Katie Jean Morris suffers from Recessive PHA type 1, an extremely rare salt wasting condition that means her body does not balance electrolytes. Severe salt loss, and dangerous potassium levels can cause her heart to stop suddenly. Even mild sweating can be life threatening. Since Katie was born in November 2010 she has spent 70%
Katie Jean Morris suffers from Recessive PHA type 1, an extremely rare salt wasting condition that means her body does not balance electrolytes. Severe salt loss, and dangerous potassium levels can cause her heart to stop suddenly. Even mild sweating can be life threatening. Since Katie was born in November 2010 she has spent 70% of her life in hospital. There is no cure and no research being undertaken to find a cure. Donations are needed to help with treatment and care for this brave but fragile little girl.
Link Digital will soon launch a site to support her appeal for donations. In the meantime, email us via info@linkdigital.com.au if you would like to make a pledge and be informed when donations can be made online.
Please also get in touch if you would like to help support Katie by participating in fundraising activities. Corporate sponsors are also welcome.
