Our January post is an update on a previous story – written by Tristan’s dad Adrian. Looking back over the last four years it’s been one hell of a ride. There have been some highs but also some lows that have had me on my knees in tears wondering how I’m gonna have the strength […]
News
Join us for Infantile Spasms Awareness Week 1st-7th December 2021
Please join us to raise awareness during the week 1st-7th December 2021 – we will be sharing regular updates on our social media. Together we can STOP infantile spasms. […]
Our December warrior Willow – beating the odds
Willow was born on Wednesday 27th January 2021 via forceps delivery after a lengthy induction. There were no complications once she was born, just pure love and joy of our beautiful baby girl entering the world. We went home the next day and started our new lives together. Around 5-6 weeks old we noticed Willow […]
Our November warrior Abby – food as medicine.
Abby was born 6 weeks early, in July 2019, and had a rough start to life. When she was 1 day old she had seizures and we were told to prepare for the worst. I’m not sure I’ll ever get over the shock of giving birth early and the trauma of those first weeks. But […]
Our September warrior Eliza – planning for the start of school after an IS diagnosis.
Eliza’s seizures started when she was 5 months old. I kept video recordings on my phone and showed them to our local GP , we were initially told it was ‘typical baby behaviour’ until I pushed my concerns that it could be Infantile Spasms. That evening we got a call and told to go through […]
Our August warrior – Tia
Our August warrior is Tia, whose story has been written by her mum Chloe Tia started displaying “strange” movements around October 2019 when she was 3 months old. We took her up to the local A&E where they said it was reflux. I knew something wasn’t quite right and kept taking her back numerous […]
July warrior – lovely Lola.
Our UKIST warrior for July is Lola, her story is told by her mum, Lisa. On 8th May 2020 we were joining in our our street party for VE day and Lola at 7 months old was not settling to sleep, which was unusual as she loved her sleep. We noticed as she was finally […]
UKIST AGM 2021
Our fifth UKIST AGM was held on Sunday 25th April 2021, via Zoom. The Trustees are delighted to report that the charity continues to grow – providing much needed support and guidance to families affected by infantile spasms. We’re also making huge strides towards increasing awareness among primary healthcare communities, and we continue to fund […]
UKIST member’s new website recommends books for children with visual impairment
UKIST would like to congratulate support group member Catherine Keeling who has set up a new book review website for children with corticovisual impairments (but likely relevant to all children with a VI). www.cvibooks.org ‘When my son was newly diagnosed with his CVI, I did lots of Google searching to try and find suitable books […]
June warrior – Madeline – diagnosed in a pandemic
My little girl Madeline was diagnosed with IS at seven months old. I had noticed some strange movements one Thursday evening during dinner. At first I thought she just didn’t enjoy my cooking! But when they happened again over the weekend I was concerned and went to A&E first thing Sunday morning after ringing 111. […]
