Can you ask your neuro what other places have meg? Are you looking for a second opinion?


I will do some searching. I am pretty sure that henry ford hospital has meg. Nyu has it in new york city. Massachusetts has one in braintree.

What is your hope for meg? It sounds like an amazing test, we have not had one though, just read about it.

Http://www.Med.Nyu.Edu/cec/pediatrics/pedi atrics.Html

i am not finding a lot searching for just the meg except info not really where they have. I will link some comprehensive epilepsy centers, you can look on those sites or contact them to see if they have meg.

Http://www.Columbiaepilepsy.Org/


http://www.Jeffersonhospital.Org/neurology /article4319.Html


http://www.Chp.Edu/


http://www.Childrenshospital.Org/clinicals ervices/site1549/mainpages1549p0.Html

http://www.Mayoclinic.Org/epilepsy/index.H tml


http://www.Henryfordhealth.Org/body.Cfm?Id =45102

Thank you very much for answers.

We need meg because it is very important to find exactly where seizures start.

We have had regular eeg, video eeg, mri, pet.

But, nobody knows why and where seizures start.

Thank you.

Andrey, I wish you well in trying to get answers. You have probably been told that for 70% of people with epilepsy, it is idiopathic and no known cause can be found? Sometimes they cannot nail down the focus either but I sure hope they can for your son.

Some other tests for you to look into are siscom (at mayo clinic) which is supposed to more precisely locate the foci, ictal spect, which is at many epilepsy centers, which can also show what is going on.

I hope that you can find a meg for your son and get him answers and control! So frustrating to try everything and not get the seizures to stop.

Hang in there....