WELCOME

We are in the process of designing this
website so that it can be a useful  
resource and a community network for
those affected by Sickle Cell Disease.  

If you are interested in sponsoring this
web site, please
contact us for more
details.
The Faces of Sickle Cell Disease
Carmani

Carmani Boozer, born on May 31, 2006, was diagnosed
with Sickle Cell Disease while still in the womb. Doctors
used stem cells from CeCe's umbilical cord for a bone
marrow transplant.  
Read more.


Submit your stories and pictures via email.  We will not
be able to use or return photos sent via postal mail.
The Boozer Family
Carlos, Cece, Cameron, Cayden, and Carmani


Carlos and Cece Boozer established
Boozer's Buddies to provide valuable
information and resources to families
affected by Sickle Cell Disease.

Boozer's Buddies also supports
treatment and research by making
grants to qualified 501(c)(3)
organizations.  

Please note, Boozer's Buddies is
currently determining its grant
guidelines. We will post them online as
soon as possible.

Have a Question for Us?

We hope that sharing our experiences
can help make your journey easier.  
Please email us questions at  
BoozersBuddies@givingback.org.

We will answer a few of your questions
online each month.
Latest News

4/17/2008

Overcoming the Odds, Healthy Utah

3/30/3008

Promising Quest for a Cure, Baltimore Sun

3/28/2008

Boozer’s Son Still Recovering From Sickle Cell Anemia

4/3/2008
New Approach To Limiting Organ Damage In Sickle Cell
Disease


12/25/2007
Boozer's Best Christmas, Salt Lake Tribune
Boozer's Buddies
Supporting Families Affected by Sickle Cell Disease
through Information, Treatment, and Research           
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Copyright ©  2007 - 2008
Boozer's Buddies at  
The Giving Back Fund