Thank You to our CURETHEPROCESS™ Campaign Partners

  • Fabry Support & Information Group
  • National MPS Society
  • Advocacy for Patients with Chronic Illness, Inc.
  • Cystinosis Research Network
  • Macular Degeneration Support
  • Myelin Project
  • International Pemphigus and Pemphigoid Foundation
  • National Organization for Rare Disorders (NORD)
  • American Heart Association
  • National PKU Alliance
  • Nomid Alliance
  • Alpha One Association
  • Association of Gastrointestinal Motility Disorders
  • Beyond Batten Disease Foundation
  • Campaign Urging Research for Eosinophilia Disease (CURED)
  • Coalition for Pulmonary Fibrosis
  • GIST Support International
  • Institute for Families
  • International Castleman's Disease Organization
  • International Dravet Syndrome Epilepsy Action (IDEA) League
  • Partnership for Cures
  • VHL Family Alliance
  • The Jain Foundation
  • National Tay Sachs & Allied Diseases Association, Inc.
  • SADS Sudden Arrhythmia Death Cardiac Syndromes Foundation
  • Reflex Sympathetic Dystrophy Syndrome Association
  • Parry Romberg Syndrome Foundation
  • Russel Silver Syndrome Advocacy and Support
  • Sarcoma Foundation of America
  • Reflex Sympathetic Dystrophy Syndrome Association
  • National Gaucher Foundation
  • ARPKD/CHF Alliance
  • Ehlers-Danlos
  • Madisons Foundation
  • Sarcoma Alliance
  • Abigail Alliance
  • Cogan's Contact Network
  • Hannah's Hope
  • MUMS National Parent to Parent Network
  • National Association for Children's Heart Disorders/Kids with Hearts
  • National Marfan Foundation
  • NKH International Family Support Network
  • Organic Acidemia Association
  • Pierre Robin Network
  • The Magic Foundation
  • Liddy Shriver Sarcoma Intiative
  • CFC International
  • United Pompe Foundation
  • Solving Kids Cancer
  • Lysomal Diseases New Zealand
  • TThe Hide & Seek Foundation for Lysosomal Disease Research
  • cMPD Education Foundation
  • National Organization Against Rare Cancers
  • Ara Parseghian Medical Research Foundation
  • MLD Foundation
  • Transverse Myelitis Association
  • Addi and Cassi Fund
  • American Chronic Pain Association
  • Association of Gastrointestinal Motility Disorders
  • Children's Alopecia Project
  • Children's Cardiomyopathy Foundation
  • CARES Foundation
  • CureDuchenne
  • Dandy-Walker Alliance
  • Dravet Syndrome Foundation
  • Fatty Oxidation Disorders (FOD)
  • Fetal Hope
  • TLGS Foundation
  • Parent Project Muscular Dystrophy
  • Erythromealgia Foundation
  • The Myositis Association
  • Dystrophic Epidermolysis Bullosa Research Association of America
  • Pediatric Hydrocephalus Foundation
  • Batten Disease Support and Research Association
  • Taylor's Tale
  • American Behcets Disease Association
  • Sickle Cell Disease Association of America
  • Pediatric OMS Research Fund
  • Invisible Diseases
  • Noah's Hope
  • Eurordis
  • R.A.R.E. (Rare Disease Advocacy, Research & Education) Project
  • Georgia PKU Connect
  • Iowa Ataxia Support Group
  • American College of Medical Genetics
  • Kids V Cancer
  • National Eczema Associ
  • Alliance SANFILIPPO
  • NAmerican childhood Cancer Organization
  • Hope 4 Bridget
  • FIRST Foundation for Ichtyosis & Related Skin Types
  • CORD Canadian Organization for Rare Diseases
  • Histiocytosis Association of America
  • Hayden's Batten Disease Foundation, Inc
  • Phelan-McDermid Syndrome Foundation
  • National Multiple Sclerosis Society
  • Nathan's Battle Foundation
  • National Alopecia Areata Foundation
  • Oxalosis and Hyperoxaluria Foundation
  • Periodic Paralysis Association
  • Mary Payton's Miracle Foundation
  • Julia's Hope - The Sanfilippo Syndrome Medical Research Foundation
  • Pennies For Nicoll Foundation
  • In Need of Diagnosis (INOD)
  • Hypertrophic Cardiomyopathy Association

Patient Organizations are partnering with us to help CureTheProcess.

