Do Our Congressmen/Women Listen? Agent Orange the Battle Continues

"ONLY THE DEAD HAVE SEEN AN END TO WAR" ~PLATO

~~*~~

Dennis has submitted his files to his Congressman.

~~*~~



Peripheral Neuropathy HELP and SUPPORT:http://www.neuropathy.orgThe Neuropathy Association is the leading national non-profit organization serving the peripheral neuropathy community. We provide support and education, advocate for patients’ interests, and promote research into the causes of and cures for neuropathy.~~*~~

Dennis Needs Help, The VA is NEGLIGENT

To whom it may concern,

My name is Dennis G. Magnusen, I used to be a mentor teacher in Hawaiian Gardens, CA. This was a hard place for a kid to grow up, gangs were well established in this area. I taught junior high during the day, home students in the afternoon, and high school "gangsters" in the evening out of a community store front school. I loved my job; I took it very seriously. I became an educator because of my experiences in Vietnam; I did not like what war did to people nor to children, therefore, I taught peaceful resolution to conflicts whenever it seemed necessary. I had to quit teaching in 1990 due to the effects of Agent Orange; I moved to Hawaii.

HERE IS THE PROBLEM: My VA doctor of 18 years (Dr. George W. Ross, Chief of Neurology for the state of Hawaii) finally admitted that he knows nothing about my medical condition. He always told me that "I should not be in so much pain" and that "it is not going to kill me". As it turns out, he could not be more wrong.

In early 2008 I was diagnosed with severe small fiber neuropathy from a biopsy that was sent to Therapath Lab,NY. This is a very painful disease that controls the autonomic nervous system; this has never been addressed by the VA. The only thing the VA has done is to load me up on drugs, that yes I have asked for to help the pain but there is another option. Most doctors are amazed that I can even get out of bed with this many medications. I need treatment (i.e. IVIG), not more meds.

In 2008 Dr. Ross recommended that I see Dr. Mandaville (at Univ. Calif. at San Diego and also with the VA in LaJolla). On January 15, 2008, I was to meet with the VA's neurologist who was going to turn me over to Dr. Mandeville. Instead, the VA's neurologist (Dr. Vivan) said that they were going to "re-test" me. It has been a year since that meeting and nothing has changed, they schedule me 4-6 months after each test to see a neurologist, and then order another test.

I need help. In December of 2009, I had to go to the ER twice. The first time I went to a local hospital, I was convulsing and could not breathe ( I was throwing-up continuously and therefore could not keep my meds down), the pain was severe. The next day it happened again. This time I went to the VA in LaJolla, a 25 mile drive. I had to wait in ER for 5 hours before being seen. Once again in severe pain. I was admitted for 3 days before being stabilized. I can't help but to think this wouldn't happen if I was not on so many meds.

In the VA's Patient Right's, it states: "You will be treated with dignity, compassion, and respect as an individual. You will receive care in a safe environment." I've never felt like I was a recipient of this kind of care, it's more like DENY, DELAY and DEATH.

So far I've been diagnosed with peripheral neuropathy, avascular necrosis ( left hip has had a full replacement, the right hip is still deteriorating), cardiomyopathy, COPD, chronic pain, chest pain, PTSD, persistent insomnia, acute sinusitis, acute tonsillitis, malaise and fatigue, cough, pyronies disease, gastrointestinal motility, and small fiber neuropathy, as well as a few others.

I need help. All I want is a doctor who can help me. There are still things in this world that I want to accomplish. I want the VA to treat me with dignity, compassion, and respect as an individual, and give me that care in a safe environment.

Dennis Magnusen


~~*~~

The image is of my (Kathy Ostman-Magnusen) painting of Dennis.

Artist's Statement:

"Mr. Magnusen", 30x40x2 oil on canvas, by Kathy Ostman-Magnusen

Artist's Statement:

Mr. Magnusen, the subject of my painting, shares many of my same memories. We grew up not far from one another In S. California and later attended the same high school.  It was in high school that I fell in love with Dennis G Magnusen. That love story was put on hold for some 30 years.

In 1967 Dennis was drafted by the US Army, and subsequently went to  Vietnam in 1968. Circumstances and follies of youth would cause us to follow separate paths.  

While in Vietnam Dennis was strongly affected by the children he saw there. "Children were never meant to experience war", he told me years later.  He decided that he wanted to do his part to change the world.  "Real  change in any society begins with the children," was Dennis' mantra, so he became a teacher.  He worked with gang zone high school kids in the evenings and intermediate students in the afternoon.  Grades of  F's and D's were bought up to A's and B's.  Mr. Magnusen reached beyond his own expectations, leading kids to an understanding of their own worth, thus opening doors to their potential futures. He created a surf club and got the community to help. He was often featured on  local TV and newspapers as someone who was making a difference in children's lives.  Dennis also became a Mentor teacher, lending help to other educators.  Being somewhat of a rebel he advised fellow teaches of  ideas that reached  beyond standard textbook techniques.  

