Donate

Patient Resources

Brave Kids– Find medical information and resources for children with special needs, chronic illness and disabilities such as: autism, cancer, cerebral palsy, ADHD, ADD and more. Brave Kids provides parents and children with information on health services, financial assistance, support groups, child care, dental assistance, camps, transportation and physical therapy to name a few (description from site).

Kids Health – If you’re looking for information you can trust about kids and teens that’s free of “doctor speak,” you’ve come to the right place. KidsHealth is the most-visited site on the Web for information about health, behavior, and development from before birth through the teen years (description from site).

When illness strikes, it affects not only the patient but the entire family unit. That impact is magnified for a child’s brother or sister. There is a powerful bond between siblings, and the realization that the connection could be lost is traumatic. It is important that the sibling understand what is happening to their brother or sister and learn to deal with it in a healthy and positive manner. The sites below can help to carry out that process.

Sibling Support Project – The Sibling Support Project is the only national effort dedicated to the interests of over six million brothers and sisters of people with special health, mental health, and developmental needs. Our mission is accomplished by training local service providers on how to create community-based peer support programs for young siblings (description from site).

Super Sibs! – SuperSibs! is dedicated to ensuring ongoing comfort, recognition and support to children with brothers and sisters who have cancer. SuperSibs! helps these siblings to redefine the cancer experience to use these life lessons for strength, courage and hope as they move into the future. No longer are these “shadow survivors” forgotten, and alone as they battle feelings of fear, insignificance, guilt, helplessness, anger and grief (description from site).

Comfort Zone Camp – Comfort Zone Camp is the nation’s largest bereavement camp. Comfort Zone Camps are offered free of charge to children ages 7-17 who have experienced the death of a parent, sibling or primary caregiver. The camps are held year-round in California, Massachusetts, New Jersey and Virginia. Comfort Zone Camps create an environment where grieving children can have fun and break the isolation death often brings, while learning valuable coping skills For their daily lives (description from site).

Everyone needs a break from all the stress that accompanies the numerous treatments and tests that a critically ill child and his or her family must endure. Whatever your wish or dream is, these organizations can help you fulfill them!

Dream Factory – The Dream factory grants dreams to critically and chronically ill children from the ages of three through eighteen. The Dream Team of volunteers roll up their sleeves and get to work making reservations, finding contacts for celebrities, sports figures and other famous people, finding gifts-in-kind and other volunteers. In essence, whatever it takes to make a dream come true that will provide a memorable and inspirational experience for the children and families alike (description taken from site).

Children’s Wish Foundation International – Wish Coordinators make up a professional team with over 20 years of experience in creating unique, carefree wishes that, depending on the type of wish, include all travel arrangements, accommodations, tickets, full detailed itineraries, expense money, volunteer support, carefully planned presentations to fit the family’s schedule, and the promise of lots of surprises along the way. Every detail is planned to perfection, allowing the family to enjoy “Family Time”, creating precious memories to forever cherish (description taken from site).

A Special Wish Foundation – A Special Wish Foundation, Inc. is a non-profit charitable organization dedicated to granting the wishes of children under the age of 21 who have been diagnosed with a life-threatening disorder. Founded in 1982, A Special Wish Foundation was one of the first wish-granting organizations in the United States, and now has chapters across the U.S. and one in Moscow, Russia. Since 1982, wishes have been granted to thousands of qualifying children (description from site).

Believe In Tomorrow – Unique healing environment of hospital and retreat housing facilities, where families find hope and comfort. Since 1986, Believe In Tomorrow has provided over 300,000 overnight accommodations, helping families stay together in the midst of a medical crisis (description from site).

Make-A-Wish Foundation – Since 1980, the Make-A-Wish Foundation® has given hope, strength and joy to children with life-threatening medical conditions. From humble beginnings with one boy’s wish to be a police officer, they’ve evolved into an organization that grants a child’s wish in the U.S. every 40 minutes (description from site).

