Friday, July 31, 2009

Re: [epilepsy] Re: Need help understanding this...what do you think

 



________________________________
From: "jenandshadow@yahoo.com" <jenandshadow@yahoo.com>
To: epilepsy@yahoogroups.com
Sent: Tuesday, July 28, 2009 3:55:05 PM
Subject: Re: [epilepsy] Re: Need help understanding this...what do you think

 
Tammy I love the T-shirt idea can someone design one?
Sent from my Verizon Wireless BlackBerry

-----Original Message-----
From: Tammy Wolfgram <tammy@maccetera. com>

Date: Tue, 28 Jul 2009 12:56:18
To: <epilepsy@yahoogroup s.com>
Subject: [epilepsy] Re: Need help understanding this...what do you think

Maybe those with seizures could wear t-shirts that say something
like, "I have epilepsy and post-ictal confusion. Transport at your
own expense." or "Do not transport unless you see blood." My daughter
and I have joked about this for a long time. Seems pointless to have
med alert jewelry if the paramedics just ignore it. She has post-
ictal confusion for a short period that gradually gets better, but it
is during that period that the paramedics are asking her questions.
Early on, she can't even speak! When she was away at college, each
transport cost over $700! And that doesn't count ER or any other
charges. I think the truth of the matter is that the paramedics and
fire departments are covering their own butts and protecting
themselves from any potential lawsuits by transporting just about
everyone they are called to see.

Tammy

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Re: [epilepsy] Re: brain surgery and driving.

I can understand the bus & bike thing. Right now I am so relieved when my medical van rides come on time. I have to say this: "I am grateful that I ran five to ten miles a day through high school.
I just felt grateful because sometimes stuck immobile for days weeks I am really so glad for that love of running. Sometimes I can think & feEl wind in my hair, pushing to get to the next water whole while my lab runs big laps around me. Jumpin in the water hole with my beloved Sambo... How did you run so far with little me my friend, without one seizure... Only had 'em at home near the stairs...Mom gave you meds twice a day. All the neighbors waited for your Visit.
22 years old, you beat all them dogs by years...You were my angel. Li'l Black Sambo~THANX
Sent from my Verizon Wireless BlackBerry

-----Original Message-----
From: TIMOTHY BALDWIN <tbb1@prodigy.net>

Date: Fri, 31 Jul 2009 20:10:23
To: <epilepsy@yahoogroups.com>
Subject: Re: [epilepsy] Re: brain surgery and driving.


Tammy,
   I'm sorry you were having so many seizures before your surgery, but my doctor and the meds. he put me since '80 have always kept at once in 3-4 wks. or what I thought was close to being controlled. I drove because of my not being aware if they were due to a seizure, but I wasn't fully aware of them. And felt at home in body shops. Since being on lacosamide since 6/08 with a different doctor, I still have one per 5-12 wks.. In Maryland 26wks. is required to legally drive. But, I'm thinking of buying a new one because I'm sick and tired of taking the bus since '98, and my public life having dropped all the way down.
Tim B.       

--- On Fri, 7/31/09, uniquepnk tds.net <Uniquepnk@tds.net> wrote:


From: uniquepnk tds.net <Uniquepnk@tds.net>
Subject: Re: [epilepsy] Re: brain surgery and driving.
To: epilepsy@yahoogroups.com
Date: Friday, July 31, 2009, 9:31 PM


 



Tim,

I had the surgery and I am glad I had it done, but it did not stop the
seizures completely. I don't see why you were driving if you were still
having seizures after the surgery. I went 9 months and thought I would get
to drive too, but then they started back. As long as there is a chance I am
going to have seizures I will not consider driving, even as much as I wanted
to years ago. It doesn't mean as much to me anymore, so as long as I am safe
and everybody around me, that is all that matters. I am not having 25
seizures a month, but since it is not near that many I am very happy about
having the surgery.I am sorry it did not stop yours or mine completely, but
that is just the way things are. Take care.

