AVM Support UK believes that it is important to share our experiences.  Not only does it enable those affected to share many of the feelings they are finding difficult to talk about with loved ones but in addition it can have encouraging consequences on others who find themselves in a similar situation.

We welcome carers, family and friends to add their experiences; in fact anyone whose life has been affected when someone they love is diagnosed as having an AVM. This page is waiting for your story.

1	7 years later and I'm okay. - Natasha Hill  submitted on  Wed 18th Jan 2012
2	Two years wait over - Pauline Shorthouse  submitted on  Sat 3rd Dec 2011
3	This was unexpected.... - Jason Sankey  updated on Sat 5th Nov 2011
4	Sharing my experience and now AVM is gone - Mary  updated on Sun 9th Oct 2011
5	AVM on left wrist - Conor Shipsey  submitted on  Sat 8th Oct 2011
6	One fight over, another one begins... - Nichola  updated on Thu 22nd Sep 2011
7	AVM diagnosed at 25 and would love to talk - Lesley Evans  submitted on  Tue 13th Sep 2011
8	HHT/AVM - Christine Nicoletti  submitted on  Mon 1st Aug 2011
9	My Son Liam's AVM - Bente  submitted on  Sat 9th Jul 2011
10	Diagnosed with brain avm - Jacquie hilliard  submitted on  Sun 3rd Jul 2011
11	On the home straight! - Yvonne Revans  submitted on  Tue 28th Jun 2011
12	Home after my GKRS treatment - Louise Pearce  submitted on  Sat 25th Jun 2011
13	M daughter - Lisa Brrett  submitted on  Fri 24th Jun 2011
14	My Son - Samantha Drummond  submitted on  Thu 23rd Jun 2011
15	My experience - R Suissa  submitted on  Wed 22nd Jun 2011
16	Pregnancy after AVM diagnosis - Lindsay  submitted on  Wed 22nd Jun 2011
17	My Experience - Darren Moore  submitted on  Tue 21st Jun 2011
18	My 8yr old son's AVM experience - JAYNIE DAVISON  submitted on  Tue 21st Jun 2011
19	Hi - Ben Stericker  submitted on  Mon 20th Jun 2011
20	AVM out of the blue! - Gemma  submitted on  Tue 14th Jun 2011