MSF Ambassador I have a new adventure that I am so excited to be a part of. I am part of a group of people who are the MS Foundation Ambassadors. This is an amazing opportunity to be part of something that is really going to help others living with MS. I have had three […]

Today at my MS treatment, I became overwhelmed with a grateful thought of how lucky I really am. While sitting there, I witnessed a women come in for a treatment for pain. She had her young grandson with her. She was in a wheelchair and unable to walk. How sad it that? She can not even

Happy Summer! With schools getting out or already out…summer is right around the corner. And that means here comes the HEAT. Now some of you like the heat but for those with MS, the heat can be a real bummer. I know personally, too hot and humid just makes me feel awful. It makes me

Attitude is everything This statement is the truth. Your attitude from the moment you wake up in the morning sets your day. If you wake up in a negative attitude or in a bad mood, your day will reflect that. Here is a little tip for you…wake up feeling positive, happy, and grateful for another

There are many emotions associated with having MS When first diagnosed with MS, I was in not necessarily denial but, ” Are you kidding me?” attitude. And then more I do not have time for this. I have things I want to accomplish and do in my life, this will be in the way. I

It is absolutely amazing how so many people inspire me each day. I am especially inspired by recent events of people being so giving and generous to my MS WALK 2013 team, Marci’s Stampede. Because of so many wonderful people in my life, my walk team has been the TOP TEAM for the Saint Charles

My life is even better now… On December 18th, 2012, my life changed the most amazing way by having my twin daughters… Harper Marie and Delani Maxine The girls are the love of my life and I could not be any happier than I am being a mommy! During the 8 months I was pregnant

This is a picture of my MS treatment called Tysaburi. I do this once a month for about two hours. This treatment has given me my life back with no weekly injections, no side effects, and no constant reminder each week that I am going to feel sick for two days like the other form

This may be a difficult area for some people and not for others. To me, I do not see the shame or reason in not telling others.  As long as this is not the only thing out talk about. It is not the first thing out of my mouth when I talk to people. But

I found this magazine clipping titled Awareness Rules. I love what it says about living with MS and I think for everyone too! 1. Take your time, deservedly 2. Nap, necessarily 3. Limit yourself, for yourself 4. Prepare, always 5. Use aids, ably 6. Go anyplace, safely 7. Research options, smartly 8. See medical professionals,