Thursday, December 15, 2005

Murderball



I recently watched the acclaimed documentary Murderball and what a great show! Murderball follows the growth of Quad Rugby as it's risen to become an Olympic sport. The members of the US and Canadian teams are the main focus as the film lays out many different interesting story lines.

The thing about this movie I really like is the realistic and honest portrayal of active adults with disabilities. It's not a pity filled "oh poor me" movie but rather a film about people living life and doing what they want.

This film not only deals with athletic competition but with the everyday life of these athletes. It shows them as regular guys who like to party, have fun, and just plain enjoy life. Alot of the quad rugby guys have girlfriends and wives and love/relationship issues are portrayed in a open and honest way.

I hope many people with disabilities and able bodied folks check out Murderball. This film shatters many misconceptions about disability and it shows that people with disabilities can do anything they choose.

If you wanna check out a little bit of Murderball visit http://www.murderballmovie.com

Peace,

Mark AKA The Nodakwheeler

Thursday, December 01, 2005

Winter/IVUN/Mark S.

The winter season has finally hit North Dakota this week. A combination blizzard & ice storm wreaked havoc on parts of the region. Oh well when you've lived in the northern plains, winter is just something that's taken in stride. The scenery sure is pretty with our first fallen snow and the feeling of the holiday season is in the air.

This week the International Ventilator Users Network put my recent newspaper article on the proposed Medicaid cuts on their website. To view the actual article please visit http://www.post-polio.org/ivun/images/BoatmanArticle.jpg It has been great to get the truth out there on the things that could devastate the lives of the poor and people with disabilities in this country. We must keep fighting and make the politicians accountable for their actions. The time for change is here and my hope is the 2006 election will bring that.

On Monday, I sadly lost a dear friend. My friend Mark Schager lost his strong and brave fight with Duchenne MD at the age of 38. He proved the medical establishment wrong by showing people with Duchenne's are living much longer quality lives. Mark had a great, funny, and intelligent personality that touched my life as well as many others.

Mark thanks for showing many of us with Duchenne's how to live strong and never give up the fight. Peaceful rest my dear friend.

The Nodakwheeler

Sunday, November 13, 2005

College Trip

Last Thursday, I made a trip over to Jamestown College to speak to the junior class of the nursing program. I spoke about what it's been like to live as a ventilator user with muscular dystrophy.

It was a unique experience to be able to share my perspectives with these future nurses. As a person with a disability, I believe it's important to educate the people around us in the communities where we live. Having a disability is just part of living life and able bodied folks need to know that we are just like them. We have the same goals, dreams, hopes, and fears as they do.

By speaking to these nursing students, I truly believe a difference is being made. It's a small step towards people with disabilities being seen for whats inside instead of outside appearances.

Mark

Thursday, November 10, 2005

In The News

On Tuesday the Jamestown Sun featured an article on my concerns over the proposed Medicaid cuts. It was a great opportunity to inform my community about the severe impact these cuts could have on folks like me and countless people with disabilities across this Nation. The complete text of the article is below.

Peace,

Mark


Boatman Concerned About Cuts

By David Maack
The Jamestown Sun

11/8/05

For Mark Boatman, the issue of Medicaid funding cuts raises life and death concerns. He has been on a ventilator since February 2003 because he has Duchenne muscular dystrophy. The Bush administration is proposing significant cuts in the Medicaid budget, a proposition that concerns Boatman over the potential effect of those cuts on people with disabilities.
The latest figures from Sen. Byron Dorgan’s office are proposed cuts of $4.285 billion from Medicaid between 2006 and 2010 and $14.184 billion over 10 years. The reconciliation bill is being considered in the Senate.

‘If Medicaid is cut at all, it will be difficult to get the things I need to live and have quality of life. Medicaid cuts would also jeopardize advancing the growth of community-based care options,” Boatman said.

“It's difficult now to get things covered under Medicaid.  Some examples of this is getting needed medical equipment and repairs done to wheelchairs and other vital items.  The money in Medicaid is stretched thin now.  I fear what will happen if that situation gets more critical,” he added.

Boatman serves on the consumer advisory committee for International Ventilator Users Network. The group recently posted a resolution, which may be located at www.post-polio.org. The resolution calls on government officials, policy makers and advocacy groups to ensure the basic rights of ventilator users to “live, to be healthy and to remain free in the community as contributing members of society.” It also requests support for Medicaid entitlements for those with disabilities, participation by those with disabilities in developing Medicaid and other health-related policies and more effort into eliminating bureaucratic waste and provider abuse.

“We have to have the money to protect our equipment and services,” Boatman said. “We need to keep living.” He said a number of states are either not funding ventilators, or are requiring those on ventilators to live in nursing homes in order to have the life-preserving machinery provided. The Supreme Court ruled in the 1999 Olmstead case that people with disabilities must be provided for in the least restrictive manner. Forcing people on ventilators to live in nursing homes is a violation of that ruling. It isn’t that difficult to train someone on the care of a ventilator and the person using it, he said.
“The saddest thing about using a ventilator is people have over-complicated it. It’s just a piece of equipment,” Boatman said.

But community care, or caring for someone in his or her home, also costs money.
“Our states need to put more money into these programs. It’s much less expensive to do community care than nursing home care. North Dakota spends 95 percent of its (Medicaid) funds in nursing home care, 5 percent care in communities,” Boatman said.

Boatman was diagnosed with Duchenne muscular dystrophy when he was a young child. At that time a person with that diagnosis was unlike to live past his teenage years. Boatman turned 30 in August. With a ventilator, he expects to live for several more years and would prefer to be someplace other than a nursing home. He has petitioned the state Human Services Department for home care.

Boatman recently opened his own Web site, http://nodakwheeler.blogspot.com/. He discusses a number of issues of interest to those with disabilities, or those interested in learning more.

If cuts to Medicaid are to be eliminated and reversed, it will be up to Congress to recognize the need. Sen. Byron Dorgan, D-N.D., is aware of the proposed cuts. “They’re cutting from the level of need,” Dorgan said in a recent telephone interview from Washington, D.C. “If you cut from that, you’re cutting from poor people.” Dorgan said that if the tax cuts President Bush asked for and got from Congress for people making more than $1 million a year was eliminated, that money would be more than enough to eliminate the cuts in Medicaid. Whether those cuts in Medicaid can be reversed or not is uncertain at the present time, he said. The president and many members of Congress favor the cuts.