Tammy

On Thu, Jul 30, 2009 at 10:29 PM, TIMOTHY BALDWIN <tbb1@prodigy. net> wrote:

>
>
> Everyone,
> Its looks like allot of people have commented about how successful their
> operations were, that's different than me. In '96 my l. temporal lobe was
> mostly removed, before the surgery I was aware of a seizure occurring every
> 3-4 weeks, Others probably happened that I knew nothing of. After my
> unsuccessful surgery my seizure rate didn't change, and I continued
> to take the same amount of medicines. In '74 I had my first few seizure and
> was diagnosed. I continued to drive and totaled my five cars each
> were repaired at least as many times as possible. In '98 I finally quit
> driving I gave up with my ridicules good luck, my crashes were always alone
> without another car involved and the police always assumed that I'd fallen
> asleep. If someone else was involved who saw that my eyes were open and the
> cop may write that the accident was due to a seizure, If people in that
> car saw lawyers could look at my past medical records and decide that I
> shouldn't have been driving in the first place...
> Tim B.
>
> --- On Thu, 7/30/09, sept161999@aol. com <sept161999% 40aol.com> <
> sept161999@aol. com <sept161999% 40aol.com> > wrote:
>
> From: sept161999@aol. com <sept161999% 40aol.com> <sept161999@aol. com<sept161999% 40aol.com>
> >
> Subject: Re: [epilepsy] Re: brain surgery and driving.
> To: epilepsy@yahoogroup s.com <epilepsy%40yahoogr oups.com>
> Date: Thursday, July 30, 2009, 7:41 PM
>
>
>
> congrats.
> my doctors asked me before they discharged me from the hospital a few days
> after the surgery if theres anything they could do.
> i said "could you write me prescriptions for my medications" ?
> they looked at me like i was crazy.
> i guess they never saw someone who wanted medication even after surgery
> talk with your dr.
> hope everything goes good
> Brian
>
> In a message dated 7/30/2009 6:20:51 A.M. Pacific Daylight Time,
> tristinspike26@ yahoo.com writes:
>
> Brian,
> Oh, I already had the surgery (Nov 12, 08). It was a cinch! I know that
> surgery isn't a guarantee, but it's worked so far. You mentioned that I
> shouldn't think of it as a way to get off of my meds. Although I'm still on
>
> extreme dosages, I do plan to talk my neuro into decreasing my dosages at
> my next visit. I know I'll probably never be fully "sober," (lol) but I do
> think I could cut back a few hundered mg.
>
> Tristin :)
>
> --- On Thu, 7/30/09,_sept161999@ aol.sep_ (mailto:sept161999@ aol. com)
> <_sept161999@ aol.sep_ (mailto:sept161999@ aol. com) > wrote:
>
> From:_sept161999@ aol.sep_ (mailto:sept161999@ aol. com)
> <_sept161999@ aol.sep_ (mailto:sept161999@ aol. com) >
> Subject: Re: [epilepsy] Re: brain surgery and driving.
> To:_epilepsy@yahoogrou pepile_ (mailto:epilepsy@ yahoogroup s.com)
> Date: Thursday, July 30, 2009, 9:09 AM
>
> it's true that surgery is not for everyone but looking into it might not
>
> hurt. I had surgery. before surgery i would have an average 50 seizures
> per
>
> day from age 2 to age 29. now after surgery ive been seizure free a little
>
> more then 9 in a half years. Just remember if you want to have it done do
> a
>
> lot of homework into what you must do(testing) how things would be done.
>
> get references on doctors. BUT REMEMBER SURGERY IS NOT A GUARANTEE IT WILL
>
> STOP OR EVEN CONTROL SEIZURES. and also you might have to stay on
> medication
>
> so dont think of surgery as a way to also being able to stop medications.
>
> Brian
>
> In a message dated 7/30/2009 5:54:22 A.M. Pacific Daylight Time,
>
> tristinspike26@ yahoo.com writes:
>
> Well Birdman,
>
> I understand that surgery isn't always perfect, and it doesn't work for
>
> everyone. But I can't criticize it. It's worked for me, so far. I'm 8
>
> months seizure-free thanks to a left temporal lobectomy. I've waited a
> long
>
> time to get my driver's license, and driving I'm gonna do. I know there's
>
> the possibility of having another seizure, and I know to take precautions
>
> if/when I start feeling strange. I have to take advantage of this time
>
> because it may not last for long.
>
> Tristin :)
>
> --- On Thu, 7/30/09, korky106_a <_korky106_a@ yahoo.kor_
>
> (mailto:korky106_ (mailto:korky1> wrote:
>
> From: korky106_a <_korky106_a@ yahoo.kor_ (mailto:korky106__korky106_ a@y>
>
> Subject: [epilepsy] Re: brain surgery and driving.
>
> To:_epilepsy@yahoogrou pepile_ (mailto:epilepsy@ To:_epilepsy@yaho
>
> Date: Thursday, July 30, 2009, 1:56 AM
>
> I am well aware the desire for people to drive- I think it may be more for
>
> a person with seizures. i am 58- I have had seizures since I was 13- I was
>
> bit by a mosquito and given encephalitis- my brain became infected-
>
> swelled up to the point I went into a coma for 18 hrs. The drs did not
> expect me
>
> to come out of it and live. I have brain damage because of this and
>
> seizures- all kinds. I have had a right temporal lobectomy to remove what
> they
>
> thought was the damaged cells and take away my seizures. Well some time
> went
>
> by without seizures- I got my license and- away I drove feeling GREAT-
> well
>
> i have totalled my Honda Accord because I had a seizure- surgery is NOT
>
> always perfect- I found this out when I totaled my Taurus as a result of a
>
> seizure accident. OKEASE reconsider driving- I will NEVER try driving
> again. I
>
> am fortunate to be alive and to have not hurt anyone as a result of my
>
> driving- I can adjust to not driving- I could
>
> NEVER adjust to hurting a person because I chose to drive when I
>
> shouldn't- THINK TWICE- Thanks- Birdman--- In epilepsy@yahoogroup s.com,
>
> "tristinspike26" <tristinspike26@ ...> wrote:
>
> >
>
> > Hi all,
>
> > Tomorrow I'm kind of going to share my epilepsy surgery testimony with
>
> my friend's (Lisa's) neurologist. I'm totally tickled that she wants me to
>
> talk to her neurologist and tell him what surgery did for me. We're trying
>
> to get her referred to the Medical College of Georgia; where I had my
>
> surgery. Surgery worked so far for me. I hope and pray that my friend,
> Lisa,
>
> turns out to be a good candidate. Maybe surgery will work for her too. It
> makes
>
> me feel good knowing that my struggle with epilepsy and my surgery might
>
> inspire someone else (Lisa). Since I got my driver's license (for the past
>
> month) I've been driving Lisa around and helping her get to where she
> needs
>
> to go. I've been in her shoes. I know what it's like. It's just my way of
>
> paying it forward.
>
> >
>
> > Tristin :)
>
> >
>
> [Non-text portions of this message have been removed]
>
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[fast5] Re: Thinking about starting the program

