2017 Dragon Magazine Winter
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potlight<br />
“In my case, the diagnosis was not made early on as<br />
it should have been, as doctors were and still are not<br />
truly aware of the signs of CMT. One doctor told my<br />
mom that she would make me neurotic if she kept<br />
dragging me around to be examined, as we had visited<br />
some really great medical institutions seeking an<br />
answer,” she said.<br />
CMT has impacted Fisher’s life in multiple ways. She<br />
had to sell her home and move in with her parents,<br />
and now uses AFOs (ankle foot orthosis), a walker<br />
and wheelchair to get around. “I’m very fortunate<br />
that my parents were willing/able to have me move<br />
back in with them, as I’ve had multiple surgeries as a<br />
result of complications from new injuries,” she said.<br />
“Due to my mobility restrictions my dad drives me<br />
to work every day and my mom is my ‘everything’ at<br />
home, as the fatigue from CMT has me benched at<br />
night and some weekends,” she said. “I hope since<br />
I just had my sixteenth surgery – an ankle fusion –<br />
that I will be able to build up strength and put a plan<br />
together to move once again towards my independence.”<br />
Despite her medical challenges, Fisher finds a way to<br />
help others. Professionally, she’s worked for Vantage<br />
Mobility International (VMI), a state-of-the-art mobility<br />
van conversion facility in Arizona since 2005.<br />
“Originally I started as an Accounts Payable lead<br />
and worked my way to manager. However, with the<br />
increased symptoms of my CMT, I took a step back,”<br />
she said. “I am very fortunate to work for a company<br />
that is supportive of me and all the changes that<br />
CMT brings to my journey.”<br />
Fisher also volunteers with the CMT and Muscular<br />
Dystrophy associations.<br />
“I try to be advocate for those with<br />
CMT and share knowledge, connect<br />
others with medical and mobility<br />
information, and provide support.<br />
Additionally I try to raise funds to<br />
help find a cure, as there are clinical<br />
trials happening throughout the United<br />
States right now, and work to bring<br />
about awareness of this little known,<br />
rare disease through various media<br />
platforms,” Fisher added.<br />
She was recently selected as the Co-Leader of the<br />
Arizona CMTA branch, and will serve in that role for<br />
a minimum of two years. Her responsibilities include<br />
organizing branch meetings, attending conferences,<br />
holding at least one fundraiser a year, and helping<br />
spread the word about CMT in the greater community.<br />
Fisher believes her desire to give back stems from<br />
watching MDA telethons on television and observing<br />
her mom volunteer at church, at the Salvation Army<br />
and at local hospitals. “These experiences somehow<br />
imprinted on me to do more and give back<br />
somehow/some way to others,” she said. “I think the<br />
confluence of life experiences has set me up perfectly<br />
for the continuation of that service platform which I<br />
continue to have in my life’s journey.”<br />
Looking back, Fisher says she missed out on playing<br />
sports in high school - and wishes she had pushed<br />
more strongly for answers. “With the right adaptive<br />
equipment I could have done anything, and I want to<br />
make sure to share that with the youth I meet today,”<br />
she said.<br />
<strong>Winter</strong> <strong>Magazine</strong> <strong>2017</strong> // 43