Has anyone experienced Multi-Connecti... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

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Has anyone experienced Multi-Connective Tissue Disease?

Lauren14 profile image
5 Replies

My sister has recently been diagnosed with this following a drs appointment with Raynauds. She has a whole load of other health issues that could be symptoms indicating how this disease will manifest itself (Lupus, Scleroderma etc). But I just hoped to find someone who may have had experience of this disease.

Any help/feedback would be great.

Thanks

Lauren

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Lauren14
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5 Replies
Dehlila profile image
Dehlila

My first symptoms were Raynaud's. The diagnosis was C.R.E.S.T later called Undifferentiated Connective Tissue Disease.

I also have overlap of Lupus. I am 65years old and was diagnosed in my late 30's

KathleenMary profile image
KathleenMary

I have had mixed connective tissue disorder for some years now and like your sister was originally diagnosed with RA.

I have traces of Lupus and also quite severe raynauds but the good news is that my rheumatologists have been great and I am now able to carry out the vast majority of tasks without a problem. i take hydroxychloroquin which seems to keep my symptoms at bay.

Do hope that the doctors find some treatment that works for your sister

146nanab profile image
146nanab

Hi, I have mixed connective tissue disorder, like your sister I have been diagnosed with raynauds(a severe one), scleroderma,lupus overlap and sjogrens syndrome, I take methotrexate for the others and a few more other meds for my raynauds. I wish your sister all the best with her treatment and hope she gets the best to help her through it.

Lady-Florence profile image
Lady-Florence

Like KathleenMary I have had mixed connective tissue disorder for some 30+ years now having been originally diagnosed with systemic sclerosis when I was aged 29. It is thought I started with this in my mid-teens, I was on prednisolone for a number of years but am now on hydroxychloroquin. In addition I now have fibromyalgia for which I take duloxetine. MCTD is an umbrella term but rheumatologists will monitor the condition carefully and I find I am able to live a fairly full life so long as I factor in some rest days.

I, too, hope that the doctors find some treatment that works for your sister

graygirl1 profile image
graygirl1

Hello There,

So sorry about your other symptoms. It is indeed a "Phenomenon" On an almost daily basis, there's something new manifesting itself, I know as I live with this everyday. It can be very frustrating but you will find some good advice here on this forum, Good luck!

graygirl1

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