Phoenix UPDATE: 2-2-2021

Phoenix UPDATE: 2-2-2021. Wow! That’s was a long time ago, BUT, Luckily, we are still here! Phoenix is now 18 years old, and while we loved him being able to push his chair around the house he can no longer do that. He actually isn’t really even strong enough to control an electric chair with standard controls. He would be able to control one with proper assistive equipment, but Im not sure I would trust his judgment in certain situations. Phoenix Is also on a ventilator 100% of the time. We were in a Gene Therapy trial here at University of Florida and we actually saw some modest respiratory gains from that trial, but the effects were short lived and we are back on the ventilator all the time. The GT trail was more of a safety trial than an effectiveness study. Phoenix still can breath on his own but maybe only for 20 min or so. And while he is weaker then he was when he was 2, he is able to use a head tracker to use his computer for school and entertainment. Its by far his favorite piece of equipment. We still go to Disney and the Movies and a bunch of other things, but currently we can’t because of COVID. Phoenix is receiving Lumizyme still and he is getting 20 mg/kg every week and so far we are hanging in there but it would be nice to see a new therapy hit the market soon! Thanks.

Photo taken at Disney Animal Kingdom Feb 2020

More Stories

McKenna’s Story

McKenna’s Story

January 2022 I am McKenna Wellner and I was diagnosed with Pompe disease at 19 years old and I am now 20.  I first noticed symptoms the beginning of...

Dwayne’s Story

Dwayne’s Story

December 2021 Hi everyone, my name is Dwayne; I am 53 years old. I was diagnosed with Late Onset Pompe disease (LOPD) in November 2018 when I was 50...

Genevieve’s Story

Genevieve’s Story

January 2022 My name is Geneviève, and I am 42 years old. I was diagnosed with Pompe disease at the age of 40. Here is my story. In my early...

Elizabeth’s Story

Elizabeth’s Story

January 2022 I was diagnosed with LGMD when I was 12 years old.  I had difficulty all my life with running, going upstairs, and doing sports, but no...

Margo’s Story

January 2022 This is Margot. She is almost two years old from Kentucky. She loves to swing, paint, and keep up with her 4-year-old brother. When she was born, there were no concerns. We went home and adjusted to our new life with baby number two. 8 days later, we...

Haley’s Story

November 2021 My name is Haley Hayes. I am from Virginia. I am 16 years old and was diagnosed with infantile-onset Pompe Disease at 6 months old.  I will be sharing my experience being a teenager living with Pompe and how it has affected me over the years. In the...

Caitlin’s Story

August 2021 My name is Caitlin Naldoza. I am 17 years old and was diagnosed with late onset Pompe Disease at 5 years old. I will be sharing my experience being a teenager living with Pompe and how it has affected me over the years. In middle school, that was when I...