Why the Foundation?

LogoBoxesRegisteredThe Meso Foundation realizes that there are numerous groups that you can affiliate with, provide your stories and attempt to raise awareness but it seems as if many are just going about this in the wrong way. To begin with, have you really looked into the Facebook pages or websites that you are supporting? Are they transparent in who they truly represent? Most often this is not the case.

The Foundation is your only 501(c)3 not-for-profit that is dedicated solely to finding a cure for mesothelioma. Our executive director and nurse practitioner, Mary Hesdorffer, is uniquely qualified to assist you in managing your disease and understanding all of the options that are available, be it a clinical trial or a more standard form of treatment. Mary spent years actively treating mesothelioma patients and writing clinical trials and papers that have been published in peer-reviewed journals. She understands the disease and brings a unique perspective to the Foundation both as a medical professional and patient advocate.

Patient advocate is a term that is widely used in mesothelioma, but who are these advocates? Who do they work for and what motivates them to advise you? Many nurses have been hired by legal entities but do you know that they have never worked in a mesothelioma clinic, and are trained in this disease by the law firm that surreptitiously pays their salary?

Hmmm… seems that we have some serious conflicts in this disease and it is about time that everyone takes a step back and thinks about what is truly best for the patient and the disease in general.

As the Meso Foundation is not a business model, we are not beholden to any institution or legal entity. We are independent and trustworthy which sets us apart from many of the “faces” you encounter on the web. Facebook is new to many of you and we ask that you think before you click the “Like” button, stop before you fill out an on-line form. Think. Where is your information going? Whose cause are you supporting?

You have more power than you realize and the capacity to effect change. We invite you to become more closely involved with the Meso Foundation, support our mission and assist us in getting unbiased information directly into the hands of those who are affected by this disease. We have a peer-reviewed research program where we provide grants which we hope one day will not only lead to more effective treatments but to a cure. We have testified before Congress multiple times. Through our direct advocacy efforts we have secured much needed federal funding for mesothelioma research. You can view this expert testimony here.

We invite you to visit our website www.curemeso.org, call us at 877-363-6376. If you’re on Facebook, please “Like” our Facebook page so you can receive the latest news about research, support, and advocacy. We are the real deal- we are your nonprofit and we need your support!

THE TOP 10 REASONS TO GO TO THE MESO FOUNDATION’S 2013 SYMPOSIUM ON MALIGNANT MESOTHELIOMA

bonnie_aMesothelioma – by now you all know how to pronounce it, and you know that being informed is important. You also know about the Mesothelioma Applied Research Foundation or you wouldn’t be reading this blog. But did you know just how amazing their symposia are?

Let me give you an example of just a few highlights that I’ve seen:

1. People hugging people just because they have this disease in common and needed a hug.
2. Meeting a man in the hotel elevator who had a meso name badge, speaking to him and finding out he is Dr. Harvey Pass, the guru of mesothelioma. (We have since had many conversations together.)
3. Hearing the top meso specialists in the world speak about treatment, hope and the future of research.
4. Meeting a researcher who knew who I was because he works on my slides in research.
5. Letting researchers know how important their work is to patients and families.
6. Giving hope to a young mother who came because she had no idea where to turn to and didn’t know what to do next.
7. Putting a face to a name for those who have and will need support.
8. Knowing you are really not alone and there are others who can help.
9. Running out the door, to grab a hold of a doctor who just gave his speech and have him listen and talk to you on a personal level to answer your questions.
10. To meet other caregivers, patients and families affected by mesothelioma.
11. To be able to sit at a table with researchers and doctors and see that they are touched to know patients and families out of a clinical setting.
12. And finally… to meet Mary Hesdorffer, the woman who has helped save so many of us.

Ok so I lied. Not 10, but so many more reasons for you to attend the Symposium. I guarantee you will be so glad you did.

By Bonnie Anderson

Erica Ruble’s Symposium Story

erica_rubleFive years ago when my dad said, “I have mesothelioma,” I sat in disbelief. What was this disease? I could barely even pronounce it. What did this mean, for my dad, for me, for our family? A flood of emotions ran through me and the panic set in as I read about this orphan disease on the web. Within weeks my dad and mom were flying to New York for treatment while I was in Florida caring for my newborn baby, who was just a few weeks old. Our lives were changed forever.

My dad underwent every treatment option available but lost his courageous battle to mesothelioma in just 12 months. Feeling sad, angry, and wanting answers, I flew to my first Symposium in Washington DC. Three days later, I left DC with a purpose and plan. Following the lead of Shelly Kozicki, who lost her husband to mesothelioma, I decided to fund a research grant. In my heart, I felt my dad suffered and died for no reason. This was my chance to give meaning and purpose to his death by helping others. My dad was the type of man who believed in “doing the right thing.” Now it was my time to follow in his footsteps. To date, with the help of my family, I have raised over $207,000.00 for mesothelioma research. Each time a dollar is raised, I think of my dad and how his life is helping someone else’s life.

