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Real members of MyEpilepsyTeam have posted questions and answers that support our community guidelines, and should not be taken as medical advice. Looking for the latest medically reviewed content by doctors and experts? Visit our resource section.

Top 10 Search Results for "大乐透12月17日 wn4 com 广发彩票平台 w6p4c8 2023年1月30日15时58分35秒 116611661"

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What Treatment For Epilepsy? I've Been On 6 Different Meds.
A MyEpilepsyTeam Member asked a question 💭

Every couple of years I have seizures then my Dr wants to try something new or ups the dosage. The meds I'm on now are making me dizzy and off balance

A MyEpilepsyTeam Member

I have been on too many meds to count. I was on phenobarbital, volume, Dilantin, Depakote, Topamax, and vimpat just to name a few. My son is on Trileptal, Keppra, Onfi, Depakote (two, 250 mg, and… read more

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How Long Have U Had Ur Disorder
A MyEpilepsyTeam Member asked a question 💭

if anyone is free to chat i am here

A MyEpilepsyTeam Member

I’ve had epilepsy since the age of 2. I’m now close to 50 yrs. Of age

How Long Did It Take For You All To Get Your License?
A MyEpilepsyTeam Member asked a question 💭

I’m a teenager and sometimes I feel like an outcast because I don’t have a license or a car. It just sucks asking for a ride all the time and they get mad at you. It’s just I’m struggling with this so much. I just want to feel like I have some control.

A MyEpilepsyTeam Member

18

Musicians... Is This Just Me? Or Is This You Too?
A MyEpilepsyTeam Member asked a question 💭

I was wondering... you folks who are lifelong musicians... has anyone's playing ability remained unaffected, or only marginally affected? Or has it spiraled downward into a steep decline? The holy grail of a performing musician is flawless execution, has your execution been affected? How severely? Tremors? Loss of muscle memory? Loss of fine motor control or dexterity? Inability to multi-task, like sight reading while you play? Did you lose your "aim" working your instrument? Have 16th notes… read more

A MyEpilepsyTeam Member

I do not have the VNS but my son does. He is now 35 years old and he got it when he was 18. His voice cracks every 5 minutes and if he is in the middle of a sentence he has to wait for it to stop… read more

Does Anyone Use The Watches That Help Detect Seizures? Are There Certain Things You Need To Take It Off To Do So It Doesn't Set Off.
A MyEpilepsyTeam Member asked a question 💭

Will it set off with excessive motion.

A MyEpilepsyTeam Member

I have heard of this but I am afraid to shell out the money only ro have it not work. I'm waiting for it to be out a little longer so I can hear how well it works. If it works well, I would be more… read more

Any Asvice With Time Difference And Travel
A MyEpilepsyTeam Member asked a question 💭

Im going on a trip soon thats a 17 hr time difference ahead of where i normally live. Ive gone through 2 hr time differences at most. Has anybody gone on far distanced trips? How did that go with the seizures? Was it harder goinng to your travel destinatiom or bacck home after? Any advice to hopefully help make if slightly easier with managing the seizures?

A MyEpilepsyTeam Member

I have travelled to Europe from NY, that’s a 6 hour difference; 17 hours is a whole other story.

The advice I would give is to adjust your meds according to your usual time intervals, and not just… read more

Vns Therapy
A MyEpilepsyTeam Member asked a question 💭

i want to know as much as possiable about it they r talking about doin this on my daughter

A MyEpilepsyTeam Member

I have a VNS also, I am not very organized so I don’t know where my 🧲 magnets have gone. The battery 🪫 in my VNS is dead 💀 right now. My neurologist recently told me there is a new and improved one… read more

Finding Friends
A MyEpilepsyTeam Member asked a question 💭

Someone on here mentioned wanting to locate old friends.
Have you tried Facebook or other social media sites?
My high school class has established such a site.
Through Facebook I was able to reestablish contact with the "boy" who used to live down the street
from me. I also re-met a cousin I hadn't seen since we were both 6 years old.
Give it a try. It's nice to contact old friends. (In my case really old LOL)
The best of luck to you. ❤️

A MyEpilepsyTeam Member

Francis2,
35 years? Wow! That's wonderful.

When You Were Told That Medication To Assist You, Did You Choose Surgery Or Alternative Solutions? How Well Did It Work For You?
A MyEpilepsyTeam Member asked a question 💭

I have heard in the past from several friends who have tried many others including surgery, implants or non-medication alternative methods. However, I think it would help if those of you who have to share your experience with those are now at the point where they have been told that medication will never allow them to reach a long-term seizure free state.

If Q + A section was better organized, then I would not have to ask this question, but we have a support site, so we have to do what we can… read more

A MyEpilepsyTeam Member

@A MyEpilepsyTeam Member Everyone gets nervous. Usually what helps is if you talk to your epileptologist/surgeon. From the surgeon, I learned there was a better chance of dying from a car accident… read more

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My 9 Yr Old With Focal Seizures And On Three Meds He Has Been Suggested Surgery … Any Thoughts On That Would Be Greatly Appreciated
A MyEpilepsyTeam Member asked a question 💭

My son has focal seizures and on three meds .. he still gets seizures auras make it very hard for him … his doctors suggest a brain surgery as he has a brain injury during birth … any advice or recent experience anyone had ….

A MyEpilepsyTeam Member

I had my first brain surgery at the age of 23. By that time my Brian was fully developed.

My Epileptologist told me that if this surgery existed whenI was younger, I would of had a better chance… read more

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