Starlight Children’s Foundation – For more than 25 years, Starlight Children’s Foundation has dedicated itself to improving the quality of life for children with chronic and life-threatening illnesses and life-altering injuries by providing entertainment, education and family activities that help them cope with the pain, fear and isolation of prolonged illness (description from site).

HopeWell Cancer Support – The mission of HopeWell Cancer Support is to create a community for all people with cancer, their families and friends, which encourages an exchange of information, the development of a support system and the presence of hope. This organization is based out of Lutherville, Maryland. (description from site).

Candlelighters Childhood Cancer Foundation – The Candlelighters Childhood Cancer Foundation National Office was founded in 1970 by concerned parents of children with cancer (description from site). This site explains clearly, in age appropriate language, what cancer means directly to the child diagnosed with the disease. It also includes support groups, upcoming events, clinical trials, reading material, and links to an incredible amount of helpful sites.

Cure Search: National Childhood Cancer Foundation – CureSearch unites the world’s largest childhood cancer research organization, the Children’s Oncology Group, and the National Childhood Cancer Foundation through their mission to cure childhood cancer (description from site). The site does a good job at directing information towards specific groups such as friends, family, parents, and of course, the patient. It also lets you customize the type of cancer you have as well as you age for more pertinent information.

I’m Too Young For This! Cancer Foundation – Founded in 2007 by young adult survivors and for young adult survivors, the I’m Too Young For This! Cancer Foundation is a global leader in the fight against cancer working exclusively on behalf of survivors and their care providers under the age of 40. Opportunities like weekend spa retreats, online forums and blogs, social networks, camping excursions, fertility education, peer counseling, college scholarships, financial aid, happy hours and more (description from site)!

Planet Cancer – Young adults with cancer slip into a lonely no-man’s land. Too old for the instant community of a children’s hospital, they still don’t fit in with the over-50 community that overwhelmingly populates adult cancer wards. Because young adults with cancer are a relatively small group, the difficulty of finding peer support is increased exponentially, forcing many to deal in isolation with issues specific to this age and stage of life: dating with cancer, disclosure to a potential employer, long-term insurance issues, moving back home, loss of fertility, or having to quit school or a newly launched career (description from site).

Group Loop (Bad Link—I can’t find a replacement) – Group Loop is a safe place online for teens with cancer away from the daily pressures of classes, after school activities, family and work responsibilities, let alone treatment schedules. Many teens with cancer are unable to leave their homes, drive cars, or attend social activities. Group Loop will serve as a unique place for teens with cancer to “connect” with other teens and forge friendships while battling unwanted aloneness, loss of control and loss of hope associated with the disease (description from site).

Young Adult Cancer Canada – This is where we “share our sh*t”, literally and figuratively. It’s for those who are ready to leave pediatrics or have already gone, but are nowhere near geriatrics. Beware, this isn’t only about ranting; while we definitely recognize the importance of a good rant. The RealTime Cancer Community is all about the open, honest, pursuit of the positive, so all the stories you find here will be from the heart and inspiring (description from site).

The Leukemia and Lymphoma Society – The Leukemia & Lymphoma Society (LLS) is the world’s largest voluntary health organization dedicated to funding blood cancer research, education and patient services (description from site). The organization provides a live chat 10a.m. to 5 p.m. Monday through Friday for patients and parents to talk to an Information Specialist. In addition to having a Peer to Peer network to connect patients and parents as well, they also have local chapters in Maryland and surrounding states.

The Lymphoma Research Foundation – On this Web site you will find valuable information about the different types of lymphoma. Here you can also learn about the latest research findings and get help searching for clinical trials that relate to your condition. The Lymphoma Support Network can help you connect with a peer who is also living with lymphoma or you can find out how to volunteer at an LRF chapter near you (description from site). They also provide a youth webcast and podcast series related to the illness.

Lymphoma Information Network – The Lymphoma Information Network provides a great detail of information about leukemia, but also provides a fantastic social network for the patients and their families. Find support groups, ask a question, use the forums – interact with others who are having similar experiences to your own.

