WWW.ALEX-CONNERTY.CO.UK

Alex's PD Friends

     
 
  Alex Connerty

Here you will find Alex's British friends with similar forms of Primordial Dwarfism.

For us as parents it's wonderful to know that there are families here in the uk that share our conerns and also have children that Alex can relate to as he gets older and understands what is he is.

Click on the pictures to view larger pictures.

John & Sue - Alex's Dad & Mum
 
 

Finn & Alex

This little princess is called Finn, she was born on the 4th February 2005, weighing 2lb 4oz. She is now 2ft 1in (62cm) and weighs 13lb 7oz's. She lives in Wrexham with her Mum and Dad (Mel and Jon). When we first met Finn, we were immediately bowled over by her size, beauty and personality. When you first meet Finn you realise what Primordial Dwarfism is all about!
Alex & Tyler

This little man is called Tyler. He lives in Calargy, Canada with his Mum and Dad (Nicki and Marv). He was born in Oxford, England on the 05/06/03and weighed 1lb 4.1/2oz. Tyler is like no typical 4 year old, he is awesome with superhuman strength and energy, Mike and Jess still bear the mental scars of racing him (he beat them everytime).
Alex & Rayth
This little cheeky chappie is called Rayth. He was born on the 11th April 2005 (same as Alex) weighing 3lb 8oz. He is 2ft 6in and now weighs 19lb 6 oz. He lives in Shildon near Durham with his Mum and Dad (Alison and Steve) along with his brothers and sister. Rayth is so so full of life and you'll need to ensure that your batteries are fully charged to keep up with him. His Cheeky Smile melts your heart!
Liam & Alex
This little fella is called Liam. He lives in Nottingham with his parents  (Joanne and Robbie) and his brother (Martin). When we first met liam, we realised this was just one boy who lives life to the full and enjoys it!.
   

Internal Links

Latest News

UK Charity set up (Walking With Giants Foundation) to help individuals in the UK with MOPD II.

Click here to visit their web site.

Short film created to help new UK Charitable Foundation raise awareness about MOPD Type II.

Click here to watch film.

American Charity (Potentials Foundation - A Cause for Chloe) set up to help individuals in the USA with MOPD II.

Please click here to visit their web site.

The work they have done over the last 12 months to help families with MOPD II, along with the support of the people of Merseyside has been instrumental, inspirational and encouraged Sue and myself in setting up a similar charity for individuals affected by MOPDII here in the UK.