Doctors say she will never get “better” because as of now there are no cures. A nap won't help. She is NOT lazy. She is…
Doctors say she will never get “better” because as of now there are no cures. A nap won't help. She is NOT lazy. She is on meds (or not) and she struggles with pain & fatigue; and no it's not the same as your cold or body aches. The most frustrating part is people look at her and say "you look fine" or “you’re faking”. While her body is attacking itself on the inside. So, I'm sorry if she misses events, and I hope one day you will understand her daily struggles. This disease affects her physically, mentally and emotionally. She needs our support not judgement. 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 Epilepsy, SARCOIDOSIS, Fibromyalgia, CFS, Rheumatoid Arthritis , Neuropathy, Knee and Hip Pain, C.O.P.D, Lupus, MS, Diabetes, Memory Loss, Kidney Diease, Herniated Disc or Myasthenia Gravis, Auto immune disease, Mental health...it's not always physical!
Copy & paste.
Prayers to those who are suffering daily
Teresha Hollis ·
@kiaraherbert24
Teresha Hollis ·
@pettybetty
Oooh! ChicanaCrazy 🤷🏽♀️·
@teresha_h 😍😍😍😍😍
Oooh! ChicanaCrazy 🤷🏽♀️·
I watch this video all the time and show it to every one that asks me about lupus. https://youtu.be/z9akaWgWd7M
Teresha Hollis ·
@pettybetty i like it. Im going to start doing that cause people really do not understand
Tara🤙🏻·
❤️❤️❤️
danielle@barton·
This gave me goosebumps. My MIL has MS.
Breauna Talley·
Мама сына (2 года)
This touched me in so many places !! Ppl just don't understand ! #lupuswarrior 💜