Mesothelioma Applied Research Foundation Inc

The Mesothelioma Applied Research Foundation helped my wife and I navigate the complicated world of mesothelioma. The Foundation provided us invaluable support and information. My wife was able to connect with other patients for support and comfort. As a bereaved member of the community now, I am able to connect with other members who lost their loved ones, and just get it.

My husband was diagnosed with peritoneal mesothelioma in 2016 and passed away in January 2019. Even though treatment wasn’t able to save his life, we never questioned whether we were making the right choices, thanks to the compassionate and expert guidance we received from the Mesothelioma Applied Research Foundation. By connecting me with other members of the bereaved community, who really understand what we went through, the foundation continues to ease my journey through the difficult world of meso.

I'm so grateful for the Meso Foundation! As the only nonprofit dedicated to serving mesothelioma patients and their families, with this tough diagnosis and confusing course to manage afterwards, having the Meso Foundation as a resource is truly a gift. From the community aspects - so no one has to go this disease alone - to the research funding, advocacy, and overall support, I cannot recommend this foundation enough.

MARF is the best source for unbiased, current, research-based information on mesothelioma. If you are a patient or caregiver, you can find person-to-person support from an extensive meso community that includes medical professionals who can put you in contact with the help you need. Not underwritten by the legal community.

Without this foundation my husband would not be alive today. We continue to rely heavily on the advice of it and use the support resources regularly.

Incredibly supportive and informative organization! As a patient, I am tremendously grateful for the team and all they do for patients and their families. I was completely lost after my diagnosis and Mesothelioma Applied Research Foundation has provided me with the knowledge, support, and direction I need to cope with this rare and scary disease. Because of this amazing organization and incredible team, I have hope again. Mesothelioma patients would be lost without them.

This organization has given us HOPE.

Mg husband was diagnosed with pleural mesothelioma in April 2021. After getting the diagnosis, we were
scared and trying desperately to find reliable information.

There is a huge amount of confusing information out there about mesothelioma- not to mention all the law firms clogging the google pages - and it feels impossible to find real, relatable stories and find other survivors and caregivers to talk with. The support groups have been amazing and so has everyone we have interacted with.

We are so incredibly grateful for this organization. They are life-giving.

I came across this wonderful organization through the research of my wife when I was first diagnosed with pleural meso in Feb 18. Since that time I have met (virtually in this crazy world) some of the finest people I have ever met. You can’t explain what it means to belong to a group like this unless you are forced to join a group like this… but, man, does it help to know we are not fighting alone.

All interactions with this foundation have been nothing short of amazing and a Godsend. Everyone is not only incredibly nice, but they go over and above to educate, help, and support. I cannot say enough good things about the Mesothelioma Applied Research Foundation and am grateful for them.

My Dad received his meso diagnosis over 10 years ago. The generally available information is frightening but the life-line we received was literally life-saving. The connections to doctors, other patients and caregivers and to researchers has created a family - brilliant, loving, caring.

This tiny organization punches SO far above its weight. Anything to raise its profile and reach so more persons can access these amazing resources to counteract the fear and give some comfort. And hope.

I cannot say enough, so I'll stop here.

The Meso Foundation has been here for our family from the time of our Mom’s initial diagnosis in 2014 through the present. It is the ONLY organization of its kind in the U.S. for mesothelioma. Patient travel grants, advice, research, information on clinical trials, a peer group of patients and caregivers, and more. Every meso patient and caregiver should make contact with the Meso Foundation.

I have fundraised for this charity for a number of years and have attended their conferences. My company is a a donor to them as well. They are an amazing resources to those that have been affected my mesothelioma.

My wife was diagnosed with pericardial mesothelioma in 2016.Not knowing where to turn and searching for help we stumbled onto the Mesothelioma Applied Research Foundation. They have been an incredible help to us,always available for us when we needed expert knowledge to help with the fight. Thanks Mary for all you and the foundation do.

I found this organization in June after my husband was diagnosed with mesothelioma. They are a great source of the most current information about the disease and treatment options. They support patients, caregivers and family members through their staff and peer support group calls. I have been impressed by their access to leading experts and the volunteers who help lead their efforts. I check in with them frequently as I know I will find good information and answers to my questions. The executive director, Mary Hersdorffer, is exceptionally helpful, knowledgeable, and accessible and was a great comfort to me when I needed it most.

A diagnosis of peritoneal mesothelioma in 2012 stopped us in our tracks. We had no idea what to do, but an internet search quickly led us to the Meso Applied Research Foundation and its wonderful staff. With a single phone call, we had the support of an expert nurse practitioner & contact information for 3 specialists located within driving distance. Throughout an 8 year battle, the Meso Applied Research Foundation was a steadfast source of science-based information, help, comfort, reassurance, & hope. I don’t know what we’d have done without it.

MARF has been nothing short of supportive, informative and makes me feel part of a loving community I never thought I would belong to as a young patient with this cancer diagnosis. MARF will always have my respect in advocating for patient safety and awareness. Thank you for all you do!

My mom was diagnosed with mesothelioma a year ago. She has no known history of exposure to asbestos. She’s currently getting chemotherapy and overall feeling pretty well. I’m an RN and appreciate evidence based info and the Mesothelioma Applied Research Foundation has been a blessing. They’ve been a trusted source of information and I feel like we aren’t alone. This is a great nonprofit organization.

Incredible patient and client support system. MesoTV is an amazing resource.

I find this foundation a great source of knowledge. It is great to hear firsthand from patients and caregivers and medical personnel about symptom, treatments and future developments regarding mesothelioma. My husband has just been diagnosed with stage 4 pleural mesothelioma and I have learned a lot from the Facebook group members.

I am honored to host the Bruce A. Waite 5k annually, with proceeds going to the Mesothelioma Applied Research Foundation. In keeping with my Dad's legacy, we wanted to ensure that the recipient agency would be one of integrity, honesty, and a focus on helping others who have lost a loved one to mesothelioma. Since the inception of the race, I have had opportunity to become a volunteer for the Foundation, through a community board and MesoTV. The Meso Foundation works diligently for mesothelioma patients and families to assist in a myriad of ways (research grants, patient care, family support), always with the understanding that we are not alone in this journey.
Jill A. Waite

This organization goes above and beyond for patients and families to not only provide resources and support, but also advocate and propel research forward for mesothelioma.

Being diagnosed with Mesothelioma was the scariest thing that has ever happened to me. This foundation has been a lifeline for me. Not only do they give you so much information, they give you hope.

Wonderful organization that provides info and support for both patients and caregivers through all steps.

This community of people gave me hope, insight, a shoulder and education on my mesothelioma diagnosis. They helped my family and myself with questions and locations. They are here to save lives and find a cure!

This foundation has helped me immensely. I have pleural mesothelioma and have learned a lot from this foundation. Thank you!

I am new in this journey with my dad who was diagnosed with pleural byphasic Mesothelioma. Mary has been nothing short of amazing in helping me navigate this journey.

