Parley
If you’re a parent or a relative of a child with a long/short term medical condition then you can sometimes feel isolated - as if nobody else understands what you as a family are going through.
Parley was set up due to the birth of my daughter in July 2007 who was born with a rare form of Spina Bifida and tethered spinal cord.
It is an information website for parents and relatives that has been created to provide support to parents with a child who has a long/short term medical condition, who has to undergo surgery or children with impairments or disabilities. Parley’s aim is to provide a network of information and contacts to support you through these difficult times so that you don’t feel alone.
Parley has become a national registered charity overnight and has had a huge demand from parents across the UK for marketing and promotional items to publicise our now registered charity.
Our aim is to make Parley extremely well known and a very useful support tool for parents and need your help to spread the word.
“You are a true angel, rare conditions have such limited support for those going through it, making what little support you can find and latch onto so vital.
So as a mum who went through hell without the support of others who knew what it was like I thank you from the bottom of my heart for starting your wonderful support network”
“We think that you are absolutely amazing to put aside your anguish to help others. Your determination and courage are an inspiration and know that you will make Parley the huge success that you’ve always dreamed of.”
“You and you’re family are an inspiration to all those in need of support. Undoubtedly, www.TheBabyWebsite.com and its members will help you to further your cause and support to those families that are in need of it.”
On behalf of Parley many thanks for your support
Victoria Paine
Charity Founder
Victoria@parleyonline.
www.parleyonline.
www.justgiving.
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