03.07.2019 Views

2017 Dragon Magazine Winter

Create successful ePaper yourself

Turn your PDF publications into a flip-book with our unique Google optimized e-Paper software.

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

Hooray! Your file is uploaded and ready to be published.

Saved successfully!

Ooh no, something went wrong!