Saw this post on Face book thought it was apt 🙂
Doctors say I will never get better or go into remission...I am not giving up, but I want to make others aware. A nap won't help. I am not lazy. I am on meds. I struggle with pain, mobility issues and fatigue every day. The most frustrating part is people look at me and say "It can't be that bad; you look fine." Despite the fact that my body is experiencing excruciating pain all over. I apologize if I miss events that I would love to attend. One day you'll understand my daily struggles. This disease affects me physically, mentally, and emotionally. I need your support, not your judgment.
With the post comes the following request:
"Please, in honor of someone who is fighting: Osteoarthritis ❤ Devic Disease (NMO) Sarcoidosis, 💜💜Lupus💜💜, Multiple Sclerosis 🧡🧡, Cancer💛💛, Rheumatoid Arthritis💜💜, psoriasis 💚💚Thyroid diseases💜, 💜Anxiety ❤️,Depression❤️❤️, Arthritis 💜💜Fibromyalgia💜💜 COPD💙💙 Crohn's disease💙💙 endometriosis 💛💛 Addison’s Disease 💚 GTPS 💖 Pernicious Anaemia ❤️ Graves’ disease 💛or any other hidden illnesses." Copy & paste.
Write 'done' in comments and thank you for your support.
Saw a Rheumy today.
Not posted in ages. Currently going through a juggling 🤹🏼♀️ act 
Ongoing post re Rituximab infusions
LUPUS/M.E/CFS/POST VIRAL could they all be the same sneaky bugger
Headache post update 🤕 
