I was diagnosed in 2000, but have had MS since 1966 when I was 16. It took research and understanding this disease before they actually said the words Multiple Sclerosis to me (do I have that spelled right).
The Doctor in Tampa Fl. that I finally connected with got hold of all of my medical records from 2000 to 1966 and found my first episode with MS was in high school when I had bad trouble swallowing and was always very tired. this problem cleared up in a month and did not return.(it was not Mono).
In 1987 my legs went numb and my balance was bad. That also cleared completely in about 6 months. I moved from Maryland to Florida in 1990 with no bad effects until 1997 when my legs went numb and tingling again. These last problems are still with me and I have learned to live with the numbness, lethargy, and sometimes double vision.
It seems now that I am in secondary progressive MS. I am now 63 and still hanging in there. If the doctors in Maryland had caught this in the R/R stage in 1987 it might not have returned (wishful thinking). My problems are now dealing with a husband with first stage Alzheimer's, and trying to do everything by myself and not get too tired. Does anyone have any helpful hints?
** Moderator's note - Post broken into paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print. **
The Doctor in Tampa Fl. that I finally connected with got hold of all of my medical records from 2000 to 1966 and found my first episode with MS was in high school when I had bad trouble swallowing and was always very tired. this problem cleared up in a month and did not return.(it was not Mono).
In 1987 my legs went numb and my balance was bad. That also cleared completely in about 6 months. I moved from Maryland to Florida in 1990 with no bad effects until 1997 when my legs went numb and tingling again. These last problems are still with me and I have learned to live with the numbness, lethargy, and sometimes double vision.
It seems now that I am in secondary progressive MS. I am now 63 and still hanging in there. If the doctors in Maryland had caught this in the R/R stage in 1987 it might not have returned (wishful thinking). My problems are now dealing with a husband with first stage Alzheimer's, and trying to do everything by myself and not get too tired. Does anyone have any helpful hints?
** Moderator's note - Post broken into paragraphs for easier reading. Many people with MS have visual difficulties that prevent them from reading large blocks of print. **
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