Is this the right site for MCTD? Does... - Scleroderma & Ray...

Scleroderma & Raynaud's UK (SRUK)

11,297 members5,733 posts

Is this the right site for MCTD? Does anybody else suffer from tenderness in their jaw?

vletchworth profile image
5 Replies

I have Mixed connective tissue disease. Symptoms hard patches on fingers, arthritic joints, fatique.

Written by
vletchworth profile image
vletchworth
To view profiles and participate in discussions please or .
5 Replies
Lady-Florence profile image
Lady-Florence

I, too, have a diagnosis of MCTD, plus Fibromyalgia. So many of the conditions have aspects in common so this site can be right for you, both to read and to support others. Just beware of thinking you may get every side effect that others have! Good luck and good health! Are you recently diagnosed? I had a whole range of possible diagnoses before they said MCTD as a term to cover a multitude of things, some more severe than others. I have had an autoimmune condition since my mid-teens, it is thought, and had dreadful chilblains and 'dead' fingers long before that. Now in my early 60's I can testify that life can be fulfilling in spite of it all ...

vletchworth profile image
vletchworth in reply toLady-Florence

Thank you for your reply. I am in my early 60s too. I was diagnosed about four years ago when they were searching why I was so tired and could barely stand. After a period of being stable on drugs have now started all sorts of 'odd' symptoms. - am ignoring them until they force their attention on me! - It's easy to think that common ailments are something more. Tiredness and arthritic joints are main issues as I am a carer for my husband (dialysis patient)and work.

Shadows-walker profile image
Shadows-walker

Hi to have tenderness in my jaw ,I have been told I have raynaulds sjorgrens ,fibro and chronic fatique , I might add it's just the right side of my face waiting on a lip biopsy and eye specialt at moment also told I have connective tissue but hasn't used the word mixed I don't think .also found lupus antibiodys but says I don't have lupus ? I have decided to stop worrying at moment as there is nothing I can do just trust the doctors look after me, the more stressed I get the worse I feel .I have stopped chatting to some of my friends as they look at me ,and I feel they don't think there is anything wrong with me and that does Wined me hope you feel better Chris

Helen58 profile image
Helen58

Hi. Yes to all of the above, my jaw was very sore carrying into my ears and cheekbones. I was told that this was linked to Sjorgens along with my Scleroderma. I am n meds which have reduced the pain unless it is very cold or I talk too much ;)

Helen

vletchworth profile image
vletchworth in reply toHelen58

Thank you for replying. My jaw bone on the right hand side seems to slip in and out of alignment and I end up talking very strangely! There are so many odd symptoms that appear that you can end up getting very neurotic!

Not what you're looking for?

You may also like...

DOES ANYBODY ELSE SUFFER FROM RAYNAUD'S LIKE I DO?

Not only do I suffer in my hands and feet but my entire body suffers...externally and internally....
LisaB356 profile image

Does anyone else suffer from arthritis?

I've been diagnosed with raynards for around 2-3 years. I've been having extra problems with my...
LiseHickin profile image

Does Anybody else have to take Folic Acid with their Scleroderma

I have Scleroderma for 10 Yrs now. I am just wondering how many others have to take Folic Acid...
horseman694 profile image

Does anyone else get really bad pains in their legs?

Does anyone get really bad pains in their legs anytime or the day but mostly at night, in the...

How many people in this forum suffer from Restless Legs Syndrome?

I saw a few posts about RLS, and Parkinsons's meds, so I know some of you do. Just wodering how...
nightdancer profile image

Moderation team

See all
JillWillSRUK profile image
JillWillSRUKAdministrator
AnnabelSRUK profile image
AnnabelSRUKAdministrator
Chicunique27 profile image
Chicunique27Administrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.