Some of you may have already heard of Teagan Appleby's story or may have seen it in the news recently
Teagan suffers from a very severe case of epilepsy where she can seizure up to 300 times a day. In April 2019 she started using a medication that isnt yet available here in the UK and it has changed her life. Teagan has gone from having hundreds of seizures a day to just a handful. This isn't the only improvement. Teagan has re-learnt skills doctors never thought she would get back. Her quality of life has dramatically improved
But, the NHS will not prescribe this medication even though it is now legal here in the UK. It is costing Teagan's parents £2500 per month and it's a struggle every month to find this amount of money.
If you can help in anyway, we would be very grateful xx

Please see updates xxxx

I have no words....I don't know how to thank everyone. Thank you just doesn't seem enough!! I need to do an update as the story on here is a little out of date. Today marks 2 years that the law was changed and the medication Teagan is on became legal. Unfortunately we still have NOT got an NHS prescription so are continuing to pay privately through a private doctor and then an import company who arranges the collection and delivery process. This all comes at a costly price. I am going to set up a new page which is more up to date x THANK YOU x

⭐THIS IS AN ONGOING PROCESS AS FUNDRAISING COSTS NEED TO BE MET EACH MONTH ⭐