Montgomery Mayor Todd Strange presented a proclamation today declaring April 1-7 as Asbestos Awareness Week in the city of Montgomery, Alabama. The proclamation supports National Asbestos Awareness Week, as established by Senate Resolution 427.

It is the purpose of Asbestos Awareness Week to raise public awareness about the prevalence of asbestos and the dangers of asbestos exposure in the United States and around the world. Microscopic asbestos fibers can be inhaled or ingested, and imbed themselves in the body where they can cause diseases such as asbestosis, a severe scarring of the lungs, and mesothelioma, a deadly cancer that can affect the chest and lungs, the abdomen or the heart.

The U.S. Congress has recognized a National Asbestos Awareness Day or Week for the past six years. The awareness effort is a project of the Asbestos Disease Awareness Organization (ADAO), which is the largest organization in the United States serving as the voice of asbestos victims. The ADAO lobbies for the complete ban of asbestos and asbestos-containing products in the U.S. It is estimated that within the next decade 100,000 workers around the world will die of an asbestos-related disease. That equals 30 deaths each day.

For more information, visit ADAO online.

It was Cheryl Cotton’s third time attending the Mesothelioma Applied Research Foundation’s annual International Symposium on Malignant Mesothelioma when I met her this past June. We were both seated in the hotel lobby, waiting for a bus to take us to Capitol Hill, where we would ask our legislators to support a complete ban of asbestos and for funding for mesothelioma research.

I think it was Cheryl who introduced herself first, and I was delighted to hear she was from my home state, Alabama, about two and a half hours north of Montgomery, in Anniston. When I told her I was from Montgomery, she was ecstatic to finally find someone with a meso connection in her home state.

Cheryl lost her husband, Virgil, to mesothelioma on May 31, 2005, just two days after their 40th wedding anniversary. She began attending the Meso Foundation conference almost immediately, urgently needing to connect with others who might understand what she was going through, and to make sense of a disease that took her best friend and love of her life before either of them fully realized what was happening.

Virgil first began to notice something was wrong in late March 2004, when he had a severe pain in his side. His hobby was restoring vintage automobiles, and he had been working on a friend’s car, so he thought he had possibly just bruised a muscle while working. But shortly after that he developed a terrible cough.

“It was a whole-body cough,” Cheryl recalls. “Like from head to toe.”

Virgil went to see his doctor, who thought the cough might be related to a drug he was taking following a heart catheterization, which he’d had earlier that year.

“The doctor said it would take 60 days or so to get the drug out of his system, so basically for two months we did nothing,” Cheryl says. “The pain in his side persisted, and the cough got worse. Right up until this time, after his heart problems, he had been dedicated to cardiovascular exercise and eating right. He was probably in the best shape he’d been in for years. He would actually get onto to me about exercising more and eating right,” she recalls with a laugh before turning sober again. “So this was just odd. He kept feeling sicker and sicker.”

He went back to the doctor, thinking maybe there was something wrong with his heart. Tests showed his heart was fine, and doctors sent him home and told him to just continue to exercise and eat right.

But Virgil began having trouble breathing. It was September by now. He visited the doctor again, and was referred to a pulmonary specialist for a thoracentesis. They found fluid in his lungs, but tests came back negative for cancer or any type of infection. But the fluid came back almost immediately.

Cheryl was getting really worried.

“He was used to being active, but now he could hardly get around. He had no energy,” she remembers. “We had requested referrals to see some doctors in Birmingham, because he was dying in front of me. I knew there was something more going on, and I couldn’t understand why nobody could tell us. We had two more thoracenteses and still no diagnosis. The local doctors said they didn’t know what was wrong with him.”

At this point, Cheryl decided to call Birmingham, and talked to a nurse at UAB Medical Center. She got a referral for a pulmonary specialist, and made an appointment for Virgil the following week. But when they got to see the doctor, he said Virgil actually should see a thoracic surgeon, and gave them another referral. They gathered all Virgil’s test results and visited the thoracic surgeon on December 14. An initial theory was that Virgil might have a collapsed lung and scar tissue.

