Find Voluntary Health Associations & Medical Disciplines Nonprofits and Charities

  Changed wrote:

This organization is affiliated with the IPA (International Parurisis Association) which helps individuals with Parurusis (Shy Bladder Syndrome). Although to many people who do not suffer from this condition (which affects daily life, multiple times... more »

  gracies19 wrote:

Invisible Disabilities Association provides a great network for people who otherwise would struggle to find feelings of community. Lives touched by disability are made easier and more enjoyable because of this amazing foundation. more »

  dyoder wrote:

I just found the MAGIC Foundation this year when I was faced with a medical mystery with my son who is now 3. He stopped growing properly when he was less than six months old and after a parade of doctors I realized that it was up to me to find out how... more »

  thoughtenergy wrote:

Since its inception in 1999, the Association for Comprehensive energy Psychology (ACEP) has promoted the goals of unifying a diverse field of professionals who utilize human electromagnetic and bioenergetic potentials to promote healing of mind-body-spirit.... more »

  dscgan wrote:

I've volunteered for this organization for 10+ years. It is amazing to see their growth over the last two years. It's fantastic that finally, in 2014, the organization will be funding meaningful multiple system atrophy research. more »

  DeborahBrennerLiss wrote:

The mission of Eating Disorders Resource Center (EDRC) is to increase awareness and understanding of eating disorders for the general public and for health professionals; to promote early diagnosis, effective treatment, and recovery; and to advocate... more »

  bbp3 wrote:

I've done some copywriting work and some volunteer work for the Worldwide Fistula Fund, and I will continue to offer my services. It's a great organization working to prevent and treat obstetric fistula all over the world, but especially in Danja, Niger,... more »

  archaeologymom31 wrote:

I have been on two missions with this charity and am preparing to go on the one in June 2015 to Equador. It is extremely well organized, not a penny is wasted, all funds raised goes to patient care, no one gets a salary not even the director. We pay... more »

  CAPkids wrote:

Bald Girls Do Lunch is a great resource for women with alopecia. The Children's Alopecia Project is proud to partner with them as they help to restore self-esteem in women living with hair loss. more »

  R.C. wrote:

AnCan is a tremendous resource offering real-world experience and actionable data. The caring folks associated with this foundation are selfless in the way they interact with those who seek their help. In my case, AnCan was largely instrumental in my... more »

  David Wolfesky wrote:

rarediseases.org is far removed from knowing the patients they serve. more »

  BattleForBattle wrote:

Our daughter was diagnosed with cancer when she was fourteen and a half. Lisa visited many times to bring care packages to our family during long weeks while our daughter received chemo. The packages were full of gift cards and words of encouragement.... more »

  Teresa wrote:

The Taylor Family Foundation provides a great service to children with a wide-range of illnesses and disabilities. The money that is given to TTFF is wisely spent and over 90% of it goes directly to benefit the children. It is a well-run and well-organized... more »

  H. Sandbach wrote:

This extraordinary therapeutic equestrian center has it all. Great underlying management strength and direction by its founders, a well-rounded board of directors reflecting the best of the community, capable and caring volunteers and, best of all, a... more »

  Justin Reilly wrote:

ME/CFIDS is a devastating neuro-immune disease. ME is a disease that desperately needs funding more than almost any other. Unfortunately CAA, one of the two largest ME orgs in the US, has failed patients and thus is not the org to which one should... more »

  Justin Reilly wrote:

Just a couple of years after its founding, WPI is the clear world leader in the science of neuro-immune diseases including ME. They were founded with a $5M donation from the Whittemore family, whose daughter Andrea suffers from ME. They do incredible... more »

  allensteere wrote:

I have served on the Ivy Hill Board of Directors for approximately 10 years. My role is to support the mission of Ivy Hill which is help individuals with disabilities gain strength, independence, confidence, and a sense of achievement through equine therapy.... more »

  Writer wrote:

Topaz Canine Services is a tremendous organization. I am a senior citizen and have been a member of the ‘Topaz Family’ since fall 2016. Topaz’s ability to access and meet the clients’ individual needs is beyond compare. Topaz possesses the great... more »

  Paula wrote:

I found the Raynaud's Association about a year ago, when I was diagnosed with Secondary Raynaud's. I have found the site to be a great source of education, information, and support. I learn more from people that are going through similar situations,... more »

  coreyrocks1994 wrote:

The NN is a fabulous organization that provides tremendous support to those afflicted by narcolepsy. We just returned from our annual conference. It was well organized, had very imformative speakers, provided a wealth of knowledge to those attending and... more »

