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Cecelia’s Story

Since Cecelia was born, she has experienced thousands of seizures. Her brain shows signs of constant epileptic activity, and much of her world has revolved around doctors’ appointments and medications.

Cecelia has been diagnosed with a rare form of drug-resistant epilepsy called KCNQ2E, which means she has several hundred severe seizures every single day. Due to the constant brain activity, she has experienced developmental delays and was unresponsive to any form of stimuli.

When Cecelia came to Dame Vera Lynn Children’s Charity for her initial assessment, she slept most of the way through, remaining in her parents’ arms, where she is most comfortable. She was distressed by being moved and even experienced a seizure during the session.

A smailing baby girl with red hair and wearing a peach coloured oneside with a bib is sat in a black supportive chair while playing with a colourful toy with bells.

Soon after her assessment, Cecelia’s medication was changed, meaning that she had to isolate from other children. This meant cancelling the plans for Cecelia to start sessions at the centre. However, our Outreach Worker Jos came up with a solution.

Because of Cecelia’s condition, it was too early for her to undertake any form of physiotherapy. She was unable to engage in play due to her lack of response to stimuli and the team did not want to overwhelm her with strange sounds and lights from toys. It was instead decided that Jos would take her baby massage training directly to Cecelia’s home. Over a 6-week period Jos taught Cecelia’s parents how to massage her in ways that would relax her and help with areas of discomfort and tension.

A baby in a peach coloured onesie is lying on a beige towel with baby massage certificate placed next to her.

Immediately, it became obvious that Cecelia enjoyed her sessions with Jos more than anything else she had experienced so far. Upon hearing Jos’ voice when she arrived for her weekly sessions, Cecelia would smile and behave entirely differently. She would close her eyes, unclench her fists, breathe more calmly during massages and would coo when deep pressure was applied to her feet.

It was the first time her parents had seen her enjoy something.  

Alongside the many health benefits, baby massage can be an excellent way to introduce positive touch to children who have experienced a large number of medical procedures, helping parents to connect with their child on a deeper, more personal level. Cecelia’s mum has expressed wanting to cry with joy when seeing how happy Cecelia is during baby massage sessions, while her dad has described how this form of outreach has been beneficial, not just for Cecelia, but for the whole family.

​“I cannot put into words what it means to have someone look past a medical label and simply delight and revel in who your child is. Jos brought genuine joy, pride, and compassion to our entire family.” – Cecelia’s mum Alisha.

As Jos has helped the whole family unlock a deeper connection with Cecelia, she has also provided a great sense of companionship and comfort to a family who felt isolated and stressed for their daughter’s health. Her presence didn’t only have a calming effect on Cecelia, but on the whole household.

An image of a baby girl with bright red hair leaning bacl in a chair and grinning. She is wearing a white onesie.

Our time with Jos has been genuinely life-changing, and we will always be deeply grateful to her and the charity

Cecelia’s mum, Alisha

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The Dame Vera Lynn Children’s Charity has been one of the places where we’ve felt completely seen, heard, and supported on Freddie’s journey. Every session has been filled with genuine care and a deep understanding of what Freddie needs to thrive.

– Freddie’s mum, Anna

Freddie was born with an incredibly rare genetic condition called Galloway-Mowat Syndrome. His happy disposition and love of music has seen him thrive since coming to the charity.

Freddie, 3 years old

A young boy with Galloway- Mowat syndrome is being held to sit up and is smiling. He has short dark hair.

With the help of the wonderful team, Jonas is constantly building his strength, stability and motor skills as well as social skills and independence.

– Jonas’ Mum, Kate

Jonas was born with an extra chromosome that causes Down Syndrome leading to delays in his development. With the support of the service team at DVLCC, Jonas has taken his first independent steps within 5 months of being here!

Jonas, 3 years old

A young boy with downs syndrome stand with a small ladder looking back at the camera

The charity provided us with hope, structure, and a community when we needed it most.

– Khanya, Alissa’s Mum

After being unable to leave hospital for 8 months, Alissa was diagnosed with a rare genetic condition called Noonan syndrome. She has made huge progress at DVLCC.

Alissa, 2 years old

A young girl with Noonan Syndrome is reaching for the camera, she is in a brightly coloured room and wearing a great top.

I don’t think there’s another service that compares. We feel so lucky to be able to access it. You can tell that the staff really want to help and want Elsie to do well. It’s just so nice to have another cheerleader.

– Elsie’s mum, Debi

Born at 23 weeks and 5 days, Elsie’s prematurity meant that her development was considerably delayed. With so many unknowns, Elsie’s parents weren’t sure what her future would look like until they came to DVLCC.

Elsie, 3 years old

A young girl playing with a sensory game.