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Undifferentiated Connective Tissue Disease

Autoimmune Diseases | Last Active: May 9, 2023 | Replies (75)

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@patyrod

I have UCTD. Luckily, I was quickly diagnosed and put on medication that has helped immensely. Yes, it would be nice to have a group for this condition. I also have FOSMN (facial onset sensory and motor neuronopathy) which is a deadly disease hard to diagnose and not included in these Mayo forums. Yet, people have gone to Mayo and have been diagnosed there with FOSMN. It's a headscratcher why they aren't recognized as conditions in this community.

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Replies to "I have UCTD. Luckily, I was quickly diagnosed and put on medication that has helped immensely...."

@patyrod if you would like to start a discussion on FOSMN, you can do so in the Neuropathy group. On the home page of the group there is a “start a discussion” place. I think it could be very interesting!
What is the treatment for FOSMN?

Hi, my wife has UCTD but we live in Ottawa where her reumatology doctor has not suggested any meds- what is the name of the medication you were treated with?
Thank you