The Mesothelioma Applied Research Foundation has been an invaluable help to my husband and to me, as his caregiver. They are excellent stewards of their funds and their resources and knowledge helped us immensely as we journeyed through this awful disease. I highly recommend them as a resource for those who have been diagnosed with mesothelioma.

A great organization truly dedicated to help mesothelioma research with fundraising activity and people affected by mesothelioma providing all the info useful to deal with this disease.

Incredible organization that truly helps people. The money is being used wisely towards research and finding a cure for Mesothelioma. As a 11 year survivor I can tell you that this is the greatest resource that I have found. The staff is fantastic and the group of people are so helpful. I only wish I had known about them sooner. This is a very wise investment of donation money. They are the real deal!

I learned about MARF 6 1/2 years ago soon after my diagnosis. My friend requested the free books and information after seeing the advertisement on television. She brought me the books and information, which answered many of the questions stirring in our minds. It gave a number to call for contact with a nurse practitioner well schooled in the latest treatments and where to find them. She put me in touch with someone who had been treated and willing to share her personal story with me. It was a great way to learn that there was hope for me and others. The nurse also confirmed for me that the cancer center I was considering was appropriate for treating Mesothelioma. I have enjoyed the educational conferences where you are able to learn the latest stats of treatments and guidance to additional new methods. You are able to meet physicians and nurses from different treatment centers you may have considered visiting. I love knowing that I can call the nurse practitioner who will give me unbiased information , and points me in the direction of choices.

This is the most amazing non-profit for mesothelioma research and patient support. There are not a lot of treatments available for this rare cancer. Because it is so rare, those with the disease (like me) need as much support as possible. Those working for the foundation have literally helped save my life. I’m forever indebted and grateful.

My grandfather and his best friend died of meso, an asbestos related cancer. It is relatively common in places with large military populations. But the general public understands little about this disease and people have few places to turn to for good information on treatment options and a community of fellow warriors. This fine organization provides guidance for people with this lethal disease and funds research, organizes conferences, puts together support groups, lobbies for a patient registry and other much-needed services. Without MARF, thousands of people would struggle alone with a fatal disease that is understood by few doctors, let alone lay people. I have attended their conferences to learn about the advances in the war against meso and am astonished that the director of the foundation, Mary Hesdorffer, personally fields calls from patients desperate for information and support. I can’t say enough good things about MARF.

Until I found the Mesothelioma Applied Research Foundation, I was floundering in a sea of misinformation skewed by legal ads all jumbled into pages and pages of internet search results, it was so overwhelming to me at the very time when I was desperate for information, support and education.. I was broken from the news that my husband was now a victim of this deadly disease. This foundation provided me the guidance in getting him the best care, the education I needed to pick the right providers, it put me in touch with survivors and caregivers and gave me a safe place to express my fears and concerns, the ability to ask all of the questions as a caregiver so I could be my best ..and understand from both ends of the spectrum what this disease process does to a family, and to the loved ones we are watching fight for their lives. I can't speak highly enough of how invaluable an advocate Mary Hesdorfer is for all of us affected by this horrific disease, from her clinical excellence in practice to knowledge of treatment options and clinical trials, to being a friend who is there for you when you're falling apart and can't find your way through the maze of medical care. Thank you Mary, for your dedication, the creation of this foundation, and what you have accomplished in getting awareness and improved treatment for those fighting Meso. By advocating for us in the fight for funding for improved treatment.. We would be lost without Mesothelioma Applied Research Foundation and the resources is has provided for us personally and for everyone In the battle of survival against Mesothelioma. Blayne Minogue, Suffern NY

This nonprofit does so much for people with mesothelioma, both patients and caregivers. They are so patient-focused and offer endless treatment resources and support groups. All of the information shared with this group is private (they don't resell your name, etc.). It's all about the patients here, which is so wonderful. The caring individuals associated with this foundation give people support, hope and roadmap for a bright future. I donate regularly as I know my money is going to a great place and will be used to help patients and fund research for a cure.

Mary and the entire team at MARF were monumental is helping my daughter find doctors and get support in order to travel to these doctors. Although she lost her battle almost two years ago at age 27, we still support MARF. Together we will find a cure! #curemeso

Diagnosed in 2010 with stage 4 mesothelioma, I faced a precarious and unknown future. The Mesothelioma Foundation provided me with guidance to physicians, centers, and treatment modalities of experience and excellence.
No other organization has the depth of knowledge coupled with the passion to support patients, their families, and critical research in the mesothelioma field.
I, and many of my peers, are alive; credit to MARF.

I have been associated with the Foundation for almost five years. I've been to their symposiums, done fundraisers, participated on their facebook groups and mentored other patients. The staff and board of this Foundation is top notch in my book. They keep things personal with all patients. We can call, meet with them or corrrespond by phone and email. Really a dedicated and caring group of people in my book. They have ceryainly helped me and I can say that I know many more patients who owe their lives to this organization. Bob Brittingham, 302-381-1292, bobbrittsemail@gmail.com . Meso patient.

This is a fantastic organisation that is committed to finding a cure for mesothelioma ..In addition it provides support for patients and their families.They are a fantastic source of the most upto date information on treatment methods and ways of managing symptoms

I am so grateful this organisation exists it gives us hope for the future.

My dad was diagnosed with Mesathemioma in July 2014. This foundation helped a lot. I know my dad must talk them since he had curemeso magnet. I got involved when I decided to do my own charity event for them. My dad past away from mesothelioma 2 months ago and this nonprofit has been so supportive

What a great source for information and support. Everyone associated with it wants to help find a cure and help you and your family.

Most amazing foundation truely dedicated to research.

My mother was diagnosed with Mesothelioma in 2014. The Meso Foundation served so many roles for us over the last two years -- expert knowledge of doctors, trials, treatments, caregiving, and side effects. Mary's straightforward, compassionate conversations and friendship during Mom's end of life this summer during my time of need was invaluable and much appreciated.

I attended the October 7, 2016 Mesothelioma Symposium in Chicago as the 'caregiver' of a patient, my husband. I arrived alone, a bit apprehensive not knowing what to expect. The group was very welcoming, it was wonderful to realize there were many other patients and families struggling with the same disease and issues.

The agenda and experts were stellar, the Q & A portions moved right along, the lunch provided was outstanding.
I learned about the Facebook group, and now have additional resources to use in the future, because that's the one thing there is available to us, a FUTURE!

I would recommend the Mesothelioma Applied Research Foundation to anyone with an interest in the disease, as a parent, caregiver, or clinician.

I cannot thank the staff at MARF enough. When my father was diagnosed with mesothelioma, we had no one to turn to at the hospital. No one was answering questions, no one was giving us resources. Then, we found MARF. My father only lived two months after his diagnosis but without the help of MARF, those two months would have been more chaotic and uncomfortable than I could ever have imagined. Thank you for being there and thank you for you support. Here is a photo of our family at our first Miles for Meso this summer, two months after my dad passed away.

