02/17/2023
Doctors say I will never get better or go into full 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 Spinal stenosis ❤️💜❤️ Sarcoidosis💜💙Lupus💜Multiple Sclerosis 🧡🧡Cancer💛💛Rheumatoid Arthritis💜Thyroid disease💙❤️💚Anxiety🖤🧡Depression🖤💙❤️PTSD 🖤❤️💜❤️Fibromyalgia🖤❤️💜❤️COPD/Asthma🖤💙💙🖤Neuropathy💛❤️❤️ Cancer🖤💜Epilepsy💚❤️or any other hidden illnesses.”💗❤️🖤💗MCTD💜💜💜 and
Crohns🖤 and ESRD💚💚💚. And Parkinson’s
Copy & paste.
Write 'DONE' in comments and thank you for your support. So many wonderful people fight hidden physical pain everyday. I can relate. I feel like I have more wrong than right...
ITS SUCKS BIG TIME
