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Join us!
We need your help to find treatments and cures for INAD/PLAN
PLAN is an exceedingly rare genetic neurological disorder causing significant challenges for those affected. It is diagnosed via DNA testing of the PLA2G6-Associated Neurodegeneration gene. PLAN is one of 10 known Neurodegeneration with Brain Iron Accumulation (NBIA) disorders, and the most common variant is Infantile Neuroaxonal Dystrophy (INAD).
Classic INAD starts early in life and progresses rapidly. It usually develops between 6 months and 3 years of age. The first signs are often delays in developing skills, such as walking and talking. Eye disease is common later on and can cause poor vision and eventual blindness. Seizures and fast rhythms on an EEG may also occur.
A loss of cognitive abilities occurs, and many affected children never learn to walk or lose the ability early on. Many affected children do not survive beyond their first decade, but some survive into their teens or later.
Research funding is desperately needed to help speed up finding a cure.
Here’s what you can do to help us:
Help bring awareness to INAD/PLAN so we can fund potentially life-saving research. It’s easy. Just create a personal fundraising page by clicking on the blue fundraise button below. Share your story and say why this is important to you. Add some photos too. Set your own fundraising goal, whether it is $40, $400 or $4,000. Choose any amount and just know: Every dollar makes a difference!
And don’t forget to promote your page on Facebook, Instagram and Twitter.
Don’t want to set up a fundraising page? How about hosting a picnic or another event to raise funds?
Only have time to send an email or two to family and friends? No problem. Tell them you need their help. Ask them to share your message with their friends and family or create their own page to raise awareness. Or they can donate directly by clicking on the lavender button below.
HERE’S HOW YOU CAN HELP. We’re asking you to please consider joining with others to fund research for treatments and a cure for INAD/PLAN.
Please know that your contributions are tax-deductible to the full extent allowed by law because we are a charitable, 501(c)(3) organization.
Neurodegeneration with Brain Iron Accumulation (NBIA) is a group of rare, genetic neurological disorders. The common feature among all individuals with NBIA is iron accumulation in the brain, along with a progressive movement disorder.
Our Mission
In our drive to find a cure for NBIA, we provide support to families, educate the public and accelerate research with collaborators from around the world.
Federal Tax ID EIN 33-0712327