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Our children’s stories

“Since Freddie has started at the charity I have been blown away by the friendliness and understanding of all the staff. I suddenly feel like our journey is not different and we are so included!”

– Freddie’s mum, Anna

Freddie was diagnosed with Galloway-Mowat Syndrome, a rare life-limiting disorder. Since starting at DVLCC, Freddie has begun to learn new skills and is making great progress.

Freddie, 2 years old

A young boy laying on the floor smiling.

“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.

“We cannot believe the difference in Lillyanna since she started at the Dame Vera Lynn Charity. We will be forever grateful for the help of this incredible charity.”

– Lillyanna’s mum, Rebecca

Lillyanna was 5 years old when her parents discovered DVLCC. She struggled with crawling, standing up and walking independently, in her short time with us she has made amazing progress.

Lillyanna, 6 years old

A young girl being supported by a physiotherapist.

Dame Vera Lynn Children’s Charity has made a huge difference to Max and to our family. I’m so grateful that this amazing charity has this centre and helps these families.

– Max’s mum, Holly

Max was diagnosed with Bainbridge-Ropers Syndrome, a rare genetic disorder causing global development delay. Since coming to DVLCC Max has learnt new skills to reach his full potential.

Max, 3 years old

A young boy in a blue jumper attending a conductive education session.

“All the consultants in the neonatal unit said repeatedly, ‘early intervention is key’ which is why we feel so strongly that all children like Jothi need access to support like we have with Dame Vera Lynn Children’s Charity.”

– Jothi’s Mum, Kate

Born by emergency c-section at 32 weeks, Jothi spent his first 24 hours on a ventilator and the first 93 days of his life in the neonatal intensive care unit. His personal growth since coming to DVLCC is remarkable.

Jothi, 4 years old

Jothi holding a microphone in a conductive education session.

“We’re so proud of the progress that Finlay has made since coming to Dame Vera Lynn Children’s Charity. It is life-changing for him to be able to communicate his needs with the family and it is amazing to hear him start to say our names.”

– Finlay’s mum, Faye

Finlay was diagnosed with rare genetic disorder, Hao Fountain Syndrome. Affecting 250 people in the world, the syndrome causes muscle weakness and developmental delay – especially impacting speech. Finlay has made amazing progress since starting at DVLCC.

Finlay, 4 years old

Finlay enjoying a stay and play session and Dame Vera Lynn Children's Charity.

We will forever be thankful to DVLCC, with their support, Albert has come on leaps and bounds. Now, our little boy runs around the park, which we never thought would happen. Without the help of the charity, he just wouldn’t be where he is now.

– Lisa, Albert’s mum

Born prematurely at 25 weeks, Albert had a tough start in life. After using all the services at DVLCC, Albert is about to start school!

Albert, 4 years old

A young boy with a fixed cleft palate playing with a xylophone.

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Your £10 monthly donation could help us to keep offering the hydrotherapy sessions with the children each week

Families playing with a parachute at Dame Vera Lynn Children's Charity's centre.

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What our parents say

Two young children laying on a carpet.

“Max has gone from strength to strength and that’s because Istvan pushes him and can see what he’s capable of.”

Holly, mum of Max

“To see Lillyanna standing independently brings tears of joy to us. We will be forever grateful for the help of this incredible charity.” 

Rebecca, mum of Lillyanna

“Since starting at the charity I have been blown away by the friendliness and understanding of all the staff. I suddenly feel like our journey is not different and we are so included!”

Anna, mum of Freddie

“As parents, we know that without the help, support and guidance that the charity has given us we would not be able to help Molly achieve the things she has.”

Sarah, mum of Molly

“We’re so proud of the progress that Finlay has made since coming to Dame Vera Lynn Children’s Charity. It is life-changing for him to be able to communicate his needs with the family and it is amazing to hear him start to say our names.”

Faye, mum of Finlay

“Coming here, I’ve seen so many changes in so many children. It’s changed our lives massively.”

Kayleigh, mum of Otis

“I don’t think there’s another service that compares. We feel so lucky to be able to access it. It’s just so nice to have another cheerleader.”

Debi, mum of Elsie

“Dame Vera Lynn Children’s Charity gave us a place to belong, unwavering support not only for Brooks but for us as parents trying to navigate all the complications that come along with having a child with additional needs.”

Aaron, mum of Brooks

Contact us

Want to know more? The team will be happy to help – get in touch today via email or phone.

[email protected]

[email protected]

01444 473274

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