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We found 29 questions associated with the 'Systemic' topic.
Posted 27 Aug 2017 by • 0 answers
What else can I take. I'm also on ketetofin for too much histamine but can't get any as stock problems. What other H1 can I take
Posted 14 Aug 2017 by • 0 answers
I am looking for a support group for people who have Indolent Systemic Mastocytosis. Any suggestions? I have found other support groups for Mastocytosis but it's too broad to be helpful.
Posted 28 Mar 2017 by • 0 answers
I have been diagnosed with a very strong on my lab work with anti ss-a or RO and anti ss-b or LA. I was wondering if it could be changed at one point down the road with a negative? I have a very bad case of lupus for years and am on meds for that as well as other problems so I was just curious if ...
Posted 11 Mar 2017 by • 0 answers
Systemic Lupus Erythematosus - Hi! I've recently been diagnosed with Osteoarthritis & Lupus. It took
Posted 11 Jul 2016 by • 2 answers
... my doc forever to figure out what is wrong with me. It's going to be another 2 months before I can get in to see a specialist. Rapid weight gain, hair loss, terrible swelling in feet-legs-limp nodes. I hurt all over my body. How do you deal with this?
Posted 13 Jul 2016 by • 0 answers
... still have an un opened bottle 2000 Units 250 mg which says expires 02/15. And, is that date too old to open and take?
Posted 1 May 2016 by • 1 answer
Posted 19 May 2016 by • 0 answers
So I have systemic lupus which causes severe tiredness to begin with . What can I do to help with the fatigue? I'm almost scared to even take this medicine!
Posted 23 Apr 2016 by • 0 answers
Drug which work localy not systemic that save for pregnant and lactation women
Posted 9 Feb 2016 by • 0 answers
I'm really wary of steroids. I had to take prednisone many times when I was a kid and it produced awful side effects. I'm dealing with allergies, chronic sinus disease, heavy mucus and coughing. The Doc prescribed this for me a day ago. I trust him I just wondered if I'll get those ...
Posted 6 Nov 2015 by • 2 answers
... My joints are so stiff and they pop in the mornings. I love sweets, I wonder if sugar could make it worse? Thanks
Posted 23 Jan 2016 by • 1 answer
During my research today i found two new drugs specific to SS. Actemra and Fresolimumab. They both appear to be in a clinical trial stage but apparently are available. Does anybody on this site have knowledge of these?
Posted 26 Jan 2016 by • 0 answers
we received an article discussing natrexone on ms; the link contained a bullet describing it as effective against systemic sclerosis. i found one technical article testing it for prunitus but it does not appear to have any clinical studies. Has anybody with ss been prescribed this?
Posted 17 Dec 2015 by • 0 answers
And are and have been on long term fluconazol therapy. What is the feel with long term meds such as this. Is there a safety factor?
Posted 4 Jun 2015 by • 1 answer
... thought it was dental, but turned out it was not, then they said glands was up, now they are saying that my saliva glands are swollen noticed that is one of the side affects, will this go over time, or does it mean I have to stop using the medication, as I have asthma and epilespy , I am ...