 

Karen,

I think that you are a pretty good success story because it sounds like you're doing exactly what you need to do at the time that you need to do it and you're not beating yourself up for not being "prefect." If any of us could be perfect, would we even be here?

Everytime I take a break from F5 I feel like garbage even though I eat pretty healthy. When I eat according to the F5 schedule I feel awsome even though half of what I eat is technically garbage. What does that tell you? It's not so much what you eat but when and that's the whole point of the book. We need to forget about the so called "Ideal Diet" because no one can follow it. Even Ori H. who wrote the Warrior Diet said in the beginning of the book that he has has done the Warrior Diet off and on for 25 years. There's a clue there, even HE can't stick to it every freekin day of his life and he's the author! We don't need to be perfect. As long as we aren't stuffing ourself with food around the clock we'll be fine. As long as we give our bodies a break from food most of the time we'll be getting the full benefits of fasting even if we don't eat perfect when we do eat. What you eat during your 5 hour window is GOING to be better than what you would have eaten if you ate between 3-6 meals a day, that's for sure, and because of that you should consider yourself a success even if you've been stuck at a weight higher than what you want for a while.

Most of us here feel amazing when we fast and that is the whole point of the book. We don't feel like that on other diets. As long as your doing it your a success. Enjoy your day, enjoy the freedom and energy and at night after all the work is done enjoy your food and relax. Life's too short to worry about all the unimportant details.

I still get newsletters from diet programs promoting 6 meals a day and the one I got today outlined a plan for breaking a plateau and it had all these steps and rules and things you had to give up and I'm like WHAT A DRAG. Thank God I don't do that anymore. If the dude would just fast once in a while maybe he wouldn't have to follow his 85 steps to dieting success.

