Monthly Archives: April 2011

My Story

National Multiple Sclerosis Society,Ohio Buckeye Chapter

Established in 1953, the Chapter is an important part of a nationwide network that advances the Society’s mission to achieve a world free of multiple sclerosis. We provide quality programs and services to over 10,000 Ohioans living with MS and their families in a 38-county area. Areas served include the Akron, Cleveland, Columbus and Youngstown metropolitan areas as well as all Central and Eastern Ohio counties. Our two offices are located in Independence and Worthington.  

Northeast Ohio
6155 Rockside Rd., Suite 202
Independence, OH 44131

Central & Southeast Ohio
651G Lakeview Plaza Blvd.
Worthington, OH 43085


National Multiple Sclerosis Society Ohio Buckeye Chapter Diagnosed with MS in 1987

Living with MS for 14 years prior to diagnosis

This is my story…

Elizabeth Thompson

What is your connection to multiple sclerosis?

I have multiple sclerosis. I am a volunteer for the National MS Society.

How has MS impacted your life?

The diagnosis of MS in 1987 gave a name to the strange things happening to me since at least 1973. Numbness, poor balance, repeated falls, vision problems and fatigue are the main issues I deal with. I was living with MS long before there was any medication proven to slow the progression of the disease. Research has now allowed four or five medications on the market for us with MS. I have used three of them settling on Copaxone almost four years ago. I even became an advocate for Teva Neuroscience, makers of Copaxone, so I could help others with MS understand the value of taking daily injections to stave off the progression of this unpredictable disease. I now use a cane, walker, or power chair, depending on the situation. In 2004, I went on Social Security Disability after working all my adult life. I was 54 at the time. It was a tough decision but now I can better manage my disease and advocate for others who have no voice in the matters that relate to us. MS slowed me down and took away some simple pleasures such as taking a walk outside or any physical activity. But I have learned to adapt and adjust. I refuse to let MS make me stop moving or living a full life.

Are you receiving or have received assistance from any services or programs?

I have received assistance from Transportation Services (COTA, Metro RTS, SCAT).

Have you experienced issues with any services or programs? If so, which ones?

I have experienced issues with caregiving, employment, home care services, medications and prescriptions, transportation, and Social Security.

Please tell us about the issue.

The Ohio Buckeye Chapter of the National Multiple Sclerosis Society provided caregiving for me two times. After two separate falls where I broke a wrist and had surgery, they provided assistance for me at home. It was wonderful and I am very grateful. Prior to going on Social Security Disability, some employers had little patience for the limitations that MS caused.

I learned to self-advocate but in the late 90s, one employer was going to let me go but I was able to leave on my own terms. The issues with medication were finding the right MS medication for me that didn’t make me sick. I have done that but now when my husband retires in April I will no longer have his insurance and will have to deal with the donut hole costs using Medicare. I am in the process of setting up assistance through Teva but nothing is final at this time.

What else should we know about your unique story?

As a result of going deaf since childhood, non-MS related, and being deaf by 50 and receiving a cochlear implant, I learned to self-advocate. When I was diagnosed with MS, these experiences made my ability to advocate and deal with MS a bit easier since it was familiar. So with the work world, I was deaf and had MS: not a great combination but just prior to my first implant, I was a reporter for Suburban News Publications. They took a chance on me, worked with me and I succeeded. I like to think that others can do the same in their fields of interest if we continue to bring awareness to the public and teach people to advocate for themselves.

Every person with MS has a unique story because MS is different for each person. I have been blessed with a supportive family, church and friends. Many don’t have even part of that. My story is unique because of that. I am a writer and advocate for people with MS every way I can hoping to reach the public with knowledge of MS and how it affects the lives of those living with it.

Thank you for listening to my story!


® • 800.344.4867


There’s more to those with multiple sclerosis

Published: Wednesday, March 30, 2011 5:40 PM EDT
Suburban News Publications

Every time my legs go numb or I stumble when I walk, I am reminded I have multiple sclerosis.

My body reminds me daily that the messages to my brain are disrupted.

MS is a central nervous system disease with no known cause or cure. Symptoms range from numbness, fatigue, vision loss and pain to the worst-case scenario of paralysis.

March is MS Awareness Month. The estimated 20,000 adult Ohioans and 400,000 Americans do not need a specific month to be aware they have MS. The public does need to understand what a diagnosis of MS can mean to a person and everyone in his or her lives.

The number is growing as one person an hour is diagnosed with MS. Between 8,000-10,000 children younger than 18 have MS.

Ohio is the only state that recognizes the entire month of March for MS Awareness. This is the five-year anniversary of the legislation passed unanimously to recognize the entire month. Thanks to State Rep. Kenny Yuko (D-7th District), also living with MS, who introduced House Bill 379.

On March 22, members from all around Ohio met with legislators at the Statehouse to discuss issues related to people with MS. Planning for the Walk MS on April 16 is in full swing. My team, Thompson’s Trekkers is one of many teams raising funds for the National MS Society.

Fundraising is mandatory to provide resources for people with MS and to support research. Ohio State University and the Cleveland Clinic each received a grant last year for researching MS.

Advocating person by person is an ongoing event.

The word advocate has many synonyms, including supporter, promoter, sponsor, believer, campaigner and activist. When we present ourselves in an honest, positive way in public or in private, we become advocates.

While I move through a store using a provided scooter, for which I am thankful, I realize I need more space than a person with a regular shopping cart. I smile, wait patiently as others move about and say, “Excuse me,” and “Thank you,” when people either need to move or have accommodated me in some way. If someone offers to get something from the shelf for me, I let them!

Many people do not know how to react to someone using a cane, walker or wheelchair. This is true, especially if you “look normal,” and as many with MS have heard, “But you look fine.” We are fine — we just have MS. So I teach and help others understand.

There is more to people with MS than their disease. By sharing, laughing, helping any way we can, moving the best we can and taking care of ourselves so we can do things that make life worth living, we are advocating and raising awareness of MS.

Then people will look past the cane, walker or wheelchair, the slurred speech or wobbly gait, and see the person first. Then we have accomplished true MS awareness and life goes on as it does every year — only better.

For more information about MS or events like the Walk MS, contact the Ohio Buckeye Chapter of the National MS Society at 800-344-4867 or

Liz Thompson is a freelance writer and former SNP reporter who lives in Grove City with her husband, Bob.