I've spent over 30 years in litigation arising from asbestos. In those years, this group stands alone - by far - as the top group advocating for scientific research and providing educational, emotional and financial support for patients and their caregivers. No other group has - or will have - the knowledge, compassion and tenacity of Mary, Melinda and the entire team.

MARF is the only place to go for Mesothelioma information. The money goes to research to help understand this very rare form of cancer. God Bless them and the work they do!

I stumbled upon this foundation in my research for patient assistance when my husband was diagnosed with Mesothelioma a year ago. The foundation provides both financial and educational assistance for patients and their loved ones. Their executive director, Mary Hesdorffer, RN is incredibly knowledgeable and helpful in advising and educating patients about the different clinical trials available for treatment of Mesothelioma. She is dedicated to helping patients getting the help they need and has been incredible helpful to us. I highly recommend this foundation.

Meso Foundation has been awesome support to my family. My husband was diagnosed with Meso in 2014 and has undergone several types of treatments. The volunteers and staff at the foundation have been helpful in directing us to other options as well as supporting us emotionally through connecting us to others who have been through this.

Mesothelioma Applied Research Foundation Inc Is THE organization that drives awareness, fund raising for research, and life saving guidance for and about the deadly asbestos- caused cancer- mesothelioma. The Foundations symposia are the resource for both scientists and patients and their families. This is truly a life changing organization. It has made it possible for me to continue to live with hope.

Cure Meso helped me understand my second "Moms" condition. It helped me understand the complexities of this disease and helped me feel connected with others who were going through the same. It helped spread the word about Meso by ordering and wearing the "curemeso" blue braclets. More awareness needs to be made an more research needs to be done and MARF is doing just that. Forever grateful for this nonprofit!!!

Did wonders for my friend who has now been free of the disease for 9 years. The research grants, patient and caregiver support, and wealth of information is second to none along with the small staff that keeps it's wheels oiled looking for better treatments and a cure.

A great resource and support for mesothelioma patients and their families.

The Mesothelioma Research Foundation was an incredible source of hope and knowledge for me when I was diagnosed in 2007. They helped my husband get me to the right doctors and gave us support and the ability to interact with others who were going through the same situation. Over the last 8 years I have been able to use their wealth of knowledge to help me whenever I have questions or concerns. They have created a community for patients and caregivers that is essential when dealing with this disease.

The Meso Foundation and its dedicated staff gave our family courage when we needed it the most - to help us through our son Adam's peritoneal mesothelioma, and to help Adam see that he was not alone with this awful illness. Every penny given to the Foundation has resulted in better treatments and hope for thousands of patients and their families. Survival rates are up, and the network supported by the Foundation allows patients and family members to access medical experts and promising treatments, and allows researchers to move forward. Thank you, Meso Foundation.

The Meso Foundation is one of a kind, literally. This wonderful non-profit serves many needs of the meso patients and their caregivers. From travel grants to the latest medical trials and research, our meso journey would not have been the same without this wonderful group of knowledgeable, compassionate people.

When I was told to contact the Mesothelioma Foundation after my husbands diagnosis I was apprehensive. Not sure if this was going to be another secretly fueled Lawyer website. I did call but was still unsure. There were so many questions about the disease and treatment. As well as the immediate unknown about how our life was going to change without an income.
It was only after I contacted another family that also had just been diagnosed with Mesothelioma and heard their first hand account of how the foundation had answered all the unknowns that I made my second call to the foundation.
And after that second call and over the next two years the foundation guided us through surgery, recovery, chemo, radiation by giving us the tools to make informed descisions. In addition, with the support (closed and private) groups online I could always ask another family a question and receive a firsthand opinion from someone or from many who have walked that mile in my shoes. The online support groups were the day to day support that helped me as a caregiver get through the best days and the worst days of my husbands treatment. As someone once told me "it's the worst way to meet the best people". I hold the Mesothelioma Applied Research Foundation in the highest esteem. The help and guidance we received was like being embraced by a family and guided by angels every step of the way.

It keeps us all up to date on the latest information on mesothelioma.

My father passed away from mesothelioma eight years ago. When he was diagnosed, it was almost impossible to find quality information about the disease or doctors who were experts, let alone familiar with this "orphan" form of cancer. Our entire family was extremely frightened, confused and had no idea how to help my dad cope with the journey which lay ahead of him By chance, my sister came across the name of the Foundation and spoke with Chris Hahn (who was there at the time) and later, Mary Hesdorffer. These individuals along with others, helped us to make sense of the available medical treatment (no cure) at the time, and gave us referrals to oncologists (and hospital programs) who were extremely experienced and who helped my father put up the most valiant fight he could and retain his dignity until the day he passed away. My dad (a Navy veteran and former Brooklyn Navy Yard employee) was put in touch with others battling the disease for information, support and friendship. The caregivers' support board and Mary were always available to answer questions and offer kind words in our time of need. I honestly do not know what we would have done without being able to turn to the Mesothelioma Applied Research Foundation and its incredible team of volunteers.

I lost my beloved husband to mesothelioma 4/10/09 and found this site after his death. I am so gratified to find people actively working to find cures, give advice and encouragement and raise funds etc. for those suffering as we did. Mesothelioma is a killer and an awful way to die. Anything that can be done to help eradicate this terrible disease and to help those suffering from it is a good thing. Please keep up the good work.

Cure Meso. Org. This organization helps get information to those who are in need of medications and Who need assistance in helping others with this horrible disease

Totally run by professionals who work with Mesothelioma patients and families by educating and supporting them. There is no organization with better medical knowledge of this disease. Their nurse practioner knows and has contact with every mesotheioma specialist and is constantly up-to-date on newest clinical trials.

The Mesothelioma Applied Research Foundation deserves a huge amount of credit for the fact that my husband is alive today.

In 2012, my husband was diagnosed with peritoneal mesothelioma. It was difficult to find resources because it's an exceptionally rare disease, and we needed someone with experience who could treat it in the abdomen -- unlike most meso patients who need treatment in the lungs. There are very few experienced surgeons in the U.S. for peritoneal mesothelioma, and it was daunting to wade through the internet to find one because even though we live in one of the largest cities in the country, there wasn't a single oncologist in town who specialized in treating peritoneal meso.

The Mesothelioma Applied Research Foundation not only helped us to find experienced onocological surgeons, but provided guidance and counsel. My husband's cancer didn't image on CT scans (it was found in the pathology after his appendix was removed), so moving forward with the drastic treatment of HIPEC--the standard of care for peritoneal meso--was scary. I can't imagine having done it without the experience, wisdom, and guidance of Mary Hefsdorffer at the Foundation.

After my husband's HIPEC surgery, there were tons of life-threatening complications. It has been and continues to be a rough road, but the Foundation has provided education and emotional support. They have helped us to attend conferences where we've learned first hand from doctors, researches, survivors and bereaved about this disease.

The Mesothelioma Applied Research Foundation has had an incredibly profound impact on my life. I'm forever grateful for everything they do!

