I am epeleptic as is DS24 and DD15. The advice you have been given is all good. I will ad though that she should not let herself get dehydrated while in the parks or to tired. This will lower the siezure threshold. So she should plan some downtime and not do the parks commando. We take a small luggage tag an attach it to our kids belt loops. DS still uses it. On it we put his name, age, height, weight, disorder, meds and dosages, and the time he takes it. In the event of a grandmal siezure the person may be extremley disoriented and not be able to tell a paramedic what they need to know. A medical alert braclet is fine but it also will not give the pertinent infor. Also the people she is traveling with should know where this is so that in the event of a seizure they can alert the paramedic or whoever is attending. They should also be told to watch for severe tiredness or stress to remind her to take a break. When I was a teen we were advised to not tell anyone, not school officals, teachers no one. Fortunatly I was savy enough to alert a group of my friends so when I was with them they would know to look for warning signs. With my kids we know enough to make others aware. You can have a very normal life living with epilepsy if you pay attention and follow your doctors directions. It has never slowed us down. It may take a little longer to get a drivers license and I cannot give blood, it is one of my triggers. If I can help with anymore advice feel free to pm me.
A friend of my DHs decided that he might not need his medication any more and wanted to see what would happen if he stopped it.With teenagers those around them need to know the warning singns and be aware. They are very capable of deciding on their own that they just do not want to take meds any more. Of my 3 kids 2 have siezures. The one that does not has a friend who decided to do this. He died six months later after having a siezure while standing at the end of a dock. He fell into the water and was not able to call for help. So please make sure that the others with her know what to do.
I know all the hospitals in my area and even the EMS people do look for and use the Medic Alert bracelets. They may not have time to call right away (which may be why the first responders and head of the EMT program told you not to bother with it - when those people are seeing the patient, they don’t need or use anything more than the very basic which you can get from a generic one).I really like the luggage tag idea! I think I'm going to use it when I go in March. I'll attach it to my purse.
I am one who thought of going with MedicAlert, but then I talked to first responders around me and know the head of an EMT program and was told by them not to bother getting one because most of the time they don't have time to call the phone number. They told me to get just a generic medical bracelet with the basics on it and then put see wallet or something like that on it with a card in my purse with all my meds and info. Even in the ER, they don't always have time to call the # or the staff to do it. It could be just a regional thing though.
hiya , i am also epileptic have ben since the age of 4 , i went to florida for the first time in 09 it was my first time with a diffrent time zone like that but all i did was switch to local time and i was fine took it easy for a few days , but its the best thing i ever did and am doing again this sep lol yeah i gt the disney bug now lol , and as for teen with epilepsy i can gt that to they do go through the stage of trying to fit it without epilepsy its hard enough but with it its even harder i went through it also , but they all get there just takes time its a lot to ajust to even if u have had it all your life . xx tinkfan72![]()