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Submitted URL: http://hunterstribe.com/
Effective URL: https://www.cmt4b3research.org/
Submission: On December 28 via api from US — Scanned from DE
Effective URL: https://www.cmt4b3research.org/
Submission: On December 28 via api from US — Scanned from DE
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0 Skip to Content HOME HUNTER'S STORY SCIENCE WHAT IS CMT4B3? RESEARCH OVERVIEW RESEARCH PROJECTS RESEARCH MATERIALS APPLY FOR FUNDING PATIENTS NEWLY DIAGNOSED DATA COLLECTION ABOUT US LEADERSHIP SCIENTIFIC ADVISORY BOARD FOLLOW OUR JOURNEY WAYS TO HELP HELP US FUNDRAISE DONATE CRYPTO FUND UNIVERSITY OF MIAMI GOLF OUTING Donate Open Menu Close Menu HOME HUNTER'S STORY SCIENCE WHAT IS CMT4B3? RESEARCH OVERVIEW RESEARCH PROJECTS RESEARCH MATERIALS APPLY FOR FUNDING PATIENTS NEWLY DIAGNOSED DATA COLLECTION ABOUT US LEADERSHIP SCIENTIFIC ADVISORY BOARD FOLLOW OUR JOURNEY WAYS TO HELP HELP US FUNDRAISE DONATE CRYPTO FUND UNIVERSITY OF MIAMI GOLF OUTING Donate Open Menu Close Menu HOME HUNTER'S STORY Folder: SCIENCE Folder: PATIENTS Folder: ABOUT US Folder: WAYS TO HELP Donate Back WHAT IS CMT4B3? RESEARCH OVERVIEW RESEARCH PROJECTS RESEARCH MATERIALS APPLY FOR FUNDING Back NEWLY DIAGNOSED DATA COLLECTION Back LEADERSHIP SCIENTIFIC ADVISORY BOARD FOLLOW OUR JOURNEY Back HELP US FUNDRAISE DONATE CRYPTO FUND UNIVERSITY OF MIAMI GOLF OUTING TOGETHER WE CAN MAKE A DIFFERENCE Hunter is battling Charcot-Marie-Tooth Disease Type 4B3, a rare progressive neuromuscular disorder with no cure or treatments. By working to find a cure, Hunters CMT4B3 Research Foundation will bring hope to thousands of children suffering from early onset peripheral nerve diseases. DONATE Hunter’s parents, Iris and Brett Schultz were told there are no treatments or cure for CMT4B3, and Hunter would eventually lose his mobility, and potentially go deaf and blind. Research and funding for CMT4B3 is virtually nonexistent. Not willing to simply watch their son deteriorate before their eyes, they founded “Hunters CMT4B3 Research Foundation” to find a cure for Hunter and all children suffering from CMT4B3 and related neuromuscular diseases. DONATE 1 in every 2500 people have CMT, an estimated 150,000 in the U.S. and 3 million worldwide. The same amount as Multiple Sclerosis (MS) and considerably more than Lou Gehrig Disease (ALS). Please donate to help us fund laboratories to research therapeutic treatments for CMT4B3. REGISTRATION NOW OPEN! 〰️ 1ST ANNUAL GOLF OUTING & CARD PARTY 〰️ CLICK HERE TO REGISTER 〰️ REGISTRATION NOW OPEN!〰️1ST ANNUAL GOLF OUTING & CARD PARTY〰️CLICK HERE TO REGISTER〰️REGISTRATION NOW OPEN!〰️1ST ANNUAL GOLF OUTING & CARD PARTY〰️CLICK HERE TO REGISTER〰️REGISTRATION NOW OPEN!〰️1ST ANNUAL GOLF OUTING & CARD PARTY〰️CLICK HERE TO REGISTER〰️REGISTRATION NOW OPEN!〰️1ST ANNUAL GOLF OUTING & CARD PARTY〰️CLICK HERE TO REGISTER〰️ REGISTRATION NOW OPEN! 〰️ 1ST ANNUAL GOLF OUTING & CARD PARTY 〰️ CLICK HERE TO REGISTER 〰️ REGISTRATION NOW OPEN! 〰️ 1ST ANNUAL GOLF OUTING & CARD PARTY 〰️ CLICK HERE TO REGISTER 〰️ HELP US FUNDRAISE Raise Money when You Shop on Amazon! Click here to setup AmazonSmile YOU SHOP, AMAZON GIVES! AT NO COST TO YOU! Did you know that Amazon has a charitable give back program called Amazon Smile and you can choose Hunters CMT4B3 Research Foundation as the charity for Amazon to give back to. This can be set up within your Amazon Mobile App as well.Open the app and find 'Settings' in the main menu (≡). Tap 'AmazonSmile' and follow the on screen instructions to turn on amazon smile on your phone. GENE THERAPY DRUG REPURPOSING MODELS OF THE DISEASE CMT4B3 Research Foundation 77 Garden Road Scarsdale, NY 10583 info@cmt4b3research.org Contact us: (917) 453-2319 Hunters CMT4B3 Research Foundation Inc. is a 501(c)(3) non-profit organization. Federal Tax ID: 85-3259676 JOIN HUNTER’S TRIBE Sign up to receive occasional updates on Hunter, and the scientific breakthroughs we are working on in laboratories throughout the world. First Name Last Name Email Address Sign Up Thank you!