Whilst the internet is undoubtedly a good source of information, please be aware that, just because it is ‘published’ on the internet, not all the information is correct or trustworthy. If you are unsure about the information you have found, print it off and discuss it with your doctor or MND clinical specialist. Some useful sites which have good, trustworthy information are:-
- NHS Inform www.nhsinform.co.uk
- International Alliance of ALS/MND Associations www.alsmndalliance.org
- Motor Neurone Disease Association (England, Wales & N. Ireland) www.mndassociation.org
- ALS Society of Canada www.als.ca
- ALS Society of Canada, specialist sections for children or teenagers www.als411.ca
- Muscular Dystrophy Association, (USA) www.als-mda.org
- The ALS Association (USA) www.alsa.org
- Patients Like Me (A social networking website for those with long term disease) www.patientslikeme.com
- Eurostemcell (for information about the latest stem cell research) www.eurostemcell.org
