Press
by Jen Reeder
"Wilson was born with a rare form of muscular dystrophy called spinal muscular atrophy. When she was 6 months old, doctors told her parents she likely wouldn’t survive past the age of 3. But she did. Over time, she’s lost the ability to eat and breathe on her own. Now 44, Wilson’s remarkable journey is featured in the documentary “Annie Loves Dogs,” a sentiment tattooed on her fingers because she wants her love of dogs to be “front and center.”
“Hear from Annie Wilson (@anniejbwilson), in her own words, about how her Eyegaze Edge has supported her love for graphic design and helping animals! 🐾
In Joanne Warden’s latest documentary, “Annie Loves Dogs,” Annie shares her journey with Spinal Muscular Atrophy (SMA) and how her strength and resilience has allowed her to continue pursuing her passions.”
by Vivian Delchamps Wolf
When asked about common misconceptions she encounters about people with Spinal Muscular Atrophy and wheelchair users, she replied, “People tend to think that wheelchair users are weak, sad, and need assistance for everything, which is not true. People with disabilities are living independently and are active members in the communities that they live in.”
Like many folks in the disability community, Annie rejects pity as a default response. When people respond to her diagnosis with “I’m so sorry,” she replies, “Why are you sorry? I’m not sorry. I’m out here killin’ it.”