While I really don't like talking about myself, I have been going back and forth for about a month now whether or not I was going to tell people about this. Then on Thanksgiving I decided to tell my family and friends.
In the spring of this year I started to have a tingling in my right hand and arm... It would feel like it was asleep. By the summer, it had moved to my shoulder and right leg. So, in Aug. I went in to the doctor. 1st they thought it was related to my traumatic brain injury, that I sustained in 2010 in Afghanistan. So, after three different doctors, In early Oct. I was diagnosed with Relapsing Remitting Multiple Sclerosis.
This is not fatal. And my life expectancy is normal.
I have begun treatments that will keep my symptoms in check. Most of the time I will be 'normal'(at least as normal as I get). But for time to time I may experience attacks, which can range from fainting to loss of the use on limbs, to confusion. But after the attacks I should return to 'normal'.
I could stay like this the rest of my life. In fact a very high percentage of this type of MS patients live normal life's. But there is a small chance it could get worse and become Secondary Progressive MS, which would mean very slow decline. But I am not there and nor do I plan to be.
But for me, This has been a real dick punch and I am not fully out of the shock of it all.
I just wanted to explain to my MFC friends what has been going on with me and why I have been a little f'ed up lately...
-applie
In the spring of this year I started to have a tingling in my right hand and arm... It would feel like it was asleep. By the summer, it had moved to my shoulder and right leg. So, in Aug. I went in to the doctor. 1st they thought it was related to my traumatic brain injury, that I sustained in 2010 in Afghanistan. So, after three different doctors, In early Oct. I was diagnosed with Relapsing Remitting Multiple Sclerosis.
This is not fatal. And my life expectancy is normal.
I have begun treatments that will keep my symptoms in check. Most of the time I will be 'normal'(at least as normal as I get). But for time to time I may experience attacks, which can range from fainting to loss of the use on limbs, to confusion. But after the attacks I should return to 'normal'.
I could stay like this the rest of my life. In fact a very high percentage of this type of MS patients live normal life's. But there is a small chance it could get worse and become Secondary Progressive MS, which would mean very slow decline. But I am not there and nor do I plan to be.
But for me, This has been a real dick punch and I am not fully out of the shock of it all.
I just wanted to explain to my MFC friends what has been going on with me and why I have been a little f'ed up lately...
-applie