VA: All veterans with ALS eligible for benefits
Late last month the U.S. Department of Veterans Affairs (VA) published new regulations granting military veterans diagnosed with amyotrophic lateral sclerosis, also called ALS or Lou Gehrig’s Disease, full access to health and disability benefits. The new rule went in effect immediately and covers all veterans serving at least 90 consecutive days no matter where or when they served. ALS is a progressive neuromuscular disease that affects about 20,000 to 30,000 people of all races and ethnicities in the United States, according to the National Academies of Science. It causes degeneration of nerve cells in the brain and spinal cord that leads to muscle weakness, muscle atrophy, paralysis, and eventually the patient may lose the ability to swallow or breathe. Life expectancy after diagnosis is generally two to five years after diagnosis. However, there have been cases where ALS stops progressing and where symptoms have reversed.
“Veterans living with Lou Gehrig’s Disease now have one less hurdle to face on an already difficult road,” said Steve Gibson, the ALS Association’s vice president of government relations and public affairs.
Citing the high incidence of ALS among Persian Gulf War veterans who were diagnosed with the disease at younger ages than had been typical, the VA granted service connected benefits to veterans of the 1990-91 war. Veterans with ALS, advocacy groups including the ALS Association, and some members of the military and Congress continued to push to designate ALS as a presumption of service connection and to expand benefits for all war veterans.
The VA cited a compilation of medical studies, Amyotrophic Lateral Sclerosis in Veterans: Review of the Scientific Literature, in concluding that “there is limited and suggestive evidence of an association between military service and later development of ALS.” The report, completed by the National Academies of Science at the behest of the VA, was released in November 2006.
According to the studies, military veterans within the last century are nearly twice as likely to develop ALS as those with no history of military service, regardless of where or when they served in the military.
“Veterans are developing ALS in rates higher than the general population, and it was appropriate to take action,” VA Secretary James Peake said in a written statement. “ALS is a disease that progresses rapidly, once it is diagnosed. There simply isn’t time to develop the evidence needed to support compensation claims before many veterans become seriously ill. My decision will make those claims much easier to process, and for them and their families to receive the compensation they have earned through their service to our Nation.”
The VA said it will try to identify and contact veterans with ALS, including those whose claims were previously denied.
Why ALS occurs more often in veterans is unclear but anthrax vaccine may play a role
Bob Evans, a reporter with the Daily Press, wrote about the anthrax vaccine-ALS connection in a December 2005 article (‘Young’ men got Lou Gehrig’s disease, Navy officers Denis Army and Brody Prieto were hit by amyotrophic lateral sclerosis soon after their shots). Evans wrote: “Both died thinking that their anthrax shots triggered - or caused - this always-fatal illness, despite military doctors’ refusal to consider the possibility, their widows say.”
Both veterans also received anthrax from vaccine batches containing squalene, which, while boosting the potency of vaccines, caused symptoms consistent with “Gulf War Syndrome,” according to a 2002 study. Squalene is also known to cause severe autoimmune problems in laboratory animals. The Army experimented with vaccines containing squalene for 50 years, Evans found.
Todd Sanders of Kingsport, TN, told a reporter last year that he and his friend, another among the nearly 2 million Gulf War soldiers to receive the anthrax vaccine, believed their illness was caused by the vaccine. ”Sanders said he believes — and that Robertson believed — their condition was caused by the anthrax vaccine, which made him sick and almost caused him to pass out when he first received it,” wrote Rick Wagner.
Other studies have looked at the possible role of genetics, physical activity, environmental toxins, trauma, chemical and alcohol use, or a combination of these factors, to explain the high incidence of ALS in military veterans. Aside from determining that 5 to 10 percent of cases are inherited, these study results have been, for the most part, inconclusive.
National ALS Registries
The VA discontinued the National Registration of Veterans with ALS in September 2007. Between 2003 and 2007 the registry collected data, including DNA samples to be made available for ALS research, from 2,090 ALS patients or their survivors. However, a national ALS registry bill was signed into law on Oct. 8 of this year. The registry is to be maintained by the Centers for Disease Control and Prevention. The law requires that an advisory board for the registry include at least one member from the VA, and that the CDC share and “coordinate with” state, local and federal registries, including the VA.
