroxysmal AFib. I now wonder...
https://connect.mayoclinic.org/comment/634699/
hydroxychloroquine which I take for UCTD
Hi woody319, I have been on HCQ for UCTD since 2018. Raynaud’s has been a continuing...
https://connect.mayoclinic.org/comment/1062255/
woody319,
I have been on HCQ for UCTD
I’ve diagnosed w/UCTD and have been taking hydrochloriquine for 3 months with no improvement. I started...
https://connect.mayoclinic.org/comment/613699/
I’ve diagnosed w/UCTD and have been
Hi there, I was diagnosed with UCTD about 4 months ago. The hydroxychloroquine and methotrexate really...
https://connect.mayoclinic.org/comment/308769/
Hi there,
I was diagnosed with UCTD
@marymaryoregon There are other discussions within this Autoimmune group. I don’t know about groups on Facebook,...
https://connect.mayoclinic.org/comment/842242/
/connect.mayoclinic.org/discussion/uctd
@bayhorse - I wrote a long reply while I was riding in the car this weekend,...
https://connect.mayoclinic.org/comment/845390/
setting up some kind of website for UCTD
I’ve been in my battle with what initiated as Undifferentiated Connective Tissue Disease & Hashimoto’s in...
https://connect.mayoclinic.org/comment/1391307/
My UCTD was officially diagnosed as
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