ALONE WE ARE RARE - TOGETHER WE ARE STRONG !

There are no WMS Medical Experts anywhere in the world - we are the 'Experts' ... 100 Families around the world - sharing decades of experience and pride in our 'Smilers'.

We are here to help and can't wait to hear from you !

We have no affiliations ... PLEASE beware funding requests or claims for a 'WMS cure' ... sharing inaccurate information undermines years of work to improve the diagnosis process for new Families !

Best wishes, Tymandra (Poppy's Mum)
Dr Tymandra Blewett-Silcock
UK