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Thanks for your message and the advice. Sorry to hear that

you are also going through this.

I have not looked into VNS for - the diet was working

brilliantly for him up until this catabolic thing kicked in, so I am

going all out to try and get him sorted through the diet again - just

going to take a bit more tweaking I feel. Instead of the diazepam I

have tried clobazam but that does nothing at all - so those have been

binned.

I am not familiar with the other medication you mention in your other

message - or maybe I am and I just know it by a different name!!! I

try to avoid as many medications as I can with - went through

a lot of them pre-diet days - not good. Normally the valium works

well for emergency use - but that particular night it took 2 lots to

stop the seizures instead of 1. Thankfully only needed 1 the

following night and hasn't had any since then (I've now probably

tempted fate and will have to give it to him tonight now - I am

getting really nervous of posting ANYTHING remotely positive!) Can

you tell me some more about this medication - I am presuming it is

another emergency med? Is it the valium that is placed under the

tongue instead of rectally?

Take Care.

Emma. Mum to .

> Emma, Mathew sounds like Stella with his seizure patterns, this

last weekend

> I was away at an Epilepsy camp w/ my older daughter and of course

Stella had

> a bad weekend.

> With Stella the fasting helps along w/ the diazepam, I hate giving

it to her

> though, we'll wait out 10-20 seizures before giving it to her, she

clusters

> too, and has both the atonic and the TC's. I'll occasionally give

her a tsp

> of OJ and see if that brings her around, her ketones have never

measured

> that high thru the blood tests at the labs but her urine/breath

always says

> high, the OJ actually helps a little, I think some kids benefit from

> slightly lower ketones. The not wanting to eat also rings a bell,

is he too

> acidotic? I've been playing around w/ giving stella different

carbs that

> are more alkaline to see if it makes a difference, (nothing too

concrete yet

> though). Also, watch out for sodium levels, stella's were really

high and

> i'm not sure why because we don't use salt, maybe the cheese? but I

know

> that can cause seizures. Remember giving the benzo's lowers his

gaba

> threshold so it's a catch 22 on that one.

> We are meeting w/ a neuro surgeon today to talk about VNS, do you

have that

> over in the UK? That is our last option w/ stella, so i'm crossing

all

> toes/fingers we have some success w/ it. She is due to start school

> (kindergarden) next wednesday and i'm a little scared of that.

> I hope things pick up for you,

> amanda

> --

> http://www.epilepsyfoundation.org/ecommunities/heroes/index.cfm?

user_id=143

> >

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