Female 5 - KISS
MOM: GODIVA          DAD:   CADENCE
Born:  1/22/11              Ready: 3/19/10

Brody's Puppy - MAYA GRIFFIN
Guntersville, Alabama
Click photos to go to parents' webpages
Brody Griffin.... so much to tell about who
he is, how he has changed lives; how he
was diagnosed with Fragile X Syndrome,
Austim,  ADHD, sensory processing
disorder, hearing loss and strabismus, only
to name a few, and how his life without
hope in a Guatemalen orphanage changed
to a life filled with blessings with his four
brothers and sisters (two also adopted
from Guatemala) when a wonderful
Christian couple I'm happy to call friends
adopted him.  Brody went home with his
new mom and dad at age 22 months
weighing only 20 pounds- the size of a six
month old baby. He could not hold his own
bottle and had never had solid food. He
had acid burns on his back from urine and
scars from feces on his rectum. He lost
half of his hair when he went home due to
stress. Such a sad start to life, but with
early intervention, he is using his own
laptop computer, wearing headphones,
even went potty for the first time in this
week (3-5-11) and enjoying life while still
taking NO medications.  A testament to a
loving family and answered prayers. You
can get to know Brody on his blog at:
http://www.whosbrody.blogspot.com
Brody and his beloved service dog,
Milo.  Millo went to over Rainbow's
Bridge on 1/23/11
What is Fragile X?
The Top Ten Things You Should Know About
Fragile X Syndrome
By Mary Beth Langan
and Sally Nantais
1. It’s genetic.
2. If a woman is a carrier, she has a 50/50
chance of passing it on to her son(s) or
daughter(s). 1 in 100 to 200 women are
carriers **.
3. If a man is a carrier he will pass it only to
his daughter(s), and they will only be carriers.
1 in 800 men are carriers.
4. Fragile X Syndrome does not discriminate;
it doesn’t care which ethnic group you belong
to.
5. Fragile X Syndrome is a spectrum disorder.
Symptoms may vary from mild learning
disabilities (including shyness and social
anxiety) to severe cognitive impairment
(mental retardation).
6. Premature Ovarian Failure, more
commonly known as early menopause, is a
condition that affects 20-28% of the female
FXS carrier population.
7. Fragile X-associated Tremor/Ataxia
Syndrome (FXTAS), discovered in 2001, is a
neurological disorder that can involve
tremors, balance irregularities, difficulty
walking and dementia which sadly is often
misdiagnosed as Parkinson's and/or
Alzheimer’s. This condition is present in some
older FXS carriers (typically after the age of
fifty), usually in males but FXTAS can also
affect female carriers.
8. There are minor physical traits noted in
many persons with Fragile X Syndrome, but
not in all. These are traits which may also be
present within the typical population, nothing
unique which would necessarily indicate FXS
testing is necessary for your child.
9. When testing for Fragile X Syndrome
(FXS), it is critical that the correct tests are
ordered – the Fragile X DNA (Southern Blot)
and PCR analysis. Inaccurate results occur far
too often with the generic chromosomal panel.
Test for FXS to obtain a diagnosis or to rule it
out. If you don’t have what may be the correct
diagnosis of FXS, then you will never be aware
of improved treatments or the cure when it’s
found.
10. Where to go for the most accurate and up-
to-date information on fragile X syndrome:
http://www.fragilex.org/, the National Fragile
X Foundationhttp://www.fraxa.org/, Fraxa
Research Foundationhttp://www.
conquerfragilex.org/, Conquer Fragile X
Foundation** American Academy of Family
Physicians, News and Publications, Vol. 72/No.
1 (July 1, 2005) http://www.aafp.
org/afp/20050701/111.html
Mary Beth Langan and Sally Nantais are both
Fragile X Syndrome carriers; each has a son
with Fragile X Syndrome. They can be
contacted at mblangan@hotmail.com and
sally_nada@juno.com