Doctors say I will never get better. A nap won't help. I am not lazy. I am on meds. I struggle with pain & fatigue every day. No it's not the same as your cold or body aches. The most frustrating part is people look at me and say "you look great!" while my body is attacking itself on the inside. So, I'm sorry if I miss events, decline invites, don't answer the phone or fail to return phone calls. I hope one day you will understand my daily struggles... or perhaps I hope you never have to, first-hand. This disease affects me physically, mentally and emotionally. I need your support not judgment and if you can't give me that then dueces. I'm watching the ones who will take the time to read this post until the end. This is a little test, just to see who reads & who shares without reading! Please, in honor of someone who is fighting Sarcoidosis, Lyme Disease, Lupus, Fibromyalgia, Osteoarthritis, Multiple Sclerosis, Arthritis, Neuropathy, muscular dystrophy, Knee and Hip Pain, C.O.P.D, Cancer, MS, Diabetes, Memory Loss, Kidney Disease, Herniated Disc or Myasthenia Gravis. Autoimmune disease, SCLERODERMA, IIH and any other health issue mental and physical. Dorris Wedding casual and informal wedding wears look flapper
Copy & paste to this list ......