“Virgil had really gone downhill,” Cheryl said. “He was aging. Things had fallen apart in nine months, since the first symptoms.”

Doctors decided to do a thoractomy, but because it was Christmastime, they decided to wait until January, telling Virgil and Cheryl to go home and enjoy the holidays with their family. He finally had the surgery Jan. 4, and they first heard the word mesothelioma. But the diagnosis still wasn’t definite until about 10 days later.

“At that point it was stage 2+ or 3-. It was already advanced. We were referred to a doctor for chemotherapy, but still nobody was really telling us much about what this diagnosis meant. We had no idea.”

Virgil underwent a series of chemotherapy treatments, and then on April 20 began receiving radiation at a cancer center in Birmingham.

“By then, his breathing had deteriorated and they’d put him on oxygen,” Cheryl said. “He’d really not been able to lie flat since September. He had to prop up in a recliner or on a pallet on the floor.”

On May 19, a Thursday morning, Virgil woke Cheryl and told her something was wrong and that he felt he needed to go to the hospital. They went to UAB. On May 21, the doctor came in and told them Virgil was not improving, and that he didn’t have long to live. She estimated two and half to three months, and advised them to get their affairs in order.

“This was the first time anyone really talked to us about dying. Everyone was telling us he had time, that there was all this time.”

They called in Hospice care, and their daughter, Pam, came to visit, bringing their grandson and making a video of Virgil and the boy. On May 30, Virgil began doing worse, and passed away the next day. This was just nine days after they’d first been told that Virgil’s condition was terminal, and about 15 months since his first symptoms.

Cheryl was in shock. “He was 60 years old and had been in prime health,” she says. “When he died, he looked like he was 90. I didn’t even realize how bad he looked because I guess I saw him every day. Months later, I watched the video Pam had made just before he died, and then I really saw it.”

Virgil’s illness had been such a whirlwind; Cheryl wasn’t quite sure what to do after his death. She still couldn’t quite believe it had even happened. She was angry, that Virgil went so long with no diagnosis and no treatment. She felt guilty, like she ought to have somehow known more, or done more. And she felt alone.

Some time after Virgil was diagnosed with mesothelioma, Cheryl found the Mesothelioma Applied Research Foundation, a non-profit organization dedicated to the elimination of mesothelioma through outreach, education and funding research efforts to find a cure. She also connected with Sue Vento, the widow of Sen. Bruce Vento of Minnesota, after whom the pending “Bruce Vento Ban Asbestos and Prevent Mesothelioma” legislation before the U.S. Congress was named.

“She emailed me and I think called me, too,” Cheryl says. “She sent me a book on meso as well. She was the calm in the middle of my storm, and has kept in touch with me during this time via emails.”

Following Virgil’s death, Cheryl decided to attend the Meso Foundation’s annual International Symposium on Malignant Mesothelioma, and packed her bags for the trip to Washington, D.C. Many of her friends couldn’t understand it, but she says it was something she had to do.

“I somehow found MARF and the main reason I went to the conference that first year was to have someone to share this pain, and try to come to some conclusions,” she said. “You feel like you didn’t do something you should have. We had never heard of the word until they told us the diagnosis.

“I really felt like … when you lose your husband, who had been my friend, before he was my sweetheart – we’d known each other since we were 12. I felt if there was some way I could reach out to someone else it would help me as much as maybe I could help them. I felt there was that need in my heart, to find out as much as I could about the disease,” Cheryl says. “It was wonderful to know that people were surviving. But it makes me angry that Virgil didn’t have a chance.”

