Please join me January 9, 2015 / 7pm, @ Romys Nitingale W5670 County Road A, Black Creek, WI 54106 for a MS FIND A CURE FUN NIGHT lots of prizes, raffles and fun! Thank you! Tracie Buchinger😘 💖cost is $10per person unless you have MS then its free! Excited to see you all there lots of prizes, raffles & FUN ! What I would like people to know about MS? Why I am like I am! By: Tracie Buchinger 2015 Explaining what it’s like to live with multiple sclerosis can often be difficult…and frustrating. This is what I do know..... MS is unpredictable No two people progress the same – it’s not one size fits all. My symptoms can change on a daily or sometimes hourly basis. It can literally & figuratively knock you off your feet at anytime. MS is like a box of chocolates you never what’s in it until you get it. It’s a roller coaster…you have ups and downs, twists and turns, except it is never fun. MS tries to steal your self worth every day by stealing little things you could do the day before. Just because yesterday was a bad day doesn’t mean today will be. MS is real – it’s not an excuse This is not something I chose. It’s out of my control. I’m not faking it. I’m not being a hypochondriac or lazy, I just hurt & need to rest. MS is exhausting and can cause extreme fatigue and horrific pain. MS is not a death sentence (and it’s not contagious!) This is my struggle and what makes me stronger. MS is not fatal, and isn’t always debilitating. It doesn’t change who I am, just what I can do. It’s a terribly frightening diagnosis to receive. But, with time and education, it’s not the end of the world. MS can be invisible I may look fine on the outside but feel terrible on the inside. MS makes you appear somewhat normal on the outside, but wreaks havoc on the inside. Others can’t necessarily see my limits, as I see and feel them and sometimes I can not push past them. Then at times I jump right over them! I have to do what I can, when I can, so I hope you understand me, a little bit better, why I am like I am! MS can sometimes be stressful and depressing Slowly and quietly it takes away my mobility, my cognitive thinking, and my dignity. It’s unbelievably hard to live with -mentally physically and emotionally. MS is a constant battle – for everyone It’s on my mind even when I feel well. MS is something you think about every day; there is never a break. It’s devastating – it is not just to me the victim but my whole family has the disease as well because, they have to live with me! MS requires those who love us to be open minded with great big hearts, and understanding. MS still has no cure MS can’t be fixed with the miracle potion they might be selling. We need research for treatment and a cure! Please join me January 9, 2015 / 7pm, @ Romys Nitingale W5670 County Road A, Black Creek, WI 54106 for a MS FIND A CURE FUN NIGHT lots of prizes, raffles and fun! Thank you! Tracie B 😘
Posted on: Sun, 04 Jan 2015 19:21:09 +0000
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