The Mesolthelioma Applied Research Foundation is nothing short of wonderful in dealing with patients dealing with this disease and their caregivers. They are ALWAYS available to answer questions and are in the know on everything about this disease, whether it is related to doctors, drugs, clinical trials, etc.. I would, without a doubt, direct anybody facing this disease their way.

I have several friends who are either battling mesothelioma, have a loved one who is (or who died from it), or are health care providers to meso patients. From them, I have learned that the Meso Foundation is the kind of nonprofit all others should strive to emulate! Its leaders are eminently ethical and professional in their operation of the foundation and stewardship of its funds -- and they provide absolutely priceless support to meso patients and caregivers. More than one of my friends have told me the Meso Foundation is the first place that gave them hope for effective treatment of their cancer, rather than just bad news. The Foundation stays on top of -- and helps fund -- the latest treatments for mesothelioma, and connects patients and families with expert doctors and nurses who are using these treatments. As a result, my friends who have the disease are alive today! The Meso Foundation also does a wonderful job of bringing patients and caregivers together in their yearly Symposium...and one of the truly healing and bonding experiences that has developed at this event is a band! They call themselves the Meso Fighters Band, and I wrote a blog post about them here. Please forgive the shameless plug...only including the link because it is absolutely an example of what makes the Meso Foundation, and all associated with it, exceptional: http://www.jcsmusicsbest.blogspot.com/2015/08/we-will-rock-you-meso-fighters-band.html

In the fall of 2007 my fiancee Brian was diagnosed with mesothelioma. Needless to say were were devastated. This being a rare cancer, we knew we had to seek out a Dr and hospital who dealt with this cancer on a regular basis to give Brian his best chance of survival.
I had read about Mesothelioma Applied Research Foundation (MARF) in a nursing journal only 1 month prior to Brian's diagnosis. I did not realize at the time how serendipitous that was. I found that article and contacted them. I spoke with the nurse practitioner, Mary, who ultimately helped guide us all the way through the 2 years of treatment with where to find resources and physicians, advice for chemotherapy related issues, and even just listening a time or 2. I believe in my heart that Brian would not have had those 2 years had it not been for this organization and their expertise, guidance, and knowledge of leading experts in this field. Thank you so much for all you do.

Incredible peer support for a rare disease that doesn't have a lot of support elsewhere. The foundation helps the entire family, not just the patient. The funding they have provided for research has truly made a differenced in the world of mesothelioma treatment. i'm proud to continually spread the word and raise money for this foundation, as I know it will be used for research.

When I was first diagnosed with Mesothelioma, the Mesothelioma Applied Research Foundation was there for me, and continues to stand with me every step of the way. I cannot put into words the knowledge and support I have obtained from this agency.

I don't know what we would have done without this organization when we discovered we needed help with this diagnosis. The support, education, and expertise is invaluable and has been a constant thread of hope when hope was hard to find. I thank God for this organization and do everything I can to let people know about it because REAL help with Meso is so hard to find. This is a charitable organization with true grit heart, compassion and up to the moment expertise.

When my mother was diagnosed with mesothelioma we got most of our information and guidance from MARF. My mother did not live very long after the diagnosis but I am thankful for the help we received from MARF.

I have mesothelioma. I have survived post-diagnosis (more than 5 years) because I have had access to and care by some of the most expert medical personnel who are dedicated to not only treatment, but also developing new medicines to beat this disease. I found those doctors and nurses because the Mesothelioma Applied Research Foundation made the connection for me. Simply put, MARF is one of the primary reasons I am alive.

Moreover, the Foundation was and is instrumental in promoting and funding the research that may allow me, and my peers, to continue to hold back and defeat meso. Additionally, it offers support tailored to patients, to caregivers and family members, and to the bereaved. The Foundation also has created systems for peer-to-peer discussions and contact among those groups, which let the affected know they are not alone, and spread information on shared experiences, what works, what doesn't, and other items that save time and reduce stress for patients or caregivers.

The Foundation stands alone as THE nonprofit organization dedicated to aiding patients in receiving care, funding peer-reviewed research into new treatments and drugs, educating patients, physicians, and those at risk of developing the disease, spreading awareness of the disease and its causes, and advocating tirelessly in Congress and the DoD for funding for research.

This is an outstanding organization.

In full disclosure, several years after the Foundation started helping me find appropriate treatments, I was pleased to accept an invitation to join the Board of Directors. This review system only allows designating one relationship with the organization, and I have received far greater benefit as a "Client Served" than I will ever be able to repay as a "Board Member".

This nonprofit is essential to all who suffer from Mesothelioma. I unfortunately have this disease and might not be alive if it wasn't for them. After my initial diagnosis they helped me weed through all of the misinformation out there and helped point me to the surgeon who has since made it so that I currently show no evidence of disease. Also once my surgeon left his practice to go somewhere else, they helped me find a suitable location to have my follow up exams that was much less stressful to get to.

The Mesothelioma Applied Research Foundation is an amazing group dedicated to helping meso patients and their caretakers around the world. The staff is so genuine and caring. They go above and beyond to help patients like me find the best treatments available. They assist with travel when needed. They're experts in the field and therefore have a plethora of knowledge to share. MARF works to bring patients together for networking and support. They're always quick to share breakthrough information related to cancer and mesothelioma. The Foundation truly cares for the wellbeing of every single patient. Their support has helped me through the various stages of my disease and I'm forever grateful for it.

Great organization that helps patients and families affected by mesothelioma to find right treatment. Also sponsors several grants for research and over 90% donated funds goes into research

Gr8 organization very dedicated to the patients and families it serves!!!

MARF is an organization that saves lives every day!!! They support patients, caregivers, provide education and most importantly they bring the Meso community together!!!

The meso foundation was there for my family from day one. They helped us find the best doctors we could for my father and helped us feel at ease. Many of the members have become close friends of ours. We will continue to support them and go to their fundraising events!

My sister was diagnosed with peritoneal mesothelioma and died seven months later. She was 45 years old, never worked with or around asbestos. We really don't know her true exposure. We had so many questions and found that MARF was the BEST source of information, help, and caring at a time when all else felt lost. I continue to follow them as I want remain informed and continue to help spread the word about mesothelioma so lives can be saved and no one will have to bury their loved ones. Asbestos kills!

My hubby was diagnosed in 2006 and at that time we did not know anyone who had had this cancer.....I found The Meso Foundation ...then MARF on line, and it became my resource for everything.....info.... counsel.... comfort ...... and courage !! They are truly a heaven sent group..... My hubby died in 2007 and I have been pleased to see they have continued to be a beacon to those affected by mesothelioma !!

As a 7 plus year survivor the Meso Foundation has been the go to place for everything meso related. It's prime directive is to fund much needed research. Available research funding puts Meso at the bottom of the list, so the funds provided by the Meso Foundation act as seed grants for proof of concept. It has funded over $8 million to date. Results from several of those grants have been awarded major funding by the DOD and other organizations. The Meso Foundation also provides patient and caregiver support 24/7, as well as having it's hand on the pulse of all the meso treatment centers and available treatment trials. A no brainer, the go to place.