• Abigail Alliance for Better Access to Investigation Drugs • Addi and Cassi Fund
• Adult Congenital Heart Association • Advocacy for Patients with Chronic Illness, Inc.
• Alliance SANFILIPPO • Alpha-1 Association
• American Autoimmune Related Diseases Association • American Behcets Disease Association
• American childhood Cancer Organization • American Chronic Pain Association
• American College of Medical Genetics • American Heart Association
• APS Foundation • Ara Parseghian Medical Research Foundation
• ARPKD/CHF Alliance • Association of Gastrointestinal Motility Disorders
• Batten Disease Support and Research Association • Beyond Batten Disease Foundation
• Campaign Urging Research for Eosinophilia Disease (CURED) • CARES Foundation
• CFC International • Children's Alopecia Project
• Children's Cardiomyopathy Foundation • Children's PKU Network
• Children's Rare Disease Network • Chronic Granulomatous Disease Association
• cMPD Education Foundation • Coalition for Pulmonary Fibrosis
• Cogan's Contact Network • Cooley's Anemia Foundation
• CORD Canadian Organization for Rare Diseases • CureDuchenne Muscular Dystrophy
• Cystinosis Research Network • Dandy-Walker Alliance
• Dravet Syndrome Foundation • Dystrophic Epidermolysis Bullosa Research Association of America
• Ehlers-Danlos National Foundation • Eurordis
• Fabry Support & Information Group • Fatty Oxidation Disorders (FOD) Family Support Group
• Fetal Hope • FIRST Foundation for Ichtyosis & Related Skin Types
• Foundation for Nager Miller Syndrome • Georgia PKU Connect
• GIST Support International • Hajdu-Cheney Syndrome Support Group
• Hannah’s Hope Fund • Hayden's Batten Disease Foundation, Inc
• Histiocytosis Association of America • Hope 4 Bridget
• Hydrocephalus Association • Hypertrophic Cardiomyopathy Association
• In Need of Diagnosis (INOD) • Institute for Families
• International Castleman's Disease Organization • International Dravet Syndrome Epilepsy Action (IDEA) League
• International Pemphigus and Pemphigoid Foundation • Intractable Childhood Epilepsy Association
• Invisible Diseases • Iowa Ataxia Support Group
• ISMRD, International Society for Mucolipidosis & Related Disorders • John F. & Aileen A. Crowley Foundation
• Julia's Hope - The Sanfilippo Syndrome Medical Research Foundation • Kids V Cancer
• LGS Foundation • Liddy Shriver Sarcoma Intiative
• Lysomal Diseases New Zealand • Macular Degeneration Support
• Madisons Foundation • Mary Payton's Miracle Foundation
• MLD Foundation • MUMS National Parent to Parent Network
• Myelin Project • Myeloproliferative Disease Support
• Nail Patella Syndrome Network Support Group • Nathan's Battle Foundation
• National Alopecia Areata Foundation • National Association for Children's Heart Disorders/Kids with Hearts
• National Eczema Association • National Gaucher Foundation
• National Marfan Foundation • National MPS Society
• National Multiple Sclerosis Society • National Niemann-Pick Disease Foundation
• National Organization Against Rare Cancers • National Organization for Rare Disorders (NORD)
• National PKU Alliance • National Tay-Sachs & Allied Diseases Association, Inc.
• NKH International Family Support Network • Noah's Hope--Batten Disease Fund
• Nomid Alliance • Organic Acidemia Association
• Oxalosis and Hyperoxaluria Foundation • Parent Project Muscular Dystrophy
• Parry Romberg Syndrome Foundation • Partnership for Compassionate Use Therapies
• Partnership for Cures • Pediatric Gastroesophagel Reflux Disease Foundation
• Pediatric Hydrocephalus Foundation • Pediatric OMS Research Fund
• Pennies For Nicoll Foundation • Periodic Paralysis Association
• Phelan-McDermid Syndrome Foundation • Pierre Robin Network
• R.A.R.E. (Rare Disease Advocacy, Research & Education) Project • Reflex Sympathetic Dystrophy Syndrome Association
• Retinitis Pigementosa International • Russell Silver Syndrome Advocacy and Support
• SADS Sudden Arrhythmia Death Cardiac Syndromes Foundation • Sarcoma Alliance
• Sarcoma Foundation of America • Sickle Cell Disease Association of America
• Society for Inherited Metabolic Disorders • Solving Kids Cancer
• Taylor's Tale • The Erythromelalgia Association (TEA)
• The Hide & Seek Foundation for Lysosomal Disease Research • The Jain Foundation
• The Magic Foundation • The Myositis Association
• The Ryan Foundation for MPS Children • Transverse Myelitis Association
• United Pompe Foundation • VHL Family Alliance
 
 
 
 
 
 
 
 

If your organization would like to join our list of endorsers and Partner with us to CureTheProcess, please call 415-884-0223.