I was asked to be on
the board of directors almost a year ago and now have the opportunity to serve as the secretary as well. This organization has become near and dear to
my heart. We were hesitant to get
involved for quite sometime because we felt like Jaxon did not "fit" .... because his hearing loss was not "severe". Although, Jaxon didn’t really "fit"in the hearing world either. Eventually, we made our way to an Arkansas
Hands & Voices activity. It was a
definite blessing to us to have that social support from
parents that had children with hearing loss and despite the severity of hearing loss a child has there are still common concerns that we all have as parents. The knowledge & support the professionals brought to the table was also a great blessing. We learned very quickly there is rich diversity in the deaf& hard of hearing world and that everyone fits!
Every October
ARH&V has their annual fundraiser Tasting at Twilight. This year they decorated the tables with
framed copies of different children’s hearing journey along with a picture. For those interested here is Jaxon's "hearing" journey!
Jax’s story is a
victory for early identification and early intervention. The first indications that Jaxon might have
hearing loss came before he even left the hospital. His hearing deficits were identified during
the newborn hearing screen and after many attempts to get him to sleep through
a hearing test – no matter how hard we tried, Jax would always fall asleep on
the way to the hospital and then be wide awake and smiley during the hearing
tests! – we had a confirmed diagnosis of bilateral sensorineural hearing
loss.
Jaxon had his
first pair of hearing aides by the time he was four months old. Thanks to an aggressive approach to early
intervention in California, Jaxon was enrolled in the San Diego Unified School
District a short time later and soon began receiving in-home (and occasionally
at our office, depending on our schedule) speech therapy. We worried that the move from San Diego to
Conway would result in a step backward in his treatment, but were delighted to
find an even more committed and caring group of providers in Sharon Ross, Jan
Stroud, and others in the Central Arkansas deaf and hard of hearing community.
Jaxon is doing
great today. We recognize how much we
owe to the support of the entire community that has supported his growth and
development.





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