Tagged: National MS Society

Get Movin’ and Walk

If you’re like me, this is about the time of the season that you’re itching to get out of the house, spend more time with friends, and maybe get in a little exercise while you’re at it.  The great thing about living in the Creative Corridor, is that you have access to a few malls that are nice enough to let local charitable organizations use them for some of their annual fundraisers.

Since there are so many worthwhile organizations that have mall walk fundraisers coming up in the next few months, I thought I would break down the upcoming walks for those who are in the Cedar Rapids/Iowa City area.

MDA Walk

Muscular Dystrophy Association | MDA Muscle Walk | February 9th @ Coral Ridge Mall | 8 AM – 10 AM

JDRF Walk to Cure

Juvenile Diabetes Research Foundation | Walk to Cure | February 23rd @ Westdale Mall | 8 AM / 10 AM Walk

CMC Mall Walk

Catherine McAuley Center | Movin’ For McAuley | March 9th @ Westdale Mall | 9 AM / 10 AM Walk


March of Dimes | March for Babies | April 28th @ Rockwell Collins | 8 AM / 9 AM Walk

Walk MS Logo

National Multiple Sclerosis Society | Walk MS | May 18th @ Kirkwood Community College | TBA

These are just the ones on my radar for the Spring.  Please let me know if I missed your favorite!  I hope you have a chance to attend one (or more!).  These are all great causes and hold a special place in my heart, so I know I’ll be at most, if not all, of these walks.  Interested in getting a team together, but not sure how to get the word out?  Have a team, but want help spreading the word?  Leave a comment on the blog or my Facebook page and I’ll do what I can to help!

See you at the mall!


World MS Day 2012

Happy World MS Day!  Multiple Sclerosis, also known as MS, is a chronic, unpredictable neurological disease that affects the central nervous system (source).

MS is a disease that I am very familiar with.  When I was in high school, my mom was diagnosed with Multiple Sclerosis.  I had never really heard of MS before so I wasn’t sure what to think.  She made the point to reassure my sister and I that she would not die from the disease, but it would slowly degenerate her mind and body.  Knowing that she wouldn’t die made me feel a little better, but I still didn’t know what it meant to live with this disease.  It wasn’t until I returned from 4 years away at college, that I would come to understand how it affected her body.  When I moved home, her energy levels were low, she often repeated herself, and she didn’t remember things well.  Watching her go from the high energy person to someone who easily fatigued was hard for me to grasp, especially since she looked fine.

The difference between MS and other diseases is that no two people have the same experience.  It looks very different from person to person.  MS can cause various symptoms, such as blurry vision, numbness, loss of balance, poor coordination, extreme fatigue, and problems with memory and concentration, along with paralysis and blindness.  These problems can come and go, otherwise known as flare-ups (source).

Watching my mom’s disease worsen continues to be heart breaking.  While you can’t really tell that she has MS when you look at her, as you listen to her speak sometimes and walk, you can see how it has affected her in both mind and body.

MS occurs in more women than men, but anyone can be diagnosed with it.  Children as young as 2 years old have developed the disease.  While it is not fatal, as the diagnosis progresses throughout their lifetime, many develop limited productivity.

World MS Day was established in 2009 as a global awareness campaign to provide information regarding MS and the 2 million plus people living with MS.    Progress is being made to treating and understanding MS, but there is no cure yet.  However, there are FDA-approved medications that have been shown to “modify” or slow down the course of MS, and there are various therapeutic and technological advances that aid in managing symptoms (source).  Learn how you can spread the word about the 1000 faces of MS on the World MS Day website, Twitter, or Facebook.

If you are living with MS, living with someone who has MS, or know someone who has MS,  please take the time and create a postcard on the World MS Day 2012 website.  Take a look at mine.  Maybe it will inspire you to share your story and join the 1000 faces of MS.

Are you or anyone you know living with Multiple Sclerosis?  What is your story?