Pediatric Brain Tumor Foundation – The Pediatric Brain Tumor Foundation (PBTF) is a 501 (c)(3) nonprofit organization dedicated to supporting the search for the cause of and cure for childhood brain tumors. As the world’s largest nongovernmental source of funding for childhood brain tumor research, they’re dedicated to not only eradicating this disease, but to providing support to families (description from site). The site offers an online conference series for parents about different elements of the illness including sibling stress, risk factors, school re-entry and much more.

National Brain Tumor Society – The National Brain Tumor Society offers top-notch resources and caring support for everyone affected by brain tumors. They offer hope to patients, families, and caregivers during every stage of the treatment journey (description from website). The organization also offers a program to put current patients in contact with survivors who can relate to what is going on and offer hope for the future.

Children’s Brain Tumor Foundation – This organization works to improve the treatment, quality of life and the long term outlook for children with brain and spinal cord tumors through research, support, education, and advocacy to families and survivors (description from site). Also offers a Parent to Parent support network as well as online conference and support information.

Aplastic Anemia and MDS International Foundation, Inc. – The Aplastic Anemia & MDS International Foundation is an independent nonprofit organization whose mission is to support patients, families, and caregivers coping with Aplastic Anemia, Myelodysplastic Syndromes, Paroxysmal Nocturnal Hemoglobinuria, and related bone marrow failure diseases. They also provide educational materials, medical information, and access to peer support via a global network of volunteers who offer hope to those struggling with bone marrow failure diseases (description from site).

National Heart Lung and Blood Institute – The Institute plans, conducts, fosters, and supports an integrated and coordinated program of basic research, clinical investigations and trials, observational studies, and demonstration and education projects. Research is related to the causes, prevention, diagnosis, and treatment of heart, blood vessel, lung, and blood diseases; and sleep disorders. The NHLBI plans and directs research in development and evaluation of interventions and devices related to prevention, treatment, and rehabilitation of patients suffering from such diseases and disorders.

Medline Plus – This link will direct you to the section on Blood and Blood Disorders. It contains a variety of information including an overview, treatments, educational games, research, and sections on children and teenagers.

Blood Typing Game – In this game, three patients need blood transfusions, and it is up to you to pick the right type of blood to give them! This educational game is perfect for teaching kids the difference in blood types.

The Leukemia and Lymphoma Society – The Leukemia & Lymphoma Society (LLS) is the world’s largest voluntary health organization dedicated to funding blood cancer research, education and patient services (description from site). The organization provides a live chat 10a.m. to 5 p.m. Monday through Friday for patients and parents to talk to an Information Specialist. In addition to having a Peer to Peer network to connect patients and parents as well, they also have local chapters in Maryland and surrounding states.

The Lymphoma Research Foundation – On this Web site you will find valuable information about the different types of lymphoma. Here you can also learn about the latest research findings and get help searching for clinical trials that relate to your condition. The Lymphoma Support Network can help you connect with a peer who is also living with lymphoma or you can find out how to volunteer at an LRF chapter near you (description from site). They also provide a youth webcast and podcast series related to the illness.

Lymphoma Information Network – The Lymphoma Information Network provides a great detail of information about leukemia, but also provides a fantastic social network for the patients and their families. Find support groups, ask a question, use the forums – interact with others who are having similar experiences to your own.

The Sarcoma Foundation of America – The SFA eliminates pains and suffering due to sarcoma by funding research, advocating for increased government funding, increasing public awareness, education patients, and making clinical trials available to those who need it.

Sarcoma Alliance (Domain Name expired? – The Sarcoma Alliance strives to extend and improve the lives of sarcoma patients through accurate diagnosis, improved access to care, education, and support (description from site). Key features of this group include a live 24/7 support chat room, and online specialist, support centers in MD, PA and DC, a peer to peer network, financial assistance and links to sites to connect young patients together.

NorthWest Sarcoma Foundation – The Northwest Sarcoma Foundation goal is to create and actively participate in the direction of a national alliance with other sarcoma foundations and affiliated groups guiding a coalition among private and public concerns furthering research for a cure of sarcomas. Although this organization is more directed towards the Northwest states, the information contained in it is pertinent to all patients.