Join our new Southeastern USA XXY Support Forum!

[pmgamer18]

I felt the need to post this here for the man with XXY
Phil
Join our new Southeastern USA XXY Support Forum!

If you live in the USA and specifically within any of the southeastern
states of North Carolina, South Carolina, Tennessee, Alabama, Georgia,
or Florida, then you are who we want to join this forum. But if you
live in a surrounding state and cannot locate on the web a support
group that covers your state, let me know and I will try to help you
find support or you can simply join in with us.

I myself live in the southeastern part of the United States. I have
Klinefelter Syndrome and my karyotype is 47,XXY. This support forum is
for those with Klinefelter Syndrome, XXY, or Variants. Your spouse is
welcome to join this forum as well including anyone else who has a
close tie or interest in you.

There have been attempts to form regional support groups for the
southern United States, but as of lately there is virtually little if
any organized support. So maybe we can change that. We will start
small and grow from this point on (even by adding more southern states
if we need to). Therefore, I invite you to join and tell others that
you know who live in your area about us.

How to join? Visit our forum within the international forum called
XXYTalk. The link is: http://www.xxytalk.com
You must first become a member of XXYTalk in order to access the
Southeastern USA XXY Support Forum.

As Forum Administrator, here are my goals for the next 12 months:

1) Get the word out among the other Klinefelter Syndrome support
groups that we now have our own SE USA Support Forum within XXYTalk.
com and that we want everyone who lives in NC, GA, TN, SC, AL, and FL
to join.

2) Sponsor a Southeastern US regional one-day conference with
qualified speakers on the subject of Klinefelter Syndrome and invite
everyone including local endocrinologists, compounding phamacists, and
other related professionals to attend.

3) Promote the Klinefelter Syndrome Awareness Day on March 20, 2007
and every year thereafter.

4) Create and maintain a database of recommended southeastern
physicians and surgeons who understand and can adequately treat our
Klinefelter Syndrome condition.

5) Organize a weekend 2-day retreat at DisneyWorld, Orlando, FL for
Klinefelter Syndrome, XXY, and Variant individuals. This is an
opportunity to meet one another face to face and form friendships as
well as enjoy one of America's greatest entertainment resorts.

6) Form alliances and reciprocal referral courtesies with KS&A and
AAKSIS. Form alliances with existing or hibernating US southern based
Klinefelter Syndrome support leaders and groups.

7) Change any of this on the fly if we want to and substitute better
ideas!

Is that enough to do in one year? I think so! I need help too. I seek
energetic individuals who want to be on the ground floor of this new
support group. Don't feel energetic? Come join us and we'll drink a
pot of coffee and do a T-shot. We can get energetic together. LOL

Don't live in the southeastern USA? We have two other support groups:
Sydney, Australia and KSA-UK (including Ireland). Want to start your
own regional support group, but don't have a website? Write me at
xxytalk@gmail.com and let's discuss the possibilities.

Yours truly,

Matt
47,XXY
www.xxytalk.com
Email: xxytalk@gmail.com