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Huntington's NSW ACT | Supporting people with Huntington's disease
Huntington's NSW ACT was established in 1975 to develop support and educational programs for people affected by Huntington's disease (HD) in New South Wales and the Australian Capital Territory. We help families understand and cope with Huntington's disease, and give families affected by HD a strong united voice. What is…
Author: Mara Milani
The International Huntington Association - Huntington's disease worldwide information and support
Huntington’s Disease Association NI providing support to individuals, families and carers living with Huntington’s disease
Huntington’s Disease Association Northern Ireland is a NI registered charity which supports people affected by Huntington’s disease. We provide information & advice to families and professionals.
Author: Platypus Consultancy Limited
Asbestos Disease Support Society
Vancouver Chapter – Huntington Society of Canada
Huntington Society of Canada
London Chapter – Huntington Society of Canada
Huntington Society of Canada
Halifax Chapter – Huntington Society of Canada
Huntington Society of Canada
Camrose Chapter – Huntington Society of Canada
Huntington Society of Canada
Huntington's Disease News Home - Huntington's Disease News
No Description.
Author: Theme Templates
Cross-Canada RVing with Huntington's Disease in 2019 – Tells the story of a couple–one of whom is Huntington's Disease positive–and their 20
Tells the story of a couple--one of whom is Huntington's Disease positive--and their 2019 Cross Canada road trip.
Huntington's Disease Association
Find out more about the Huntington's Disease Association here!
At Risk for Huntington's Disease
HD is a genetically caused brain disorder that causes uncontrollable bodily movements and robs people's ability to walk, talk, eat, and think. The final result is a slow, **** death. Children of parents with HD have a 50-50 chance of inheriting the disease. There is no cure or treatment.
Author: Gene Veritas
Durham Region Chapter – Huntington Society of Canada
Huntington Society of Canada
Southern Alberta Chapter – Huntington Society of Canada
Huntington Society of Canada
Huntington's Disease Association - Cyprus
Ο Κυπριακός Σύνδεσμος για τη Νόσο του Huntigton έχει ως σκοπό την υπεύθυνη ενημέρωση και στήριξη σε όλους όσοι επηρεάζονται άμεσα ή έμμεσα από τη Νόσο.
Huntington's Disease Youth Organization
Huntington's Disease Association Tasmania
What is Huntington's Disease? Huntington’s Disease (HD) is a degenerative brain disorder that results in the progressive loss of mental and physical capacities. The hereditary and complex nature of HD means that it’s not just patients, but an entire community that’s affected. Read more... Who we are Huntington’s Disease Association
Author: HD Association Tasmania
ACN Canada – We are helping those who help!
We Had Faces Then
A **** man of a certain age and a certain sensibility searching for meaning in the flickering images...
Other sites like huntingtonsociety ca
Ectodermal Dysplasia Society | Supporting those affected by ED
The Ectodermal Dysplasia Society is a charity dedicated to improving the health and well-being of people whose lives are affected by Ectodermal Dysplasia.
Free support for those facing cancer | Gilda's Club Middle Tennessee
Free of charge to everyone, Gilda’s Club Middle Tennessee provides a gathering place where people with cancer, as well as their families and friends, can join with others to actively involve themselves in building social and emotional support as a supplement to regular medical care.
Trained, caring volunteers offer support to those facing terminal illness.
Horizon-Timmins Palliative Care Inc.
We Do Those
Huntington Research Nederland – Dutch Huntington's Disease Research Network
Die Huntingtonkrankheit - Chorea Huntington - Huntington´s disease
Ein Ort der Hilfe und des Austausches für Angehörige, Betroffene und Risikopersonen der Huntingtonkrankheit.
Huntington's Disease Associations of New Zealand
A site for people affected by or interested in the Huntington's Disease scene in New Zealand.
Author: Jan Pickering
Promising New Treatment for Huntington’s Disease
Author: Sons
Home - Huntington’s Disease **** Works
Education and support for people with Huntington's disease
About European Huntington's Disease Network
Huntington's Disease Association of Ireland - Home
Axion Hellas – we support society
Support those who support seniors
The Alberta government promised small increases to staff at seniors' homes, but they haven't seen a dime. It's shameful treatment of front line heroes.
Menieres Disease Society of Western Australia – Help Support Locals wiith Menieres Disease
NWDC Resistance | Supporting those facing deportation inside the Northwest Detention Center
We’ve got a new name and a new website! As of April 2019, Northwest Detention Center Resistance is now… Click here to take you to our new website. #AbolishICE !! Share this:
Huntington Lighthouse Preservation Society
European Huntington Association – Inspiring and empowering people affected by Huntington Disease
Educational Support | Project Amigo Canada Society
Project Amigo Canada Society has been in existence since 2009 and has applied for charitable status, Project Amigo Canada Society provides educational scholarships, material support, enrichment activities, and health care to disadvantaged youth in Colima state.
