Forty-five minutes left in Day 6; this will be a short one!
Dear Multiple Sclerosis,
Thank you for providing me with the opportunity to make changes in my lifestyle to improve my health. I was not taking care of my body and you alerted me to the fact that I was harming it. You may very well have prevented my body from experiencing future illnesses, such as cancer or heart disease. I am so happy to learn about nutrition, the human body and brain, and the immune system. My only regret is that you did not come along sooner so I could have more time teaching my children about proper nutrition before they left the nest. I can only hope they learned something they can draw from in their future years. While you have been a blessing in disguise for me, I do not wish for my children to know you or your cousins.
I also want to thank you for instilling in me an awareness of others with health problems. I now can appreciate the fact that John Doe slowing me down on the sidewalk may be moving slowly because he could be living with you too. Before I met you, I could not have known what it might be like for him. If John isn’t living with you, one of your cousins might have moved in and become a part of his life. I have shared this awareness with my children and hope they too can be patient with those who may be slowing them down.
The life lessons I have learned as a result of having met you are priceless.
As part of WEGO Health’s third Health Activist’s Writer’s Month Challenge, I am challenging myself to write 30 posts in 30 days using prompts provided for the event. Wish me luck, or join me!
Image by seannalexander via Flickr
I came across an article on Caring.com that succinctly explains why I ought to be moving a whole lot more than I am now. Have a look.
Improved cognitive function
I could use some of that!
Less deterioration of brain white matter
I’ll take some of that too!!
What the heck am I waiting for?
Ugh, what a lame excuse. Even before I was diagnosed, I knew I should be exercising.
So… how to incorporate exercise in bad weather?
Well, there are 10 flights of stairs in the building at work. That’s a start… but not all 10 of them on the first try!! Oh goodness me, no! I’ll start with 5 and see how that goes.
A perfect time to do it is around 3:00, when the afternoon slump hits. Once I make this a regular activity, maybe after a week or two, I’ll probably be motivated to look into other activities.
You just gotta start somewhere!
Image via Wikipedia
I created a custom Google news category for Multiple Sclerosis and check it every once in awhile. Currently, the big MS news is that reality TV celebrity Michaele Salahi claims to have had MS for years. Due to the controversial figures she and her husband have become, people are debating whether or not it’s a publicity stunt. There’s nothing to debate – they are getting a lot of publicity. It’s no coincidence it was announced yesterday, the same day their ebook was made available.
I’ll be honest, I’m curious to know what is said about Michaele’s MS in the book. I have yet to come across any reports about what detail, if any, is provided about how she’s been living with it for so long. Surely there has to be more to it than, “Michaele has had Multiple Sclerosis for years.”
But I’m not falling into their trap and spending my money on the book to find out.
I just hope she isn’t making it up. If she is, if Michaele does not have MS, then I have to give the Salahis props for choosing a disease that can easily be faked. She could lie that she’s been on the Swank diet for years, which can greatly reduce the disease’s progression. It’s true for people who have MS and choose to treat it with diet and nutrition. Thus, Michaele’s claim to have MS is certainly a believable lie. If she does have it, she’s done a good job managing it, helping to prevent further disease progression. She could be on the Swank diet!
What truly shocked me was how people with MS were so quick to judge Michaele. The last people on earth who should be judging the validity of her claim are those with MS. As we know, it affects everyone differently. Some of us are in wheelchairs, some use canes, and some get around fine without either. This is actually a great opportunity to help educate people about invisible MS, how we can have a disease but “look so good.”
Regardless whether or not Michaele has MS, turn their publicity stunt into an opportunity to explain how someone can have MS and what appears to people on the outside as a normal life. Get the word out and make your contribution to MS Awareness.