Category Archives: MS and Assistive Devices

MSAA: Multiple Sclerosis Association of America

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

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

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.

Traveling with a Medical Condition

***I’m off to Las Vegas for a few days: a much-needed break from the “slow” life. I wrote this traveling tips article a few years ago, but it still holds true. I’ve found many of these ideas to be very useful and energy-conserving and I hope they help you too.

I’m Vegas, baby!.. LUCK be a LADY….

When traveling with MS or any medical condition, it’s good to take steps to make the journey as smooth and enjoyable as possible. Follow some or all of these ideas on your next trip to save time and energy. The list is not exhaustive, but it pinpoints basic tricks that can help those with medical conditions get the most out of traveling:

Pre-Trip

  • Leave your destination phone number and address with a friend or family member
  • Get doctors’ notes for any injectable or questionable medications you bring on a train or airplane
  • Carry a small, portable sharps container for injectables
  • Keep all meds and prescriptions in your carry-on case in the event that your luggage is lost
  • Bring extra prescriptions in case you lose your medications en route
  • Give yourself extra time to avoid unnecessary stress and fatigue
  • Use luggage with wheels/ long handles to avoid carrying it from place to place
  • Use the bathroom right before boarding the plane or train (airlines make you sit with the seatbelt on for a while after take-off)
  • Avoid excess drinking of any liquids before boarding or going on a road trip and also just before landing
  • Make use of assistive devices such as canes and wheel chairs to avoid fatigue
  • Ask for seats near an exit if you are physically handicapped

During Trip

  • Use assistive devices to avoid fatigue on such journeys as nature walks, amusement parks, and all-day excursions
  • Keep hydrated to avoid fatigue
  • Avoid prolonged sun exposure
  • Keep medications with you in a convenient place such as a purse or backpack
  • Know where local hospitals are
  • Ask theme parks if there are special services for those with disabilities
  • Wear ID bracelets that indicate medical conditions (example: epilepsy) in case of emergency
  • Be prepared and patient enough to make pit-stops— Hey, at least you’re out there!

Post-Trip

  • Repack early for less stress
  • Do the same things that are listed for the pre-trip
  • Have your taxi or ride pull right up to the curb of the airport or train station for luggage transport
  • Have your ride come nice and early
  • If there are baggage porters, utilize them (remember to tip well!)

Keep an open mind when traveling and you can have a fantastic time. Just because you have a medical condition, you don’t have to miss out on the fun and adventures of traveling. Give yourself extra time, know the information about your destination, and utilize any assistive devices to make your journey easier. Don’t be hard on yourself and expect perfection because even those who are in “perfect health” sometimes need assistance. Lastly, ENJOY!

Large-Print and Audio Books for MS Patients

I often find myself listening to audio versions of my favorite print books. As an MS patient, I have some mild cognitive impairments that make me easily distracted when trying to read. My attention span has gotten shorter as the years have gone by, and instead of throwing my hands up in frustration and giving up on reading, I pop a CD or cassette book into my portable stereo and put on a headset. This has worked well for me because I can really only concentrate on the speaker as I’m relaxing on my bed. I’ve found this works well for any abstract reads where I have to give my full attention to the subject matter.

Audio and large-print books are also great for those with residual visual impairments due to optic neuritis or double vision. Large-print books allow for reading with less eye strain and audio books eliminate this hindrance. Libraries are good, free sources for both of these options. Many libraries have extensive sections for each, with both popular and not-so-known selections available. If you are unable to get yourself out to the library, many systems will deliver library materials to your home.

Library Books for Homebound MS Patrons

I’ve been volunteering at a few library branches for the past five years and one of their greatest free services is a “home borrowers” program for homebound library patrons. Volunteers and staff make deliveries of print books, audio books, DVDs, CDs, periodicals, and pretty much anything else someone can borrow as an in-person patron. Volunteers are often matched with patrons to establish consistent, steady bonds when bringing books to and from their homes. Volunteers also provide services to managed-care facilities, usually delivering items to several people. If the program involves staff, a library “bookmobile” or van provides the transportation. No need to worry about returning library materials: volunteers or staff return to pick them up.

*To learn more about the home delivery of library materials, contact your local library branch.

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