Recommended reading:
Afflicted with Lou Gehrig’s disease, they fight for military benefits as science hunts the cause , Josh Mitchell, Baltimore Sun, May 19, 2008
ALS in the Military: Unexpected Consequences of Military Service, ALS Association, May 13, 2008
Department of Veteran’s Affairs disability compensation program www.va.gov
Gulf War veteran believes illness related to anthrax vaccine, Rick Wagner, Kingsport (TN) Times-News, Sept. 3, 2007
Presumption of Service Connection for Amyotrophic Lateral Sclerosis, Final Ruling, Federal Register
‘Young’ men got Lou Gehrig’s disease, Bob Evans, Daily Press, December 5, 2005
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My husband, kenneth f. shearer died from ALS on 09/04/2008. He is a US Navy Vet and I need to know how to get more info about ALS being service related and are there any spousal benefits avail
Anne,
I'm so sorry for your loss. A dear friend lost her father to ALS a couple years ago. The ALS Association has a whole section on the military and ALS. http://tinyurl.com/56jqfs Go to their site, call them and arm yourself with info. Good luck.
My husband served as a corpsman in the Viet Nam War. He was assigned to the USS Okinawa (hospital ship). He started having memory problems (short term) in 2001. He worked in a Psychiatric Facility in Pittsburgh and was also a Paramedic and taught EMS/Advanced Life Support. In 2002 He had a CT of the brain which showed atrophy indicative to Alzheimer's. To me (I am a nurse) he did not present with the typical Alzheimers behavior. I did not accept that diagnosis and sought additional medical testing/neuro/etc. for him. He then was diagnosed with frontal/temporal lobe dementia and the doctor made reference to his being in contact with agent orange while in Viet Nam. Gary continued to regress, lose weight, had difficulty swallowing and in 2006 was unable to perform his job thus, we applied for disability for him. Gary used to weigh 232 lbs. and was in excellent physical shape (worked out, ran, etc.) His weight kept dropping drastically and he got to the point he was unable to speak in sentences, was unable to read, write, ambulate without difficulty, was incontinent. In otherwards, he was total care. I had hospice in for him plus, I took out loans for daily attendants to come into the home (I work full-time). I had applied to the VA on 4 separate occassions for the Aid and attendant stipend but, was turned down due to the fact that Gary never c/o these symptoms while on active duty. His MD had ordered EMG studies on him to r/o ALS. Gary had the test and the results were positive for motor neuron disease. Gary passed away on February 6, 2008 with cause of death being frontal/temporal lobe dementi - motor neuron disease his weight at his death was 104 lbs.. My husband was a VERY PROUD VETERAN and gave all to his country. I am angry and saddened that he received NO HELP from the VA while he was still alive. I now am told that ALS is a compensatable service related disease and I am entitled to compensation. During Gary's life, the VA abandoned him and I feel that it will be this way with me. Who or where shall I turn to for assistance in receiviing benefits. The Order of the Purple Heart did submit the ALS info to the VA in April 2009. I have not heard anything as of this date. Gary died at age 61 as a result of Agent Orange and other herbicides contacted in Viet Nam. I lost my husband, my children lost their dad and everyone who ever had any contact with Gary lost a wonderful, giving human being. Will look forward to your reply. Thank you, Rosemarie
Rosemarie, please send your email address to fleshandstone @ gmail dot com and I can forward it to another veteran with an Agent Orange-related illness who will be able to give you better advice than I can. Also visit http://www.VietNow.com, a resource for Vietnam veterans and their families. Thanks for sharing your experience. KS
Just had a diagnosis of ALS yesterday and will see one more Specialist Friday. I served in the Army from 1972 to 1975. I'm wondering if there is any link to ALS and the nerve gas training most received and was asked to take off our masks and take one breath for effects?
My first husband, Ronald E. Korsman, died Nov. 19, 1994 from ALS. He was 61 years old. He had served in Korea from 1953 to 1955. I don't know if their are any benefits due. I just wanat to say what a horrible disease this is. When he first started losing weight, he was so proud of himself. Then when one foot started dragging, I knew something was wrong. He was diagnosed wwith ALS and that was the worst day of our lives. The disease progressed very fast. He was then a retired postal carrier. Because Social Security was not taken out of their checks at that time, there was no help anywhere. When he was bedridden, I took out a loan to pay in-home hospice. All hospice and medication came out of pocket. He had a feeding tube and after he managed to pull it out for the third time, I knew that he did not want it in any more.It was like he had pulled his own plug,
I would not wish this disease on anyone. It is a very cruel and demeaning disease. It is horrible to watch someone you love die from ALS.I would just like to know if there are any benefits from this time.I will be waiting for your reply.
Yours truly,
Jean Korsman Davis
I am a Viet Nam era vet (1967-1969)who was diagnosed with PLS (Primary Lateral Sclerosis) about two years ago. This disease is covered under ALS and I'm wondering if it will also allow me to qualify for VA benefits including disability.
