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211 Manitoba
Health Information from the Winnipeg Regional Health Authority
MyRightCare (WRHA)
Winnipeg Public Library's Health Information Guide
WRHA Health Services Directory
Newborn Screening "Screen Positive Fact Sheets" (WRHA)
Argininosuccinic Acidemia (ASA) or Citrullinemia (↑ citrulline)
Beta-Ketothiolase Deficiency (BKT) (↑ C5OH)
Biotinidase Deficiency
Carnitine Uptake Defect
Inuit Carnitine Palmitoyl Transferase 1A Deficiency
Carnitine Palmitoyl Transferase 1A Deficiency
Cystic Fibrosis
Elevated C5OH
Galactosemia
Glutaric Acidemia Type 1 (↑ C5DC)
Homocystinuria (↑ methionine)
Isovaleric Acidemia (↑ C5)
LCHAD or TriFunctional Protein
Maple Syrup Urine Disease
Medium Chain Acyl CoA Dehydrogenase Deficiency (MCADD)
Phenylketonuria
Propionic Acidemia or Methylmalonic Acidemia (↑ C3 or ↑ C4DC)
Short Chain Acyl CoA Dehydrogenase Deficiency (SCADD) (↑C4)
Tyrosinemia
Very Long Chain Acyl CoA Dehydrogenase Deficiency (VLCADD)
General Information, Advocacy and Support
Best use of medicines in pregnancy (BUMPS)
Canadian Association for Community Living (CACL)
Canadian Organization for Rare Disorders (CORD)
Centre for Genetics Education (NSW)
Consumer Health Information Service (U of M)
Cook for Love (low protein recipes)
Council of Canadians with Disabilities (CCD)
CyDAS karyogram drawing tool
EuroGentest [32 languages]
Genetic Alliance
Global Genes
Kids as Self Advocates (KASA)
My46 (University of Washington)
National Organization for Rare Disorders (NORD)
Rare Disease Foundation
Rare Diseases Europe (EURORDIS)
Save Babies Through Screening Foundation
STAR-G Newborn Screening Parents' Fact Sheets
Syndromes Without a Name (SWAN)
Unique: Understanding Chromosome Disorders
Your Genetic Health: Patient Information (NSGC)
Patient Organizations - General
AboutFace
Accord Alliance [DSD]
Alzheimer Society of Canada
Canadian Cancer Society
Canadian Hearing Society (CHS)
Canadian Liver Foundation
Canadian Mental Health Association (CMHA)
Canadian National Institute for the Blind (CNIB)
Cancer Genetics Support Group of Canada
Children Living with Inherited Metabolic Diseases (CLIMB)
Chromosome Disorder Outreach
Epilepsy Canada
Facial Palsy UK
Facing our Risk of Cancer Empowered (FORCE) DTC
Hearts in Rhythm (HiRO)
Immune Deficiency Foundation
InterACT: Advocates for Intersex Youth
Kidney Foundation of Canada
Little People of Canada
Magic Foundation for Children's Growth
National Ataxia Foundation
National Scoliosis Foundation
Society for Treatment of Autism
Willow Breast and Hereditary Cancer Support
Bereavement/Palliative Care
Courageous Parents Network
KidsGrief
Light the Shadows Project
MISS Foundation
MyGrief
Now I Lay Me Down to Sleep
Virtual Hospice
Walk to Remember
With love, Aydrah
Women's Health Clinic
Patient Organizations - Condition Specific
Angelman Syndrome Foundation
Association for Glycogen Storage Disease (AGSD)
Association for X and Y Chromosome Variations (AXYS)
Beckwith-Wiedemann Children's Foundation International
Canadian Angelman Syndrome Society
Canadian Association for Williams Syndrome (CAWS)
Canadian Down Syndrome Society (CDSS)
Canadian Fabry Association
Canadian Hemochromatosis Society
Canadian Hemophilia Society
Canadian Marfan Association
Canadian PKU and Allied Disorders
Children's Tumour Foundation [NF1]
Cooley's Anemia Foundation [Thalassemia]
Cornelia de Lange Syndrome Foundation
Curehht (HHT)
Cystic Fibrosis Canada
Ehlers Danlos Society
Facioscapulohumeral Muscular Dystrophy Society
Familial Gastrointestinal Cancer Registry (FGICR)
Families of Spinal Muscular Atrophy Canada Society
Fatty Acid Oxidation Disorders Family Support Group
Foundation for Prader-Willi Research Canada
Fragile X Research Foundation of Canada
Hereditary Breast and Ovarian Cancer Society
Hereditary Hemorrhagic Telangiectasia Foundation
HLRCC Family Alliance
Huntington Society of Canada
Joubert Syndrome and Related Disorders Foundation (JSRDF)
Leukodystrophies Foundation
Loeys-Dietz Syndrome Foundation
Manitoba Down Syndrome Society (MDSS)
Manitoba Neurofibromatosis Support Group (MBNF)
MitoCanada
Muscular Dystrophy Canada
National Foundation for Ectodermal Dysplasias (NFED)
National Gaucher Foundation of Canada
National Organization for Albinism & Hypopigmentation (NOAH)
National Urea Cycle Disorders Foundation (NUCDF)
Ontario Rett Syndrome Association (ORSA)
Organic Acidemia Association (OAA)
Osteogenesis Imperfecta Foundation (OIF)
Proteus Syndrome Foundation
Rubenstein-Taybi Syndrome Canada
Sickle Cell Association of Ontario
Soft Bones Canada [Hypophosphatasia]
Sotos Syndrome Support Association
Spina Bifida and Hydrocephalus Association of Canada
Stickler Involved People (SIP)
Sturge-Weber Foundation Canada
Support Organization for Trisomy 18, 13 & Related Disorders (SOFT)
Thalassemia Foundation of Canada
Tuberous Sclerosis (TS) Canada
Turner Syndrome Society of Canada
Understanding a Down Syndrome Diagnosis
United Mitochondrial Disease Foundation
Williams Syndrome Association
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