Help Albie Access Life-Changing Treatment!

We are fundraising on behalf of our dear friends Georgina & Nathan and their beautiful little boy Albie, a brave 3-year-old who has faced more challenges in his short life than most of us ever will still holding the most contagious smile.

Albie lives with multiple, severe and complex medical conditions, including cerebral palsy, Lennox gastaut syndrome, West syndrome (infantile spasms), severe microcephaly, and severe hypoxic ischaemic encephalopathy (HIE). He experiences four different types of seizures:

• Vacant episodes

• Epileptic spasms

• Focal seizures

• Tonic seizures

Recently, Albie’s condition has worsened significantly, with seizures lasting anywhere from 48 minutes to over an hour, leaving him extremely unwell and vulnerable.

Albie is also registered blind due to severe visual impairment, has dystonia and spasticity, and requires a PEG feeding tube as he has an unsafe swallow. Every day is a battle, not only for Albie, but for Georgina & Nathan, who fight tirelessly to give their son the best possible care and comfort. Albie is adored by his siblings and he’s taught us all so much as a family!

Despite everything, Albie continues to show incredible strength, and his family refuse to give up hope.

We are raising funds to help Albie access Cytotron treatment, which is not available within Europe. This treatment offers hope in improving Albie’s quality of life, reducing suffering, and supporting his comfort and wellbeing.

All funds raised will go towards treatment costs, travel, accommodation, and essential care associated with this journey.

Any donation, no matter how small, will make a meaningful difference. If you’re unable to donate, sharing this page would mean the world to Albie and his family.

Thank you for taking the time to read Albie’s story and for supporting this little warrior and his family!