Lyra Can: help Lyra to walk & talk

Lyra Can: help Lyra to walk & talk Lyra is a happy, bright girl who Global Developmental Delay and other neurological problems. Some tr

My name is Lyra from Cannock and I’m 2 in February, and I love to laugh, roll like crazy on the floor and play with my big brother, Joseph. As I grew older, my Mummy and Daddy noticed I wasn’t doing things I should. We saw lots and lots of doctors who say I may have Cerebral Palsy, but I am still having tests. It means that I can’t walk or talk, and really struggle to sit on my own. I have to do l

ots of physio everyday – even if I don’t want to – I also have muscle spasms which means my little body can’t move and locks up. But I started to crawl in September, and now Mummy has put up special gates, but they smile and say they ‘love it’. Mummy and Daddy want to take me to have intensive Oxygen Therapy in Slovakia which helps children with neurological problems. It will be hard work because I will have to do about 5 hour’s physio a day and I’ll miss my Daddy and brother. I’ll also need to find someone to help me do my extra physio in between my sessions with the nice ladies at the hospital. Mummy and Daddy are planning lots of events and you can find them on my page ‘Lyra Can’… and my brother is even going to do a sponsored silence!?! He really wants me to shout his name and chase him, as much as I want to chase him too!

Address

Hednesford

Alerts

Be the first to know and let us send you an email when Lyra Can: help Lyra to walk & talk posts news and promotions. Your email address will not be used for any other purpose, and you can unsubscribe at any time.

Contact The Organisation

Send a message to Lyra Can: help Lyra to walk & talk:

Share

Our Story

My name is Lyra from Cannock and I’m 4, and I love to laugh, sing and play with my big brother, Joseph.

When I was little Mummy and Daddy noticed I wasn’t doing things I should. We’ve seen lots of doctors who say I have Global Developmental Delay and other issues with how my brain works. I am still having lots of tests.

I had to work really hard to learn to walk and I still can’t say much more than ‘Mummy’ or ‘Daddy’. I have muscle spasms which mean my body can’t move and locks up and I struggle to chew my food. I do lots of physio to help me improve how I get around and I’m working hard to learn how to tell people what I want.

Mummy has taken me to Slovakia three times now for treatments which help children with neurological problems. I might have to go again! It’s hard work because I do about 5 hour’s physio a day and I miss my Daddy and Brother.