My husband was given 6 months to live after being diagnosised with peritoneal mesothelioma. This was in 1998. Thankfully we found a trial in NY and he survived 11 years. It was after the first or second year that the Meso Foundation opened it doors and we found them on the internet. They immediately began to give us the support we so disperately needed. They knew about about the disease and offered us hope. We began going to symposiums and meeting many other patients and caregivers. Craig began giving others hope as he continued to beat the odds and live a strong productive life. I found my niche in fundraising for the Foundation. It empowered us against a monster. The Foundation helps people get the help they need and provides much more than information. They provide support of other patients and that is priceless.

The Meso Foundation has been an incredible support in my life. In 2009, my mom was diagnosed with Mesothelioma. She passed away 2 years later when I was 24 years old. She was the third person in her family to die from Mesothelimoa, and also not the last. Her sister, my Aunt passed away a year later in 2012.

Mesothelioma is a cancer that has literally destroyed my family. It can often be an isolating disease. Few people have heard of it, even fewer know what it truly is. The Foundation has been there for my family in every way, for my mom & aunt who were patients, for me as a loved one and now as a bereaved.

This nonprofit was instrumental in its early days as families like ours watched a loved one suffer so much before death. Whenever I called there was a friendly person to provide advice. Our loved one has been gone for 11 years now. However, this nonprofit is still helping others in so many new ways! We continue to support their efforts for a health issue that is so devastating. This organization is top notch!

When my father was diagnosed with mesothelioma we had no idea where to turn. I stayed up researching on the internet through the night, fighting my way through the law firm sites to try to get REAL help! Within 36 hours I was on the phone with MARF. It was a Sunday afternoon when Mary Hesdorffer answered the phone. That same Sunday, she had us on the phone with the top thorasic surgeon at New York University Medical Center in Manhattan. By Tuesday, my dad was in his office and Friday he was conducting a surgical biopsy.

This organization is the real deal! They have been there for us from the diagnosis and even now. The mission is to help patients and their loved ones to advocate, fight, survive and live well with mesothelioma. Of course, they also want to find a cure so pivotal research is funded.

My dad was with us for 20 months after his diagnosis. All of my initial research said that we would be lucky to get six months. There is not a doubt in my mind that we would not have had all of that time had we not found MARF. Even now that my father is no longer here, Mary and the foundation are still there trying to support us in our grief and loss. My mom calls Mary her angel: for without that support it would have been impossible to carry on.

I have family members & thousands of families are in the US Asbestos Exposure Health Emergency of Libby, Montana. In seeking Life Saving Medical Treatment for my family, I called the National Cancer Institute (NCI), and explained my families health situations. The NCI informed me that there are Zero Designated Cancer Treatment Centers in the Whole State of Montana, and Referred me to the Mesothelioma Applied Research Foundation aka CureMeso. This said everything to me, that CureMeso is the Best.
To this day, I'm still working with Mary Hesdorffer at CureMeso, in obtaining help for my family members, and appreciate all the time and effort she has given to my family members. Asbestos exposure not only affects the Lungs, it also affects other vital organs of the body. My brother Diagnosed by Dr. Brad Black of Libby CARD Clinic, has had to have a Kidney removed, and his wife is in Double Kidney Failure, so not only am I appreciative of CureMeso, but also The Kidney Foundation and UHCancerCenter whom also is now working with my family to save their lives. I appreciate all whom are helping to save the lives of my family members, and others with Asbestos Related Diseases.

I subscribed to this foundation after my beautiful Mum was diagnosed with Meso last year. It gives me hope & feels like there's a whole community of people who care out there as I read their regular social media updates. They are always extremely positive & do a great job of updating us all on trials & research from all over the world.

This non profit organization has helped so many others. Whether you are fighting for your life, caring for a loved one, lost a loved one or want to support research, the great people at mesothelioma applied research can help guide, direct and comfort you in your personal journey!

My husband is a stage 4 Mesothelioma patient and this site has helped us both greatly.

When my husband was diagnosed with meso in March of 2006, we knew nothing--what it meant, where to go for treatment, etc. The resources we found here were enourmously helpful, and so were the boards/forums. The support and comfort we received there cannot be quantified. Although my husband passed in 2008, I continue to keep up with the research. No one should have to die from meso--it's preventable, if ONLY we could get asbestos banned--but in the meantime, the research MARF funds goes a long way to helping find viable treatments, if not a cure.

My husband was diagnosed in June 2012, we were devastated with the diagnosis of Mesothelioma and really needed someone who was in our shoes to walk through this with. We inquired at the hospital if there was a support group for this cancer and that evening we received a call from a patient who was willing to talk about their experience with Mesothelioma. In that conversation we were introduced to MARF and were invited to participate in a private group atmosphere. This place of comfort took on so many different roles in our fight. At first it was a place to ask and receive answers from our peers, it included an opportunity to have private conversations with people you relate to and share a common mind set. Then it was our lifeline to ask and understand medical issues so foreign to us in the beginning. Finally, it was our research link to our persistent stretch for a cure. It is a non profit research foundation that only wants a cure and it is given freely. Privacy and Respect

My husband, John, was diagnosed with peritoneal mesothelioma a year ago. We frantically searched for help, but it seemed there was no place to find information or support for this rare type of cancer. So when we found MARF online it was God-sent! Mary was so encouraging! She was kind with a wealth of knowledge. She added us to a survivors and caregivers support group - an ongoing blessing! We were moved from fear to hope as knowledge gained from MARF's research helped us navigate to the best possible treatment options. John had a 14 hr. surgery with the only dr. in our area having the expertise to perform it. Today John is doing very well! Only those that have walked this road know what is needed for survival. We are grateful to the MARF staff for all they do to fight this terrible disease and their mission to find a cure for mesothelioma, including grants for clinical trials.

When my husband was diagnosised with Mesothelioma naturally fear set in . But somehow I/we found
Our way to MARF. This nonprofit is a godsend! They are not associated with any attorney's. The volunteers
Who call & talk with you, help you find the best care possible for your love ones. They are awesome people. The staff at MARF are always willing to help you. The caregivers support groups are super . I can go on & on. Simply put they saved me. Thank you to all the staff especially, Mary H...

I am a medical oncologist who treats a large number of patients with mesothelioma. From a physician's point of view, perhaps the most important aspect of the organization is the grant support they provide to fund research. Too few grant opportunities are available for this uncommon disease, yet MARF has been a consistent source of funding over the years for the top, scientifically peer reviewed projects in mesothelioma. Equally important, though, is, the tremendous emotional and educational support that MARF provides to my patients. I give each of my mesothelioma patients information about the foundation, and everyone who contacts them has benefited. I have been involved with MARF for about 10 years, and have seen dramatic change in organization over that time. The foundation has clearly established itself as the leading advocacy, educational, and scientific organization fighting this disease.

