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dd has to see a neurologist.

2 replies

brokebuthappy · 13/06/2007 14:32

I'm new to mn so i don't know if anybody has any experiance with epilepsy,but thought i would ask.My dd has got to go to birmingham children's hospital to see a neurologist.There is a chance she has been having fits and gp wants her checked.My fil has epilepsy,but hasn't had i fit for afew years.Also his brother has it to but he has no contact with him so unsure how bad he suffers.Anybody know what i should prepare my dd for when we go to hospital.I should add we have to wait for a appointment,so i'm taking that has a good sign.

I have posted on heath too,but thought somebody might have some advice on here.

OP posts:
mm22bys · 13/06/2007 17:26

Hi,

my DS saw a neurologist, attached to the Royal London in London.

He was lovely, and I felt like I could talk to him and trust him.

My DS's background - he wasn't responding to visual stimuli and was not smiling, so my GP referred him to a neurologist who referred him to an opthalmologist.

At the initial appt with the neurologist, he did a basic physical exam to test his reflexes and muscle tone. At the time we were told he didn't have an underlying neurological condition, but he was referred for an MRI.

For that, because he was so young (six months), he was anaesthetised with gas, but he was done within an hour and a half of having the anaesthetic, and apart from being a little sleepy for the rest of the day you wouldn't have known that anything had happened to him.

He went back to the neurologist two weeks later for the results of the MRI, and also another physical exam to check his eye movements and muscle tone (head control, etc).

He is going to be followed up again in six months.

It sounds like your DD's case is different to my DS's but I found it really reassuring dealing with the neurologist.

All the best,

mm22bys · 13/06/2007 17:30

BBH,

I have just seen your messages on Health. I misread your first message and thought you were a "new mum", not new to MN!

Your dd is a lot older than my DS, so sorry for the irrelevance of my DS's experiences.

The neurologist was still very good though, hope the one you see is just as good (if not better!)

All the best,

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