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Funding
We receive a small grant from the Primary Care Trust
for our Newsletter but otherwise rely solely upon annual membership fees, public appeals and
donations for running the Group.
Aims
To
help all those people whose lives are affected by ME/CFS by:
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Providing
accurate, effective and high quality information on ME/CFS to members. |
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Providing
support to ME/CFS members, their families and carers. |
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Offering
members appropriate advice on ME/CFS to enable them to make informed
decisions. |
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Offering
guidance for attaining fair diagnosis and treatment of ME/CFS with regard to
employment, benefits, insurance and other related issues. |
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Increasing
awareness, stimulating interest in and disseminating high quality
information on ME/CFS to all relevant individuals and organisations,
including medical professionals. |
Or, can we help you:
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