Campaigns

Cancer

Curebound is a San Diego-based 501c3 philanthropic organization that raises and invests strategic funding in translational cancer research projects aimed at accelerating new discoveries to clinical application.

Curebound

Curebound is a San Diego-based 501c3 philanthropic organization that raises and invests strategic funding in translational cancer research projects aimed at accelerating new discoveries to clinical application.

The F C Cancer Foundation fights cancer by raising awareness and educating about prevention and early cancer detection, ultimately putting an end to late stage cancer diagnosis. As a 501c3 non-profit, the Foundation also coordinates experiences for cancer fighters.. Dyin 2 Live Dreams is a wish-granting program committed to helping those who are currently in the fight against cancer by giving them a one-of-a-kind “VIP Experience” that may be a source of hope, joy, and inspiration while they continue in their fight against these terrible diseases. Through our extensive network of friends, supporters, and partners, we put together our VIP Experiences, focusing on select music festivals, concerts, and sporting events throughout the year. We take our Dyin 2 Live Dreams recipients backstage and behind the scenes at these events to meet their favorite bands, artists, athletes, and celebrities. Meet-and-greets, signings, watching their favorite bands side stage, backstage access, media interviews, photo ops, and more are all apart of the VIP Experience! Our Dyin 2 Live Dreams recipients walk away from the experience with the will and determination to continue in their fight against cancer. We want to show them that life is worth fighting for and that no one fights alone.

F C Cancer Foundation

The F C Cancer Foundation fights cancer by raising awareness and educating about prevention and early cancer detection, ultimately putting an end to late stage cancer diagnosis. As a 501c3 non-profit, the Foundation also coordinates experiences for cancer fighters.. Dyin 2 Live Dreams is a wish-granting program committed to helping those who are currently in the fight against cancer by giving them a one-of-a-kind “VIP Experience” that may be a source of hope, joy, and inspiration while they continue in their fight against these terrible diseases. Through our extensive network of friends, supporters, and partners, we put together our VIP Experiences, focusing on select music festivals, concerts, and sporting events throughout the year. We take our Dyin 2 Live Dreams recipients backstage and behind the scenes at these events to meet their favorite bands, artists, athletes, and celebrities. Meet-and-greets, signings, watching their favorite bands side stage, backstage access, media interviews, photo ops, and more are all apart of the VIP Experience! Our Dyin 2 Live Dreams recipients walk away from the experience with the will and determination to continue in their fight against cancer. We want to show them that life is worth fighting for and that no one fights alone.

Friends of Jaclyn aims to improve the quality of life for children and families with a pediatric cancer diagnosis. Friends of Jaclyn (FOJ) pairs children with pediatric brain tumors and other childhood cancers with local sports teams, clubs and community groups. The teams provide a unique support system for the family during all stages of their journey. Friends of Jaclyn started in 2004, nine year old Jaclyn Murphy was diagnosed with a medulloblastoma, a malignant brain tumor. Through chance events she became connected to and later adopted by a collegiate lacrosse team as an honorary team member. Jaclyn’s strength, courage, relentless spirit, and joy for life inspired the players. The team went on to a perfect season, winning their first NCAA national championship in 64 years. Later, Jaclyn shared her dream of helping all of the sick children in the hospital with her family. In 2005, the Murphy Family created the Friends of Jaclyn Foundation to improve the quality of life for children battling pediatric brain tumors, allowing them to: Live in the Moment…Play in the Moment. Today, Friends of Jaclyn has helped over 950 families with brain tumors and other childhood cancers.

