ARCHIVE # 4: 554 ARTICLES (NOV -SEPT 2006)
Dr. Timothy L. Vollmer


Chairman, Division of Neurology

Barrow Neurological Institute
St. Joseph's Hospital and Medical Center
My Educational Video on MS and MS Trials
Produced by www.MDhealthChannel.com
UNDER CONSTRUCTION
Visitors Since 03/2006
Click here to read messages from our MySpace Friends
HERE'S A FEW OF OUR 1,404 MySpace FRIENDS
CLICKING ON THE RED BUTTON BELOW COULD SAVE TOUR LIFE IF THERE'S A PROBLEM WITH A MS DRUG!
WE WILL SEND YOU BREAKING NEWS ON MS DRUGS IF YOU CLICK ON THE RED BUTTON BELOW.....Scroll down & read what we did last year...within 24 hours of the 1st death from Tysabri!
IMPORTANT: We filmed the video below within hours of the 1st death from Tysabri and e-mailed it to everyone who clicked the Flashing Red Button above!...WATCH THE VIDEO...THEN CLICK THE FLASHING RED BUTTON ABOVE!
Timothy L. Vollmer M.D.
Chairman, Division of Neurology
Barrow Neurological Institute
St. Joseph's Hospital and Medical Center


BARROW NEUROLOGICAL INSTITUTE'S
GRAND CANYON
RIM-RIM-HIKE


Organized by Dr. Robert F. Spetzler - Director, Barrow Neurological Institute

250 Photo-Slideshow


Click to view 1280 MS Walk photos!

"Join a trial at Barrow & receive all medication & study based procedures at no charge!"
Stan Swartz, CEO, The MD Health Channel

"WE PRODUCED THE FOLLOWING 9 VIDEOS FOR YOU!"
Simply click the "video" buttons below:

.

"MS Can Not
Rob You of Joy"
"I'm an M.D....my Mom has MS and we have a message for everyone."
- Jennifer Hartmark-Hill MD
Beverly Dean

"I've had MS for 2 years...this is the most important advice you'll ever hear."
"This is how I give myself a painless injection."
Heather Johnson

"A helpful tip for newly diagnosed MS patients."
"Important advice on choosing MS medication "
Joyce Moore

"OUR TEAM IS WORKING ON A CURE FOR MS"
Runtime: 54 sec
Runtime: 54 sec
Susan N. Rhodes
Multiple Sclerosis Research
Barrow Neurological Institute

"'The 2006 Barrow Neurological Institute at St. Joseph's Hospital MS "Walk on the Wild Side" raised more than $460,000 with 3,500 walkers! Click on the blue link above to view photos"

Chris Uithoven
President
National Multiple Sclerosis Society
Arizona Chapter


"THE MS SOCIETY OFFERS MANY PROGRAMS TO HELP...EVERYTHING FROM PILATES & SUPPORT GROUPS TO HORSEBACK RIDING"
Jerry Turner
Program Director
National Multiple Sclerosis Society
Arizona Chapter

Previious Posts

MS NEWS ARCHIVES: by week
September 2006  
October 2006  
November 2006  
July 2013  
April 2014  

This page is powered by Blogger. Isn't yours?

Sunday, November 12, 2006

 
{DEPRESSING STORY FROM THE UK} "Please help me to die" The Weston Mercury
"A MULTIPLE sclerosis sufferer is begging for someone to help him end his life after battling with the severely debilitating condition for nearly 20 years.

Every morning Neville Badger wakes up he says he makes the same determined wish - for someone to send him back to sleep for good.

The 45-year-old, of Vale Crescent, Weston, says he has lived a full life and wants to end it while it is still his choice, and is pleading for someone to help him find a way he can be euthanised.

He said: "I just want someone to tell me how to die. Why hang around for it to get worse?

"There will be a time where I won't be able to make decisions any more and I want someone to give me euthanasia while I can still have my say."

Mr Badger has asked everyone he can think of for advice, his doctor, social services, even the Samaritans. He has now turned to a solicitor for help but holds out little hope. Multiple sclerosis is a chronic degenerative disease of the nervous system.

"Everyone says I should go to Holland because it can happen there, but how am I supposed to get there? I don't have access to the internet and I can't find any information," he said.

"I've led a full life. I have had two good marriages and I've travelled to America and Iceland and met some fantastic people.

"I have to smoke cannabis all the time just to stay supple. I don't even like the stuff and I don't believe in it at all but I have to smoke it otherwise my body goes all stiff. It's the only thing that takes the pain away.

"I spend all my time either in bed or on a chair. It's not like I'm depressed, I was diagnosed when I was about 26 and I just want it over with now. It's no life and it's going to get worse.

"So much money is being thrown away caring for me. Social services has spent £12,000 on a bathroom I don't need, there's no point. I've got a £2,000 toilet which is a waste of money.

"I have to keep bothering the neighbours when I need help or fall out of my chair and it's not their job. I've got nothing left to live for."