  RobbieRob wrote:

This Organization changed my family's life about 16 years ago. This diet program is for children with ADHD and many other disabilities. By tailoring the diet you see a major difference in abilities both physically and mentally. Thank you Feingold... more »

  happyjack wrote:

I am a ET sufferer and have to say the IETF are the biggest and best non profit organisation i know of for ET and help a lot of people around the world with this condition and make them feel better about themselves. keep supporting the IETF so they can... more »

  Stacy Benton S. wrote:

PMG Awarenesss organization has been amazing for our family. We have been able to connect with other families around the world that have someone with PMG! We also got to attend our first PMG conference this last July in Colorado. We talked with lots of... more »

  lynnmanning54 wrote:

Although my family member has myositis, I say please, please do not donate to the Myositis Association. It is an outrage that they get three stars. The Director's lofty salary represents 20% of the revenues! It's shameful how a few people who control... more »

  dnl1231 wrote:

I have been coordinating events and running the Brad Kaminsky Foundation for the past 10 years. It was started after Brad Kaminsky passed away from brain cancer at age 29. Brad's family and friends came together vowing to end this disease as a way to... more »

  Tracy wrote:

I was called by the Breast Cancer Prevention Fund, and encouraged to schedule a mammogram. Since I was uninsured, this is not something I could afford to do. They told me that they would pay for the mammogram and helped me get scheduled with a local clinic.... more »

  Danster092 wrote:

I worked at NEDA this past summer as a social media intern. I was able to respond to individuals with eating disorders and individuals who know of someone with an eating disorder. By updating NEDA's Facebook tattoo page and responding to Facebook messages,... more »

  jimgundlach wrote:

After the doctor who has treated people who have had their brain infected with encephalitis told me that I was his first patient to survive this infection in twenty-fours of treating about two cases every three years, I understood why he did not know... more »

  Writer wrote:

Music Sweet Music has made an even greater impact than imagined in my life when visiting the Shriner's and St. Joseph's Children’s Hospitals in Tampa, FL with Ted Wagner. We shadowed Music Therapist Jennifer Miller during one of her days of providing... more »

  MyKidsSccrMom wrote:

I discovered Rest Ministries about 8 years ago. it became a big source of support and information in my physical battles with Fibromyalgia, IBS, Depression and Anxiety. Lisa Copen has a heart of service to those within her organization. It provides a... more »

  Momof1MS wrote:

Loosing a child is one of the most difficult things I have ever had to deal with. My husband and I were never able to afford a tombstone for my son's grave. The people at the Luca John Foundation were generous enough to donate the stone. From the first... more »

  kschoen wrote:

The Foundation is VERY committed to its goal of raising awareness of LGS, providing support for LGS families, and raising funds for additional research. As a board member, and participant in the many LGS foundation events, I have first-hand experience... more »

  Maurice F. wrote:

I was told about Breast Friends from a Dear Friend who has battled and beat breast cancer....I was not sure what to expect or what was expected from me....but I went to help mail out letters and forms.....Who knew that the people and organization was... more »

  Dreamweaver13 wrote:

I have been donating to the National Fibromyalgai Association since I attended their first national conference held in southern CA in 2000. If it weren't for the efforts of this organization people would still think that this terrible chronic pain illness... more »

  tritter wrote:

My husband of 35 years of age had his 3rd stroke in May of 2012. He was sent to Barnes Jewish Hospital in St. Louis, MO. It was there where he was finally diagnosed with Fabry. The doctor being a stroke specialist did not know much about this disease... more »

  Polarseltzer12 wrote:

This is a small but mighty organization. I appreciate the patient stories and also being able to find accurate research on MAS! more »

  Jennifer596 wrote:

My 9 year old son has idiopathic Syringomyelia and this organization has been so helpful. I love Beth's passion to help spread the word and help others more »

  tedthartley wrote:

I was on dialysis and had to quit working and lost my insurance. The AKF stepped in and helped me by paying the extra that my wife's insurance was charging us to have me on her policy. You have enough to deal with when you are on dialysis waiting for... more »

  Tracy A. wrote:

I am a 14-year Breast Cancer survivor and was introduced to ABCD in the early years! My Breast Health Coordinator suggested that because I was relatively young at the time of diagnosis, I might want to consider helping other younger women with my story... more »

  milindacleft wrote:

