How I want to treat Multiple Sclerosis | Fall 2020 video
With employment in 2022, I changed my MS treatment plan. Well, not changed, I abandoned my wellness routines.
In the 18-months of pain killers, muscle relaxers, fusions, physical therapy, occupational therapy, and other forms, I've declined.
I miss having energy throughout the day. I miss being present. I miss the way I felt, how limber my body was. I miss sleeping all night, spooning my wife.
My chronic illness is Primary Progressive Multiple Sclerosis. There is no cure. No medication heals or repairs the physical damage to my body. The medical professionals offer expensive drugs hoping to slow the progression of disabilities and limitations.
Comparing my wellness routines to the medical programs can be tricky because I can't view them in a vacuum.
Still, I prefer the former. There is no if, and or but. I'm busting my ass to create a lifestyle grounded in wellness routines and mental health.
This is why I started a GoFundMe. My goal is earn disability, SSI, food stamps and Medicaid.
Please use the link to donate, purchase products, order services or simply share. Any help is greatly appreciated.
#wheelchair #disability #chronicillness #multiplesclerosis #limitations