Calling all professional Boxers get behind a great cause
I have been contacted today by a friend who has asked me to use my influence in the Birmingham & Black Country boxing scene to ask for help form the professional boxing community. There is a charity event being held on Saturday 16th November at the Crosswells Inn Whyley walk Oldbury to raise money for research into the disease. I have been asked to ask any Midland professional boxers who could help by attending the event as a guest or maybe donate some memorabilia for the charity to raffle or auction off. I have been informed already that the new English Light è champ Shaken Pitters will be making appearance at the event. This is a very worthy cause to get behind and anything the pro boxing community could do would be fantastic. If you would like to help, contact the column and I will put you in touch the appropriate people. Below is Daisy’s story and also a link for more information, to anyone who does get involved I would like to thank in advance. Daisy was born to myself Toni & father Adam on the 4th June 2019 at 40+6 weeks after an uneventful pregnancy by a forcep delivery. Daisy Initially appeared to be a healthy baby passing all her newborn screenings and was able to go home once I was discharged. The next morning I raised my concerns to the doctors as Daisy appeared very sleepy, was feeding poorly and didn’t cry! Later on that day Daisy was transferred to Neonatal intensive care unit. It was here where our nightmare began. Over the next few days Daisy deteriorated was feeding poorly and having difficulties breathing on her own. After trying different breathing aids it was decided Daisy needed to be ventilated. She was moved to the most intensive care room, she was ventilated for almost 3 days. On Day 9 (diagnosis day) Daisy was doing much better she was now completely breathing on her own we thought she was getting better, little did we know the next conversation with the doctors was about to change our life’s forever. Daisy was diagnosed with a rare metabolic condition Non ketotic Hyperglycinemia (NKH for short) NKH affects 1 child in every 76,000 born there are approximately 50 kids in the UK and 500 worldwide living with this condition. Sadly the mortality rate for children born with NKH is high and many die before they make it out of toddlerhood. Those that survive are often extremely disabled with uncontrollable seizures. There is no cure, however there is research underway looking at gene replacement therapy, which may in the future hopefully save our babies life and prevent any parents in the future having to go through the nightmare and the heartache we have. Any donations will directly go to helping researchers find a cure to this awful disease!