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Help coming for veterans with Lou Gehrig’s disease

by SUSANNAH FRAME / KING 5 News

Bio | Email | Follow: @SFrameK5

KING5.com

Posted on January 16, 2012 at 10:00 PM

Updated Tuesday, Jan 17 at 6:06 AM

LAKE STEVENS, Wash. - No one knows exactly why, but serving in the military can actually cause the progressive, fatal disease of ALS. Those who’ve served in any branch of the military are twice as likely to contract ALS as those with no military service.

Last year the KING 5 Investigators exposed how the Veteran's Administration (VA) was failing some vets with ALS by being slow to get them benefits such as pieces of medical equipment and grant money to adapt their homes for wheelchairs. Since those stories aired the VA has made a major rule change. Beginning January 19th, benefits should arrive much sooner.

Rich Knapton of Lake Stevens is a decorated Viet Nam veteran diagnosed with the disease who waited for months for items to help him get through his days, such as a hospital bed. And with ALS there's no time to waste. Rich's disease is progressing quickly. When KING reporters first met Knapton in November he was able to slowly walk with the aid of a walker. Now he’s lost his ability to walk at all. He’s lost mobility in his arm that still functions, which means he often needs help to eat. It’s getting harder to press the keys on his computer. And his throat muscles are weaker which causes him to choke on food.

“My legs don't work anymore. I’m a bit more depressed. I’ve grown weaker, and that’s frustrating,” said Knapton. “So you sit around and you wait, and you get weaker.”

That is the reality of ALS. It progressively destroys the cells that control muscle function. Eventually patients can't walk, talk or breathe. Just a year-and-a-half ago Knapton was jogging six miles, four times a week.

“It’s devastating to watch someone deteriorate. It's hard, very hard," said Knapton’s wife, Rietje Knapton.

KING 5 first interviewed the Knaptons as part of series on veterans with ALS who were having problems getting badly needed benefits from the Veteran's Administration (VA).
 
They’d been waiting for months for a motorized wheelchair and a hospital bed the VA promised were on the way.

"I may be dead in three months, so why is it taking so long?" said Rich Knapton in November.

Since that story aired the VA has stepped up. They delivered the wheelchair and the hospital bed. KING 5 viewers responded as well.

"Your viewers were wonderful. They just opened up their hearts and sent us cards or money or offers of beds and things like that. There are a lot of nice people out there." said Rich Knapton.

One hold-up for many veterans with ALS is the VA’s use of what's called a Schedule for Rating Disabilities; a disability rating system. Benefits are approved based on how disabled VA doctors consider the patient to be. A rating of 100% disabled is needed for expensive items like a wheelchair accessible van and grant money for home adaptations, such as the installation of a shower to accommodate a wheelchair.

In November the KING 5 Investigators aired a story about another veteran with ALS, Barry Mangan of Tacoma. Mangan died waiting for his benefits. For months he wasn't considered disabled enough to qualify for the money to adapt his home. Without the adaptations he couldn’t live at home with his family. He died alone in a VA nursing home.

"I was so upset that we couldn't get him home. That he could not die with his loved ones at his bedside," said his widow Debby Mangan.

That shouldn't happen again. The VA will now rate veterans with ALS 100 percent disabled upon the diagnosis. The change means veterans won’t have to be constantly re-evaluated to determine a rating and benefits should arrive much faster.

"We’re thrilled as an association,” said Kathy Holt, Board President of the ALS Association, Evergreen Chapter.

“Every vet will now not have to fight to get that additional compensation, will not have to go back and be re-evaluated and will not be constantly trying to catch up with the system," said Holt.

The automatic 100% disability rating doesn't necessarily mean all the wait times are over. Currently the Knaptons are waiting for a wheelchair accessible van and grant money to adapt their bathroom to make a shower that will accomodate Rich's wheelchair. It could be several months before those things arrive.

"It's such a devastating blow to be told you have ALS, and then to have them (the VA) drag their feet, so this is great. This will help," said Rich Knapton.

Since the KING reporters visited the Knaptons on January 5th, Rich's health has declined. He's been admitted to the hospital with breathing problems; a common ailment for those with ALS because of the deterioration of the diaphragm and other respiratory muscles.

 

 

 

 

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Comments: Displaying 1 - 5 of 5

gloski1947 said on January 17, 2012 at 7:35 PM

Thanks so much for this incredible, positive news for V.A. ALS patients. My brother was stricken with ALS, 31/2 years ago, and passed away 1 year later. The V.A. was a very slow, painstaking, frustrating process, for my brother Vic and all of our family, as we, with broken hearts, watched his rapid decline. Thankfully we had the Evergreen ALS Chapter for constant moral support and to help in getting the needed supplies. I can't say enough good things for them. Vic, was an incredible human being and even when he was no longer able to talk, he worked on a system to communicate with us. He used a lazed ligh,t up until his final days to comfort and encourage all of us, family, friends and care givers alike. The Toby Kieth song 'He taught us how to live and he taught us how to die". certainly applied to my brother Vic. He was a fantastic inspiration to all of us.

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theo980 said on January 17, 2012 at 12:15 PM

My sympathies to anyone that is diagnosed with this dreaded disease. My brother in law passed from ALS and the VA were dragging their feet until the day he died!

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bigdaddyof4 said on January 17, 2012 at 8:46 AM

While I applaud the efforts the folks of King5 are making, their really is little help on the way. The VA system is so bogged down in it's own antiquated red tape that veterans filing claims are regularly waiting over 15-16 months to get those claims decided. Even when a Veteran asks for "Expedited" status, they rarely get done in less than 10 months without congressional or presidential intervention. The politicians are quick to get the photo ops and sound bites proclaiming their support for veterans, but when it comes time to fund the programs and effect real change, they are nowhere to be found. Including our own Patty Murray. Her office is of little help when a veteran is having trouble traversing the system and she's Chairwoman of the Senate Veterans Affairs committee!! If the Veterans of this country followed up on their promises like the politicians have, we would all be speaking German, Japanese or the Queens English!

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regnrob said on January 17, 2012 at 12:46 AM

Bev, I am so sorry for your husband's passing. May you find strength in all around you during this difficult time. I knew of one individual, Captain Joho as many knew that passed from LGD, not too long ago actually. I can't imagine how his family has felt, and still don't. Only they must hope that this disease finally is erradicated. God Bless.

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BevSwartz said on January 16, 2012 at 11:01 PM

This is excellent news. Unfortunately, it was not in time for my husband. He was diagnosed with ALS in February 2011 and passed away in September. His progression was rapid. In addition to ALS my husband also had Frontotempural Dementioa (also service connected). The ALS and the FTD both progressed rapidly. VA didn't "get it." They kept thinking that we could run all over for all these appointments and evaluations that went nowhere. To date, they still haven't rated his lungs. At the time of diagnosis. His his lung capacity was 44%, later it was 34% sitting up and 24% laying down. He was unable to breathe because of ALS, he died because he he couldnt breathe, yet they still can't rate his lungs. It was a horrible ordeal. One that I wouldn't wish on a healthy person, let alone one that is dying with every breath they take. Shame on the VA. They have forgotten that there are real people involved and not just the papers that they are pushing around their desks.

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