3
out of 5 women SAL interviewed said they believe they have always had
lupus. Although they couldn't get a confirmation something was
wrong from their doctors, they felt the ongoing pain they knew was
not normal. Even when they went to their doctors to get tested, they
were told they were fine (when they weren't fine). They battled with multiple lupus symptoms before they were correctly diagnosed. Being educated and knowing the symptoms can save you the headache some of these women experienced before they found out, they too, had lupus.
SAL hopes you take something and learn from their stories......
Lupus
is already a hard disease to diagnose and treat. We hope that sharing symptoms of lupus will push you to get tested for lupus, especially if you are
experiencing any of the symptoms. You know your body most, so do
everything you can to ensure your body is well.
Interviews will be shown during the
'Singing For A Cure' Lupus Benefit Concert
Oct 16th 6PM at Tabernacle MBC.
Press on the link below to become a fan of Sisters Against Lupus on facebook
SAL on FB
