Sorry I'm really late to this but we went to a one day family event and it was great. How soon is it? The only reason I ask is that the amount of information at these things can be overwhelming, and there will likely be people from different areas who are all getting slightly different advice so whilst it can be extremely useful - and was for us - if you are very newly diagnosed it may throw a little more at you than you need right now. My experience of it was that you get more out of it once you have found your feet.
Also, don't underestimate the emotional impact - one of the kids at ours spoke about her experience of it all and I was in floods of tears. If you're grieving the diagnosis it can be tough.
Having said all that, we found it really useful. It can be a great way to meet other parents, share some experiences and the kids have a complete ball. I can't stress their value enough for making the kids feel 'normal' again.
Thank you! There are a few weekends over the coming year. I was thinking May but I might go for the September one now?!?
I'm glad you mentioned grief, that's exactly how I have been feeling. I'm picking up a bit now though x
I would definitely recommend this to every family the sooner after the diagnosis the better - we have been on one 12 weeks after my son was diagnosed it was fantastic we learned so much from all the professionals and so much more from the families & the kids - it was the first time my son aged 9 at the time had seen any other children injecting & using pumps & for me meeting & talking to other parents going through the same thing was exactly what I neededHi, I am thinking about booking on to the family weekend. My daughter was diagnosed last week. Has anyone been to one of these events? Did they find it beneficial?
Well done to you & your Son Caz ! 😉I would definitely recommend this to every family the sooner after the diagnosis the better - we have been on one 12 weeks after my son was diagnosed it was fantastic we learned so much from all the professionals and so much more from the families & the kids - it was the first time my son aged 9 at the time had seen any other children injecting & using pumps & for me meeting & talking to other parents going through the same thing was exactly what I needed
Please let us Know how it went Hnorcy !Thank you! There are a few weekends over the coming year. I was thinking May but I might go for the September one now?!?
I'm glad you mentioned grief, that's exactly how I have been feeling. I'm picking up a bit now though x
It was absolutely fantastic. The whole family got so much out of the event. The volunteers were amazing, the kids had a fab time and we even had a 'date night' while they were at a party. We all learnt so much and came away with new friends and lots of useful information. I strongly believe this event should be mandatory and free to all newly diagnosed children and their families. I hope to help at an event like this in the future.Please let us Know how it went Hnorcy !
That's really good to hear 🙂It was absolutely fantastic. The whole family got so much out of the event. The volunteers were amazing, the kids had a fab time and we even had a 'date night' while they were at a party. We all learnt so much and came away with new friends and lots of useful information. I strongly believe this event should be mandatory and free to all newly diagnosed children and their families. I hope to help at an event like this in the future.
I am really pleased you & your family enjoyed. You do learn off others & the pros. They take kids in one area & parents in another & both sets LEARN. Double well good !😎😉It was absolutely fantastic. The whole family got so much out of the event. The volunteers were amazing, the kids had a fab time and we even had a 'date night' while they were at a party. We all learnt so much and came away with new friends and lots of useful information. I strongly believe this event should be mandatory and free to all newly diagnosed children and their families. I hope to help at an event like this in the future.
They are good ! 😎It was absolutely fantastic. The whole family got so much out of the event. The volunteers were amazing, the kids had a fab time and we even had a 'date night' while they were at a party. We all learnt so much and came away with new friends and lots of useful information. I strongly believe this event should be mandatory and free to all newly diagnosed children and their families. I hope to help at an event like this in the future.
They are good !I would definitely recommend this to every family the sooner after the diagnosis the better - we have been on one 12 weeks after my son was diagnosed it was fantastic we learned so much from all the professionals and so much more from the families & the kids - it was the first time my son aged 9 at the time had seen any other children injecting & using pumps & for me meeting & talking to other parents going through the same thing was exactly what I needed
May be someone from Duk could elaborate ?Have a look at Parents section. Post about "Kids Events". I & others have volunteered on them. They are a great way of meeting others & you will learn a lot. Good luck Honrcy. Welcome