Basically I have an autoimmune disorder called multiple sclerosis. The wiring in my brain "short circuits" and some signals don't get sent properly to the rest of my body. Symptoms of MS can range from muscle weakness, loss in coordination, fatigue, vision problems and even paralysis. Some people experience acute symptoms and others have chronic symptoms that don't always go away. There is no way to know when another relapse can happen or even what part of the body it will affect.
Neither a cause or cure is known and I take a medication that slows down the progression of the disease. It is taken by subcutaneous injection (just below the skin) three times a week and there are a few side effects which I try to sleep off with an ibuprofen. I'm not contagious nor am I dying. I've learned to accept this disease and am in a much better place than I was over a year ago (proof of this is in my very first blog posts). I can finally talk about MS and I am always willing to answer questions to the best of my knowledge. If it wasn't for the support of my friends, family, colleagues and twitter crew, I would not be in the zone I am today. I'm so grateful; everything happens for a reason and you must learn to adapt and overcome.
#beatMS
way to go :) great to hear! I remember the summer I realized I could talk about MS matter of factly to strangers. It took me longer than a year :( because I stayed isolated -- but I dont regret being open about MS whatsoever. I've had the unfortunate experience of being the reference point for several concerned parents as their young adult child goes through an MS diagnosis. Ya never know how telling your story will help. So many people are affected and the stigma of the disease is out there. Let's change it :)
ReplyDeleteWay to go girl! I am happy that you are gaining strength and confidence every day! I'm here for your support... when can we go to starbucks?
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