I’ll Run Again in Heaven 2
This is the story of my life with multiple sclerosis. In the past year my MS has taken my balance and walking. I feel my life is still good and with the Internet I can now earn a good living!
This is the second article in a series of articles that came from my ebook.
I feel I can talk about my Multiple Sclerosis with confidence because my body has experienced just about everything MS can dish out. I’ve only been in my current condition for the past two years and I feel it’s still not that bad! I’m still looking forward to the future! That is not a bunch of bull, either! My life is good! I get up in the morning and I go to my computer to check my emails. Then I write articles about my MS or telemarketing. I’ve been telemarketing for 19 years now.
When I was healthier it was a way to get more business for my businesses but now it has become a large portion of my income. In 2007 I started a business from my apartment where I teach people how to telemarket. Telemarketing is a great way for homemakers, students and the disabled to earn money. After that I can rest, watch TV or whatever. I don’t have a boss overlooking my shoulder which I’ve never really liked!
Now I ride my electric scooter (Max) 100% of the time when I’m outdoors. I figure as long as I have Max who needs legs! I joke with people that walking is overrated anyway! lol Max will be my legs for the next 30 years and I know it sounds weird but that’s OK with me. I also use a walker (Sally) in my apartment. I now find that I’m using Sally as soon as I get up each morning! This has all happened in the past 6 months and I’m using Max or Sally more and more everyday! I’m continually amazed at what the human body can do or not do to itself! It’s kinda weird to experience losing your legs first hand. I didn’t get shot in a war, I didn’t have a bad diving accident and I didn’t have a bad car accident. Multiple sclerosis just happens to people!
Everyday people are getting more accepting of disabled people. I feel disabled people are the new minority of the world. Everywhere I go is handicapped accessible. If I need to go to a Wal-Mart, a Home Depot or a large grocery store they have doors that open automatically making access easy. In my little town where I live there are no automatic doors but I can still get in the buildings I want to. I can easily get into my small grocery store, the drug store, the post office and my favorite pizza place. I’ve been opening doors for 8 years now while riding my scooter and I’m proud to say that there is no building as of yet I haven’t been able to get into.
When I was diagnosed with MS my neurologist always told me that how I was after 5 years was how I would probably be for the rest of my life. My magic year to get to was 1996. I thought if I could make it to “96 I”d be alright. Well, I made it to “96 and I was still very active. Things looked pretty good for me! However, in the past 7 years doctors have changed their thinking on that 5 year rule. They’ve noticed some of their patients have a worsening of their MS in years 5-10. They call this type of MS secondary progressive. In “96 if I had an exacerbation which is a worsening of the symptoms I’d still work and everything but I’d feel miserable. In “98 or year seven for me I had a bad exacerbation which I”ve never fully recovered from. I like to think I’m walking on a hill and there’s only one direction to go and it isn’t up.
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Post CommentAthlyn Green
On July 29, 2008 at 6:56 pm
Hi Jon,
How do heat and evenings affect you? I find that my jolts get so much worse in the heat and that at around 4PM I can count on the “orchestra” starting up: jumping, buzzing, tingling, jolting, zapping, etc.