MS Strength

Within every Multiple Sclerosis Patient there Lies an Indomitable Strength.

Archive for the ‘MS Assistive Devices’ Category

MSAA: Multiple Sclerosis Association of America

Posted by Jen On April - 15 - 2009

A great multiple sclerosis resource has been around since 1970: the Multiple Sclerosis Association of America (MSAA.) Headquartered in Cherry Hill, New Jersey, the association has various regional offices throughout the United States and its main functions are to inform, empower, and assist MS patients and their families/friends. The following are some of the MSAA’s main services:

Programs and Services:

This is a link to such services as a toll-free telephone helpline, reassurance calls, a lending library, information about support groups, events and classes, an MRI assistance fund, information about barrier-free housing, an equipment (including cooling devices) lending service, and program applications.

News Center:

Access the latest multiple sclerosis information here. Learn more about the MSAA, find out about current research, MS-related organizations, frequently asked questions (FAQ’s), and access the MSAA’s news archive.

MSAA Publications:

The Multiple Sclerosis Association of America has a quarterly, free publication: The Motivator. It also has various, free booklets and brochures that cover such topics as depression, complementary and alternative medicines, wellness tips, cooling devices, the MRI assistance program, and MSAA’s services and programs.

Life Lessons: MSAA’s Life Coaching Blog:

This is a fairly new component to the MSAA’s website. A group therapist and life coach provides life coaching sessions (via telephone) and she writes about helpful tips and tricks to live fully and realistically with multiple sclerosis.

Regional Offices:

Contact an MSAA regional branch near you.

Website that Focuses on MS Technology

Posted by Jen On March - 31 - 2009

I recently received this email about a website that connects MS patients with technology solutions to better adapt to daily living. Check it out:

Hello Jen,

My name is Ellen Kampel – I work for Microsoft and am a person living with multiple sclerosis (MS). I am reaching out to you on behalf of a great program in which I’m involved: The MS Technology Collaborative. The Collaborative is a partnership between the National MS Society, Microsoft and Bayer HealthCare Pharmaceuticals, dedicated to connecting people living with MS to technologies that can help them overcome MS-related challenges and live better.

The goal of the Collaborative is to provide technology solutions for people living with MS, many of which are affordable or free. Our Web site, www.MyMSMyWay.com, offers an online interactive tool called “Snapshot” that prompts users to answer a series of questions, after which they receive a customized report with technology solutions specific to each person and his or her particular challenges. We also offer technology tips submitted by members of the MS community, a monthly column that I write with a leading accessible technology expert, and information on the types of technology available.

Lastly, I wanted to share with you a bit of a preview about our newest and most exciting initiative – we’re in the process of building a free online game that addresses the cognitive challenges of people living with MS. The game will provide cognitive exercises that target some of the main cognitive challenges faced by the MS community. It’s being developed in consultation with individuals living with MS as well as medical experts who specialize in researching and treating this condition.

With so many people finding strength and courage through your blog, I thought that both you and your readers might be interested in the resources available at MyMSMyWay.com.

I’d also like to invite you to be one of the first to preview our game this spring. Do you think that you’d be interested in reviewing the game prior to its official launch and providing your feedback? If so, please let me know. I’d love to have you involved in our efforts.

Thanks for your time, and I look forward to hearing from you soon.

Best,
Ellen Kampel

Keeping an MS Medical Journal

Posted by Jen On February - 23 - 2009

When I first developed multiple sclerosis, it was so vague and weird that I couldn’t quite describe the sensations to others, particularly to my family and friends. How do you explain fleeting neurological symptoms that sound like you’re having a stroke? Explaining to my then-primary doctor what was going on seemed even more challenging: he wanted to know WHAT kind of numbness I had. Did it feel like pins-and-needles or did the area lack ALL feeling? When did it come and when did it go? Was it restricting any of my activities and did it ever become painful? At this point I began a medical journal where I logged symptoms, durations, my feelings about these symptoms, dates, things that worsened these symptoms and so on. This journal has become my guide to my history with multiple sclerosis and a basic reference that I bring along with me to my doctors’ visits.

Keeping an MS medical journal is easy. Here’s what I find helpful:

Narrow a Medical Journal Down to One Topic

If you have more than one ailment— many of us do— then separate the problems into different journals within a notebook. Keep MS information in one area and (for example) low blood sugar, or hypoglycemia, in another section. Sometimes it’s difficult to tell where symptoms are coming from (particularly in the case of multiple autoimmune diseases) but if the illnesses are unrelated try to keep them unrelated in the journal to focus on what is precisely going on with each illness.

Be as Specific as Possible

I look back at my medical journal and my memory is jogged: I had this episode of vertigo at this point in time, I took this medication, my neurologist said such-and-such, the vertigo tapered off at such-and-such time. I would never remember this on my own and I’m glad that I took such descriptive details. Referencing entries with specific dates, durations, performed tests, my feelings about the symptoms, what medications I took, whether said medications helped or did nothing, and my doctors’ opinions has helped me to keep a mental idea of my MS journey thus far. It’s still of course mysterious, but I feel a little more in control of what’s going on.

Regularly Update Your Status, Including the Good Times

Being well is a point of reference within the journal. It’s important to document this as part of the journey. Just checking in every few months keeps the journal updated and current.

Record Feelings about the Attacks and the Symptoms

I was able to see a pattern of anxiety and depression which I shared with my therapist because of my noted feelings within my medical journal. The psychological elements are definitely a part of the greater whole.

Remember to Bring the Medical Journal Along with You to Doctors’ Visits

This journal aids not only you but your treatment team in better knowing your disease history and present status. You can also immediately record what your doctors say, requesting proper spellings and exact information. Sometimes it all sounds like mumbo jumbo if you wait until you get home.

Stick to the Basics

I don’t know about you but I prefer to keep this sort of journal in a standard wide-ruled notebook. I don’t get fancy and I keep to the basics of my case. This isn’t my autobiography; it’s a book of facts I need to keep. A basic notebook works for me.