As a mother of three and my youngest born with a cleft palate and other conditions, I have found the Cleft Lip and Palate Foundation of Smiles a orgainzation that "real" people, a family cares so much for each person that wants some support. Just to know... more »

  petha wrote:

They have a flourishing message board that has helped thousands of people. In addition they provide education to medical providers, patients, caregivers and the general public. They also develop educational programs for clinicians who treat viral hepatitis... more »

  shelley3 wrote:

We are a passionate group of volunteers working towards a cure for paralysis and in the mean time we provide adaptive scuba diving as a quality of life program with Cody's Dive Team, operation Deep Down. The Dive Team is composed of 100% volunteers,... more »

  bobbidaly wrote:

The ERC has been an absolute godsend for me. I was diagnosed with endometriosis early this year after suffering symptoms for an extended period of time. I felt so confused and alone and had no idea what my options were. The ERC provides support and extensive... more »

  Writer wrote:

I am a researcher in this field and have been for 6 years. This organization is one that actively brings together the top minds in the clinical and research areas in order to bring the most recent information and awareness to those afflicted with Lp(a)... more »

  mcelhina wrote:

I was diagnosed in 2008 with IIIC ovarian cancer. After being incompletely debulked, I had carboplaten, taxol, and Avastin. I had my molecular profile done in 2010. It showed my tumor would best respond to Avastin, the drug I’d already had. I’ve... more »

  Talitha McGuinness wrote:

Fetal Hope is unique that it is one of the only organizations to serve as a liaison between both families affected by fetal syndromes such as Twin-to-Twin Transfusion Syndrome and other fatal syndromes, and the medical teams that provide their care. The... more »

  frank5 wrote:

EARS is a top notch, very efficiently run organization. The staff really is very caring and concerned for all they assist. There tapes are very professionally done and do the job they were created for. Their website is very easy to use and has a database... more »

  adiegrey wrote:

Lymphedema is a tricky condition that is little understood by much of the general population as well as the medical community. As a patient and a therapist in this realm, I am always grateful for excellent education on the subject, and I get that from... more »

  kevgal wrote:

The organization has done a lot of work with volunteers who have raised funds to support hospice care in the Missoula area. They have been in business for over 30 years and are fiscally responsible stewards of thier donatio ns. As they turned from a... more »

  Tom_29 wrote:

I've observed how one young woman, who is herself inflicted with Ehlers-Danlos syndrome, has taken this nonprofit from the ground up to potentially raising worldwide awareness of this previously misunderstood condition. EDSers United not only serves... more »

  ellie4 wrote:

The AARDA is a org that helps people by giving them information about AI diseases. They are also involved in reaching the medical profession to spread info, increase awearness and help get laws passed to aid in funding and research. There are over 50... more »

  wbguard wrote:

CAPPS is a great organization that has helped my family tremendously from day 1, through the surgery, recovery, and beyond! I don't know where we would be without their support and knowledge. My family has met other great families and we have made life... more »

  Charles Hummer Jr wrote:

Good mission, badly needed services for its clients made up of terminally ill ALS patients. Disappointing trend in all aspects and particularly in view of the superb performance of some of the chapters who are more successful in demonstrating responsible... more »

  NADER KAY wrote:

This is the best non profit orgnization that will help us to save this world we live in it from falling appart by educating the people in the wold about the laws of cration. more »

  jj wrote:

I have traveled to Africa (Uganda) with this group to participate in a medical mission trip, and it was simply outstanding. I highly recommend checking out this group if you are interested in foreign medical missions, tropical disease, international... more »

  maryvinpdx wrote:

My involvement with this organization began over six years ago, first by volunteering, then donating, and eventually becoming a Board member. Having had family members with Parkinson's disease gives me a deep understanding of the needs of not only the... more »

  sally9 wrote:

I came into contact with Canavan Research Foundation in 2005 when my son Ben was 2 years old, at the age of 18 months he had been diagnosed with Canavan disease. To say that this diagnosis completly broke our hearts does not nearly cover the depth of... more »

  caharris wrote:

My son suffers from anxiety and OCD. The teenage anxiety support group that he was a part of, gave him a positive role model, coping mechanisms, and most importantly, showed him that there were others much the same. The group leader was always willing... more »

  tkozman wrote:

This organization is the *only* existing resource whose purpose is to provide direct relief to individuals who find themselves in a state of economic emergency as a direct result of their narcolepsy, a rare, potentially debilitating neurological disorder... more »

  mikelang1313 wrote:

This is why I work with Angel Eyes and what this organization means to me. A Facebook post on my sons 21st birthday. As I have attended support group meetings for that past year or so for parents who have lost children to SIDS and other early... more »