Sadly the ghost of Vietnam took away Mr. Magnusen's strength in the form of Peripheral Neuropathy, caused by Agent Orange.  By 1990 he was too ill to continue his beloved teaching career. It broke his heart.   Seeking rest, relief from stress, needing a special place to deal with the physical pain that comes with Small Nerve Fiber Neuropathy, he relocated to Hawaii.  Hawaii has been his solace and a cool breeze when memories of who he once was for kids becomes faint.

About three months ago "Mr. Magnusen"  was contacted by a former student.  Amy had been looking for him for eighteen years.  She had heard he had died from Agent Orange complications, but still hoped that  she would find him.  You see, Amy became a teacher and she wanted to find Mr. Magnusen to tell him how much he had affected her life. While working on her Masters in Literature, Amy wrote a paper describing the most influential person in her life.  That person was Mr. Magnusen.  Amy called to tell Mr. Magnusen that she wanted to make a difference in this world too. For a teacher there can be no greater reward.  

As for me? I found Dennis once again after 30 years, through a miracle of circumstance, but that I guess is another story. 


~~*~~

How can you help Dennis? Speak out for Vietnam Vets. And the next time you pass someone who is homeless and you think they were probably a Vietnam Vet? Give them a dollar or two.

Also SUPPORT THE NEUROPATHY ASSOCIATION:



Peripheral Neuropathy HELP and SUPPORT:

http://www.neuropathy.org

The Neuropathy Association is the leading national non-profit organization serving the peripheral neuropathy community. We provide support and education, advocate for patients’ interests, and promote research into the causes of and cures for neuropathy.

~~*~~

Spray Yourself With a Can of Raid For One Year-Would it Affect You?

My love story with Dennis is bittersweet. I found him after 30 years, we had been high school sweethearts, gone on separate paths.

Joan Baez sings this song about her sister and brother in law... Denny has always been my "Sweet Sir Galahad".



Dennis, my Denny is disabled with Small Nerve Fiber Neuropathy due to Agent Orange exposure while in Vietnam. He bathed in the Mekong Delta everyday so it was always on his skin for his nine month term.

If you sprayed a can on Raid on your skin every single day for nine months do you think it would affect you?

The US Government says no.



Peripheral Neuropathy HELP and SUPPORT:

http://www.neuropathy.org

The Neuropathy Association is the leading national non-profit organization serving the peripheral neuropathy community. We provide support and education, advocate for patients’ interests, and promote research into the causes of and cures for neuropathy.

~~*~~

Agent Orange Effects

WARNING- disturbing images, but then the truth when one has hoped for the best, believed the best and finally realizing that you have been deceived is disturbing. This is not the America soldiers fight for in this video. Use your voice to protest wars that are wrong. Be patriotic.

Alternative Treatment for Peripheral Neuropathy - Agent Orange - Vitamin B12 Supplements BELOW

~~*~~

The Effects of Agent Orange

The effects of Agent Orange on the people of Vietnam and to our very own soldiers is heart wrenching. USA has never accepted responsibility for its spray missions. People are often surprised to know that the US Government does not accept most US soldiers claim of being affected by Agent Orange by saying their complaints are not "Service Connected". Peripheral Neuropathy is ONLY accepted by US Government if it was reported within the first year after leaving Vietnam.

Back then, people were not putting little yellow decals on their cars saying they,

"Support the Troops",

no, they were spitting on many of them, angry, and not supportive,

so who would have noticed a little tingling, a little vomiting and weight loss? They were just happy to be out of Vietnam.



Watch this video and ask yourself if the US Government should admit to responsibility.

Do not look away.

Know that this is one of the things that war does.

All you anti-choice people? Know that war kills and maim babies too. Think twice before you agree and support the next war. US now has business' in Vietnam.. business as usual I guess.

Ask yourself just how many wars you plan on supporting from a distance.

Many Vietnam Vets ARE out homeless and discarded... think of them next Veterans Day, next Memorial Day or maybe the next time you see a homeless man on the street around 60 years old.



Peripheral Neuropathy HELP and SUPPORT:

http://www.neuropathy.org

The Neuropathy Association is the leading national non-profit organization serving the peripheral neuropathy community. We provide support and education, advocate for patients’ interests, and promote research into the causes of and cures for neuropathy.

~~*~~