Jump to content
RemedySpot.com

CA Connection photo book

Rate this topic


Guest guest

Recommended Posts

Well folks it's finally completed. Thanks to all of you who send me your

snapshots and digital photos. Any one who wants their photos returned

please email me directly. I regret to say this photo album is not as complete

as I would like. So many of the local Californians did not attend the meals

portion of the weekend and that was where the majority of the pictures

where taken. I'd like to continue the tradition of asking for a donation for the

photo book. This time to be sent to the Symposium fund. I'd like to see us

give a little more than the usual $10.00 even if it's only a dollar or two more.

$15 would be great but whatever you can afford will be appreciated. I feel

like the Public Television stations on their annual fund raising drive. But what

ever works and I do think the books are wonderful momentos of the events

and great chronicles of our group. We've come a long way. I will do as I have

done in the past and send along the donation forms and envelope with the

books. Even if you didn't attend the connection the book is an excellent way

to connect a face with the names you see every day on the PLSFriends.

Back issues of the Connecticut Connection, Oct 2000 The pioneer connection

that brrought 20 PLS'ers and their famly/caregivers and friends together) and

the North Carolina Connection, Oct 2001 (18 PLS'ers),and even 5 pages of

Spring Fling, WV #1, 2001 & #2, 2002, (no programs) photo books and

program booklets are available upon request. email me direct.

dixsign@...

I know these are tight economic times but the upcoming symposium is a big

step toward speeding up research. Research that will benefit all of us

regardless of where we live, how much money we do or don't make, how old

or young we are and what stage or type of PLS we have.

Every little bit helps and I welcome the opportunity to give my time and

resources to help us reach every new goal and challenge. It's my way of

fighting my disease. Here's an opportunity to get to see what most of us look

like (a truly fine looking bunch if you ask me) and to get to know every one a

little better and help fight your battle against PLS. Let's put that thermometer

over the top.

Link to comment
Share on other sites

Join the conversation

You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.

Guest
Reply to this topic...

×   Pasted as rich text.   Paste as plain text instead

  Only 75 emoji are allowed.

×   Your link has been automatically embedded.   Display as a link instead

×   Your previous content has been restored.   Clear editor

×   You cannot paste images directly. Upload or insert images from URL.

Loading...
×
×
  • Create New...