Most of you know that I  was diagnosed with Sjogrens a little over 10 years ago.  

Sjogren's is one of the most prevalent autoimmune diseases in the country affecting 4,000,000 Americans with 9 out of 10 being woman. This little known, yet severely disabling disease can be devastating to the individual as well as family members.

All instances of Sjögren’s syndrome are systemic, affecting the entire body. Symptoms may remain steady, worsen, or, uncommonly, go into remission. While some people experience mild discomfort, others suffer debilitating symptoms that greatly impair their functioning. Early diagnosis and proper treatment are important — they may prevent serious complications and greatly improve a patient’s quality of life.

Since symptoms of Sjögren’s syndrome mimic other conditions and diseases, Sjögren’s can often be overlooked or misdiagnosed. On average, it takes nearly seven years to receive a diagnosis of Sjögren’s syndrome. Patients need to remember to be pro-active in talking with their physicians and dentists about their symptoms and potential treatment options.

 

This disease has  affected how I live my life.  I am learning how to make these adjustments.

  I want my daughters and grandchildren to have a chance, so I am asking you to donate whatever you can.  In time, these and other donations will put this disease to an END. 

 

Thank you for visiting my  fundraising page.  If you find it in your heart  to donate, thank you.  If you can't please remember us in your prayers. 

Donating thru this website is simple, fast and totally secure.

 

Thanking you from the bottom of my heart.  May God bless you for your generosity.

Lynn