Hertfordshire / North London

Find a support group in your area or find out if there are others with whom you could start up a group.

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Hertfordshire / North London

Postby Pre-Raphaelite » Sat May 24, 2014 11:55 am

Hello, I would be glad to hear from anyone in a similar situation living around South Herts / North London.
Thanks
Trevor
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Re: Hertfordshire / North London

Postby Pre-Raphaelite » Wed Jun 04, 2014 12:49 pm

44 views and not as single reply!
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Re: Hertfordshire / North London

Postby HazelB » Thu Jun 05, 2014 9:29 am

Perhaps no-one in your area has read the post, and that is why you've not had a reply. Xxx

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Hazel xxx
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Re: Hertfordshire / North London

Postby FluppyPuffy » Thu Jun 05, 2014 10:54 am

Sometimes a post doesn't appear on the "View New Posts" option. The first I knew of you asking about people in your area was after it appeared with Hazel's reply. Not sure why this happens, we tend to blame the Gremlins, and, as Hazel has already said, it may not have been read by anyone in your area.

Wrt to the number of views, as well as us huu~mons, posts are also read/scanned by various bots, crawlers etc that can access open parts of the forum, which adds to the number of views shown.

Have you had a look at the Support Groups page on the main UKFM site to see if there are any around where you are??? Also Mr Googley can be helpful in finding such groups. As well as searching using FM, trying things like CFS/ME and phrases like "invisible illness" can throw something up as it's not unusual to find that a groups' membership covers a number of conditions.
As a Public Moderator of this forum my opinions/views expressed are personal and are no more valid than those of other members and not necessarily those of UKFibromyalgia.

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Re: Hertfordshire / North London

Postby *Lisa* » Thu Jun 05, 2014 11:58 am

Im in Hertfordshire but North Herts so I cannot help you there apart from checking the linky out fluppy has given you.

I do know that not many members seem to come from your side of the country. You can ask your GP if there is any support groups around or the Rhumatology/physio department at your local hospital
As a Public Moderator & Admin of this forum my opinions/views expressed are personal and are no more valid than those of other members and not necessarily those of UKFibromyalgia...Lisa
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Re: Hertfordshire / North London

Postby Pre-Raphaelite » Thu Jun 05, 2014 1:44 pm

Hi, thanks for the replies. Yes I have searched, the closest one was at the Royal Free but is now defunct. There is a North London ME group though they only meet quarterly and attendance seems to be very low.
Seems we've been cast into austerity isolation, for such a densely populated area there is quite literally sod all going on. :yikes:
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