The Mesothelioma Applied Research Foundation (MARF) will hold its International Symposium on Malignant Mesothelioma 2008 in Washington, D.C., June 26-28. The annual event highlights the latest advances in research and treatment for patients and caregivers, offers psychosocial support to them as well as those who have lost someone to the disease, and provides significant advocacy and volunteer opportunities for those who are intent on eradicating mesothelioma.
According to Rob Grayson, director of marketing for the Meso Foundation, the event actually started as a purely scientific event, geared toward researchers and scientists, with technical presentations. However, at the time, there were no informational or educational events like it, and they found that patients, families and caregivers wanted to attend.
“Initially, these people would come and sit in on these high-level presentations by scientists, with very technical presentations. We saw the interest and our meeting has now evolved into more of a patient meeting, the scientists speak in more layman’s terms, and we’ve added programs to reach out to people who are also interested in the community of support and the activism that takes place,” Grayson said.
The advocacy element is a new piece of the symposium, added last year when the meeting coincided with debate in the Senate on the Ban Asbestos in America Act, S. 742, sponsored by Senator Patty Murray (D-WA).
“The day we lobbied, they took an administrative vote, and it passed in the Senate. So we’re going back to Washington this year,” Grayson said.
Advocacy efforts this year will include a rallying cry to the House of Representatives to move quickly to pass the legislation in the House, which bans asbestos and provides research funding for mesothelioma. Last week, the Foundation issued an action alert in support of The Bruce Vento Ban Asbestos and Prevent Mesothelioma Act of 2007 (H.R. 3339), the companion to the Senate bill. The bill includes $10 million for mesothelioma research.
“Normally we’d hold the Symposium in a different city each year, but it’s almost the same timing as last year, with the bill pending, this time in the House, so we’re back to Washington,” Grayson explained.
Those attending the Symposium can register to participate in the advocacy efforts, and the Meso Foundation will arrange for them to meet personally with their congressional delegate, and will provide a training session to help advocates prepare for the meeting.
In addition to lobbying for passage of the House bill, Symposium advocates will request that the Senate’s Defense Appropriations Subcommittee maintain, for the second year, mesothelioma’s eligibility to compete for medical research funding from the Department of Defense. In 2007, the DoD appropriated $50 million and included mesothelioma as a research priority for its Peer Reviewed Medical Research Program, effective in the 2008 budget. The Meso Foundation is working for continuing and increasing funds for mesothelioma research in the 2009 defense appropriations bill.
“There currently is no ban on asbestos, so companies can use it however they see fit. We’ve pretty much stopped mining here, but asbestos is still used in about 3,000 products that you could go out and buy right now. Even if we banned asbestos tomorrow, it probably won’t change the rate of sickness for the next 50 years, due to the latency period of asbestos. That’s why the funding for research is so important,” Grayson says. “Advocacy and the call for a ban on asbestos raises awareness, and raises money for research, which is what we need to deal with the illness itself,” he said.
In addition to advocacy, the Symposium again will feature an educational program, with sessions covering topics including Peritoneal Mesothelioma, Pleural Meso Surgical Options, Emerging Therapies, Optimizing Patient Care, and Scientific Advances in Meso Research. Other educational programs will provide instruction on outreach topics including volunteerism, fundraising, peer support and advocacy, to help those who want to make a difference learn how to be most effective.
A Gala Dinner will honor those people living with meso, and recognize outstanding volunteers and advocates for their hard work and dedication to raising awareness. The dinner will feature a unique guest speaker – Seventh grader Lexi Miletto, the granddaughter of Joseph Miletto, who died in 2005 of peritoneal mesothelioma.
Scholarships for Symposium registration fees, as well as for transportation and accommodations, are still available for patients, family members and caregivers who would like to attend. Contact the Meso Foundation at www.curemeso.org or call 805-563-8400 for details.
The Mesothelioma Foundation was started in 1999, by attorney Roger Worthington. Unfortunately, Grayson says, there was an initial stigma because of his association, with people suspicious the Foundation was attempting to gather clients for his firm, so he removed himself from the Board of Directors and the Foundation was re-established as a non-profit, 501(c)3 organization. Today, with 8 staff members, the organization raises $2.5 million annually and funds more than $1 million in research projects.
“Currently, most of our funding goes to seed money to help researchers who have good ideas for treatment to validate their work, and take it to the NIH to get additional funding for the next step of the research,” Grayson explained. “We hope very soon that we’ll be able to fund clinical trials.”
View Comments to “Girl honors grandpa at Mesothelioma symposium”
Great post. This is a very uplifting story. I wish Lexi the best of luck as she pushes forward.
Thank you, asbestosnews! What a remarkable girl to speak out on behalf of her grandpa at such a young age! It just goes to show that anyone can be an advocate – it just takes a willingness to speak up.
