Raymond Gaudlap

By Alexandra Gaudlap

Why I’m doing it

Raymond was born on June 20, 2016 at Camp Lejeune Naval Hospital in Jacksonville, NC. Pediatricians and specialists in North Carolina were not concerned about Raymond’s well-being because he appeared to be a “happy boy who is just taking his time hitting his milestones”. Motherly instincts told me it was time to take steps to become an advocate for my son’s wellbeing.

In August 2017, we returned to our home state of New Jersey to have Raymond evaluated by top notch specialists in our area. At this point Raymond was 14 months old and still unable to roll over, crawl, walk or talk. In the first few months back in NJ Raymond saw a Geneticist who did genome testing which came back normal. When visiting Neurology at Alfred I. duPont Hospital for Children, we did a routine EEG and were told Raymond was having seizures all day, everyday and this was causing his developmental delays. He was put on Keppra, a seizure medication, and we immediately saw a difference. He began sitting up almost immediately. Unfortunately, Raymond was severely allergic to the medication causing a reaction called “erythema multiforme”. Once he recovered from the reaction Raymond was prescribed Topamax as his seizure medication. As of September 2021, he takes this twice daily.

In November 2017, we began Early Intervention Therapy Services through our county. Raymond received in-home physical therapy, speech therapy and occupational therapy. He was eligible to receive therapy until his third birthday when he became eligible for early pre-school.

In March 2018, Raymond’s Neurologist at Alfred I. duPont Hospital for Children recommended we research CBD Oil through Charlotte’s Web in Colorado. We started the CBD within a few months and within six months noticed an improvement on Raymond’s EEGs. He improved from having seizures to having abnormal spikes putting him at risk for seizures. Around this time, Raymond’s geneticist also recommended that we apply for the National Institute of Health’s Undiagnosed Disease Program which would allow us to be introduced to expert doctors and receive advanced medical treatment.

Raymond became a big brother at 18 months old. Raymond began meeting developmental milestones with Ryan. They started sitting independently and crawling around the same time. When Raymond turned two in June, he was diagnosed with Cerebral Palsy and also started receiving weekly outpatient physical therapy. It was summer 2018 when Raymond got accepted into the National Institute of Health’s Undiagnosed Disease Program. Due to weight and age guidelines for the program our trip was postponed until February 2020.

September 2018 Raymond sat at the table for the first time without assistance. He finger-feeds since he is unable to use utensils. Over winter 2018 and spring and summer 2019, Raymond continued to work hard in his therapies to pull to stand. Although we were not quite ready for the gait trainer, we continued to take the steps to get there.

Fall 2019, Raymond started ABA preschool with a one-to-one aide. He received physical therapy, occupational therapy, and speech therapy in school. In February 2020, Raymond was finally ready for his gait trainer. “Crocodile walker”. He made great progress.

In June 2020, we got huge news. Raymond’s genetic testing was sent for reanalysis through Ambry Genetics where we received confirmation on a diagnosis. He was one of eight children in the world that have been diagnosed with a VAMP-2 Gene Mutation. This was huge news for us, and although it did not change our treatment plan we were glad to finally receive a diagnosis.

Summer 2021 was a great summer for us with a lot of new milestones. In June, Raymond began walking independently. There was a lot of hand coordination improvement and consistent new sounds being vocalized. In July, Raymond’s baby sister was born. He loved her from the start. Raymond is now interested in books and toys. He gets out of his bed independently and we are working on getting in his bed by using therapy steps. In August we decided to take a six-month break from outpatient therapies to allow Raymond to start school full-time without having to be pulled out. We all agreed it would be more beneficial to have him exposed to other children in school during this big burst of milestones. We continue to see improvements and are hopeful for the future.

Currently, Raymond continues to progress each day with his walking. He is now walking with his hands at his sides which shows he is gaining confidence. He initiates play with his siblings and has his own way of communicating what he wants. He is continuing to improve his fine motor skills as well. Every day we notice new sounds and we are slowly being able to understand his language. As of now, Raymond can say about 5-10 words and is working hard to put words together clearly. His newest is “hold my hand”.

Raymond is a very happy and social little boy which makes things so much easier when it comes to struggling with the parental feelings of having a child with a newly discovered and rare genetic disorder.

Although we do not know how Raymond’s future may be, we continue to remind ourselves that nobody’s life is predictable. Our mindset from the beginning was that we would provide Raymond all the tools he needs to be the best version of himself. He will achieve them when he is ready. In the meantime, we celebrate every milestone big or small because that is something to be proud of.

Thank you to my Sponsors


The Lynch’s

In honor of Raymond’s Great Great Grandfather who is turning 100 years old this month we will donate $1 for each of his years well lived! #PowerOfCommunity


Philip Natale Jr

Keep kicking ass Raymond you are an amazing young man with a great family and a lot of people rooting for you💪💪💪💪💪


Elise Morgan

What a beautiful, extraordinary family. You are an amazing inspiration. I do wish this contribution could have many more zeroes on it, but it's what I can do for now.