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Experiences with
Mixed connective tissue disease (MCTD)
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Has anybody suffered a chest pain leading to Pnemonia?
Last year, I was diagnosed with
MCTD
by Rheuma and have had a symptoms of chestpains, difficulty in breating due to pain & tiredness. Prescribed of steroids to reduce inflammation in my lungs.
Last year, I was diagnosed with
MCTD
by Rheuma and have had a symptoms of chestpains, difficulty in breating due to pain & tiredness. Prescribed of steroids to reduce inflammation in my lungs.
anya_marie
in
Scleroderma & Raynaud's UK (SRUK)
12 years ago
MCTD - is it genetic?
I have recently been diagnosed with Mixed Connective Tissue Disease and I forgot to ask at the appointment whether it is genetic? Will I pass this on to my kids?
I have recently been diagnosed with Mixed Connective Tissue Disease and I forgot to ask at the appointment whether it is genetic? Will I pass this on to my kids?
Jennie_103
in
LUPUS UK
12 years ago
MCTD help please...
No one seems to know very much about
MCTD
and I have never met a fellow 'sufferer'. Is there anyone else out there like me? Is it right to feel like this all the time with no release? Surely I should have periods where things are fine like I did when I was first diagnosed?
No one seems to know very much about
MCTD
and I have never met a fellow 'sufferer'. Is there anyone else out there like me? Is it right to feel like this all the time with no release? Surely I should have periods where things are fine like I did when I was first diagnosed?
MCTDGus
in
LUPUS UK
12 years ago
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Does anybody else have Mixed Connective Tissue Disease with scleroderma?
Hi does any body else have
MCTD
with Scleroderma? I was recently diagnosed after being treated for RA for two years and would like to know more about it. I have read websites and booklets from R and S Ass but would be good to have some first hand, forgive the pun, information.
Hi does any body else have
MCTD
with Scleroderma? I was recently diagnosed after being treated for RA for two years and would like to know more about it. I have read websites and booklets from R and S Ass but would be good to have some first hand, forgive the pun, information.
AMDP
in
Scleroderma & Raynaud's UK (SRUK)
13 years ago
Anyone with hot, not cold, hands and feet?
I have only recently been diagnosed with
MCTD
and Scleroderma but my hands and feet are always hot and I mean really hot - so hot I have to soak them in cold water from time to time. I have never had Raynaud's, well one finger a couple of times so that hardly counts. Is this so usual?
I have only recently been diagnosed with
MCTD
and Scleroderma but my hands and feet are always hot and I mean really hot - so hot I have to soak them in cold water from time to time. I have never had Raynaud's, well one finger a couple of times so that hardly counts. Is this so usual?
AMDP
in
Scleroderma & Raynaud's UK (SRUK)
13 years ago
Good News and Bad News
I presume there might be a
MCTD
society as well so I might have to join that too. I’m devastated and I don’t really know where to turn now. Thank you all for your help and advice over the last couple of years. Good luck and best wishes to you all. Ax
I presume there might be a
MCTD
society as well so I might have to join that too. I’m devastated and I don’t really know where to turn now. Thank you all for your help and advice over the last couple of years. Good luck and best wishes to you all. Ax
AMDP
in
NRAS
13 years ago
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