My son was diagnosed with mesothelioma in December 2006, and died in September 2009. Between his diagnosis and his death he sought information on the nature of the disease and possible treatment options. The most useful, honest and unfiltered information he received was from personnel and contacts at the Mesothelioma Advanced Research Foundation. My son contacted the Foundation numerous times for advice on potential treatments and clinical trials, and relied on them for important guidance. He came to believe they were the preeminent source of this information, and they provided this information with a caring attitude and strong psychological support as well.
As I began to learn about the Foundation, it was apparent to me that their stated focus of guiding the patient victims and providing funds for research was more than an altruistic goal. They really live that mission. As a result I have joined the Board of Directors and committed my time as well as monetary resources to their very worthy efforts.

I came into contact with MARF in January of 2009 and started to volunteer in September 2012. This is a group of people who care about the whole person, not just the diagnosis, or the part of the body with Meso. They care about you and your family and all those affected by the diagnosis. And they offer support to each one. And unlike other Meso organizations, they are not a front for a law firm whose real interest is is getting you to sign on with them so they can get part of your money. This is THE go to place for the most current information on treatment and trial, for details on advocacy and legislation, and for people coming together in love and support. Read the other reviews! There is no finer organization. And I simply would not volunteer my time with any other organization.

I had heard about the MARF for a number of years and was impressed by what I had read. However, in recent months I have been privileged to meet some of the key staff at MARF and was truly overwhelmed by their compassion and expertise. At the MARF conference in July 2012, there was an enormous amount of support for sufferers and carers as well as the opportunity for closed sessions where people could speak openly about their own situation. There are many people who talk big and deliver little but MARF IS THE REAL DEAL!

Where do you turn when you've diagnosed with a deadly disease you can't even pronounce? The Mesothelioma Applied Research Foundation Inc., helped by dear childhood friend by providing her and her family with up-to-date research materials, treatment options, an incredible support system and hope.

My husband was diagnosed December 31, 2001 with meso at the young age of 39. We were told the same by our local physician, get your affairs in order, travel to Europe etc....you have 6 to 8 months to live. I immediately hit the internet that New Year's Eve night and located the Meso Foundation. Left them a message and received a call from Chris Hahn, the Executive Director that January 2, 2002. I contribute that initial contact to my husbands' survial of 5 years. He succumbed to the disease December 21, 2006 at the age of 44. The outstanding caring, knowledge, assistance this foundation has given my family is beyond words. My heartfelt thank you and gratitude to this wonderful organization.

The Mesothelioma Applied Research Foundation (MARF) or Meso Foundation as it is commonly known looks after the interest of patients and families that are victims of this deadly but preventable disease. As there is virtually no research funded by the government or by any other groups the available treatment arsenal hasn’t changed much over the last 30 years contrary to the progress seen in eg Breast, Colorectal, Non-Hodgkin’s lymphoma, and Multiple Myeloma to mention just a few malignant diseases that have seen the impact of newer treatment modalities. The other side of Mesothelioma is the money, due to the asbestosis litigation which makes every patient a potential gold mine for those few law firms that are selected to represent the patient. Thus, there is a lot of advertisement from respectable and less respectable trial attorneys trying to attract a potential client. For a person with a newly diagnosed deadly malignant disease, with a name you can hardly pronounce, it’s not an easy task to navigate the turbulent waters of the excessive but not always necessary information flow. No wonder patients and families feel lost and confused in a time of significant stress and chock. MARF was founded to be a non-biased support group, initially helping patients with the information flow, supporting patients who can ill afford to travel for a consultation with the few and far apart clinical experts, supporting the family in difficult times and not least trying to find money for the much needed basic and clinical research, compensating for all the lost ground that the years of neglect and ignorance has caused. The Meso Foundation has as it’s ultimate long term goal to find the tools that will cure the disease and to work with other organizations to find ways to eradicate this preventable disease. As an Oncologist, Clinical Research Physician and Scientist working within the Meso Foundation finding a way to make the public, the medical community and the “government” aware and engaged in taking on the fight against Mesothelioma and reaching out to the many patients and families that are victims of this deadly but preventable malignant disease to help and support them is a noble and important task. I call on you to help me/us in doing the same, we are long overdue with dealing with this disease and you can make the difference.

I fully credit the Foundation with saving my life. I was diagnosed with peritoneal mesothelioma in August 2006, and was told by my local physicians that I should get my affairs in order. I found the Meso Foundation and they led me to a specialist, and I will be celebrating my 3 year survival anniversary soon. their work in research and advocacy in this field is unmatched. I am honored to be affiliated with them.

My grandfather was diagnosed with mesothelioma in 2007. I found the Meso Foundation by accident through a Google search. I was so lucky. From day one, the Meso Foundation provided me and my family with loving support, advice on multiple treatment options for my grandfather, and a community that simply inspired our entire family. Without their outpouring of love and support (to a total stranger nonetheless), there is no way I could endured the process of trying to help my grandfather get well while caring for him the best I could in the process. The Meso Foundation is first class all the way. It's too bad this site only provides five star ranking. They truly deserve at least 100 stars!

My diagnosis of mesothelioma was a shocker. Trolling the internet for information turned up MARF--a source not only of information but also of hope. Even though I had been to a major cancer center for a second opinion, I had been offered nothing but symptom treatment. MARF showed me the way to one of the few medical centers that actually treat mesothelioma. The staff has been extraordinarily supportive and the organization's work continues to offer hope.

This is a great foundation with purpose. It has helped many families that are going through an unbelievably tough time. Trying to provide answers, where there are none. Trying to provide solutions, where they are needed. They have played a very influential role in members of my families lives. We all appreciate everything they have done.

The Mesothelioma Applied Research Foundation is a remarkable non-profit organization that truly helps and cares about patients and care-givers. My mother was diagnosed with pleural meso about a year ago and we have found so many resources and information from MARF. We have utilized the resident nurse, Mary Herdorffer, with her plethora of information on doctors, medicinal information, and overall treatment options. She is available via phone or email basically every day of the week for patients to access for questions or data. My father and I attended the International Mesothelioma Symposium, which MARF has organized for the past few years, in Washington D.C. and received so much information, contacts, and feeling of hope! We were able to travel to Capitol Hill and voice our stories and ask for help with research funding, awareness, and support in banning asbestos legislation to our state's representatives. We learned valuable information from the top researchers and doctors from around the world who focus on this disease. I plan to attend this Symposium year after year, and I vow to stay involved with the foundation because it creates hope for a cure for this terrible disease. It funds research grants, is in the process of making September 26 a Mesothelioma Awareness Day nation-wide, and helps thousands of people.

I attended the Mesothelioma Applied Research Foundations Symposium in Washington DC in June 2009. I was impressed by the dedication of all involved. The Symposium was for patients, caregivers, doctors and researchers. Whatever the persons involvement, they were there with their whole heart. I was surprised to see so many people who have lost loved ones to Mesothelioma still so involved in the Foundation. It speaks alot to their dedication to finding a cure for meso. I was there as a volunteer and I know I will continue to help the Foundation in their fight to help ban asbestos and help to fund research to find a cure.

