Art For Hope|Love|Cure

It’s Rare Disease Day. I had never heard of it until my son was diagnosed with CDKL5 Deficiency Disorder. This will be our sixth Rare...

{this blog is written by G’s mom} Hello! I understand that your child has been diagnosed with CDKL5 Deficiency Disorder. Even though we...

{this blog is written by G’s mom} I fought getting a G/J tube for my son for too long because I thought it meant that I couldn’t blend...

{this blog is written by G’s mom} When my son got his g-tube placed in May 2019, I was adamant that I was going to continue to feed him...

{this blog is written by G’s mom} Exciting news! Our Rare Starfish Collection is currently on display at NORD - the National Organization...

{this blog is written by G’s mom} When you have a typically developing child there are endless resources to explore about what are the...

{this blog is written by G’s mom} 2018 was all about getting out there and sharing G’s art and our story. It was a great year! *We gained...

{this blog is written by G’s mom} We had our first show! Art for Hope/Love/Cure was at Open Studio Hartford this past weekend and we had...

We are so excited to share that Art For Hope/Love/Cure is a participating artist with Open Studio Hartford! This is an amazing...

{this blog is written by G’s mom} I have always loved art. Many of my electives in high school and college were art related. I almost...