Friends of Jaclyn Programs

Friends of Jaclyn aims to improve the quality of life for children and families with a pediatric cancer diagnosis. Friends of Jaclyn (FOJ) pairs children with pediatric brain tumors and other childhood cancers with local sports teams, clubs and community groups. The teams provide a unique support system for the family during all stages of their journey. Friends of Jaclyn started in 2004, nine year old Jaclyn Murphy was diagnosed with a medulloblastoma, a malignant brain tumor. Through chance events she became connected to and later adopted by a collegiate lacrosse team as an honorary team member. Jaclyn’s strength, courage, relentless spirit, and joy for life inspired the players. The team went on to a perfect season, winning their first NCAA national championship in 64 years. Later, Jaclyn shared her dream of helping all of the sick children in the hospital with her family. In 2005, the Murphy Family created the Friends of Jaclyn Foundation to improve the quality of life for children battling pediatric brain tumors, allowing them to: Live in the Moment…Play in the Moment. Today, Friends of Jaclyn has helped over 950 families with brain tumors and other childhood cancers.

It all began with a few symptoms a week prior to her diagnosis. We were planning to take her to the pediatrician on the Monday coming up to have her checked out but she started a nose bleed that Easter Sunday that we could not get to stop. We rushed her to the local children's hospital and the tests ensued. She was at a critical level and immediately had to have multiple blood and platelet transfusions. After many blood tests, a spinal tap and bone marrow biopsy the results came back positive. On April 16, 2017 our beautiful baby girl Dakota Rain was diagnosed with B-Cell Acute Lymphoblastic Leukemia (ALL) at only 3 years old.  She started treatment immediately and we began our battle.Dakota spent the next 26 days in the hospital. Doctors had to make sure her immune system was stable enough for her to safely go home. We returned 4 days later to remove her picc line and place her port. Our weekly trips to the hospital have become a regular routine. She endures countless pokes, chemo treatments, spinal taps and oral medications. For a 3 year I can only imagine how confusing and scary it is for her. She will be in treatment for the minimum of 2 1/2 years so this means she will be close to the age of 6 before we are officially done.  Dealing with Dakota's Leukemia has dramatically altered our family's lifestyle and daily activities. We can no longer have the freedom to go wherever we want due to her fragile immune system. There is a constant worry and stress not only about her health but also financially. Mom had to resign from her job to immediately assist with all of Dakota's medical necessities. We worry that we simply will not have enough to make ends meat and keep a roof over our heads while trying to take care of Dakota. She is our priority now and  we want to make sure she has the best care.  All funds donated will primarily go towards any medical costs related to her treatment. Due to the fact mom is no longer working we will also need help with utilities and everyday items like food. Please help our family while we fight for our babies life. Thank you!

Help Dakota Defeat Cancer

It all began with a few symptoms a week prior to her diagnosis. We were planning to take her to the pediatrician on the Monday coming up to have her checked out but she started a nose bleed that Easter Sunday that we could not get to stop. We rushed her to the local children's hospital and the tests ensued. She was at a critical level and immediately had to have multiple blood and platelet transfusions. After many blood tests, a spinal tap and bone marrow biopsy the results came back positive. On April 16, 2017 our beautiful baby girl Dakota Rain was diagnosed with B-Cell Acute Lymphoblastic Leukemia (ALL) at only 3 years old.  She started treatment immediately and we began our battle.Dakota spent the next 26 days in the hospital. Doctors had to make sure her immune system was stable enough for her to safely go home. We returned 4 days later to remove her picc line and place her port. Our weekly trips to the hospital have become a regular routine. She endures countless pokes, chemo treatments, spinal taps and oral medications. For a 3 year I can only imagine how confusing and scary it is for her. She will be in treatment for the minimum of 2 1/2 years so this means she will be close to the age of 6 before we are officially done.  Dealing with Dakota's Leukemia has dramatically altered our family's lifestyle and daily activities. We can no longer have the freedom to go wherever we want due to her fragile immune system. There is a constant worry and stress not only about her health but also financially. Mom had to resign from her job to immediately assist with all of Dakota's medical necessities. We worry that we simply will not have enough to make ends meat and keep a roof over our heads while trying to take care of Dakota. She is our priority now and  we want to make sure she has the best care.  All funds donated will primarily go towards any medical costs related to her treatment. Due to the fact mom is no longer working we will also need help with utilities and everyday items like food. Please help our family while we fight for our babies life. Thank you!

