Hello All,
I don't want to write an exhaustive story that has everyone wishing it would just be over and I can add more details as we go, but thought that some of my learning and insight over the years might help new sufferers.
I have primary Sjogren's with organ involvement, most particular kidneys--renal tubular acidosis and medullar tissue disease. I was diagnosed while living overseas when I was 23 Years old--I was the youngest diagnosed Sjogren's patient at the time and an anomaly because I had recently given birth. I have had positive titers every year for the ensuing 30 and have experienced that Sjogren's, like many other auto-immune disorders, does have periods of remission and active state.
1. When I know that I am getting sick, I am better prepared to deal with the pain. For instance. I have therefore learned not to ignore the following:
Intense muscle tingling or "heat" when tired
Immediate and overwheling fatigue particularly a couple of hours after I wake up
Dramatic change in appetite; for me it is usually getting very hungry but it can also be the complete loss of appetite.
My immediate response now to any of these symptoms is:
Increase my sleep to 10 hours a night; go to bed, read, do breathing exercises; you will fall asleep
Increase the amount of outside activity; usually walking or bike ridiing; gentle but persistent and consistent exercise reprograms the muscle tissue and helps you sleep which helps you heal
Eliminate all alcohol except for one glass of red wine a day
Immediately eliminate all foods from my diet that tend to increase inflammation.
My goal is to nip my body's auto-iimmune response in the bud. I've learned the key to this is to reduce the inflammatory response which is cyclical and gets worse as the inflammation gets worse. The inflammation is also responsible for most, although not all, of the pain that I have from Sjogren's.
I hope this first post helps. I'll keep contributing and please feel free to ask any questions you want. If it relates to Sjogren's I've generally been through it and am living pretty healthy and happy and looking forward to aging gracefully and having lots of fun with my GKids for years to come.
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Thank you so very much for your post!
July 17, 2013 - 11:28amMy mother is struggling with this disease and has terrible sores in her mouth.
She has trouble eating, swallowing and speaking.
The more I learn about this disease the more baffled I am by it.
Thank you for your information I will continue to share all the great tips I get on EmpowHER and hopefully we will find her some relief!
Marta
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Jean,
THANK YOU for the positive post! I was just diagnosed with sjogren's. I am scared, I think "what will be my quality of life, how long will I live?" I have changed my diet to an anti-inflammation diet. I am 36, but had symptoms since May 2011. Are you taking any supplements,any additional advice? God Bless!
September 25, 2012 - 4:00pmThis Comment
I actually don't use any medications for my Sjogrens. I did for some years but found that I did not get enough relief to make it worth taking the meds. I am very proactive with my health and especially in relation to my kidneys. My highest recommendation is an anti-inflammatory diet. Dr. Weil has a great one in his book, but essentially it is the Mediterranean Diet. I get exercise every day, but avoid getting exhausted.
September 28, 2011 - 3:12pmThis Comment
Jean, what medications or medical treatments have you had good luck with? Thx. J
September 22, 2011 - 9:44pmThis Comment
Hi Jean in Oregon,
April 11, 2011 - 6:17amThank you for sharing your story. I'm sure you will be able to provide comfort and information through your experience to another member. Welcome to the community! We're glad you're here.
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