Helping families in NC affected by Huntington's disease
HD Reach is working to improve the care and quality of life for people affected by Huntington’s disease.
Author: Dr Myriam Sollman; PhD; ABPP; Board Certified Clinical Neuropsychologist; HD Reach Affiliate
ALS Canada – ALS Society of Canada
ALS doesn't stop. Neither will we.
What else huntingtonsociety.ca alternative websites
Roshini Welfare Society – We Value Your Support
Faces and Voices of Recovery Canada
OCD SUPPORT – A monthly support group for those with OCD or for those who affected by it.
Swiss Society for Infectious Diseases
Author: BlueMouse GmbH
Asbestos Diseases Society of SA | ADSSA
International Society for Disease Surveillance
The European Society for Diseases of the Esophagus
Society for Disease Control and Research
MPS Society | Support for MPS, Fabry and related diseases in the United Kingdom
The Society for Mucopolysaccharide Diseases (MPS Society) provides professional support to individuals and families affected by MPS, Fabry and related lysosomal storage diseases. Contact our helpline Monday-Friday 9-5pm on 0345 389 9901 or email us at advocacy@mpssociety.org.uk
MPS and ML Disease Information, Donations, and Support - National MPS Society
The National MPS Society exists to cure, support and advocate for mucopolysaccharidosis and mucolipidosis. Our mission serves individuals, families and friends affected by MPS.
PBC Society Canada – PBC Society Canada
Vegan Society of Canada - Vegan Society of Canada
Welcome to the Vegan Society of Canada, from links to local association, current events, resources and discussion on issues of interest to vegan living in Canada we aim to provide it all. If you have some free time come and volunteer with us or help us with our mission with a donation.
Author: Vegan Society
For Those Affected By Celiac Disease | Celiac Chat
Epitrack: we love diseases, but we have to **** them.
A Epitrack é uma startup que atua no segmento de Digital Health, focada no desenvolvimento de soluções que buscam contribuir com a melhoria da saúde.
Author: Epitrack; Hi Tech
Epitrack: we love diseases, but we have to **** them.
A Epitrack é uma startup que atua no segmento de Digital Health, focada no desenvolvimento de soluções que buscam contribuir com a melhoria da saúde.
Author: Epitrack; Hi Tech
Genetic Support | Rare Diseases | Genetic Alliance Australia | Support for those affected directly or indirectly by genetic conditions s
Support for those affected directly or indirectly by genetic conditions/rare diseases throughout Australasia. Information, support network, personal stories, news and events.
Inn Churches – Practical support for those that need it most
Author: Innchurches-Admin
Annexon Biosciences | Neurodegenerative Disorders, Alzheimer's, Huntington's Disease
Annexon Biosciences is creating and developing proprietary therapeutic products that modulate the classical complement pathway.
Ross Support - Support for those affected by the collapse of Ross Asset ManagementRoss Support | Support for those affected by the collapse
Support for those affected by the collapse of Ross Asset Management
Author: Admin
The New Zealand Acromegaly Society – Supporting and educating those affected by acromegaly and their families.
Supporting and educating those affected by acromegaly and their families.
Other websites similar as huntingtonsociety.ca
Lyme Disease Support & Consolation
Chronic Lyme Disease is a vastly misunderstood reality in society, and as a result, much of the information needed by those to overcome it is ridiculously hard to find. Within its capabilities, Tired of Lyme strives to remove this confusion and frustratio
The Ecclesiological Society - for those who love churches
Whether you are an expert on church history and church architecture, or merely curious our society provides lots of information, publications, images, news & events.
Lincoln County Humane Society | We speak for those who cannot speak for themselves
The Lincoln County Humane Society is a charitable not-for-profit organization dedicated to the humane treatment of all animals; to alleviate their suffering and neglect, support the human-animal bond…
The Knowledge Management Institute of Canada | From Those Who Know to Those who Need to Know
The John Howard Society of Canada - The John Howard Society of Canada : The John Howard Society of Canada
Pacific Post Partum Support Society - Vancouver, BC Canada
PPPSS provides telephone support, weekly women's support groups, partner education sessions, community trainings and resource materials.
Lyme Disease, Science, And Society: Camp Other
Lyme Disease, Science & Society: Camp Other
Author: Camp Other
Parkinson’s Disease and Movement – Disorder Society
Societi - The UK Kawasaki Disease Foundation
Kawasaki Disease is the leading cause of acquired heart disease in children in the UK. It’s time we changed that…together we will.
Author: August
