Help keep this bug running
Bay of Plenty
One in every 3,000 children is born with neurofibromatosis (NF), a genetic disorder that causes tumors to grow all over the body. We need to take action now so that no child or adult has to face the challenges of NF – learning disabilities, blindness, pain, deafness, cancer, disfigurement, bone defects and cardiovascular problems. There is no cure for NF, but as a parent of a child suffering from this disfiguring and painful disease and also a member of the Running Bug - NF Endurance Team (a fundraising support arm of the Ladybug Foundation) we are fighting to change that through raising awareness.
My daughter Mikayla was diagnosed with this disease when she was only 5 months. What was first diagnosed as a mosquito bite turned out to be a tumour on her back which has now latched onto her spine. She also has scoliosis of the spine (curvature of the spine) which has lead to her first operation this year. The pain she was in for the first 2 years of her life was horrendous. She is now on medication to help with the nerve pain and she is now able to get out of bed like any other normal 11 year old.
I am wanting to help find a cure for this disfiguring and painful disease so I am currently training for various NZ Half Marathons throughout 2018 and 2019. I need your help, your generosity and your support. A mascot has joined me this year which will be with me every event around NZ please help me keep her running - The Running Bug
The Ladybug Foundation, via the Running Bug Endurance Team, has set a goal of raising $5,000 and I am asking YOU to please make a contribution.
The Ladybug Foundation is a New Zealand non-profit organization dedicated to raising awareness for Neurofibromatosis and helping NF families in need.
Your donation will ensure continued funding these families and people struggling with the daily pain of NF.
When you donate to the Ladybug Foundation, you become part of a team driven to provide hope for the more than 3,000 people who suffer from NF in NZ including 11 year old Mikayla.
Thank you in advance for your generosity. If you have any questions, please contact me at ladybugfoundation@xtra.co.nz or 0275257303.
The Ladybug Foundation is a charity focussed on supporting families dealing with Neurofibromatosis.This Foundation is dedicated to making a real difference for not just the NF community but the wider community of NZ - awareness is the key to finding a cure
To keep our website up and running to help raise awareness and provide a place for our NF heroes to go to for resources
To help raise awareness for NF
To help fellow NF heroes through tough times ie hospital stays etc
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