Immunotherapy Foundation (IF) is a non-profit organization that strategically funds the most promising cancer immunotherapy research, focused on HPV-driven cancers. IF works directly with world-class researchers to accelerate the discovery and development of new and improved immunotherapies for patients, by translating multiple research projects into the clinical setting and creating a robust portfolio of preclinical immunotherapies and award-winning research at the University of California - San Diego (UCSD) and the La Jolla Institute for Allergy and Immunology (LIAI), as recognized by the Cancer Research Institute. IF is building educational programming around HPV vaccination and screening, with a focus on the link to cancer. IF is also creating a digital portal of the latest news and resources regarding HPV, HPV-related cancers, and immunotherapy treatments. The organization is investigating partnerships and alliances to help amplify existing education and advocacy initiatives, and build out regional, national and international efforts to reduce incidence of HPV and thus HPV-related cancers. IF is a 501(c)3 non-profit organization founded by the Whitworths in 2015.

Immunotherapy Foundation Cures for Cancer Campaign

Immunotherapy Foundation (IF) is a non-profit organization that strategically funds the most promising cancer immunotherapy research, focused on HPV-driven cancers. IF works directly with world-class researchers to accelerate the discovery and development of new and improved immunotherapies for patients, by translating multiple research projects into the clinical setting and creating a robust portfolio of preclinical immunotherapies and award-winning research at the University of California - San Diego (UCSD) and the La Jolla Institute for Allergy and Immunology (LIAI), as recognized by the Cancer Research Institute. IF is building educational programming around HPV vaccination and screening, with a focus on the link to cancer. IF is also creating a digital portal of the latest news and resources regarding HPV, HPV-related cancers, and immunotherapy treatments. The organization is investigating partnerships and alliances to help amplify existing education and advocacy initiatives, and build out regional, national and international efforts to reduce incidence of HPV and thus HPV-related cancers. IF is a 501(c)3 non-profit organization founded by the Whitworths in 2015.

Thirty-two days after saying I do to Jeff, Laurel Chaney was diagnosed with a fast-growing Stage 2B invasive ductal breast cancer. While still attempting to pay off their wedding, 40 days later they hit their out-of-pocket maximum for the year, and will again by 2/2019.

Laurel faces off against Breast Cancer

Thirty-two days after saying I do to Jeff, Laurel Chaney was diagnosed with a fast-growing Stage 2B invasive ductal breast cancer. While still attempting to pay off their wedding, 40 days later they hit their out-of-pocket maximum for the year, and will again by 2/2019.

To cure leukemia, lymphoma, Hodgkin's disease, and myeloma, and improve the quality of life of patients and their families.

Leukemia & Lymphoma Society

To cure leukemia, lymphoma, Hodgkin's disease, and myeloma, and improve the quality of life of patients and their families.

Libby’s Legacy Breast Cancer Foundation was formed in 2007 just a year after Robin and Marty lost their mom, Libby Maynard to Stage IV Breast Cancer. (Libby would never say she lost her battle, she would say she WON her trip to heaven!)

Libby's Legacy

Libby’s Legacy Breast Cancer Foundation was formed in 2007 just a year after Robin and Marty lost their mom, Libby Maynard to Stage IV Breast Cancer. (Libby would never say she lost her battle, she would say she WON her trip to heaven!)

The LIVESTRONG Foundation fights to improve the lives of people affected by cancer now.

LiveStrong Foundation

The LIVESTRONG Foundation fights to improve the lives of people affected by cancer now.

The Pancreatic Cancer Action Network is a nationwide network of people dedicated to working together to advance research, support patients, and create hope for those affected by pancreatic cancer.

Pancreatic Cancer Action Network

The Pancreatic Cancer Action Network is a nationwide network of people dedicated to working together to advance research, support patients, and create hope for those affected by pancreatic cancer.

