Story
In February, my family are going to be walking through the Peak District to raise money for the Aplastic Anaemia Trust and celebrate Rare Diseases Day.
In August 2022, my mum, Gail, was admitted to hospital. Tests later identified that she has a rare blood condition called Severe Aplastic Anaemia. Severe Aplastic Anaemia is a condition where a person's bone marrow completely fails and their body is no longer able to make blood and platelets.
Following her diagnosis my mum has received a course of advanced ATG treatment and continues to be closely monitored by her consultant. The care and treatment she has received from all of the doctors and nurses at Manchester Royal Infirmary has been fantastic. My family and myself are so grateful for the NHS and the care she has received.
When we see our loved ones sick, it can feel overwhelming to think we are unable to help. This walk is our way of supporting not only our loved one but also all those who suffer from such life-changing diseases. The more we support charities like the Aplastic Anaemia Trust, the closer we get to understanding and treating rare diseases.
The Aplastic Anaemia Trust is a fantastic, small charity which relies on public donations. Not only do they aim to raise awareness and fund research but they also provide support to families during times of great need.
https://www.theaat.org.uk/event/peak-district-walk-2026
Thank you so much for your donations.
