I live in Ealing and was hoping I might be able to attend one of your social gatherings. I have had ME for a number of years and would like to have the opportunity to meet others who understand the condition and be able to socialise for an hour or so. Do you have any forthcoming events I could attend?
Hello Karen, I will add information about social events on this page once they have been agreed. They are also advertised on our newsletter if you are a member.
Heidi (editor of the website)
Hello there, I have recently been diagnosed with Post viral Chronic fatigue syndrome and i am looking for a support group within the Ealing area and wondered if you may be able to help?
hello James, you’ve come to the right place as we cover the whole of West London, including Ealing (although many of our social meetings take place in Chiswick). If you would like to join our group, please use our membership form here:
I am diagnosed with CFS / ME. I have been directed to you by the Hillingdon CFS/ME clinic. I am looking for a group in which I can share experiences with similar people. Please can you let me know what meetings you have planned in the Chiswick area in the near future. Do you have a meeting I can come along to before your advertised summer party on 23 July?
I’m afraid the summer party in July is the only one that has been planned so far, but as soon as new dates are planned, I will update the website. If you want to come along to the summer party, you are very welcome to join our group! 🙂
Pls can you advise timing and location for your summer party tomorrow. Apologies, I can’t find the info on your website.
The summer party details can be found in the Network MESH newsletter which has been circulated to all Network MESH members.
Thanks. Please can you mail me a copy of the newsletter or send me the address of “Maggie’s garden” (privately, if necessary) so that I can come along to see if I want to join the group formally. Thank you.
Tim, I will contact you privately.
Thanks Heidi. Standing by for your message.
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