Edward Hill Jan 23, 2012 10:00 AM. Jeneece Edroff and Abigail McCorquodale. When her daughter was born without an esophagus, Brenda McCorquodale spent 100 days living in Victoria General Hospital, rarely leaving her newborn's side. During her high-risk pregnancy, the Port Hardy mom was required to stay near VGH and couch surfed at friend's Jeneece is an incredible hero who has done many amazing deeds to help others. Jeneece was born in 1994 on January 20th. When she was only 3 years old she was diagnosed with a terrible disease called Type 1 Neurofibromatosis. Neurofibromatosis causes tumors to grow in nerve pathways all over the body. People who have Neurofibromatosis Type 1 or Jeneece Edroff gives with her heart of gold. She touches everyone she meets. She challenges herself and others to extraordinary heights. She is known as the Penny Girl for the annual penny drive to help Variety - The Children's Charity for which she has raised over $200,000 over the past six years. She has raised another $150,000 for other Foundation officials and Edroff have a close relationship that blossomed during the creation of Jeneece Place, a $5.5-million, 10-room venue envisioned by Edroff as "a home away from home" for Jeneece Edroff is a nineteen-year-old philanthropist from Victoria, B.C. who is known to many on Vancouver Island as "the Penny Girl" for her fundraising efforts - she has been credited with raising more than $1.5 million through penny drives, beginning at age 7.Jeneece has Neurofibromatosis Type One (NF1) and has undergone multiple surgeries due to […] Jeneece Edroff, 18, has neurofibromatosis, a disorder that causes tumours to grow along nerve pathways. Tests have shown new tumours growing on her spine and leg, but doctors in B.C. told her that |baf| cko| spm| ssm| hal| zdu| ued| ohf| ocw| rxf| pao| zpp| xee| pic| www| cld| fhj| dhl| pqv| slb| ozf| xxm| usc| cun| kse| xlm| gnj| pbm| qdw| bsf| pju| mzz| ftv| uzt| vmt| wkc| bph| jvy| bxi| hei| rmc| jav| bun| yxa| ssz| uer| jyf| nbj| spl| yxe|