Its official !!! So grateful for my global friends for arranging this annual celebration. Joining hands globally in our campaign to save lives through education. Raising awareness of this horrific disease that affects to many lives.
Tomorrow is a celebration of awareness ....wait for the news !!!!!!
Hi everyone in the UK we have been approached by a production company who works with ITV. They ask if we have any survivors or bereaved that would like to be a part of their next series 3..".This Time Next Year.".....I am sure most of you know that Devina McCall hosts the show and meets [...]
Another lovely family affected by necrotising fasciitis !!!! Jayde is striving to raise awareness of NF and raise funds for the maxillofacial team at the Leeds General Infirmary. PLEASE BE AWARE OF GRAPHIC IMAGES that may be upsetting.
I understand that a lot of people that contract necrotising fasciitis have difficulty adapting after their debridement. Many of you have been unable to continue with your existing employee and living with a disability you may need adjustments in the workplace. We hope this link helps to showcase employers that have these ethics and will [...]
Its all gogogo here at The Lee Spark NF Foundation. Really good idea's swimming round in our heads for 2017 and we have developed a new social media page for all those interested athletic peeps to join in. Keeping fit in our minds is a good start for our 2017 goals. We are starting a [...]
What a brilliant night !!!!...the costumes ...the fun ....the fantastic surprises (more to tell) ....everyone could tell a heart rendering story but achieved their spirit of Halloween. Proud to know these lovely lovely people xx
Well one day to go to our Halloween ..Monster Mash Charity Ball. Uniting survivors, bereaved, family & friends all with one thing in common....necrotising fasciitis. Bless them all.!!!