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Support Freddie in His Fight Against MPS1

Meet Freddie, a bright and energetic young boy who recently received a life-changing diagnosis: Mucopolysaccharidosis type I (MPS1). This rare genetic disorder, also known as Hurler syndrome, affects approximately 1 in 100,000 babies and is caused by a deficiency of an enzyme called alpha-L-iduronidase. This enzyme is crucial for breaking down complex sugars in the body. Without it, these sugars accumulate in various tissues, leading to a host of health challenges.

Freddie's journey with MPS1 has been filled with both hope and challenges. Despite his diagnosis, he continues to light up every room with his infectious smile and boundless enthusiasm. Whether he's playing with his favourite toys or blabbering away sharing stories with us, Freddie's resilience and spirit are truly inspiring.

MPS1 is a progressive disease that can impact many parts of the body, including the heart, bones, joints, respiratory system, and central nervous system. Symptoms can range from mild to severe and often include developmental delays, difficulty breathing, vision and hearing loss, and joint stiffness. Early diagnosis and intervention are critical in managing the symptoms and improving quality of life.

To support Freddie and other children like him, I will be running the London Marathon on behalf of the MPS Society. This incredible charity is dedicated to supporting individuals and families affected by MPS and related lysosomal storage diseases, including:

- MPS II (Hunter syndrome)

- MPS III (Sanfilippo syndrome)

- MPS IV (Morquio syndrome)

- MPS VI (Maroteaux-Lamy syndrome)

- MPS VII (Sly syndrome)

- MPS IX

- Mucolipidosis II and III

The MPS Society provides vital support services, funds critical research, and advocates for better treatments and a cure for these devastating conditions. By raising funds for the MPS Society, we can help ensure that children like Freddie receive the medical care, therapies, and support they need.

Your support can make a tremendous difference in Freddie's life and the lives of many other children facing similar challenges. Donations will go directly to the MPS Society to help fund their essential work, including medical treatments, therapies, and research initiatives. Every donation, no matter how small, brings us one step closer to making a positive impact.

Let's come together to support Freddie and his family during this challenging time. Your generosity will not only help Freddie but also countless other children who are battling MPS and related diseases.

Thank you for your support!

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