Find Neurology & Neuroscience Nonprofits and Charities

  ClusterHead wrote:

This is by far the largest non-profit organization working toward better treatment options for cluster headache, specificially. It is also the most giving and caring organization I have had the pleasure to engage with, and they do it all on a volunteer... more »

  Amy_89 wrote:

CSF has been incredibly helpful to myself and my family as we faced my daughter's diagnosis of Chiari and Syringomyelia in early 2012. They have wonderful resources with all the information you could possibly ask for regarding both and much more! My... 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 »

  hazelw wrote:

Everyone in the organization understands and focuses on what helps those with auto-immune and other diseases that affect mobility and balance. Some come in in wheel chairs, others have no apparent problems. more »

  Rys Gamma wrote:

It was a few weeks after Christmas 20011 that my Grandson Ry was diagnosed with Hydranencephaly. My Daughter and Son in-law were told after Ry was airlifted to Denver Children's Hospital that they felt they needed to run a brain scan on Ry. The results... 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 »

  ABJMom wrote:

Parkinsons Resource Organization (PRO) is a small nonprofit with a huge heart and a huge mission. As a caregiver for my husband, who battled Parkinsons from a relatively young age, and now as a CNA in a skilled nursing facility, I have found that PRO... more »

  Tina M. wrote:

I developed the symptoms of Dystonia 3 yrs ago this August. This disease is rare (probablly not as rare as they think); so all of the numerous doctors I went to shuffled me from here to there. I went through every kind of medical test. My original... 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 »

  dkhulvey wrote:

Hope for HIE has been an amazing support for me and my family! It is a place where I have found emotional support, a community that encourages forward thinking, administrators who want to provide the most accurate information, and a they have given us... more »

  7173trees wrote:

All my life I've known my feet didn't have the strength and capability of most of the people I knew. It wasn't until after my brother and I were diagnosed after I retired from 34 years of elementary teaching that I found out why. I was diagnosed with... more »

  mmkstl wrote:

Magic Mirror, a CD for patients going through chemotherapy to promote healing is fabulous. This is possible due to Amy Camie and the Scientific Arts Foundation. We have had great feedback from our patients abou this CD. Please recognize the fine work... more »

  RayNorshine wrote:

Without this organization, we wouldn’t have a lasting source of support and resources in our community for brain injury survivors/caregivers. Thanks for the great work you’re doing in Southwest Florida. more »

  Power of Pain Foundation wrote:

The NAF is a great foundation with outstanding leadership. They are dedicated to neuropathy education and deliver quality materials to the pain community. Thank you for all you do. more »

  Wayne wrote:

I am writing this review both as a client served and a volunteer. When my wife was diagnosed with MS three years ago and we sought out information and assistance, this organization was the first one to step forward with the programs and services... 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 »

  prueann wrote:

I started volunteering with the Mid-Atlantic Chapter of the National MS Society as a way to help one of my best friends who was diagnosed with MS. She lives in Texas and it was hard for me to be able to help her from so far away. I called the local chapter... more »

  LT1270 wrote:

This organization is a lifesaver. Literally. The CJD disease is very rare and no one is prepared for it. The disease is always fatal. The lives saved are the families affected. The CJD Hotline and founder Florence Kranitz in particular, helped guide my... more »

  condesa wrote:

This organization is very helpful in providing information to patients and caregivers of those with facial pain. A fabulous resource on the phone, through newsletters and at their conferences. more »

  flossie wrote:

More than 95 cents go toward finding a cure for Parkinson's disease which we desperately need. It is very important to me that the maximum amount of my donation goes to research. I am extremely impressed by the quality of this organization's contributions... more »

  Nannette H. wrote:

Tremor Action Network is the best objective source of information for Essential Tremor. more »

  brainsearch wrote:

This charity is a volunteer run recognized 501 (c). There are no slaries, so the money raised goes to the Foundation and its programs. One of the programs: The Summer Student Fellowship Program attracts bright, motivated college students to... more »

  krothrock wrote:

We have only attended two events but both were spectacular and my kids enjoyed them immensely. The events are creative and appealing but we have had many sport conflicts that don't allow us to participate. I think this is a worthwhile group so my kids... more »

  kinder1 wrote:

This used to be a wonderful caring organization with excellent doctors and friendly supportive staff. All that changed last year when they got a new president. All the doctors have left, the new doctor is very unpleasant and uncaring. They used to... more »

  Mike164 wrote:

This is a superior NP. Feel confident when you give. Often your donation it matched by the major donor. This groups creates impactful fundraising, by incorporating compelling events and including people to form comradely and interest, the Parkinson Alliance... more »