  Joy and Happiness wrote:

This Non Profit does great things for this orphan disease of Essential Thrombocythemia. As well as for the MPN community in general. Orphan diseases are mostly neglected by the scientific community. Thus, non profits like this that raise money to fund... more »

  anniepedret wrote:

I donated a Cpap machine with the understanding that I would get a donation letter for tax purposes. I also donated the shipping at their request. I have asked for the letter 3-4 times over a year and they have promised, but not sent it to me. It makes... more »

  Frederick1 wrote:

I have been an MRF volunteer for over 5 years. I've had MS for over 14 years. My experience with MRF has been very positive. MRF is truly the best organization when it comes to advancing research directed at finding better treatments for MS. The commitment... more »

  Pattie_D wrote:

The National Kidney Foundation of Maryland inspires me to give because the work that this organization does makes a huge difference in the lives of patients with kidney disease. Kidney disease impacts 73 million American adults (1 in 3) are at risk for... more »

  Grandma Concerned wrote:

I have been a consistent donor to the Juvenile Bipolar Research Foundation since its inception. It is the only organization that it totally focused on research - not intervention/politics/policy-making/advocacy/counseling. I have a son who has severe... more »

  Win C. wrote:

Breast Cancer Emergency Fund provides quick and compassionate short-term emergency financial assistance to low-income breast cancer patients and their families. I volunteered at Whiskey of the World and This Old Bag event. Both of these events... more »

  angelface wrote:

I reached out to The Connie J Goodale Breast Cancer Foundation after receiving my breast cancer diagnosis. It felt like a punch in the stomach! In addition to being "under insured," I was unable to work after the surgery. Prior to beginning radiation,... more »

  Natalie V. wrote:

The ALSAOC is so supportive to everyone they care for. If you ever need anything they are just a phone call away. more »

  jboone7117 wrote:

I have been dealing with Anxiety and depression for more than half of my life. I hid it and always felt as if I kept it a secret, no one could see this invisible illness I was facing. I ended up finding 3/31 on Facebook and they talked about living not... more »

  kevinm wrote:

I came to the alano mens Pine house from phoenix in november of 2009 and have found a new way to live . the program set out there gave me the structure and acountability to get a hold of my drug and alcohole issues and the safe clean enviroment to do... more »

  Vickee wrote:

I asked myself, "How many charities are actual charities?" I know the National CFIDS Foundation is because there are no employees to pay, no secretaries, and every last penny of my donation went toward funding research into my disease: Chronic Fatigue... more »

  WOMBAT wrote:

I have been volunteering with Project Kindle for over 5 years. I learned about Kindle when I went with my sister to a fundraiser in Nebraska. I was immediately impacted by all the people who were involved and the cause they stood for. I submitted my application... more »

  pscky wrote:

There's something unique in receiving a diagnosis of a chronic illness, such as Parkinson's disease. In fact, PD is such a strange, complex and baffling disease that despite the many educational resources we can throw at it, each human's experience is... more »

  cindy18 wrote:

The ALS Association has been a wonderful place to volunteer. Through working in the office collating mailings all the way to doing Autograph Parties and Walks, it has given me the opportunity to help those in need while at the same time bringing my family... more »

  Postreview01 wrote:

The Reggie White Foundation is amazing! I found the organization while desperately searching for a replacement CPAP. The CPAP my husband used had caused problems and was ultimately recalled by Philips, the manufacture. I contacted our insurance and... more »

  8677 wrote:

I was married to The Love of My Life for close to 46 years, until ALS took him from us. I wear a ring to this day with the word HOPE on it, in hopes , I can in some small way, raise awareness of ALS, so no others will have to go through what my husband,family... more »

  jomitch wrote:

I do not recommend the Hospice House or Respite. This is a critical review about the Hospice House. I have no criticism of the in-home care portion of this hospice. I felt they did a good job over past year and especially appreciated the visiting... more »

  Corbly wrote:

These guys have been donating their time and fund raising skills to Prostate Cancer awareness and research for years now. I was honored to be asked to join the BOD about a year ago while we were launching our fall events, Pints for Prostates and Save... more »

  Michael B.20 wrote:

I have donated many times to Out of the Closet. However, I never will again. I wanted to donate a gently used sofa. The first scheduled pick-up was cancelled because the driver was 'sick.' The next pick up was scheduled several days later, between 8 to... more »

  orange1 wrote:

