After learning of our son, brother, husband, father, colleague and dear friend Peter Van Wyk's diagnoses with ALS (Amyotrophic Lateral Sclerosis), we decided to embark on a fund-raising campaign in support of Peter and his immediate family's fight against this debilitating disease.

ALS, also know as Lou Gehrig's Disease and Motor Neurone Disease (MND), is a progressive disease that affects the nerve cells responsible for controlling muscle movements like chewing, walking, breathing and talking. Although the mind is not affected, gradually all muscles controlling voluntary movement are affected. At present, there is no cure for ALS, and no effective treatment to halt, or reverse the progression of the disease.

According to a case study conducted by the Motor Neuron Disease Association, the average monthly cost of care is £16,500 per month, with cases known to be as high as £28,000 per month depending on the patients requirements. That's a staggering £198,000 per annum. The quantum of the care, medication and equipment is enormous ranging from Neuro powered wheel chairs, Wheel chair adapted vehicles, Breathing support, Recline and lift chairs, Electrical beds, Electrical Hoist and lifting belts, Augmented computerised communication devices, Non FDA approved compassionate medications and Palliative nursing care both day and night.

To support their fight against ALS, all funds raised will be used towards a pro-active treatment plan and long term living expenses.

Your donations, however big or small are greatly appreciated!

Thank you from all us!