Are there any Cardinal Fans out there?
SUPPORT THE FOUNDATION FOR CHILDREN WITH ATYPICAL HUS FOR AS LITTL AS $5
Hi again...it's that time of year for The Foundation for Children with Atypical HUS, St. Louis. This might be a long shot, but I know the Cardinals have far reaching fans. This year you may want to participate in our raffle, it is chance to win
a David Freeze autographed and framed picture of his walk off home run this year OR third prize, a Whitey Herzog ouautographed baseball-second prize is a autographed St. Louis Blues Jersey with nearly the whole team signing it, including the big names, and this might be their year to go to the Stanley Cup!
FIVE DOLLAR RAFFLE TICKET COULD WIN FOR YOU AN
AUTOGRAPHED & FRAMED PICTURE OF THE DAVID FRIEZE WALK OFF HOME RUN
AN AUTOGRAPHED STL LOUIS BLUES JERSEY WITH NEARLY THE ENTIRE TEAM
THE HALL OF FAME-WHITEY HERZOG-SIGNED BASEBALL IN A PROTECTIVE CASE
NOTE: Wouldn't any of these look awsome in your sports fanatics, "Man Cave"?
PS: Don't forget Mother's Day and Father's Day is coming up!
Just contact me, Cheryl Biermann and reserve your ticket today! I'll give you your ticket number/numbers at that time and snail mail the actual ticket, if you like, after receiving payment. Easy - Peasy!
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WELCOME - Friends, Family Members, Patients, and Researchers - JOIN US!
The Foundation for Children with Atypical HUS encourages patients and investigators to share information and explore options/resources as we work together to gain insight into this rare complement disorder. By increasing contact opportunities with researchers and medical personnel interested in helping the aHUS community, our stories foster a better understanding of atypical hemolytic uremic syndrome.
Sharing information, inspiration and support for one another, we seek to gather together people and knowledge as we strive to improve the lives of patients and families dealing with a diagnosis of aHUS.
NEW DIAGNOSIS OF aHUS?
Be proactive! Get the medical basics of aHUS, what lab values to monitor, and areas of concern...check out the "aHUS Bootcamp" and "About aHUS" tabs at the top of this page!
If your doctor has never treated a case of aHUS, please print out our 'Doc to Doc Registry' and ask him/her to contact a physician versed in the complexities of aHUS and new options for 2011 genetic testing and treatment.
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NOTE: Our 'Send a Message" function on each Member's page allows for private discussion of personal content. As with any social network, be cautious about giving personal contact information (home email info, phone number) until you have an established relationship with another person, organization, or associated website.
Did you know...
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It is estimated that there are about 300 cases of aHUS in the U.S., and it is most common with young children. The condition is life threatening and either can be chronic or can recur at intervals.
more factoids...
Help us fight the battle
Your tax-deductible purchase of one or more bracelets will directly fund research to help end the tragedy and heartbreak that aHUS families live with every day. Each bracelet has an appraised value of $825, but your purchase price is only $295.
Or you can donate a specific dollar amount-every dollar will help the Foundation for Children with atypical HUS atypicalHUS.50megs.com
Donations may be made via credit card or Paypal. If you prefer, checks made payable to The Foundation for Children with Atypical HUS may be mailed to:
Atypical aHUS Foundation
19 Olde Colony Lane
Cape Elizabeth, ME 04107
For pearl bracelet orders, please allow extra time for processing checks.
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