This young boy here is Kaije, my son, he is 32 months old and although he may look happy and well, he suffers from a rare kidney disease, congenital nephrotic syndrome. At 4 weeks old he had his first kidney removed due to his kidney dying and now at 31 months has had his second kidney removed and placed on temporary haemo dialysis which filters out his blood, currently expecting an upcoming transplant in February, awaiting the long haul in the future with daily hospital visits and blood tests. Medical supplies, medication and daily living expenses are quite the daily battle when living away from home and was just hoping to ask your support, any questions, feel free to ask. Thankyou and please give generously.
Kaije was born with a rare kidney disease called congenital nephrotic syndrome which in short had been taking life from this small child, now 32 months on, with no kidneys left and expecting transplant some time in February, kaije and his family are in more need than ever.
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Gregory Archer
GA
Campaign Creator
Gregory Archer
Kings Meadows , TAS
Sun, 1 May 2016
Janet Jewson
$ 20
Best wishes Kaije. Go strong young one!
Wed, 2 Mar 2016
Kylie Coleman
$ 10
Sending my well wishes x
Wed, 2 Mar 2016
Judanne Simpson
$ 50
I hope all goes well. I know how difficult it is to be away from home with expenses at home ongoing, along with the new ones from being in Melb - although in my case it was Adelaide.
I hope he gets back here very soon.
Wed, 2 Mar 2016
Julie Wise
$ 50
Hope you are both feeling better soon. Xx
Tue, 23 Feb 2016
Bakers Delight Glenorchy
$ 30
Tue, 23 Feb 2016
Robyne Williams
$ 10
Tue, 23 Feb 2016
Michael Peters
$ 20
Good luck to this little fellas and his family, lets get behind them people. A little from many makes a big difference.
Sun, 7 Feb 2016
Bev Deane
$ 30
I hope all goes well ☺
Sun, 7 Feb 2016
Tammy Donohue
$ 20
Thinking of you all. Goodluck with the big op Kaije xx
Wed, 3 Feb 2016
Brad Homan
$ 25
I know it's not much but hopefully it helps in some way
Kaije was born with a rare kidney disease called congenital nephrotic syndrome which in short had been taking life from this small child, now 32 months on, with no kidneys left and expecting transplant some time in February, kaije and his family are in more need than ever.
Best wishes Kaije. Go strong young one!