She had a chance to meet her “rock,” Sue Vento, at that first conference as well. Since that time, Cheryl has attended the Symposium for three years in a row, where she is active, joining others in visiting Capitol Hill to ask Congress to ban asbestos, and to fund mesothelioma research. She is also active in her community, talking to people about the dangers of asbestos exposure and about mesothelioma. She takes brochures about mesothelioma to doctors’ offices, hoping to increase knowledge among the medical community, hoping that someone else may be diagnosed early enough for treatment.

“Now I have contact with more people who are battling mesothelioma, and I learn that most people also have never heard of it. At the time, you just have to hang in there, and you can fall apart later. So I try to connect and just try to help someone, to let them know that someone is there who understands what they are going through. And it helps me too,” she says.

“I share my story every chance I get. I wear an awareness pin. People need to know asbestos is out there and it’s killing people.”

Outreach is hard. Every time she shares Virgil’s story, the pain is fresh again. But Cheryl is determined, and she’s willing.

“Mesothelioma patients and their families are victims,” Cheryl says. “They are victims of asbestos. And all of this COULD and SHOULD have been avoided!”

Montgomery Mayor Todd Strange has officially designated Saturday, Sept. 26, as Mesothelioma Awareness Day in Montgomery, Alabama. The recognition goes hand-in-hand with a nationwide Mesothelioma Awareness Day campaign under the direction of the Mesothelioma Applied Research Foundation (Meso Foundation).

Mesothelioma is a deadly cancer that most often affects the lining of the chest and lungs, but which also may affect the lining of the abdomen or, more rarely, the heart. It is caused only by exposure to asbestos. The latency period for mesothelioma is generally long, spanning 10 to 50 years from the time of exposure to any symptoms developing, making it hard for mesothelioma sufferers to pinpoint when they were exposed. There is currently no know cure for mesothelioma.

In the past, mesothelioma was seen primarily in older men, who had worked in factories, as insulators, or in shipyards, where asbestos was commonly used. However, today, the disease is being diagnosed more frequently in younger people and more often in women. Most of these cases are the result of secondary exposure, such as family members exposed to asbestos dust on the clothes of someone who worked with the substance. It could also be the result of environmental exposure. Mesothelioma has become everybody’s problem.

Asbestos is still not completely banned in the United States.

The folks from this web site, www.myMeso.org, are excited that we will have a table this weekend at the American Cancer Society “Bite the Tail Off Cancer” Crawfish Boil event. The event is presented by the ACS Junior Executive Board and Riverfront Facilities, City of Montgomery. If you are going to be in Central Alabama on Saturday, please come by and see us!

The event is planned to be held at Riverwalk Amphitheater in Downtown Montgomery, Ala., on Saturday, April 4, from 2 p.m.-8 p.m. and will feature all the crawfish and sides you can eat, live music, and activities for children. Tickets are $20 in advance or $25 at the door, with proceeds benefitting the American Cancer Society. (Advance tickets can be purchased through etix.xom)

myMeso‘s sponsor, Beasley Allen Law Firm, is also a sponsor for this event, along with Alfa, Alfa Dental, Morgan Keegan, Jackson Thornton, Dr. Kynard Adams, Price Trailer Sales, Southeast IV, ServisFirst Bank, Harmon Dennis & Bradshaw, Cumulus Broadcastin, Seay Seay & Litchfield, AKD Printing, and AAF-Montgomery.

It is particularly fitting for myMeso to present information about mesothelioma and asbestos awareness during this event, as April 1-7 has been declared Asbestos Awareness Week both in the City of Montgomery and nationally, by U.S. Senate Resolution.

In case of inclement weather, the event will be held at the historic Train Shed, which is located adjacent to the Riverfront and Riverwalk. Come see us, rain or shine!

Mayor Todd Strange today signed a proclamation declaring April 1-7 as Asbestos Awareness Week in Montgomery, Alabama. This proclamation supports National Asbestos Awareness Week, as established by Senate Resolution.

