
It was not in our heads... it was under our skin. Because of this debilitating disease we feel each others pain as it will strip your life right out of you. The symptoms & damage is HORRENDOUS. Most of us went undiagnosed as cases were not being reported. We never got the bullseye rash that shows that one has Lyme. 80% never get it. Besides Fibromyalgia & Lyme Arthritis (which I can ignore) I was damaged very badly Neurologically. I also have chronic sinusitis which knocks me to my knees post Lyme symptoms like to reek havoc & make all of your other symptome act up worse. In 9+ years I have had 11 piklines-yes that is what you see in the picture, an IV threaded to my heart. I can get 1-3 infusions a day of antibiotics -I have had them in for up to 3-4 months. 11 piklines in 9 years. My art was my saving grace as staying home in bed was not an option. I decide after I could stand up & focus (8 months) I would concentrate on my art. I sold 1400 Wall Dancers dolls each made 1 at a time on Ebay then I went to Etsy. So this be knows what one goes through. the reason for this ugly picture & story is because people tell me Keri if you can do it I can try... I always wanted to paint... I would like to sew ............so my heart & prayers are with you all & I will stand by your side. This is MY story. Last week I was written up in Artizen Magazine. I know everyone wants to ask questions but I do NOT do support groups or get all over Lyme websites. I KNOW what the disease so please try & respect my right to not want to talk sick talk with anyone. I have met great people & learned many lessons on my journey. I cannot change the Lyme Disease but I can choose how I want to live my life & I do! To all of you that have gone through so much of this with me over the years-I love you to pieces! Hugs,
Keri