I was diagnosed 28 yrs ago symptoms at least five or six before with bladder and left leg no feelings, doctors telling me their was nothing wrong with me.
1988 vertigo which put me in the hospital and the diagnose of ms. I was happy the doctors finally found out what was wrong with me even though I had no clue what ms was.
1995 optic neuritis
Ever since 1995 all my symptoms are the legs, bladder and bowels no problems with the top part of my body,
I have been on a lot of medications, they either didn't work or I had an allergic reaction The best medication was the IVig it worked for at least 2 yrs. That was the last time I was on meds and that was over 10 yrs ago the drs told me they had nothing to help me I also had plenty of pt, aquatic exercises and massage.
Shortly after diagnose I became Sp. I had a lot of good yrs even though I had problems with the left leg and leaky bladder.
I am now home bound either in my bed or recliner, hubby helps me.
In the last few yrs I met a lot health care people and they told me they never seen anybody with ms like mine. Last yr I had an occupational therapist who couldn't believe I had so much upper body strength, he told me somebody should do a study on me ad my ms
It is so frustrating cause my upper body wants to go but the lower body can't go anywhere. I always say if you cut me in half and give me a new lower half you wouldn't even know I had ms
So anybody out there like me?
Thank you if any body read this or responded
Shoo
1988 vertigo which put me in the hospital and the diagnose of ms. I was happy the doctors finally found out what was wrong with me even though I had no clue what ms was.
1995 optic neuritis
Ever since 1995 all my symptoms are the legs, bladder and bowels no problems with the top part of my body,
I have been on a lot of medications, they either didn't work or I had an allergic reaction The best medication was the IVig it worked for at least 2 yrs. That was the last time I was on meds and that was over 10 yrs ago the drs told me they had nothing to help me I also had plenty of pt, aquatic exercises and massage.
Shortly after diagnose I became Sp. I had a lot of good yrs even though I had problems with the left leg and leaky bladder.
I am now home bound either in my bed or recliner, hubby helps me.
In the last few yrs I met a lot health care people and they told me they never seen anybody with ms like mine. Last yr I had an occupational therapist who couldn't believe I had so much upper body strength, he told me somebody should do a study on me ad my ms
It is so frustrating cause my upper body wants to go but the lower body can't go anywhere. I always say if you cut me in half and give me a new lower half you wouldn't even know I had ms
So anybody out there like me?
Thank you if any body read this or responded
Shoo
Comment