Lola Hope was born on the 2nd November 2018. Sadly she was born very poorly and was diagnosed with Edward’s Syndrome. Her Mum and Dad (Becca and Chris) wanted to not only share their story, so that more people are aware of Edward’s Syndrome but so that family and friends can celebrate the happiness and love that having Lola has given them.

Very sadly little Lola went to fly with the angels at 5 months old. Lola was a true miracle and a fighter just like her parents who are still continuing to raise money and raise awareness. All that know the family and met Lola know that the world has become a better place having had Lola in it 💔💕

For those who aren’t aware, Edward’s Syndrome (also known as Trisomy 18) is a rare but serious genetic condition that causes a wide range of severe medical problems. Sadly most babies die before birth and of those who survive birth 20-30% die within one month.

The family are asking for your support to not only raise awareness of Edward’s Syndrome but to donate as generously as you can to give something back to the nurses and doctors who helped them to take Lola home and so that other parents can be given the same amazing support from the NNU that they have received.

Donations can be made via the Just Giving page (HTTPS://WWW.JUSTGIVING.COM/CROWDFUNDING/HOPE-FOR-LOLA ) or by attending the Charity Football match and Family day (£5 entry fee on the gate or whatever you would like to donate), where there will be an auction of signed merchandise and a raffle with amazing donations.

L.O.L.A – Lola, Our Little Angel