PUBLISHED FOR FRIENDS OF CONQUER FRAGILE X FOUNDATION
Fall 2006 Newsletter
PHILADELPHIANS HOST BENEFIT
GET-TOGETHER FOR CFXF
CFXF FAMILIES RAISING MONEY
FOR RESEARCH

On October 18th, Dr. and Mrs. Harold Yaffe hosted a
fundraising event at their lovely home in the historic
Barclay, on Rittenhouse Square. The event was sponsored
my Marion and Elliot Fisher. It was co-chaired by Barbara
and Mickey Black, Iris and Igal Hami and Sande and
Harris Hollin. The 60+ guests were enlightened about
Fragile X by members of our Scientific Advisory Board,
Dr. Karen Usdin, of NIH and Dr. Jason Dichtenberg from
Albert Einstein School of Medicine. The guests had a
special treat in meeting our CFXF Poster child, Matthew
Hollin. He was his usual charming and warm self. To see
him is to be taken with him and to want to help. The
event raised about $40,000 for CFXF.

Recently, CFXF Family Group members Mark and
Kimberly Grimmel decided to send a letter to family and
friends explaining their experience with fragile X and how
important it is to support research through CFXF. With a
simple mailing that included donation envelopes, they
raised over $4,000 for CFXF research, so far, with
donations still coming in. Through their efforts many
more friends have been introduced into the CFXF
community. Thank you Mark and Kimberly.
Also, the CFXF Family Group, led by our own Patti Neal,
participated in the Bloomingdale’s Shopping Benefit on
October 26. The day included entertainment, refreshments
and lots of shopping. Participating charities will share a
portion of the funds raised and the total amount CFXF will
receive will be announced at a later date. Thank you to all
who worked so hard to make this event a success.



DRS. FRY AND USDIN COLLABORATE ON NEW BOOK

CFXF grantee Dr. Michael Fry of the Technion-Israel Institute of Technology and one of our Scientific advisors,
Dr. Karen Usdin of the National Institutes of Health, have recently edited a book together entitled "Human Nucleotide
Expansion Disorders" published by Springer-Verlag. Fragile X Syndrome is, of course, a human nucleotide expansion
disorder since it results from a dynamic expansion of a CGG-repeat in the FMR1 gene. The book consists of a series of
chapters on the different repeat expansion diseases each written by a different expert or set of experts in the field. It
includes a chapter on Fragile X syndrome and FXTAS written by Drs. Flora Tassone and Paul Hagerman of the School
of Medicine at the University of California, Davis. A chapter on the neglected Fragile X mutations, FRAXE and FRAXF
was written by Drs. David Nelson and Yanghong Gu of Baylor College of Medicine. Drs. Fry and Usdin authored an
introduction to the field and a postscript on future therapeutic prospects. The book can be purchased on amazon.com.
 
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Harris Hollin, Chairman & Founder ¤ Karen Fay, President
PO Box 128Palm Beach, FL 33480
Telephone: 561-833-3457 Fax: 561-833-8791
Email: mail@cfxf.org

CFXF is a not-for-profit tax exempt 501c3 organization
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