Vikki Marsden

10K Steps a day with Alfie!

Fundraising for CDKL5 UK
£1,325
raised of £500 target
10K Steps a day with Alfie
CDKL5 UK

Verified by JustGiving

RCN 1207922
We are fighting to give our kids a chance to live long, happy and healthy lives

Story

Thanks for taking the time to visit my JustGiving page.

I have decided that I want to fundraise for CDKL5 by walking 10,000 steps a day all the way up until Alfies 1st birthday on 12th December! That way on his 1st Birthday we can hopefully donate this money as a little first birthday donation for him! Anyone is free to join us in doing so if you fancy it! Ha!

The reason I'm wanting to fundraise is because Alfie was recently diagnosed with CDKL5. We've always known he was behind developmentally but we didn't know how much of a shock we were in for.

He started with seizures September 2024 at 9 months old. He was diagnosed with Infantile epilepsy with Infantile Spasms at this point. They did a genetic blood test and unfortunately 2 weeks later it came back that he had a rare genetic disorder called CDKL5. We definitely didn't expect this as it usually affects 1 in 60,000 births and nearly always girls. They also say it affects boys more severely also unfortunately.

Everyone who loves Alfie was obviously devastated. Its a devastating diagnosis for us all and poor Alfie who will have to live every day fighting to do things most other kids find easy and he will have to take multiple medicines every day to try keep medicine resistant seizures at bay.

I basically just want to do everything I can to help support CDKL5 and finding a cure for my little Alfie and others. I don't want to just sit round expecting others to.

CDKL5 deficiency disorder is a rare developmental epileptic encephalopathy caused by mutations in the CDKL5 gene, and this can manifest in a broad range of clinical symptoms and severity. The hallmarks are early-onset, intractable epilepsy and neurodevelopmental delay impacting cognitive, motor, speech, and visual function. Although rare, the occurrence is believed to be ~1:40,000 -60,000 live births, making it one of the most common forms of genetic epilepsy.

The CDKL5 gene provides instructions for making proteins that are essential for normal brain and neuron development. The CDKL5 protein acts as a kinase, which is an enzyme that changes the activity of other proteins by adding oxygen and phosphate atoms (a phosphate group) at specific positions. Researchers have not yet determined which proteins are targeted by the CDKL5 protein.

CDKL5 was first identified in 2004, it stands for cyclin-dependent kinase-like 5, and its location is on the X chromosome. The X chromosome is one of the sex chromosomes; females have two X’s, and males have one X and one Y chromosome. The letters are an abbreviation of the scientific name of the gene, which describes what it does. The CDKL5 gene was previously called STK9. Many cases have been identified in boys, but because of the location of the gene, CDD mainly affects girls.

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About the charity

CDKL5 UK

Verified by JustGiving

RCN 1207922
CDKL5 deficiency disorder is a rare condition which manifests in the first few months of life with rare and complex epilepsy. Children and adults with CDKL5 require life long support. CDKL5 UK aims to support families through direct support and patient advocacy. #Togetherwearestronger

Donation summary

Total raised
£1,324.64
+ £257.25 Gift Aid
Online donations
£1,324.64
Offline donations
£0.00

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