Re: Support Group in Boston??
From: Krissy (anonymous@obgyn.net)
Sun Nov 23 18:57:33 2008
Stephanie,
I know your post is old, but I am trying to get a support group together
around Boston. Nothing associated with the EA, but more like a time to
have dinner or coffee and talk with some women who know what they're
going through.
If interested, email me: kristinemunroe AT yahoo DOT com
At Sat, 12 Jul 2008, Stephanie wrote:
>
>Wow! That's rough! You have to pay to talk to people??? Seems a little
>crazy to me but hey maybe thats just my crazy opinion lol.
>
>At Fri, 11 Jul 2008, anonymous wrote:
>>
>>The EA will not give any info out without you paying to become a member.
>>They say you will receive helpful newsletters, etc but you only get more
>>requests for money from Mary Lou. They also get paid a hefty sum of
>>money from TAP the makers of Lupron.
>>
>>At Fri, 11 Jul 2008, anonymous wrote:
>>>
>>>The groups don't always meet because sometimes women have pain
>>>issues...but they can help you start one :)
>>>
>>>At Fri, 11 Jul 2008, Stephanie wrote:
>>>>
>>>>I haven't checked anything out yet but everyone here has had some really
>>>>good info so I thought I would ask here first. Thanks for the info Ill
>>>>call them up!
>>>>Steph!
>>>>
>>>>At Fri, 11 Jul 2008, anonymous wrote:
>>>>>
>>>>>have you heard of the Endometriosis Research Center? I think they have
>>>>>online support groups, and the Endo Association has local groups that
>>>>>meet in person
>>>>>
>>>>>oh wait, the ERC might also meet in person :)
>>>>>
>>>>>have you seen this doctor's site?
>>>>>
>>>>>endoexcision.com
>>>>>
>>>>>At Fri, 11 Jul 2008, Stephanie wrote:
>>>>>>
>>>>>>Hi My name is Stephanie, I just joined this forum a couple of days ago
>>>>>>and love it but thats besides the point! I was wondering if anyone knows
>>>>>>of a support group in the Boston area that helps for patients with Endo?
>>>>>>Thanks!
>>>>>>S
![[ endo@obgyn.net ]](../../images/endo_at_obgyn.gif)