It is the purpose of Asbestos Awareness Week to raise public awareness about the prevalence of asbestos and asbestos-related diseases and the dangers of asbestos exposure. Asbestos can still be found in many products in the United States, which consumes nearly 7,000 metric tons of asbestos each year. Asbestos also is present in insulation produced prior to the 1950s and building products used well into the late 1970s, all of which can still be found in homes and public buildings.

Microscopic asbestos fibers can be inhaled, where they imbed themselves in the body and cause diseases including asbestosis, a chronic scarring of the lungs, and mesothelioma, a deadly cancer.

Asbestos Awareness Day, and later Asbestos Awareness Week, was established nationally by the Asbestos Disease Awareness Organization (ADAO), which was founded by asbestos victims and their families in 2004. ADAO works to give asbestos victims and concerned citizens a voice as they fight for a total and complete ban on asbestos in the United States.

Mayor Bobby Bright has officially declared Sept. 26, 2008, as Mesothelioma Awareness Day in Montgomery, Alabama!

We appreciate Mayor Bright for his continued support in promoting awareness of this deadly disease and the dangers of asbestos exposure.

Read the Mesothelioma Awareness Day Proclamation.

This is a reminder to those who haven’t yet contacted their representative in U.S. Congress about H.R. 3339, the Bruce Vento Ban Asbestos and Prevent Mesothelioma Act. Please take the time to do this right now! It’s very important to let your Representative on Capitol Hill know that you support this measure to finally ban asbestos in the U.S. and provide funding for mesothelioma research.

The bill is currently in committee, with the House Committee on Energy and Commerce. Even if your district’s representative is not on this committee, it is important to let him or her know that you support the bill so that they know how to vote. The more voices they hear from their constituency, the better chance they will pay attention when this finally comes to the House floor.

If your representative IS a member of this committee, it is even more important. Many bills “die” in committee, never making it to a vote of the full House or Senate. Please make sure your representative helps get this bill approved in committee and to the floor for its vote.

My representative, Terry Everett (2nd District, Alabama), acknowledged his receipt of my request with a letter, in which he said he will keep my thoughts in mind should the bill make it to the floor, although he is not a member of the Committee on Energy and Commerce.

According to information provided by Everett’s office, H.R. 3339 would require several actions to be taken by the federal government in addressing asbestos and its harmful effects. The Environmental Protection Agency (EPA) would establish a plan to increase awareness of the dangers posed by asbestos-containing materials in homes and workplaces and encourage participation in research and treatment endeavors of asbestos-related disease patients.

The bill also would require the disposal of asbestos-containing materials within two years and the prohibition on the importing, manufacturing, processing or distributing of asbestos-containing materials, except for specific exemptions sought by the Department of Defense and National Aeronautics and Space Administration.

If you are not sure of the representative for your Congressional District, visit the House of Representatives online. You can also find out here if your representative is a member of the House Committee on Energy and Commerce.

Please take the time to do this today. Your one voice is SO important. Let it join thousands of others to finally make a real difference.

The Mesothelioma Applied Research Foundation (Meso Foundation) has issued an “action alert” urging its constituents to call on their House Representative this week to support prompt passage of The Bruce Vento Ban Asbestos and Prevent Mesothelioma Act of 2007 (H.R. 3339), sponsored by Rep. Betty McCollum (D-MN).

In October 2007, the Senate companion bill, sponsored by Sen. Patty Murray (D-WA), passed. The House bill toughened the legislation, under the direction of the Environment and Hazardous Material Subcommittee of the House’s Energy and Commerce Committee, eliminating an exception for asbestos present at 1 percent or less by weight, making the ban a matter of federal statute rather than EPA regulation, and adding enforcement provisions.

The Meso Foundation reports the critically needed medical research funding provisions from Sen. Murray’s and Congresswoman McCollum’s legislation have not yet been added to the Committee Print.

In a statement released yesterday in support of including the research funding, the Meso Foundation said, “for the sake of all those already exposed, those now sick, and those who will be exposed in the future to asbestos already in place, we call on the Health Subcommittee to follow Sen. Murray and Congresswoman McCollum in recognizing the necessity of a robust asbestos disease research program, and to adopt the research funding provisions included in their legislation.”

