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Hi everyone
many thanks for your welcomes and support.
Robster65 thank you also. I agree completely with what you say about Kurtis being influenced by my behaviour. It is for that reason that I never let him know how this affects me. He looks after his own care with a little help from me and has done so since just after diagnosis. We put a positive spin on anything that is happening and explain how it will benefit him in the long run.
 
Hi everyone
many thanks for your welcomes and support.
Robster65 thank you also. I agree completely with what you say about Kurtis being influenced by my behaviour. It is for that reason that I never let him know how this affects me. He looks after his own care with a little help from me and has done so since just after diagnosis. We put a positive spin on anything that is happening and explain how it will benefit him in the long run.

That sounds like a brilliant way of facing things.🙂

The potential consequences of every decision made can feel overwhelming at times. I'm sure he'll come through fine and will be chilled out by it all in a few years time.🙂

Rob
 
Hi firewalker 🙂

I'm 23, diagnosed when I was 2.

I know of a family in Mansfield, the son is 13 and has had type 1 for several years. He is really proactive with raising funds for JDRF and raising awareness of type 1 - he might be a good person for your son to get in touch with.

They organise a Walk to Cure in Nottingham which is taking place on Oct 2 this year, if you look at the bottom of this page you can see the details:

http://www.jdrf.org.uk/walk/landing...tionTitle=Volunteer+organised+Walks#Mansfield
 
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