Discussion in 'Action Alerts and Advocacy' started by Countrygirl, Jan 16, 2017.
Your excellent me/cfs blog will have an important place in the history of this disease. Thanks so much for your costly
(in terms of this illness) and elegantly written contributions. Best of luck in your new sunnier location. I agree that legal action will be needed. The US may be the place for this to begin rather than the UK. UK mecfs patients are in a strangle hold at present compared to the US patients.
You can also try a Google Site Search
Separate names with a comma.