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To answer your question: There is a hyperbaric therapy center in San
Diego close to Sharp Hospital in clairemont. The people there are
very helpful. It's not at the hospital but about 5 minutes away. You
should give it a try and I might see you there.
I don't know anything about it. Is that hyperbaric oxygen? Don't you have to go to Mexico to have that done?
--- On Mon, 6/9/08, feelgr8t <feelgr8t@yahoo.com>
wrote:
From: feelgr8t <feelgr8t@yahoo.com> Subject: [SAN-DIEGO-COUNTY-CFIDS-MCS-FIBROMYALGIA] Hi I'm a new member looking for advice To: SAN-DIEGO-COUNTY-CFIDS-MCS-FIBROMYALGIA@yahoogroups.com Date: Monday, June 9, 2008, 6:32 PM
My friend did hyperbaric therapy for another reason but informed me that while he was getting treated at the faciliy there were paitents get hyperbaric therapy with firomyagia he said that they said they felt so much better. What are your thoughts??? I was thinking I might give it a try. Thank you
I don't know anything about it. Is that hyperbaric oxygen? Don't you have to go to Mexico to have that done?
--- On Mon, 6/9/08, feelgr8t <feelgr8t@...> wrote:
From: feelgr8t <feelgr8t@...> Subject: [SAN-DIEGO-COUNTY-CFIDS-MCS-FIBROMYALGIA] Hi I'm a new member looking for advice To: SAN-DIEGO-COUNTY-CFIDS-MCS-FIBROMYALGIA@yahoogroups.com Date: Monday, June 9, 2008, 6:32 PM
My friend did hyperbaric therapy for another reason but informed me
that while he was getting treated at the faciliy there were paitents
get hyperbaric therapy with firomyagia he said that they said they felt
so much better. What are your thoughts??? I was thinking I might give
it a try.
Thank you
My friend did hyperbaric therapy for another reason but informed me
that while he was getting treated at the faciliy there were paitents
get hyperbaric therapy with firomyagia he said that they said they felt
so much better. What are your thoughts??? I was thinking I might give
it a try.
Thank you
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The study is taking place on 12/9 or 12/10. It is a 2 1/2 hour group and
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Thank You,
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CFIDS/Fibromyalgia victims are trying to get a million letters
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If you'd like to participate but are not up to writing out a full
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consider using this form: http://cfids.home.att.net/million_letters.htm
This link: http://www.fms-help.com/letter.htm
explains the plan and gives the addresses of those they feel
should be contacted.
And for Americans trying not to be legislated out
of their disability here's a way to have your voices heard:
http://www.aarp.org/tools/partner?url=http://capwiz.com/aarp/home/
"To travel hopefully is a better thing than to arrive, and the true
success is to labour." Robert Louis Stevenson
Hello,
The moderator of the SAN-DIEGO-COUNTY-CFIDS-FIBROMYALGIA group has changed the
group's name.
This means that both the group's email address and the group home page
location have changed.
The group email address:
SAN-DIEGO-COUNTY-CFIDS-MCS-FIBROMYALGIA@yahoogroups.com
The group home page location:
http://groups.yahoo.com/group/SAN-DIEGO-COUNTY-CFIDS-MCS-FIBROMYALGIA
If you have links which point to this group or an address book entry
for the group, you should update them, as the old addresses will no
longer work.
Regards,
Yahoo! Groups Customer Care