Mowing of the Mullet
EVENT DETAILS - Mowing The Mullet will take place 5pm Friday 26 March 2021. RSVP below if you would like to attend.
https://www.eventbrite.com.au/e/mowing-of-the-mullet-tickets-142387812781
For those of you who don't know, our son Ezra was diagnosed at one month old with Cystic Fibrosis (CF) - a serious genetic disease that causes severe damage to the respiratory and digestive systems.
People with CF develop an abnormal amount of excessively thick and sticky mucus within the lungs, airways and the digestive system. This causes impairment of the digestive functions of the pancreas and traps bacteria in the lungs resulting in recurrent infections, leading to irreversible damage. From birth, a person with CF undergoes constant medical treatments, takes a large amount of medication and requires daily physiotherapy. There is currently no cure.
Our amazing and generous friend Troy has committed to cutting his mullet (over 700mm!!) off to raise awareness and funding for ACT Cystic Fibrosis.
ACT Cystic Fibrosis is there for our family and many others like ours by providing essential equipment, nutritional supplements, grants and significant peer support to local people with CF.
Keen to support Troy, any donation will help make an impact!
Much Love
Luke, Ness & Ezra
xo
https://www.eventbrite.com.au/e/mowing-of-the-mullet-tickets-142387812781
For those of you who don't know, our son Ezra was diagnosed at one month old with Cystic Fibrosis (CF) - a serious genetic disease that causes severe damage to the respiratory and digestive systems.
People with CF develop an abnormal amount of excessively thick and sticky mucus within the lungs, airways and the digestive system. This causes impairment of the digestive functions of the pancreas and traps bacteria in the lungs resulting in recurrent infections, leading to irreversible damage. From birth, a person with CF undergoes constant medical treatments, takes a large amount of medication and requires daily physiotherapy. There is currently no cure.
Our amazing and generous friend Troy has committed to cutting his mullet (over 700mm!!) off to raise awareness and funding for ACT Cystic Fibrosis.
ACT Cystic Fibrosis is there for our family and many others like ours by providing essential equipment, nutritional supplements, grants and significant peer support to local people with CF.
Keen to support Troy, any donation will help make an impact!
Much Love
Luke, Ness & Ezra
xo
Organizer
Luke Tulenew
Organizer
Reid, ACT
CYSTIC FIBROSIS ASSOCIATION ACT INC
Beneficiary