If I had a connective tissue disease..would this show up on a blood test testing for all auto immune diseases?

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I can't be bothered going into all the symptoms because I've done it loads before..but the main ones are loose skin,arthirits looking bones..chest pain etc...

ANYWAY...IF I did have a connective tissue disease..would this show on a test for all auto immune diseases...I've already had a rheumatoid test that came back ok..

Thanks
Well the great thing about the rheumatoid test is that it is a great screening test for rheumatoid but also provides some false positives as well. Normally the test used to screen for lupus is the FANAS test but once again that only screens for lupus. As for symptoms of lupus, they tend to be fever, weight loss, malaise, and arthritis. Also people who have lupus tend to show a "butterfly" shaped rash. just schedule an appointment with your doctor and write down your symptoms before you go in so that you remember all of them.  (+ info)

What nsaids can i take if i have mixed connective tissue disorder with the lupus anticoagulant antibody?

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Absolutely talk to your doctor or pharmacist before taking any additional medications. Chances are you're already on prescription medication of some kind. Not all medications get along with one another. Complications could be severe. Please don't play with this and be your own doctor. Get advice.  (+ info)

what happens if mixed connective tissue disorder is left untreated?

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Systemic multi-organ failure similar to lupus, only even more severe and rapidly progressing.  (+ info)

what exercises are good for someone with connective tissue disease?

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are there specific exercises
try this one
http://www.youtube.com/watch?v=nbgsJXa9SRE  (+ info)

where is the best hospital to treat undifferential connective tissue disease in New york City?

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Mayo Clinic, maybe?  (+ info)

I have just been diagnosed with a connective tissue disease (lupus). Can I claim disability living allowance?

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I applied in July & was knocked back but since then I have had a diagnosis & my knees have got a lot worse with lupus arthritis & I can't walk without being in a lot of pain. I phoned the DWP to inform them of the new information but I was told they don't consider the illness, just the effect it has on my ability to walk. I told her I can't walk without being in pain but she basically said I still have the ability to walk so in their eyes things haven't changed since July. It's going to the decision maker again anyway but it does not sound promising at all.

Any advice on tackling these people would be much appreciated!
The criteria is that if u cannot walk (think its 25 yards) then u r eligible, but check this out. I would say u wld be entitled to it from what u have said. Have a word with yr gp, he/she will know and they will always help u and sign yr form. Good luck. The CAB will always help u too to fill in the appropriate forms. Dont be deterred from what the call centre tells u, go ahead. The form is pretty horrendous, its like a book!! But do go for it, u r entitled to it.  (+ info)

living with connective tissue disease,is it ok to wear an arm sling when the arm muscles are tired and painful?

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Here i s an excellent site with some wonderful options for you. It will definitely help you. Have a look. http://webmd1.notlong.com/AAoZ0wQ  (+ info)

I have been diagnosed with Undifferiented Connective Tissue Disease?

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I really don't understand what's going on. I had a low positive for Lupus, Vit D & calcium def. I can't understand the triggers of flares. This time was emotional upset for no reason at all, and the next day I can't hardly walk. I have worry that's irrational. I don't get it. I also have sun sensitivity, dry skin, swelling, mouth sores, etc. I'm not sleeping well at night. What's going on???
Try & stay away from caffeinated products like Soda pop, it breaks down & prevents absorption of Calcium & Vitamin D. Also, aspartame in diet drinks can cause liver toxicity in alot of auto-immune diseases. I have auto-immune problems too & I really advocate taking at least 15,000 IU of Vitamin D a day & 1200 mg of Calcium Citrate daily. It should really help cut down on your symptoms.Also, check the webm.d. website on Lupus, they have an interesting article on the use of low dose DHEA (available at health food stores) helping cut down on flares in patients.

As far as the trigger of your flares, if you are staying out of the sun then I would say it would be from your diet or medications. Are you taking any antibiotics or on the pill? Also, I have read to stay away from dairy products, tobacco, red meat, caffeine, salt, & sugary products. Tomatoes, peppers,& white potatoes contain a substance called solanine, which can contribute to pain & inflammation. Eggs, garlic, & onions are really good for you to eat, as they contain sulfur which is needed for the repair & rebuilding of bone, cartilage, & connective tissue.Fresh pineapple( not canned )is highly recommended because it contains Bromelain, an enzyme that is excellent in reducing inflammation.

Environmentally, they say that for some reason fluroscent & halogen lighting at home or work, can aggravate Lupus symptoms. Lack of sleep can also make symptoms worse too. Call your Dr. & see if they can give you a short term sleeping pill prescription, to use during your flares when the pain is the worst. Frustrating that the pain causes the insomnia & then the insomnia causes the symptoms to worsen!

I hope this helps! I know how frustrating auto-immune illnesses are & I feel like alot of physicians diagnose you & that's it.....they leave you hanging! In my case, I have spent the last couple of years researching all I can, otherwise, you go crazy with pain wondering what you did to cause your symptoms to come back. Hopefully, some things on this list will ring a bell with you & you can make some adjustments in your life. Hang in there! Good luck!!  (+ info)

Apart from rheumatoid arthritis, what are the auto immune connective tissue disease, and are they common?

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also - if you hv time, I asked this question earlier, if you want to have a crack at any of these:)

If anyone knows the below answers, it would be much appreciated!
(ps- i study RA a bit, so dont really need overview/web site referral, just these spec questions thankyou)
1) What are the biological agents used to treat RA(Rheumatoid Arthritis)?
2) RA causes anaemia of chronic disease - what does this blood picture look like?
3) Late surgery for RA may mean joint replacement/etc - what is the early options for surgery in RA?
4) Whats the role in splinting for RA?
Scleroderma is the only other one I know and it is very uncommon and occurs mostly in women.

Sorry I can't help you all that well :S

Best of luck!  (+ info)

Have you ever heard of connective tissue disease and if so what do you know about it?

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Well, I have Sjogrens Syndrome and it is called a connective tissue disease....so is lupus...rhuematoid arthritis...and other autoimmune diseases as well. Hope this points you in the right direction.  (+ info)

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