I have been very blessed to meet and work along side the group of very inteligent and careing people at WFFRC. The work untiredly with the community, leaders and churches and the people of west Fresno and beyond to bring awareness and information about... more »

  SylviaOblak wrote:

www.hwvt.org Healing Winds Vermont (Respite Sailing for Cancer) is an AMAZING cancer support nonprofit organization! Giving those with cancer, their loved ones, and caregivers free, private sailing excursions on Lake Champlain in Vermont, they provide... more »

  jory1961 wrote:

Hope Instilled is such an amazing source of information for people living with chronic pain. I have never seen so many alternative treatment options explained in one place, and no one is trying to sell me anything. You are able to get a better understanding... more »

  kostam wrote:

I am writing to wholeheartedly recommend the BTER Foundation for its exceptional dedication and impactful work in the field of education and treatment of patients using biotherapy. Having had the privilege of closely following the activities of and collaborating... more »

  ____724 wrote:

Thank you to the National Multiple Sclerosis Society for setting up a chapter in the Central PA area. This disease is devastating and violent and the more we can spread the word about a cure, the better. We would like to introduce you to a great... more »

  katiemag16 wrote:

In July, I attended a full day workshop through my clinic at Albany Medical. The purpose of the workshop was to educate and encourage patients (and families) about PKU. This is the third year I've attended, however just a few weeks before the date our... more »

  AFFTER fms wrote:

AFFTER is a volunteer run, charitable nonprofit, founded in 1999. Our mission is to advance research, educate and advocate for FMS, offering hope to those suffering with this illness. more »

  CrystalCox wrote:

Do Not Trust Bill Lenhard, Randall Boyte, Ken Coleman.. this foundation was the Elder LifeCare Foundation... they are thieves. EthicsComplaint.com more »

  Writer wrote:

Aim For Success is an excellent organization that helps young people learn about and avoid the risks of sexual activity, drugs, and bullying. I am totally blown away by how professional and relatable the speakers are. The presentations are educational... more »

  Sabounchian wrote:

The self-help reflexology workshops with the World Reflexology Foundation always remind me that I do have the ability, to a degree, to take care of my own health. Recently I had tweaked my lower back. To know how to work on my ears for fast pain relief... more »

  dw101 wrote:

The only organization worth going to for help in the Porphyria's. You can get answers to questions that are difficult to find elsewhere. The USPA has helped me get a lot of my life back by recommending sources to go to and people that understand the... more »

  James Lamberti wrote:

The Grace foundation of Staten Island is for Autistic children . They provide social skills classes , gym classes,swimming ,bowling , baseball &, parent support groups . They provide help for all kids of the Autistic spectrum from severe to high functioning... more »

  Holley S Jacobs wrote:

After meeting with Raina from Easter Seals of Nebraska, I have such hope and even more determination to finish what I started in 2011. She is so great at explaining complicated in a way that I can understand. I appreciate it very much as anything dealing... more »

  Alley wrote:

This is the Best' ALS support plus group in Florida You can count on your donation going to Pals " People living with ALS " Cals," their caregiver" and research. No paid employees , no wasted money. more »

  lj1989 wrote:

I am so grateful for the work you have done in my community. The horses that have been donated to our community are helping tremendously. Together we feed them each day and through our interaction with them we are brought to a better state of mind. Thanks! more »

  AZcommunityGal wrote:

NO STARS NOT AN OPTION -This organization exists in name only. Someone maintains the tax id number and there is no way to contact them other than to make donations and no one knows where that money goes. At one time they had been associated with a statewide... more »

  KIBA wrote:

Global soap project is an amazing concept by a group of dedicated people who decided to help others despite the fact that they did and do not have much themselves. It is a sign that every one of us can use the resources around us to help others live a... more »

  sunshineforyou wrote:

A very horrible disease. Help a patient be comfortable and help the caretaker to be free once in a while to deal with what she or he watches each moment. Caress the pain per say. Do a bit of research before you show up on the details. Good luck to all... more »

  beckster011 wrote:

I joined in a private fb support group and have also completed my patient survey. This group has pros and cons. Pros : The entire purpose is to "find a cure." This is almost impossible as the rate genetic disease is within our DNA. It gives me hope they... more »

  snyderbc wrote:

I have been a volunteer with AFED for over a year now, and I am so impressed with the passionate people volunteering their time to provide support and awareness for everyone affected by eating disorders. AFED volunteers have also done an incredible job... more »

  Beccaboop wrote:

