Penny Biggs
Hi Iām Penny ~ Married to James
We live in a village called Pyrford in Surrey near Woking, we are the Parents of twins ( boy / girl so non identical) Jack & Olivia who are 14 years. Jack who has 22q & was diagnosed with 22q ( 22q 11.2 deletion/ di George syndrome / vcfs ) at age 9 months old, we were given a Max Appeal card then by Muruel Mcentarget his Geneticist.
We then found that we were not alone & we had an extended family our 22q family.
I feel passionate about empowering, informing, encouraging & helping 22q families and children & young people be the best they can be. To fulfill their potential & see their light & parents be informed so they can be armed & confident to help their 22q superstars like everyone at Max Appeal.
I have always been eager to be as informed as possible & part of the 22q family & events to help Jack as much as we could. Our first Max Appeal meet up was in the lake district camping weekend when our 2 were babies . The first conference I attended was in London led by Max Appeal where I learnt so much & international conference in Birmingham , the 22q Ireland Dublin conference as part of our holiday & we have always loved over the years the 22q at the zoo days.
Jack has had a lot of hospital stays & surgeries since tiny at GOSH like so many families which has helped Jack be the amazing superstar he is today.
I am thrilled to now be on the Amazing Max Appeal team & so thankful to Julie & Paul in all they do for us all connecting to the wider 22q family & campaigning.
I was honoured to be part of the Max Appeal campaign for the 22q consensus at Parliament a few years ago.
This last year since covid even though apart we have become even more connected helping each other through via various fun zoom sessions . Baking. Quiz nights . Mens virtual pub. Ladies night . Afternoon tea and evening drop ins to help with any concerns.
I am excited to help our children, young people & families to connect & feel empowered as part of the Max Appeal team