Hi Guys,
There are some good queries there and a great suggestion (Si asking his oncologist Jamie to attend again...we haven't seem him for a few years, and he's a great bloke!).
Rich, the are quite a few singletons there every year, and as Janet says, you'll be given the warmest of welcomes.
I have often told people that since my diagnosis in 2005, I have made more good, true friends than I did in all the years previously.
Meeting up every summer and winter since 2007 has formed strong bonds, and the mutual support is amazing.
We make lielong firends.
It's certainly not a clique, it's a family of us all in the same struggle and making the very best of it.
Ann will be providing badges with Forum IDs and your real first names.
We've done that from the start, because it makes it so much easier to mingle and chat to folks you may have known only online.
Graham and Mary, there is an ideal spot for your camper van. At the entrance to the venue ther is very large car park which always has loads of spaces, since our folks in the rooms have parking bays by our doors.
Barry (I'm not going to call you 'Old Barry'https://community.prostatecanceruk.org/editors/tiny_mce/plugins/emoticons/img/smiley-tongue-out.gif) has summed up the weekend well, and Janet has given a good picture of the 'laid back' friendliness of it all.
And I'm chuffed to hear there may be a fellow Geordie there too? That will make at least four of us now.
For the first five years, I was only one, and we had to have an interpreter to translate my welcome messages and announcements.
Finally, Chris and Shirley, I am glad you have that downstairs room 8.
It just far enough away from my room that Lynn, Kat and I won't hear your world renowned snoring throughout the night!https://community.prostatecanceruk.org/editors/tiny_mce/plugins/emoticons/img/smiley-tongue-out.gif
Really looking forward to seeing you all in 3 months time.
Stay well my friends,
george