I couldn’t agree more Wendi. I hope that Lexi becomes an example to others and more people rally behind a great cause.
wow, not many people stand out at such a young age, but the ones that do may change the world. Great post.
Let me see how this works: In 1966 My family moves to Libby,Mt from Ohio.There is six kids and ma and pa. Ma and Pa are in their30s. I am 12 and the oldest. Us six kids get married and we have kids. My kids are 27 and 24 right now.They too were born and raised in Libby.And then our kids, have children.You know, the generation thing. So , I am talking 4 generations created since 1966 to 2008. That is a bunch of Family. Then in 1999, we all were told why we are sick and dying.We were told that a latency period comes with this death sentence and that it takes anywhere from 10 to 40 years befor you begin to slowly die. And since that day in 1999, the truth is taking all of us to our grave.Ma and Pa are gone now, I and my sises and bro are next and then our children will follow me. And this is how LIFE is till death for all of us.This is what we all wake up to everyday of our lives.The knowing of how each of us will/are dying…no cure,no life where the only thing to look forward to is death.Because you suffer for years befor you die from suffication/Meso.So ma and pa were close to 70 when they passed.I am 54 and on my way out and by kids are old enough to see and understand what they have to look forward to when their kids will be faced with the same truth and reality that is and has and continues to kill all of us and millions today.My grand child to be born in April of 2009, a boy and my only grand child, never ever will my grandchild breathe Libby Mt air and I will go to my grave knowing that they may have killed/murdered 3 generations of my family tree…They won't get my forth generation.This is why I ,since 1999 continue to save all who will listen by telling all who will listen to stay away from Libby Mt. What a holocaust…….that was done to us…..
I want to say thank you for the work taht is being done to find a cure and to help families and individuals that are fighting to find a cure and to those that are having to say good bye to their families….
I am from Alberta Canada, my husband Ken Cardinal Sr lost his battle to mesothelioma on Dec 31st, 2008. His dream was that he could meet others who were going througth the difficulties like him and his family were and to help in some way to find a cure…He was 42 years old, he does not know how or when he came in contact with the asbestos? Although it has only been almost 5 months of his passing I am struggling to find out how to bring the awareness to people? I want to honor his battle and his strength but keeping his promise to do this. Any information that can be passed on to me would be greatly appreciated.Thank you.
Pam Cardinal-Desjarlais (May 2009)
Hello Pam,
Thank you so much for your comment. I am so sad to hear of your
It is so frustrating that asbestos is still a
husband's passing.
threat and, as you said, so many times people don't even know it's
there, so they do not even know to protect themselves.
I admire your willingness to carry out your husband Ken's desire to
raise awareness and connect with others who are battling mesothelioma. I
would be happy to send you some mesothelioma awareness bracelets – they
are bright green – hard to miss, and a great way to get people to ask
you about mesothelioma so that you can help spread the word about meso
and the dangers of asbestos. You can email me directly at
wendi.lewis@beasleyallen.com to let me know where to mail them if you
don't want to post your address in the comments. (they are free) I'd
love to hear from you!
Thank you, again, so much, for sharing a little of Ken's story here, and
for your desire to continue his efforts to raise awareness and help find
a cure. God bless you and your family!
Sincerely,
Wendi Lewis
http://www.myMeso.org
I want to say thank you for the work taht is being done to find a cure and to help families and individuals that are fighting to find a cure and to those that are having to say good bye to their families….
I am from Alberta Canada, my husband Ken Cardinal Sr lost his battle to mesothelioma on Dec 31st, 2008. His dream was that he could meet others who were going througth the difficulties like him and his family were and to help in some way to find a cure…He was 42 years old, he does not know how or when he came in contact with the asbestos? Although it has only been almost 5 months of his passing I am struggling to find out how to bring the awareness to people? I want to honor his battle and his strength but keeping his promise to do this. Any information that can be passed on to me would be greatly appreciated.Thank you.
Pam Cardinal-Desjarlais (May 2009)
Hello Pam,
Thank you so much for your comment. I am so sad to hear of your
It is so frustrating that asbestos is still a
husband's passing.
threat and, as you said, so many times people don't even know it's
there, so they do not even know to protect themselves.
I admire your willingness to carry out your husband Ken's desire to
raise awareness and connect with others who are battling mesothelioma. I
would be happy to send you some mesothelioma awareness bracelets – they
are bright green – hard to miss, and a great way to get people to ask
you about mesothelioma so that you can help spread the word about meso
and the dangers of asbestos. You can email me directly at
wendi.lewis@beasleyallen.com to let me know where to mail them if you
don't want to post your address in the comments. (they are free) I'd
love to hear from you!
Thank you, again, so much, for sharing a little of Ken's story here, and
for your desire to continue his efforts to raise awareness and help find
a cure. God bless you and your family!
Sincerely,
Wendi Lewis
http://www.myMeso.org
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