Sjögren’s Syndrome: how do you manage the symptoms?
Hi
I see a rheumatologist next week for sjorgens syndrome. Last summer a sinus doctor I saw mentioned it to me and recommended I see a rheumatologist. I never had heard of sjorgens and I have never been to a rheumatologist. At the time last summer. My only symptom was very dried out mouth. I developed dry eyes only a few months ago. The otc drops for dry eye stopped working unless my eyes were just getting worse so my eye Dr recommended something stronger otc. It's better. He did prescribe me restasis but unfortunately even with my insurance it was too expensive so I could not get it. But my other concern is the body/joint pain I ha e been having. It's gotten so bad tonight is the first time I have been up all night. I do have a unrelated degenerative changes near my lumberspine which is causing other embarrassing issues but my other pain started actually even way before the dry mouth. It started very soon after my gallbladder surgery last January. It started in my upper back spasms and just painful. Worse now then last 6 months went to my shoulders that's very tender, my neck. Arms. I read a article about sjorgens pain being similar to fibromyalga pain. I wondering if anyone thought it was sjorgens related being this painful or maybe something else? I have wanted imaging, preferably a mri bur been unable to get it. I'm hoping next week the rheumatologist will order something. Also last summer my sinus doctor did order bloodwork some sjorgens antibody bloodwork 5 of them and they were all normal. Although now with my symptoms progressing I wonder what bloodwork now would show. Any feedback would be greatly appreciated. Thank you.
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Thank you. Please don't let your autoimmune disease get you down. Find a way to live with this disease that allows you to find joy in your day.
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I have mild RA after nearly a year on methotrexate I noticed a change in my eyes I developed sjorgens syndrome. For the past 3 weeks I have itching from my scalp, ears , neck breast and rash develops , I also have sweating . A doctor told me I might have Lupus and to have my rheumatologist have it tested. I am taking prednisone and plaquinil. I am very scared I don’t know how to cope or where to begin with 3 autoimmune disease. Can someone please share there story of hope and help me cope.
Good morning, when first ill I saw a grief counselor which I found very helpful. I use the Calm app every morning and do 3 short meditations daily, I also do the treadmill (very slow:) almost daily. I have good friends that I chat with daily too..... and I drink lots of fluids. Medicine has become one of my good friends. My life has changed so drastically but so have I. I am sorry you are a member of the multiple autoimmune club. Oh yes Sjogren's advocate is a great website and offers lots of education and support as well as the Sjogren's Foundation. In my opinion you have to be your own advocate with autoimmune diseases especially Sjogren's. Sending hugs.
I had it one time one ago but overcame it!
Hoe did you overcome it
Thanks for hugs when I’m hurting. Great tips, I will start with the grief counselor. It’s hard to accept the downhill turn in my life. Thanks for sharing.
You Guys r great! Thanks for all the support 😉 it really helps. I have several autoimmune issues, one being Sjogrens. I use Restasis 2x a day, Sustain 3-4 x daily, Salagen for the dry month. Does anyone have hot flushings, Not flashes. Usually at night out of the blue🤔❤️.