#worldTSCconference - Day 3 update by Clare Kassa

So another packed day of conference. We have been totally immersed in TSC for the last few days, I haven't left the hotel since I arrived on Tuesday. 

Networks are definitely being forged, friendships made and access to the big picture of TSC around the world firmly implanted.
So after a breakfast of biscuits and gravy (not the Bisto variety, something entirely different!) the day today began with Shelly Meitzler's story about being parent to two children with TSC. She held the audience in the palm of her hand, and there wasn't a dry eye in the house as she recounted the dreaded blue lighted trip to the ER. She paid tribute to all of the parents who have gone before and have paved the way for parents today to have access to more information and better treatments.

Then we were expertly informed about where we are up to with the use of cannabanoids in treatment of epilepsy. In the UK there have been a number of news stories and pressure on government to allow the use of cannabanoids and I see whilst I have been away there has been an announcement on this front.  People with TSC need a range of treatment options that much is clear, but early intervention is key and has a major impact on the outcomes for people with epilepsy. 

I have been to a number of sessions today on TAND - the psychological and psychiatric impacts of TSC. I was lucky enough to hear Petrus de Vries speak with such humour, candour and humility. He recounted that less than 20% of people with TSC receive any assessment or intervention for psycho-social difficulties. From the parents I have talked to these are some of the biggest challenges in day to day life with TSC. Petrus said "Families and Mums are always right." A good reminder that the expertise lies with parents and carers and something professionals should heed and act upon.

I have also had the pleasure of sharing this experience with two marvellous TSC parents, AnneMarie Cotton and Carole Hagan. Here are are a couple of their thoughts on the past few days.

"What has stood out for me are the  Mums and Dads speaking to the conference. And hearing amazing professionals talking about great advances in early treatment and progress towards a cure," said AnneMarie Cotton.

"What a privilege to have been at this International TSC conference in Dallas and see the big picture. So much excellent and collaborative research happening across the globe to advance therapies to alleviate the clinical manifestations of TSC1 and 2" said Carole Hagan.

So it's last night dinner tonight and everyone has to dress in blue (the colour of TS Alliance In the US). I am hoping for a bit of blues music too, we are in the south after all!

Last thoughts tomorrow before flying back home.