BSEM is an information website that promotes the study and good practice of allergy, environmental and nutritional medicine. The society publishes various reports and a regular newsletter for its members.
The main aim of the Chemical Sensitivity Foundation is to raise public awareness of Multiple Chemical Sensitivity.
Address: PO Box 283, Topsham, ME 04086
ME/CFS and Fibromyalgia Information Exchange Forum. Information on ME and CFS. The Co-Cure website has been gone for a few years now but messages can still be read at https://listserv.nodak.edu/archives/co-cure.html.
HEAL provides information to those concerned about the health affects of chemicals and to alert the general public about the potential dangers of chemicals. They provide a publication published quarterly, reading list and a support service. They are based in America.
Address: P.O Box 509, Stockbridge, Georgia, 30281, U.S.A
MCS International was founded in August 2005 as a "not for profit" volunteer based organisation. It provides MCS information, research, newsletters, forum and telephone helpline.
Helpline no: 01466 794700 (Tues and Thurs: 2pm to 4pm and 6pm to 7pm)
Address: The Founder, MCS International, PO Box 11529, Huntly,Aberdeenshire, AB54 8YJ, Scotland, UK
Useful information on Multiple Chemical Sensitivity (MCS) and Electromagnetic Sensitivity (EMS).
Research, support and information on ME.
Also ME Connect Telephone Helpline service open every day 10-12 am, 2-4pm, 7-9pm: 0844 576 5326
Address: Apollo Office Court, Radclive Court, Gawcott, Bucks. MK18 4DF
An information website on MCS
Tel no: 0044 (0)1524 852371
Address: Unit 34, Heysham Business park, Middleton road, Heysham, Lancashire, LA3 3PP
Useful page of links to MCS information and resources in the US.
Information and resources from a lady living with MCS.
Scent Smart is a services & resources hub on the issue of scents in the workplace.
Information on a book "Severe ME/CFS: A Guide to Living" providing help to patients with severe ME as well as the loved ones and professionals caring for them. This guide sets out to answer questions on severe ME and how to cope with it. It is based on the collective experience of patients, carers and professionals and covers a wide range of topics.
Email (to provide feedback about the book): firstname.lastname@example.org
The CFS Report shares information, updated news and research on ME/CFS.