This club is a nonprofit organization that has 12 step meetings daily. Its mission statement reads " The Backstreet club provides a safe place for those seeking recovery through 12 step programs.. It saved my life and continues to be a safe haven from... more »

  corrine wrote:

The founders are down to earth good people with two sons who are autistic. The foundation helps with needs of parents who have financial struggles with special needs children. more »

  FoxyAdvocate wrote:

The Lupus and Allied Diseases Association, Inc. was founded in 1978 in Utica, N.Y. and is now a national non-profit organization dedicated to enhancing quality of life by enlightening and empowering those impacted by lupus and allied diseases and other... more »

  Christian J. wrote:

Beautiful well produced events to create awareness about Endometriosis. I will volunteer again! more »

  leliz127 wrote:

I worry that Stepping Stones might not be living up to its own standards. A summer program I taught for had us take our classes to Stepping Stones as a service project/field trip. Each of our students was paired with a camper to supervise... more »

  Tami wrote:

In less than one short year this nonprofit has generated thousands of dollars to assist those affected by Breast Cancer and HIV/AIDS. We work with great sponsors and have started a wonderful pool of benefactors that due tremendous works. We... more »

  Blessed parent wrote:

Kids in Action is a terrific organization. My son use to take therapy through this organization as well as participate in recreational activities before we moved to Clarksville. I recently referred a friend to KIA who helped her despite their change of... more »

  Connie101 wrote:

This is a five star organization that cares about the direct impact it has on its consumers and those who utilize its services. I am one such individual. I learned that I had a bleeding disorder and a myriad of rare health issues after a vehicle accident... more »

  Inpiring by people who cares wrote:

I have personally met the President Of this Organization . She had a booth face painting and making glitter tattoos on children. I Had never heard of this disease before and learned a lot from the information Angela shared about this disease. I will... more »

  Mich2849 wrote:

This organization employees 14 people. Very little of their donations go for research. The ED is paid more than other nonprofits who raise millions, i.e. Union Gospel Mission. The ED of UGM makes less than the ED for this nonprofit. When I donate,... more »

  Litarcha C. wrote:

this organization helped by cousin while she was in treatment with breast cancer more »

  Writer wrote:

Science with a Mission, Inc [SMI] is dedicated to sending medical diagnostics to developing countries. It is a very small organization that has helped tens of thousands of people in countries around the world that relies almost entirely on small donations... more »

Persons with CFS or FM can be as impaired as those with MS or AIDs. However most people are not aware of the symptoms and few... more »

Nash austism seeking hope (nash) was established to help raise money to assist families with autistic children. Many of the items... more »

The Mission of the Spina Bifida Association of America is to promote the prevention of spina bifida and to enhance the lives of... more »

The mission of Sudden Infant Death Services of the Mid-Atlantic is to reduce the numbers of infant deaths in Washington D.C.,... more »

Pmrf is dedicated to the study, treatment, and eventual cure of diabetes. more »

The ALS Association Northern New England Chapter (ALSA NNE) is one of 47 chapters, under the umbrella of The National ALS Association,... more »

The primary goals of the ALSA Nevada Chapter are: * To help the ALS patient and family to live as full and as normal life as... more »

To provide comprehensive pediatric healthcare, that recognizes the special needs of children, through excellence and the continuous... more »

To facilitate the delivery of optimal ems and trauma care in new mexico. more »

The specific purposes for which the corporation is organized and shall be operated are supporting and undertaking research that... more »

The Child & Adolescent Bipolar Foundation educates families, professionals, and the public about pediatric bipolar disorder; connects... more »

Organization's mission is to improve the quality of life of children with cancer and their families in georgia by extending hope... more »

To provide support and advocacy for children with complex medical conditions, their families and the disenfranchised, medically... more »

We mobilize people and resources to drive research for a cure and to address the challenges of everyone affected by ms. more »

The foundation's mission is to improve the oral health of all californians by supporting the dental profession and its efforts... more »

The American Urological Association Foundation partners with physicians, researchers, health-care professionals, patients, caregivers,... more »

Raise public awareness: we believe that one of the most important things that should be done to aid in the fight against brain... more »

Advocating for addiction awareness and providing recovery support for those affected by the disease of addiction more »

To support and advocate for individuals and their families diagnosed with rare neuro-immune disorders of the central nervous system;... more »

The baker gordon educational symposium provided support for research and education from the net proceeds of the annual conference... more »

The autoimmune encephalitis alliance improves the lives of patients with autoimmune encephalitis by promoting collaboration in... more »