Opportunities & Possibilities- Alana Gohn

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By Angela Gartner   •  Photography by Kim Stahnke

We highlight individuals and families who are inspiring others by sharing their experiences in the workplace, participating in fun and meaningful activities, and demonstrating how advocacy can create a more inclusive community for everyone.

Finding Your Community — Alana Gohn

Alana Gohn, 17, of Solon, was initially diagnosed with

microcephaly as an infant, but there were still missing

pieces of Alana’s development that didn’t match

completely. It wasn’t until 2024 that she was diagnosed

with a rare neurodevelopmental disorder called HUWE1.

For the first time, her parents Scott Gohn and Elaine

Eisner, who helped to  create LiveSpecial.com because they wanted to pull together resources since their daughter Alana was so unique, were able to connect to parents with children who had this diagnosis.

Due to the rarity of HUWE1, the support group,
which has families from the U.S. to the U.K., is still a small community.

“The scientific community finally caught up,” Gohn

says. “We were the early adopters in the group. We saw

the website initially, and then we found the Facebook

group and started interacting there. At the time when

we joined the Facebook group, she was the oldest one.”

He notes that since then, more have joined and they

have been able to see adults with HUWE1, which gives

Gohn and Eisner hope for Alana’s future. He notes in a community group, you see the challenges, but also the goals achieved.

“Finding a community is great, as you will no longer

feel that you are going at this alone,” he says. “However,

what we have found is that everyone is unique and no

two HUWE1 kiddos are the same. It’s a spectrum, some

individuals are high functioning and presenting as

typical individuals while others are low functioning and

requiring great assistance with all aspects of life. We see

and understand that there are individuals that may be

similar to Alana and who achieve goals.”

Gohn says as families who have children who are

newly diagnosed come to the group looking for answers,

he’s one of the first to respond.

“I respond simply because it’s comforting — to say

hey, it’s OK, you’re going to be OK,” he says. “From

that standpoint, I am the one getting the most out of

it because I am able to interact with individuals to say

here’s what the road may look like. So, maybe that is

giving me a little bit of therapy.”

For Gohn and Eisner, while the support group provides

a community aspect, it doesn’t change how they will

advocate for Alana.

“She is living her best life,” Gohn says. “She had a great

summer with camp. She enjoys school so much and it

provides a structure. She also gets the opportunity to

interact with her peers, which is fantastic for her.”

Alana doesn’t just go to school, but she is involved in

swimming, skiing and riding bikes.

“There’s a lot she continues to do and accelerate at,”

Gohn says. “Her accomplishments are at her own pace.

She gets what she needs, because Elaine and I advocate

for her at every single turn.”