Leaciesmum

Hi there Aggierose, it's heartbreaking when we realise there is something amiss with our dear little ones, and we want answers NOW. Unfortunately there is so much waiting involved with doctors appointments, testing, getting results, physio and OT and any aids and equipment they need. It's SO frustrating.

I'm not sure if you've googled CP, I know that's how I knew my girl had it even before she was diagnosed. But my daughter's CP is 'spastic', her muscles are very stiff, but there are other forms of cp, one of which is hypotonia, which is floppy muscles. But this alone by no means she has CP, there are many differing disorders that can have similar symptoms. Trembling could also be a symptom of cp, my daughter suffers 'clonus' this is where her legs will shake uncontrolably up and down in little jitters, the only way I can stop it is to reposition her. She gets this when she's laying on her change table or sitting in her car seat.

You haven't mentioned if you've been in contact with a paediatrician yet, for us the paed doctor did an extensive check up, took brain scans and did an MRI, did blood tests and then extensive metabolic testing because Leacie's MRI came back normal. I'm not sure what country you're in, but here in Australia we have a fantastic public hospital system and all Leacie's tests and treatment (operations and botox) have been free of charge. We are still trying to get a definate diagnosis, but unfortunately sometimes there never is one.

I wish you luck, I hope the wheels get in motion for you soon and you find some answers for your darling daughter's condition.