Things I’ve Done Since I was Diagnosed with Multiple Sclerosis

I started making a list of some things I’ve done since I was diagnosed with Multiple Sclerosis. When I showed the list to my husband and told him I wanted to post it on my blog he said, these are cool things but make sure it doesn’t seem like you are trying to brag. Then I was worried; of course that wasn’t my intent.

So I thought about why I was making the list. I realized that I made it because I’m proud of myself. After I was diagnosed with MS I spent two years struggling with depression while trying to come to terms with my situation. It was the most difficult time in my life. I’m so grateful that I made it out of that dark place.

The purpose of this list is two-fold. For me, because I can be my harshest critic. I sometimes feel like I should be able to do anything and it’s hard at times to cope with my limitations. This list shows me that I’ve done some awesome things despite living with MS. The second is for others. I want everyone with MS to know that they can live a happy and fulfilling life. I want others to stay out of the dark place and live with me in the light.

So here goes. Since I was diagnosed with MS I’ve…

Graduated from college three times
Lived on my own
Got a dog
Found several jobs
Received a promotion at work
Swam in the ocean
Got married
Traveled to other countries
Adopted two cats
Rode in a helicopter
Visited four national parks
Traveled alone for business and pleasure
Went camping
Moved to two different states
Bought a house
Saw a humpback whale in Mexico
Jumped off a boat into a lake
Watched the sun rise and set in the Grand Canyon
(This spot reserved for the future)

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The Wheelchair and Me

Will I be in a wheelchair? That might be the ultimate question that someone who is diagnosed with Multiple Sclerosis wants answered. Gait problems are common in people with MS and as the disease progresses physical disability is possible.

When I was first diagnosed, I went through a phase of fear. I was certain that I’d end up in a wheelchair and couldn’t see any real future for myself. This bleak outlook contributed to the two years I spent battling depression after my diagnosis. After I started to move forward with my life, I refused the idea that I’d ever need to use a wheelchair. Then I started to have problems walking long distances.

A couple of people had suggested using a wheelchair when I declined social activities that involved walking longer distances. The thought was horrifying to me. I wasn’t using any type of assistive device at the time so the idea of hopping into a chair was inconceivable.

After I got married my mother-in-law gave me a transport wheelchair that she had used in her house after breaking her foot. At this point I was a bit more open to the idea, but not completely ready. Then one day my husband had planned a surprise. He wouldn’t tell me where we were going but said we would need to use the wheelchair. I was reluctant but curious, so we loaded up the fashionable red and black chair and headed out. We lived near Detroit, Michigan at the time and when we arrived downtown I saw the signs directing people to the dog show. Long a lover of dogs, I was thrilled with the surprise activity.

At the show my husband pushed me around in what we came to affectionately refer to as “hot wheels”. I didn’t have to worry about getting tired, or my legs just giving out. I took notice of other people in wheelchairs both young and old. I realized I didn’t care how I might appear to other people as I rolled by. It meant more to me that I could enjoy the event without worry. In fact, I was ecstatic when breeders plopped puppies into my lap who were therapy dogs in training.

After that day I welcomed using “hot wheels” when needed. We’ve done some cool things together including going to a baseball game, a vacation to Mexico, and to National Parks. I’ve also used it to participate in three National Multiple Sclerosis Society Walk MS events in two different cities.

“Hot Wheels” and me. Look close!

There have been times when I’ve dealt with insensitive comments from others while using a wheelchair. I’ve also encountered social situations where I’ve felt embarrassed and left out. I’ve also had my fair share of cries in that wheelchair, faced with the limitations imposed by the chair itself. Despite these things, I know that I’ve been able to experience more of life with it than I could without it.