The doctors told my family that my father had about 6 months to live, and that he should get his affairs in order. When it seemed like all hope was shattered, I stumbled upon the Mesothelioma Applied Research Foundation. Their supportive staff helped my family to find specialists, learn about clinical trials, connect with others battling this cancer, and most importantly this foundation gave us hope.

The Mesothelioma Applied Research Foundation is THE source for mesothelioma awareness, medical guidance and other support for anyone impacted by mesothelioma. Mesothelioma awareness and research for better treatments and a cure are desperately needed, and only MARF can meet these needs. MARF is also attempting to establish September 26 as an annual Mesothelioma Awareness Day and assists individuals who are working with their state legislators for state recognition of this date. My 39-year-old son died of mesothelioma in 2006, and MARF continues wto support me and my efforts to promote mesothelioma awareness in his memory.

Amazing group of people. The support they have given our family is overwhelming. They are advocates for patients and continue to fight for a cure and legislation to end this disease. My uncle lived 10 years with this disease. During that time MARF became a part of his daily life. He touched others with the disease thru MARF and gave them support. Hi wife also became part of MARF. She went from organizing school fund raiders to becoming a leader in national fund raising for MARF. She also supports patients and their families today. MARF helps those that are given a diagnosis that to many is a mystery.

MARF has been a tremendously helpful resource for our family. When my mother was diagnosed with mesothelioma, we had no idea what it was or knew anything about the disease. Now we have a network of people for support, info on the latest developments, and lots of hope.

I believe that MARF has truly helped my family members deal with the tragic news of having cancer in a way that I admire. The organization has helped them become members of a community of hope in a time when hope isn't easy to come by.

When my husband was diagnosed with Mesothelioma, we knew nothing about this disease.Even after his lung was removed until his death 8 months later, we knew very little.After I found MARF,I realized how many people are diagnosed with meso each year.I also found out about major treatments available for patients and tons of support for patients and the families. I have hope that one day with the work that is done by this non-profit organization [ Marf]and the funding for research that a cure will be found.

this is a great organization that has helped by friend Bonnie Anderson to be here for her grandaughter. thank you

When my father was diagnosed with Mesothelioma in October 2008, not knowing anything on the disease, I quickly began researching on the internet, which led me to MARF. I cannot say enough about MARF. I would give it 1 million stars if I could. Their website is the greatest resource for anyone seeking information on the disease or just moral support. Not only does their website provide an astounding amount of information on the disease, their boards connected my family and I to others who were once in our shoes, providing us with support and guidance. Additionally, Mary Hersdorffer, the medical liason, provided more help than imagineable. She connected us to medical resources we didn't even know existed! I credit her and the site's promptness in contacting my family to part of why my dad is still alive and fighting today. The site has provided inspiration, understanding, and hope to my family, as I'm sure with others as well. I don't know what we would have done had we not found MARF. Thank you from the bottoms of all our hearts!

it is okay but there is another california foundation that seems to do more and has higher visibility.....can't remember the name but they have high profile people to make their case

Our son was diagnosed with Mesothelioma two and one-half years ago. Since there are only approximately 300 cases annually of the type of meso from which he suffers, it is known in the medical community as an "orphan disease". This designation has been applied because it receives very little funding from the typical sources to help find a cure. Additionally, information about treatment options is hard to find. The resources of M.A.R.F. have assisted us to locate the limited number of medical doctors in the United States that have expertise in treating the disease. It is one of the most valuable services offered because of the scarcity of information. In addition, the Foundation solicits private money for research and lobbies Congress to provide public funding as well. M.A.R.F. has a very small staff that is able to make a substantial impact. They plan and conduct an annual symposium attended by 300+ people in which the leading physicians present the most recent advancements in treatment and survivors share their stories. The staff is very efficient and able to offer services well beyond the limited resources provided to them.

My Uncle Mike died of mesothelioma and my mother found MARF and told me about it. They help patients and their familes learn about mesothelioma, connect them to resources, have wonderful support in their online community, have a team of researchers and doctors who work tirelessly to try to improve treatment and find a cure, and are always there when a victim of meso, or their family needs them, or when a loved one of someone who has lost the battle needs them. They are an excellent organization and so deserving of every award available

When my husband was diagnosed with mesothelioma in Jan 1997 and told to go home and die."which is what he did 5 months later," we knew absolutely nothing about this disease. Or about the evil of asbestos. The heartbreak it was to cause for so many families. And the shame of it all is because there are still many places where this product still is in existence, the killing will go on and on for a long, long time. Thank you for the Mesothelioma Applied Research Foundation Inc for being there for so many people. I just wish we had had a place to go to in 1997 for the help you give so many people. There was no where here in New Zealand, Deidre vanGerven

MARF is responsible for helping to keep my friend Bonnie alive. She was diagnosed with meso 7 years ago and is still alive today. She credits this foundation with many good things and because she is STILL alive today, so do I.

To suffer with cancer is a difficult task at best; to suffer alone is unconscionable. My husband was struck with mesothelioma in September of 2007. Internet searches for information about mesothelioma were dismal at best until I happened upon MARF. It’s difficult for me to see MARF as an organization but rather a group of people who are truly passionate about helping those afflicted with mesothelioma as well as their caregivers, families, and medical personnel associated with this disease. MARF not only offers much needed information about meso in a straightforward, easy to understand manner, they offer hope. And as anyone associated with cancer will tell you, we should all be allowed hope. The folks at MARF are quick to return phone calls, knowledgeable with answers and work diligently to support and fund research that may one day offer a cure for this terrible cancer.

When my husband of thirty-eight years was diagnosed with mesothelioma back in 2000, we were told by the first doctor we went to that he had approximately six months to live. Though that doctor didn't say, "Go home and die," he wanted to operate and he'd had only twelve meso patients before my husband -- none of whom lived more than a month or two past the surgery. Someone told us that the Mesothelioma Applied Research Foundation had a packet of information about the disease and meso doctors. We got that packet, learned there was more to fighting meso than letting a doctor with no experience practice on a loved one -- that there was a chance to lengthen my husband's life even if meso couldn't be cured. We got four years of being together instead of six months thanks to information about Dr. Sugarbaker and other doctors we found through the Mesothelioma Applied Research Foundation. There was even helpful advice on dealing with "ambulance-chasing lawyers" and on avoiding scammers -- interesting because it was founded by a lawyer whose father, I believe, had contracted meso. The Foundation has come a long way in the last nine years. I see it connecting people into a network of assistance with all manner of questions that meso victims and their families have to deal with. MARF responds to real needs! (Bec Gilbert)

The Mesothelioma Applied Research Foundation has been and remains an important organization in my fight with mesothelioma. Upon receiving my diagnosis in July of 2007, my wife and I were in a state of chaos. Definitive information about this disease, its treatment and contact with another person who was fighting this battle was non existent for us until we found the Foundation. Within 24 hours of placing a call to the 800 phone number, we received a call from a staff nurse who was willing to spend time answering all of our questions. The additional resources provided by the Foundation did, and continue to provide support and information for us. This is truly a deserving, client centered, organization which should be supported in any way possible.