Did you know that each day, 43 children are diagnosed with a form of childhood cancer? Or that the average age of children diagnosed is six? How about the fact that 12% of children diagnosed with cancer do not survive? Little do we know, there is not a single child who is cancer exempt! Help us support the mission of Childhood Cancer Research. Let's raise awareness to the world and let them know that it's an illness that is taking the lives of innocent children. I get it.... your kid is not sick, but what if your child was? Together we can fight the fight!! I have teamed up with CureSearch ( www.curesearch.org ) to fight the fight and with your pennies, together we can save lives!! To learn more about us, go to our personal site: www.pgcountry.com

PGcountry Childhood Cancer Awarness

Did you know that each day, 43 children are diagnosed with a form of childhood cancer? Or that the average age of children diagnosed is six? How about the fact that 12% of children diagnosed with cancer do not survive? Little do we know, there is not a single child who is cancer exempt! Help us support the mission of Childhood Cancer Research. Let's raise awareness to the world and let them know that it's an illness that is taking the lives of innocent children. I get it.... your kid is not sick, but what if your child was? Together we can fight the fight!! I have teamed up with CureSearch ( www.curesearch.org ) to fight the fight and with your pennies, together we can save lives!! To learn more about us, go to our personal site: www.pgcountry.com

The Prostate Cancer Foundation (PCF) is the world’s largest philanthropic source of support for prostate cancer research to discover better treatments and cures for prostate cancer.

Prostate Cancer Foundation

The Prostate Cancer Foundation (PCF) is the world’s largest philanthropic source of support for prostate cancer research to discover better treatments and cures for prostate cancer.

Runway to Hope’s mission is to provide direct support and aid to Central Florida children and their families impacted by pediatric cancer.

Runway to Hope

Runway to Hope’s mission is to provide direct support and aid to Central Florida children and their families impacted by pediatric cancer.

Precision Medicine for All - At SOTERIA, we support a superior approach to cancer treatment, where the patient is at the center of globally curated resources to implement precision medicine and generate better outcomes despite geographic location, treating institution, or socioeconomic status. The founders and supporters of SOTERIA are personally familiar with a cancer diagnosis and believe that every cancer patient deserves access to the best care. SOTERIA challenges the one-size-fits-all approach to cancer treatment by leveraging the power of an individual's data to identify personalized, targeted treatment plans and provides access to the most relevant advanced technology and treatment options from the convenience of your own home. Advancements in genomics have enabled personalized, targeted cancer therapy, leading to better outcomes. As medicine becomes more multi-modal, no one individual or institution can be the leading expert in all areas., nor can we rely on existing institutions to lead this effort because there is no economic incentive. SOTERIA is a neutral entity that is required to synthesize medical & scientific experts to bridge the gap to navigate the complexities of precision medicine and help alleviate patient and physician burden to generate better outcomes.

SOTERIA Precision Medicine Foundation

Precision Medicine for All - At SOTERIA, we support a superior approach to cancer treatment, where the patient is at the center of globally curated resources to implement precision medicine and generate better outcomes despite geographic location, treating institution, or socioeconomic status. The founders and supporters of SOTERIA are personally familiar with a cancer diagnosis and believe that every cancer patient deserves access to the best care. SOTERIA challenges the one-size-fits-all approach to cancer treatment by leveraging the power of an individual's data to identify personalized, targeted treatment plans and provides access to the most relevant advanced technology and treatment options from the convenience of your own home. Advancements in genomics have enabled personalized, targeted cancer therapy, leading to better outcomes. As medicine becomes more multi-modal, no one individual or institution can be the leading expert in all areas., nor can we rely on existing institutions to lead this effort because there is no economic incentive. SOTERIA is a neutral entity that is required to synthesize medical & scientific experts to bridge the gap to navigate the complexities of precision medicine and help alleviate patient and physician burden to generate better outcomes.

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