Local Reviews
In February 2014, Carole T said about Annabelle's Challenge
Living with eds in the family is so very hard, every day a gift because everyday takes so much out of our bodies, and yet Annabelle's challenge finds the strength and time to not only raise awareness but to raise funds for the eds charity, there kindness and strength helps show all eds'ers great things can be achieved.
Source: thebestof.co.uk
In February 2014, Jennifer P said about Little Holcombe and Tower View Nursery
The staff at Tower View Nursery are exceptional. The care that our daughter gets there is above and beyond what is the norm. She has come along way with her speach since she's been there and the staff have been so great in all things educational also. We feel lucky our daughter goes there.
Source: thebestof.co.uk
In February 2014, Peter E said about People Matters HR
Niel offers a real personal service and goes out of his way to help giving me employment law or practical management advice. He gives 100%. People Matters have had to support me through disciplinary, appeals, grievances and redundancies as well as the more positive side of managing people. Niel understands our issues and has always been there on the phone and in person to take away the anxiety, by sharing his knowledge and calming us down in a crisis!
Source: thebestof.co.uk
In February 2014, Kathleen C said about PAW Plumbing and Heating Services
I recently asked Paul for help with a leak which was located from the bathroom. Paul investigated this and rectified the situation also re tiled the back kitchen wall as this had been saturated with water. Many thanks for you help Paul.
Source: thebestof.co.uk
In February 2014, Leanne B said about Annabelle's Challenge
Within weeks of my daughter's and my diagnosis of vascular ehlers danlos (the same condition as sweet Annabelle) I stumbled on their website. Through their website they provided advice, support and friendship through a very difficult time in our life. I thank the Griffin family for their understanding, kindness and passion to help others when already dealing with so much with their beautiful little princess. This site is an invaluable source of information for a condition that is so rare that even most doctors don't know about it. Keep up thr amazing work!!
Source: thebestof.co.uk
In February 2014, Elizabeth W said about Annabelle's Challenge
Within barely weeks of AJ's diagnosis, the Griffin's focused on turning their trauma into triumph...raising over £14k in just 12 months and in the process making this life-threatening condition visible, not only to the public but medical professionals who had never seen a case before. Annabelle's Challenge has grown to become an authoritative source of knowledge for sufferers all over the world, not only a source of support, but a source of happiness and joy as the Griffin's show that against all odds, life goes on.
Source: thebestof.co.uk
In February 2014, Cathy B said about Annabelle's Challenge
I thnk most people will do anything for their children and Annabelle's Challenge proves that. What sets them apart from the rest is how much they are prepared to give to the hundreds of other families all suffering with this same or similar conditions. I came across AJ and her family just as my daughter was diagnosed with EDS Hypermobility Type and it was an inspiration to read their posts on Facebook and see what they are doing. Faced with the awful truth of having a child with a life limiting illness has got to be every parents nightmare but they approach it with positivity, determination and courage. They have done so much for raising awareness of the condition and any recognition they receive is not only well deserved for them, but also serves to bring EDS in to the spotlight.
Source: thebestof.co.uk
In February 2014, Emily L said about Annabelle's Challenge
Wonderful people doing a wonderful job. Nothing phases this family. They have so much determination.
Source: thebestof.co.uk
In February 2014, Alicja W said about Annabelle's Challenge
AJ and her perents are like angels holding my hand in the darkness.Because of them we feel safe through the of my sons Ehlers Danlos Syndrome. Alicja and Michal
Source: thebestof.co.uk
In February 2014, Em C said about Annabelle's Challenge
Fantastic information About EDS and a great way of raising awareness. Especially for me as since hearing about it via annabelle's challenge im being tested after 21 years undiagnosed
Source: thebestof.co.uk