The Mesothelioma Applied Research Foundation, was extremely helpful during my husbands battle with Mesothelioma cancer. I was heartbroken after my husbands diagnosis and went searching for some info. about this cancer that I had never heard of. From my first contact with MARF I was introduced to a nurse who listened to all my questions and then answered them one by one. She put me in touch with a Mesothelioma patient in my area and I was able to meet this person, hear about her treatments and make informed decisions. I have developed a strong bond with this wonderful lady. I was able to take my husband to see several doctors that are experts in Mesothelioma because of the information I had attained. This saved us precious time. We met the best doctors on the East coast and we were able to make the most informed decisions on treatments, because this cancer has no cure each doctor has a different theory on treatment. I believe with out the help of MARF, my husband would have never survived for the 17 months he did. Most patients are given a 6-9 month life expectancy. MARF is heavly involved in getting the laws in the United States changed so everyday people will not be exposed to asbestos. Exposure to the deadly mineral is the main cause of Mesothelioma. Once Mesothelioma has taken a hold it is a terrible painful death. Ithink this is a wonderful Foundation and in much need of public exposure.

MARF has been a wonderfully supportive organization, providing links between patients and doctors, researchers, and other patients as well as information on the latest research into the treatments and causes of mesothelioma. Patients with this rare disease often have little local access to information, and this is the one organization with links throughout the country that can provide help that is often not available through doctors and hospitals. MARF also lobbies for legislation to eliminate the danger of asbestos, which still exists, despite the widespread notion that it has been removed.

It was by accident that I found Mesothelioma Applied Research Foundation, (MARF) actually. My brother was sick many years and had been repeatedly misdiagnosed and sent home every time he went to the doctor or hospital begging for help, pleading for more tests. He told me he thought he was dying. He was right. Michael died in a hospital clinic, and wasn't diagnosed until his autopsy. The coroner described his lungs as "just a mess..." It was after his death that I found MARF while trying to learn everything I could about mesothelioma, and to become an advocate to fight the fight my brother couldn't win. I don't know what I would do without my beloved friends and the wonderful staff at MARF! The sincere love, support, wealth of information and resources, and the advocacy one finds at MARF is almost unbelievable, and has helped me through the devastation of losing my brother. The victims themselves, the loved ones of those fighting, the loved ones of the warriors who have passed away from this horrible disease...we all find love, strength, support and lasting friendships within each other. It is sad indeed that we must come together from the tragedy of mesothelioma, but without MARF, many of us would not have the strength we have to fight for a total ban on asbestos, for mesothelioma funding to support research so that improved treatments and a cure can be found, ongoing treatment, support for the meso warriors and their families, and information resources. They have been a godsend to me!

As the caretaker of a meso patient, I found this site to be a God-send. I received hope, encouragement and the name of a meso specialist that I could take my husband to for a second opinion. During the course of his illness I received hope and encouragement by the patients and caregivers on the MARF discussion board. I shared our experiences, hope and knowledge gained bcz of the disease, and used that to encourage others and also at times to vent the grief that was welling up within me - by trying to end entries on a lighter or laughable note. My husbands 27-month long battle with meso ended just 3-1/2 weeks ago.

Until I found the Mesothelioma Applied Research Foundation, My wife and I had no hope in the treatment of her peritoneal mesothelioma. The information that was available through MARF was a lifesaver in that they were able to give us a direction and purpose in our battle, giving us above all else, HOPE that was not available to us anywhere.

Mesothelioma has affected a dear friend of mine. Knowing about this disease, where it comes from, how we as Americans can stop others from being diagnosed and hopefully finding a cure. . . . has changed my life significantly. Julie Gunlach, a Mesothelioma "diagnosee" loves life more than almost any other person I know. She is an intelligent, loving, beautiful, courageous, brave, mother, daughter, sister, wife and wonderful friend. She deserves a cure as does everyone else diagnosed with this disease and everyone else in the future diagnosed.

MARF brings patients & families from the dark pit of no knowledge about a diagnosis of mesothelioma into the light of hope & treatment! Most patients diagnosed with meso are told there's no effective treatment available. There is & MARF has the connections to it! They have a talented, tuely caring nurse/practioner to work with patients & their families. The best specialists for this terrible cancer can be found through MARF. My daughter is a survivor & I am now a volunteer offering support where & how ever I can. I also advocate for awareness about asbestos & mesothelioma. The MARF staff genuinely care for their cause & the people they help. They do a great job of funding research to find better treatments &, hopefully a cure. The on-line community formed on the MARF web site really care for each other & offer hope, support, knowledge, comfort, & love. Everyone with a horrific illness like meso should be so lucky as those who find this foundation! Whether or not my cancer recurs I will continue to work as a volunteer & stay connected to my MARF "family".

When my 48 year-od husband was diagnosed with this disease, I was told he only had two years to live, MARF provided me with the information I needed to give him a shot at a cure. Their MESO Community Blog is an invaluable method of support for people dealing with this very rare and unique form cancer. This foundation works tirelessly to educate the public about this disease and to pass laws to decrease the number of people who continue to be exposed to asbestos.

In 2002, I was at what I thought was the peak of my life. I was a 52 year old nurse with a great career. I was weeks away from marrying the love of my life, and we had just bought our dream home together. I was physically active, an avid hiker, biker, snorkeler and free diver, and my fiancee and I looked forward to traveling the world together. My happiness was boundless. The only problem was a nagging cold that I couldn't seem to get rid of - my doctor felt antibiotics would do the trick, but took a chest xray "just in case". That xray was the key to a nightmare whose name was malignant pleural mesothelioma, a lethal type of cancer. My professional training, my doctors, and every thing I read on the Internet told me I was doomed to die within months - maybe a year if I was lucky. I have never felt so alone or so afraid, or so without hope. I could not stop crying. But then I found MARF - the Mesothelioma Foundation, and a small light began to shine in all the darkness that surrounded me. Here were people who gave me hope, information on treatment options that could help me, and put me in contact with other patients like myself. And they stayed with me, every step of the way, cheering me on and telling me not to give up. That was over 7 years ago. It has not been an easy road to travel, but I have never had to travel it alone - not for an instant. My fiance stuck with me (and became my husband) and so did the people at MARF. The clinical information they provided never failed to help me identify cutting edge treatments that gave me a fighting chance to live. Their unwavering support and encouragement saw me through the rough spots. They buoyed my spirits by sharing both my highs and my lows with unconditional compassion. Without this organization, I am certain I would have curled up into a terrified ball, given up, and died. I will never be able to adequately describe what they gave me: they gave me HOPE, the sweetest gift there is. They gave me back my life.

my parents home was insulated with asbestos. My mother was badly burnt when trying to clean it and her breathing has been difficult for year. No one would agree it was dangerous, no one would agree that it was the cause of all the issues. We knew better, their home was rebuilt from brick to drywall, to rid of this from the home. There needs to be a cure, we need to find that to help those who suffer.