Read the full story about this important legislation at Yahoo! News.

Supporters are urged to contact their Representative in Washington, DC, to urge inclusion of the research funding and swift passage of the complete bill once the funding is in place.

In Alabama, House Representatives are Robert Aderholt (4th Congressional District), Jo Bonner (1st), Mike Rogers (3rd), Spencer Bachus (6th), Robert E. “Bud” Cramer (5th) and Terry Everett (2nd). If you are not sure which is your congressional district, to locate contact information for your representative or to locate the representative for your state, visit the United States House of Representatives online, and click on your state for a list of your representatives.

Please contact your Representative NOW to let them know you support this legislation and to ask for their support. Please email me if you’d like any help!

About 5 minutes into Linda Garmon’s documentary about cancer, titled The Truth About Cancer, which aired last night on PBS on Alabama Public Television, I started crying. I was a mess through most of it. Garmon films her husband, Larry D’Onofrio, who is diagnosed with mesothelioma, and records his journey. Within two years, he has died.

About six years after his death, Garmon revisits some of the cancer centers where Larry was treated, and talks to doctors, patients and family members of those suffering from a variety of cancers – pancreatic, lung, breast, prostate.

The documentary explores the complicated maze of cancer treatment, which is so widely varied partly due to the many variations cancer takes within the human body as it mutates genes. It also looks at how cancer affects people’s relationships, with the person battling cancer oftentimes also feeling the pressure to “beat it,” to “win” over cancer, a feeling of pressure that it’s somehow up to them to get well.

Garmon touches on the issue – why are people still dying of cancer? She shows news footage of President Richard Nixon declaring war on cancer. And here we are still fighting.

Larry D’Onofrio built his family’s home, and worked on other construction projects. It is suspected he contracted mesothelioma as a result of asbestos exposure in that work. Garmon wonders, “why him?” when others who worked alongside him are healthy today.

I write about mesothelioma every day because it’s my job. But I’m touched by the people I meet who share their stories. I’m amazed by the patients who agree to clinical trials even when they understand that there probably won’t be a miracle cure for them, but because they understand that by doing so they might help someone after them.

And I’m touched by the people affected by mesothelioma who work for awareness. To reach out from their place of pain to try to bring the issue to light – that’s strength almost unimaginable. Thank you, Linda, for having the strength to share your story, the story of you and Larry and the hardest battle you ever had to fight.

PBS will air the documentary several more times in the coming weeks. If you missed it last night, I urge you to check your local listings and make a point to see it. It’s powerful, and it’s a message more people need to hear.

As part of its “Take One Step” health campaign, PBS will air a documentary titled “The Truth About Cancer” tonight (Wednesday, April 16, 2008). Award-winning filmmaker Linda Garmon shares the story of her husband’s battle with and death from mesothelioma.

During the program, which strives to answer the question “Why does anyone still die of cancer?”, Garmon visits the facilities where her husband was treated, and interviews people who are undergoing treatment for various types of cancer, and interviews doctors and researchers working for a cure.

PBS describes the film as, “Part science, part personal catharsis, part character-driven storytelling, this powerful documentary uncovers the truth about cancer and tell us where we stand in fighting the battle against the disease. ”

The program is slated to air in most markets at 9 p.m. ET. In Montgomery, Alabama, where I am based, the show is scheduled for 8 p.m. CT on WAIQ, Alabama Public Television (APT).

Following the film, journalist and breast cancer survivor Linda Ellerbee will host a 30-minute follow-up panel discussion covering topics including the importance of early screening, what to expect if a loved one is diagnosed, and how to live with cancer.

Please check your local listings for this very important program! It is critical to realize that cancer is an issue of national importance in public health, and that much more needs to be done to enhance funding and research for all types of cancer.

Find more information about this program at the official PBS site for the film.