Sjogren’s Syndrome – Introduce yourself and meet others
I have been diagnosed with this and I'm in pain most days and would like to have discussions.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
I have been diagnosed with this and I'm in pain most days and would like to have discussions.
Interested in more discussions like this? Go to the Autoimmune Diseases Support Group.
@gemmax True. I have always had the 'Village' mentality. We humans are by nature social beings, and are where we are today (not in caves) by standing by one another.
@gemmax Sounds like you have an interesting lineage. I have a photo of an oil painted portrait of one of my great greats going back to 1470. His face and hair look exactly like me. When I show it to friends, they think it is me and that I had it done at one those boardwalk shops. You know the ones that take sepia tone old-timey photos? It was bizaar to see such a strong resemblence after so many generations.
@windwalker I have a large family, but I look different from most and had always wondered where my appearance came from. Then I came across a gggrandmother who is ¾ cherokee and although my skin is English like my mother, I looked so much like her that I couldn't believe it. I loaded the two pictures one of her and one of me on top of each other in a program that i have and changed the transparency and there we were a perfect match! I find genealogy very interesting. I started years ago and collected documents as i went along. I love to restore old photos too.
Gem...Where did you learn all these things like genealogy and restoring old photos. Did you take classes or teach yourself
@gemmax I find genealogy very interesting as well. I think it would be great to also have health history in that data bank so that future generations can learn what to watch out for.
I have just been diagnosed with primary Sjogren's via a lip biopsy. I was Ro and La negative. I have very dry eyes which I am managing reasonably well with eyedrops and dryness down below which I am using topical oestrogen for, I have been started on Pilocarpine (Salagen) 2-3 times a day. I was led to believe that I would not get any systemic symptoms but I do have some symptoms of fatgiue - not crippling but enough to make my working life difficult, I am 53 years old and have been told the fatigue is just part of the menopause but I am not convinced. What are the best ways to help with the fatigue or is it just a case of accepting it and pacing yourself? Any advice would be very much appreciated.
Dear
I was diagnosed by lip biopsy and I have a dry mouth and dry eyes. I use eyedrops regularly and also take Pilocarpine (Salagen) to help my salivary glands be more productive. I have no other auto immune diseases. I was diagnosed a year ago but have had dryness symptoms for many years. I was Ro and La negative on a blood test so my rheumatologist is hopeful that I will not develop the joint problems and tiredness.
Jean,. Good news for you. I have had RA for at least 10 yrs. The drugs are hard on me. I try to get thru the episodes with only Tramadol. Very very light drug. Recently my ocologist is finding something suspicious in my blood. He is not ruling out multiple Myeloma. I am doing one more blood test which somehow was damaged. I truthfully believe I do not have Myeloma. I suspect what you have. I fogot the name of disease. We can survive that. I am so sick of taking pills and being so tired and low energy. God Bless. Lee
I find it so hard to accept the time it takes doctors to determine disease. What are they teaching in dr school. I have had so many hard to stand tests with promise that after THIS test we will have a determination. They never do. I must have a new disease or need new doctors.