26/05/2020
No one knows jack about my life and what illness’s I have and what we go through. 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. I'm watching the ones who will take the time to read this post to the end."
With the post comes the following request:
"Please, in honor of someone who is fighting ❤️❤️Lyme disease 🧡🧡Autoimmune Devic Disease (NMO) Sarcoidosi🧡💙 Ehlers danlos syndrome 💚💚Scleroderma 💚💚💜💜Lupus💜💜, Multiple Sclerosis 🧡🧡, Cancer💛💛, Rheumatoid Arthritis💜💜Gastroparesis 💚💜Thyroid diseases💜💛lipoedema ❤️💜Chronic Pain💜🧡Anxiety❤️❤️Depression❤️❤️Fibromyalgia💜💜 Endometriosis 💛💛COPD💙💙 Crohn’s💜💜DIABETES💚💚scoliosis 💚💚 M.E 🧡🧡or any other hidden illnesses. Copy & paste. I get it if you don't copy and paste. It's ok!!!
Write 'done' in comments and thank you for your support. Always here, right? I'd like to see five of my friends post this message (Not share) to show you are always there if someone needs to talk. I think I know who will. x
