My TM Story.
January 1998 was when my initial bout with Transverse Myelitis surfaced. I was in 8th grade and after arriving home from school I started experiencing increasing chest pain. I curled up from the pain and needed to be carried to the car and rushed to the hospital. Luckily both my brothers were home and able to take me otherwise I don't know if I would have made it. The ER doctors and nurses had treated the chest pains but I had very limited sensation and movement from my chest line down to my feet. I was released from the ER because the chest pains have subsided but my upper body was extremely tender and painful. Also my mid to lower body had very little movement/sensation. The next day I was taken to another hospital to see a neurologist and for further testing. After a few days of testing including a spinal tap and 2 MRIs they concluded that it was Transverse Myelitis with the spinal area affected being around level T-6 or 7. I was paralyzed for a couple of weeks before initially gaining movement back on the left side first then a short time after the right side began movement again. I feel I'm in the more lucky percentage of individuals with Transverse Myelitis residuals that are more manageable in an independent manner.
It's been a little over a decade since I've used my wheelchair or walking cane and am continuing to show positive progress in handling any physical challenges due to my altered nerves. More importantly I've been able to accept and appreciate the emotional residuals that occur after a condition like this. I've had and still have the most incredible support system and I would like to do something to honor the work and care that others have put into me.
Here is a link to my youtube page where I have been posting some of my progress with my therapy the past year or so:
Overall though I just want to open myself to more experiences with positively strong minded individuals who have had a similar experience with the kind of struggle that these conditions spawn.