Attending the Symposium four years ago was one of the best decisions I ever made. Connecting with the community and sharing stories made me realize two things. First, I am NOT alone. Second, we CANNOT give up. We have to keep fighting for not only those who are sick but also for ourselves. If we don’t do this, who will?

I encourage the mesothelioma community to attend the Symposium in Las Vegas on March 7th and 8th. It is undeniably the only Symposium to encompass all facets of mesothelioma through advocacy, community, and research. Whether you are a patient, caregiver, supporter, or have lost a loved one, the Symposium will touch your life. We all have an opportunity and a chance in life to help others. This is your chance to not only help yourself but to make a difference and leave your imprint on the mesothelioma community.

Notes from Mary Hesdorffer, Executive Director of the Mesothelioma Applied Research Foundation

mary1The past four months have rapidly flown by and I had hoped to correspond with you more often and in greater detail since assuming my new role. I am enjoying this position and I must confess it has its challenges, but each day, with the assistance of the Foundation’s talented staff, we make progress and work toward fulfilling our mission. Our mission statement is posted online and was crafted with the input of board and staff. We feel that we have clearly stated the objectives of the organization and are anxious to hear what your thoughts about the direction of the Foundation. I have scheduled a town hall meeting for next week as I have not had an opportunity to thank many of our supporters and to hear their viewpoints on the mission of the Foundation and how it is meeting their current needs.

Right now my focus is on the peer-reviewed grants program. I meet with the Board of Directors (BOD) on Thursday night for a decision on the number of grants to fund. As you may recall, the Foundation administers a robust peer-reviewed research grants program which is one of the major focuses of our Scientific Advisory Board (SAB). Please view the bios of this talented group of scientists who review the grants in great detail in a process based upon the system used by our National Institute of Health. Why such a laborious process? Simple – without a strong scientific review, and oversight following funding, your research dollars would have little value. We ensure that each dollar donated to our research program is treated with respect and good faith that it will be used as intended, with oversight and transparency. The SAB recommends the grants that are worthy of funding and the BOD has the fiscal responsibility to allocate budgeted funds for this purpose. I want to personally thank Dr. Lee Krug, Chair of our SAB for leading the process and keeping us informed of progress of the grant review. His strong leadership and scientific knowledge guided this rigorous process.

It is with great excitement that I await Thursday’s meeting and we will share this news with the community quickly and with great enthusiasm.

TOWN HALL MEETING
WHAT: Town hall meeting (conducted via conference call)
WHEN: 8:00 p.m. EST Wed. Jan. 23rd
WHO: Everyone is invited
WHY: To discuss Foundation updates and its programs and to allow for question/answer with executive director
WHERE/HOW: Conference call in number: (605) 475-4000
Participant Access Code: 216145

Hope in the Big Apple: The Meso Foundation’s “Knowledge Is Hope” Conference

It doesn’t seem that long ago that we were all in Washington D.C., coming together for the 2012 Symposium. After such a successful and inspirational event, what does the Meso Foundation plan for next?

How about a one-day event on the week of Mesothelioma Awareness Day? That is exactly what we plan!

On September 28, 2012, on the heels of Mesothelioma Awareness Day, the Meso Foundation (with a generous educational grant from Levy Phillips & Konigsberg, LLP) will proudly present “Malignant Mesothelioma: Knowledge Is Hope.” This is a one-day conference in New York City, NY, focusing on patients, families, doctors, and anyone wanting to understand more about malignant mesothelioma. It’s a jam-packed day-long agenda includes:

  • A return to the Plaza for raising awareness during the Today show
  • Sessions on standard treatments, ongoing research, complementary therapy, environmental/occupational exposure risk, and legal implications
  • Morning presentations featuring Lee Krug, MD; Marc Ladanyi, MD; Harvey Pass, MD; Kenneth Rosenzweig, MD followed by a questions and answers panel
  • Afternoon presentations by Garrett Nash, MD; Robert Taub, MD; Mary Hesdorffer, NP; Kathleen Wesa, MD; Jacqueline Moline, MD; and Robert Komitor, Esq.
  • Musical entertainment by Leon Pendarvis, musical director of Saturday Night Live
  • …and much more.

“Knowledge Is Hope” brings top experts in mesothelioma from the New York area to the Harvard Club of New York City, located on 35 West 44th Street, New York, for a day of education and awareness. This event promises to be a day of information, a day of science and research, and a day of discussions over the recent advances in mesothelioma treatment.

Registration is $25 per person (includes all sessions, breakfast and lunch). Register by clicking here or by calling the Meso Foundation at (703) 879-3797. Registration fees will be donated back to the Meso Foundation. Availability is limited. You must register before our deadline of September 10.

Knowledge is hope. Join us for this incredible day in New York City.