Tuesday, July 31, 2007

BONANZA

The news broke and I put it on my list of topics. Today, as I read through my Google Reader choices, 27 out of the 30 items were about the genome breakthrough.

One item was about the Manchester Bike Tour and two told of a quest to rid the world of artificial sweeteners.

But the big news was identifying two genes common to MSers. This discovery makes the cause of MS a "mix of genes, environment, and immunology" and may lead to new treatment options.

Here are some choices of articles from around the world.

Don't expect a new pill tomorrow. These were two major research projects studying a large number of subjects, and it is widely heralded as a key factor, but there is more work to be done. Jonathan Haines, the director of the Center for Human Genetics Research at Vanderbilt University said, "The hope is that new knowledge will lead to the development of more targeted treatments."

To read the study as published in the New England Journal of Medicine, click here.

To read the study report in Nature Genetics, click here.

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Sunday, July 29, 2007

Leveling the MS Field in Europe

There are so many differences in needs, demands, opportunities, and treatment options among countries in the European Union. The European MS Platform (EMSP) is working to eliminate barriers to improve MSers quality of living.

For example, MSers treated in Poland include 1%, while in Sweden, approximately 50% of MS patients are treated. And while Ireland has 16 neurologists for 7000 MSers, Iceland has
18 neurologists to treat only 330 MSers. Wow.

The EMSP's mission is to exchange and disseminate information relating to multiple sclerosis considering all issues relevant to people affected by MS.


Read the current projects and scheduled events. One event, scheduled in Prague in October, will be hosted by the MS International Federation and the Czech MS Society with the European MS Platform. This is the first time an event of this type will be held in the Czech Republic, giving Czech MSers and medical professionals the opportunity to learn about current and future developments in living with MS.

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Resources

Aapo Halko is a Finnish mathematician who was diagnosed with MS as a young man in 1980. He has been collecting links to sites that have information of interest to MSers.

MS Crossroads has been available since 1994. There are MS sites, FDA approved MS drugs, MS in the news, support, tips, research, and more.

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Saturday, July 28, 2007

Here's Another Good One

I found this blog when she left a comment. She found me through Shirl. I found I recognized many of her commenters. But mainly, I enjoyed her posts.

Merelyme writes in a clear, poignant style about her MS experiences, symptoms, living with MS. Multiple Synchronicities & Sclerosis is definitely worth a visit. Be sure to pack a lunch because you will find yourself reading the previous post and the one before that and before that, too.

Click on her MS Diary link in the sidebar categories to read about the bully we all call MS. Keep reading about her diagnosis -- long, but familiar.

Good luck, Merelyme. Please keep writing for those of us who would like to keep reading.

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Thursday, July 26, 2007

Clarify the ADA

Today is an anniversary - seventeen years ago, Congress passed the Americans with Disabilities Act (ADA), and President George Bush signed the bill on July 26, 1990.

Today, Rep. Hoyer from Maryland and Rep. Sensenbrenner from Wisconsin are introducing the ADA Restoration Act of 2007 to clarify and strengthen legislation to eliminate discrimination of the disabled.

Following the examples set by African Americans in the Civil Rights era and by women in the Women's Movement, disabled people began working to correct problems after years of discrimination and devaluation. Discrimination in this case introduced new challenges and required opportunities for education, employment and even independent living.

The law was written very broadly and does not provide enough protection for individuals with disabilities.
MSers who manage their symptoms too well may not appear to be disabled enough to be covered by the ADA. In recent years, courts have been quick to side with employers; in effect saying people are not able to do a job but not disabled enough to qualify for ADA protection.

Urge your representative to co-sponsor and support this bill. If you do not know, click here to identify your representative and send an email that may include a personal story.

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Friday, July 20, 2007

The International Federation

Today I am thinking about the MS International Federation (MSIF). Of course we get regular notification of research around the world, but sometimes it's a good idea to visit the old faithful source of information, the MSIF web site.

There is basic information about the disease for the 2,500,000 people affected, particular symptoms and treatments, research and news from around the world. There are links to the MS societies in particular countries, so everyone can find help nearby.

There are stories of MSers and caregivers. The featured MSer for July is Dr. Hitaishi Weekrakoon from Sri Lanka.
The 2007 MSer is Ann Langley of Australia, and the 2007 caregiver is Susana Carballido Perdogon of Uruguay. But here's a delightful touch -- you can read diary entries from more than two thousand individual MSers, and you can even find diary contributors from your country or with similar symptoms and choose to correspond through email. In order to search through the diarists, you have to register.

Publications are available for download, including a comprehensive treatment guide. The current issue of MS Focus covers pain, but there are back issues available on other topics.

And because this is a truly international site, readers can change the text language into a choice of nine languages.

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Thursday, July 19, 2007

Sometimes You Just Don't See It

I have secondary progressive MS and the progression is slow. Some friends and family tell me they don't see much difference in my ability over the last several years. Maybe they are being kind and don't want to tell me if I look pathetic. Maybe the changes I feel are more the effort that goes into the daily routine. They don't see what I see.

Conversely, I don't see what they see.

I was reading Julie Stachwiak's excellent MS blog on About.com, and she suggests we MSers recruit our friends to tell us about symptoms when we may be unaware. Her examples include different size pupils and fuzzy thinking.

I can see how I might not realize when I repeat myself, but it never occurred to me to watch my pupils. When my left pupil is larger than the right one, my vision is probably not good enough to notice. I would never know, but my doctor might be interested.

Okay, friends, look me over. Do you see anything that looks a bit strange? Now that could be a dangerous question.

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Tuesday, July 17, 2007

MS Video



I found this on My Journey with MS, a blog I wrote about in February last year. She has changed her look since I wrote that first post and included several videos like this one as well as a play list for our listening pleasure. It is definitely worth a visit.

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Sunday, July 15, 2007

Goat Serum

It has been over a year since I first read about goat serum used to enhance nerve activity in MS.

For two years t
he MS Society has been asking for clinical trials to prove safety and efficacy before it is offered to the public. But there are 'roadshows' actively promoting the goat serum drug Aimspro.

Now there is concern that UK MSers are being seduced into buying the expensive treatment that has not been proven to be effective in treating MS. Daval, maker of Aimspro, is under investigation by the Medicines and Healthcare Products Regulatory Agency.

It all sounds pretty sleezy . . but, wait. There is an update. Two clinical trials are scheduled to start in October and a third is awaiting approval. They are targeting patients who have already proved resistant to current treatments. Maybe this goat serum is not so bad after all.

Research and Development are now the focus of Daval International. We'll, know more when the tests have been completed, but it sounds promising.

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Saturday, July 14, 2007

Coping with MS

How well you cope with your MS may be directly related to the information you received when you were first diagnosed.

Several Norwegian agencies, including the Competence Centre, the Centre for Movement Disorders, and the Centre for Behavioural Research joined together for a research project. They studied the relationship between information garnered in the early stages and the coping style used.

The result was that better information led to better coping with and living with MS. That made sense to me, but the really interesting thing was some of the data used to reach that conclusion. Almost half of the people studied were dissatisfied or very dissatisfied
with the information they were given at diagnosis.

People who were satisfied were less likely to deny their disease and more likely to seek more information. Hmmm. The better the information they get, the more they try to find out.

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