What to Expect When You’re Not Expecting…

By Scott Cremeans

As a seventeen-year veteran MSer, I am sometimes asked to advise the newly diagnosed. Sometimes I am the one to welcome the recently initiated into the fraternity or sorority of MSers. Questions get posed to me all of the time typically asking the same queries in different forms. Is MS a death sentence?  No. You have MS, how do you look so good?  Oil of Olay. What now? Live your life.

Then one gentleman’s query put me in a quandary. He asked: What should I expect from an MS life? I thought for a moment and came up with this answer. The following is my way of looking at it. My explanation had elucidated our strange medical condition in this simple sentence. With multiple sclerosis you must expect anything and be ready for everything.

There are a plethora of variables that make planning for MS an impossibility. To give you an idea of some of these variances: age, how healthy you are, and your geographic location, to name a few. Multiple sclerosis newbies need to know there are many similarities yet even more differences between symptoms. If you ask any ten people with MS, you will see commonalities in the symptoms. However, the impact of these symptoms on their lives can vary drastically.

People will gladly share their stories of how they dealt with the adversities that they faced. The problem is that you will not understand until you experience that symptom. However, even if you have the same symptom your body will likely respond differently.

All of that being said focus on several things in your new MS life. First and foremost, keep your bodies moving! Keep as active as you can by moving anything that you can for as long as you can. No matter if it is running, walking, swimming or something in between, stay in motion. I always say that if you sit still for too long, your body will rust. A rusty pair of scissors do not work correctly and neither will you. I went for nearly ten years without moving, and I deteriorated so much that I am currently in a wheelchair. Learn from the mistakes of others.

Food is life, but the wrong food can be the opposite. There are plenty of MS focused diets from which to choose. It is more important to pay attention to the similarities of the menus and not the differences. They all tell you to eat reasonably and smartly. Portion control is imperative just like not overdoing the unhealthy food. Although many argue what they look like, health and wellness are both critical.

When something unexpected happens, do not panic! Someone has gone through it before you, and they will deal with it after you as well. Remember that life with multiple sclerosis is the new normal so adapt and overcome. Do not give up doing things but find a workaround for you. Wear a cooling vest or carry a notepad for reminders. Just do not deprive yourself of life and take it one day at a time.

No matter what happens, keep a positive attitude and always wear a smile. When you need help, and you will require help, people will be willing to assist you if you are wearing a smile. Grumpy Gus’s get a bitter rejection when assistance is needed the most. Learn your limitations, but never give up. Live your life to the fullest using any adaptations required. Do not ruin a good today thinking about a bad yesterday, let it go.

Build a stable support system filled with family and friends who are supportive and understanding. Find a multiple sclerosis support group and in that group find a MS buddy. Stress and MS are mortal enemies so do not let them use your body as a battlefield. Avoid stress but if you cannot avoid it then find ways to manage your stress. Meditation, music, or religion might help.

I feel that these are some of the most important facts for those new to MS. Experience removes fear and builds your MS confidence. Remember: today you are better than yesterday but not as good as you will be tomorrow.

To thrive in this MS life you need three bones: a wishbone, a backbone, and a funny bone.

*Scott Cremeans lives in Central Ohio.  He is a US Marine who was diagnosed with RRMS in 2001 at the age of 27.  Scott has successfully managed his MS symptoms on his own with his faith, friends, and humor.  You can read more about his MS journey by visiting his blog www.myramblings.blog where he muses about life in the slow lane with his literary wit.

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About MSAA

The Multiple Sclerosis Association of America (MSAA) is a national nonprofit organization and leading resource for the entire MS community, improving lives today through vital services and support. MSAA provides free programs and services, such as: a Helpline with trained specialists; award-winning publications, including, The Motivator; MSAA’s nationally recognized website, featuring educational videos, webinars, and research updates; a mobile phone app, My MS Manager™; safety and mobility equipment products; cooling accessories for heat-sensitive individuals; MRI funding; My MSAA Community, a peer-to-peer online support forum; MS Conversations blog; a clinical trial search tool; podcasts; and more. For additional information, please visit www.mymsaa.org or call (800) 532-7667.

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