Veterans with ALS or survivors of a veteran of any service who died of ALS in the Long Beach, or Orange County California area needing help with filing for benefits, especially RETROACTIVE benefits (which must be filed for BEFORE September 23, 2009), contact Mike At AMVET at the Long Beach Veterans Hospital 562-826-5915. Room W210 Bldg 126. 8AM to 3PM M-F. Take marriage certificate, death certificate, separation papers. If you file AFTER 09/23/2009, you will lose one year of benefits. Please tell all veterans and survivors you know in case they know anyone who qualifies.
My husband was a navy vet and died of ALS on January 2, 1998. I have applied for DIC but I keep hearing and reading different versions of eligibility. Several have mentioned boots on the ground. Several things that I have read indicate that with ALS it is not a requirement. Does anyone know for sure?
I have to see five Neurologist's and I have Dysathria,and most of them said I had a stroke,they last one said I had possible Als. He did some tests inserting needles into the muscles of my legs.I have an appointment with him the 11th of March for follow-up tests. Iam a retired veteran of the Vietnam War Era.
My husband just passed away on March 5, 2010 from ALS. He was an Air Force Vet, Viet Nam era veteran. He probably had the condition for 7 years, but wasn't officially diagnosed until January 2007. The VA does grant service-connected disability benefits to veterans with ALS and there is a spouse survival benefit as well.
My dad passed away from ALS in 2004. He served in the Navy during Vietnam. My mom received a call from an advocate and qualified for this benefit. Please apply if you feel you qualify.
My husband, Vietnam Era,was diagnosed with ALS,12/08.Passed 2/10.Devastating diagnosis ,horrible disease.The best thing we did was got a representative with the PVA to be our advocate.That is what they are good at,and paralyzed is what our veterans become .Paralyzed Veterans of America know the benefits due you, and help you with all processes.They are in Washington when policies are written concerning your rights to medical care, equipment and assistance.Read the Publication on-line,read your Benefit Handbook,contact the ALS assoc.,and they will send you informative and educational materials about ALS to help you know the stages of progression of this fatal disease our veterans lives are stolen from them even 40 and more years after serving their country.Where are the Purple Hearts and added names to the Memorial Wall?
My husband served in the Chu Lai area (Americal Div.) in Vietnam 1970 - was forward observer with the infantry and then on several remote fire bases.
He was diagnosed with frontotemporal dementia in 2006 after searching for years for answers to his mental confusion, loss of executive function, inability to learn new things. He wasn't diagnosed until his speech problems were so evident. He was fired from his professional job in 2003.
So far he has shown no signs of motor neuron disease but I wonder if FTD isn't part and parcel of neurological atrophy caused by Agent Orange.
VA turned our claim down saying there is no connection established between dementia and agent orange. Hmm. Any thoughts?
My husband died Nov 1995, and he was in the army, and was stationed in France. in 1964 - 1966 I have applied for widow's benefits, and have not remarried. He was 53 at the time of his death. He also lost weight, and started stumbling and couldn't talk.
Receiving benefits for ALS since September 2008, diagnosed with disease in 1992 at VA hospital. Filed a notice of disagreement because I feel I am due from 1992, VA hospital disagnosed in 1992, any help trying to get the additional 16 yrs. of compensation. Gulf War Vets who have ALS get it from that timeframe but not me a Vietnam War Vet. I refuse to give up because I know individuals have won these type of appeals
My husband was diagnoised with ALS on March 5th 2010. He was given 30% disablity, I have appealed this desision and we are working for 100% disablity. ALS only gets worse over time. Why do we have to fight for everything that the VA gives him. He gave his life for our country now our country need to take care of him!!!!
this is amazing to find! my father was diagnosed with ALS in 1984, and from the very beginning was always suspicious of it having something to do with chemical exposure, he was an airman in the USAF, unfortunatly he died in 1993, I was only 9 years old. now that i am older I have found myself being more curious about his condition, we have a ton of paperwork of his and medical records, not to mention a huge resume of his including bases he was stationed at, in my research lately, I am amazed to see the connection between vets and this disease and think there is way too much of a coincidence here! maybe there is more of a connection to the bases, any info I can receive would be greatly appreciated! My father was proud to be in the service and was proud of his rank as a SGT. he was honorably discharged in 1982 and by 1984 had this disease full blown which completely paralyzed him in a matter of months at the young age of 26! he was lucky to beat the odds and live 10 years! he died at only 37! like I said my renewed interest in my Father's case has me asking many questions and finding a lot of odd links, any additional info would be greatly appreciated!
I was in the Navy for 12 years and got out in 1992In September 09, I started getting the first ALS symptoms. I got my "official" ALS diagnosis in Oct. this year from the V.A. hospital here in San Diego. Am I eligible for any disability benefits due the recent congressional acts? ANY guidance or assistance would be GREATLY appreciated!