Loved Ones With Ataxia or SCA - Spinocerebellar Ataxia

SCA is a neurological hereditary disease known aswhat the future holds, unfortunately because SCA is
Spinocerebellar Ataxia.so rare, there isn't much research being done on it.
Some symptoms of SCA are:There are many different types of SCA, but only a
- Loss of balancefew genetic tests exist, and the types that he did
- Speech difficultiestest for, he didn't have.
- Muscle spasms and weaknessEveryday we hope and pray that they will invent
- Swallowing problemsmore tests so that we know what type he has and
These are just a few of the debilitating problemswhat his prognosis is for the future.
that SCA patients endure each day.There is no cure for SCA and all that they can do for
My husband was diagnosed with SCA five years ago.SCA patients is to make their lives comfortable.
We thought that he had an inner ear infection,andMy husband is lucky being that we thing he has one
after a few months went buy and he wasn't gettingof the more slower progressive types, however
better, we were referred to a neurologist. Aftereveryday is still a struggle. He lives on over the
seeing many different doctors and specialists andcounter pain relievers everyday for his sore muscles,
enduring many painful tests, we were at a loss notand muscle relaxers at night before he goes to
having any answers as to why he was having all ofbed.All of his food needs to be cut into small pieces,
these problems. Finally our doctor asked if anyand eating solid and liquid foods together is a big NO
neurological diseases ran in the family, and afterNO! We also have to make sure he is supported
talking to some family members we found out thatwhen he walks, so he doesn't fall, but most
SCA did run in the family. My husbands paternal greatimportant we are just there to love him and make
grandmother,grandfather and many aunts, uncles andhim smile.
cousins did or do have the disease. While it wasIf you want more information about SCA, you can
scary to get diagnosed with such a debilitatingcontact the National Ataxia Foundation.
disease, we were also relieved to finally know whyMy family and I cherish everyday we have with my
he felt the way he did.husband. We don't take one minute for granted.
Since then we have done some research to find out