--- In fast5@yahoogroups.com, "Karen" <laurvick@...> wrote:
>
> I'm not much of a 'success' story in the point of losing weight.
>
> But I do feel successful in the fasting part!
>
> I have my own issues that I'm trying to learn to deal with and work around,
> so have not been on Fast5 at one time for any great length of time.
>
> Last fall, did F5 for about 3 months, but, honestly, I used my 5-hr window
> to eat junk.
>
> And since I'm close to desired weight, I did not lose weight.
>
> Then I had to take a medication w/food every 12 hrs so got off F5.
>
> Now I only need to take the meds once/day so am trying F5 again.
>
> But I mixed the days; some days I would fast, others days I would eat
> 'normally'.
>
> I was choosing not to fast on the days that I was doing my hardest work
> outs.
>
> But a week ago, I got the courage to fast past my morning workouts.
>
> I feel I have been doing fine.
>
> I do my work outs (weight lifting 4 days/wk; cardio 2 days/wk) about 10 hrs
> fasted.
>
> Now I'm making better food choices during my eating window (except the past
> two Saturdays!!! Grrr on me!!)
>
> -----Original Message-----
> From: fast5@yahoogroups.com [mailto:fast5@yahoogroups.com] On Behalf Of
> kris10_ross
> Sent: Wednesday, July 29, 2009 10:30 AM
> To: fast5@yahoogroups.com
> Subject: [fast5] Thinking about starting the program
>
> So I am thinking about the starting the program and I would like to lose
> about 25lbs in total.
>
> The biggest problem for me is simply the change in my daily routines. The
> best time for me to eat is from 1-5 or 2-6 based on my schedule, however
> weekends that might change.
>
> Do any of you find it a problem to change your window on weekends?
>
> I would love to hear some success stories and feedback on any additional
> helping points to help the weight come off. I have been working out quite
> hard the last few weeks to really jumpstart the weightloss, so I need to eat
> during the day to keep up my enegery for the evening.
>
> Let me know some thoughts, feedback, etc....
> I am very intersted in starting, just need a little help!
> thanks!
>
>
>
> ------------------------------------
>
> Yahoo! Groups Links
>

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Re: [epilepsy] Question?

 



--- On Fri, 7/31/09, Wendy Baur <wendy.sue@gmail.com> wrote:

From: Wendy Baur <wendy.sue@gmail.com>
Subject: Re: [epilepsy] Question?
To: epilepsy@yahoogroups.com
Date: Friday, July 31, 2009, 10:37 PM

Tristin,
 
Please get a hold of your neuro and do what wendy is saying what to do, just
 
for your safety and those around you. Because I'm having the same problem
 
my care taker is taking of this with my doctor too. Please do it. 
 
Rodolfo 
 
 

Tristin,

Please call your neuro all you may need is your meds adjusted. I
am worried because you could be driving when you have your next one
and you could hurt yourself and god forbid someone else, so please
make the call.

wendy

On Fri, Jul 31, 2009 at 6:31 PM, Tristin
Seagraves<tristinspike26@ yahoo.com> wrote:
>
>
> Right now, I'm just trying not to over react.  If it happens again, I'll
> tell my neurologist, but for now, I think I'll keep my mouth shut.
>
> Thanks,
>      Tristin.
>
> --- On Fri, 7/31/09, vanessa <velvet_chrome@ yahoo.com> wrote:
>
> From: vanessa <velvet_chrome@ yahoo.com>
> Subject: Re: [epilepsy] Question?
> To: epilepsy@yahoogroup s.com
> Date: Friday, July 31, 2009, 6:21 PM
>
>
>
> I once went 6 yrs without having one. You might just need your meds
> adjusted. I would certainly tell your neuro. It doesnt mean you will lose
> your license. Ive been driving since I was 16 and Im now 46. Ive had epi
> since age 14. Never had one while driving.
>
> ____________ _________ _________ __
> From: tristinspike26 <tristinspike26@ yahoo.com>
> To: epilepsy@yahoogroup s.com
> Sent: Friday, July 31, 2009 6:00:45 PM
> Subject: [epilepsy] Question?
>
> My boyfriend, Jamey, claims that I had a seizure today.  He said we were
> talking, and I suddenly paused and started making moaning noises.  He said I
> was unresponsive and was pinching myself.  I find this hard to believe.... I
> don't even remember having an aura.  Should I tell my neurologist about this
> and risk losing my driver's license?  I mean... I just bought a car last
> week!  I already swore Jamey to secrecy, and I'm surely not going to tell
> any of my family.  They will totally freak out!  After 8 1/2 months of being
> seizure-free, I have a seizure?  This can't be right.  I guess you could say
> I'm in denial.  If another one happens, I'll tell someone, but until then, I
> think I'm going to keep this to myself.
>
> Tristin
>
> ------------ --------- --------- ------
>
> Just a friendly reminder: Please remember to sign your post and remember to
> clean up messages when you reply to them.  This is especially important if
> you are on digest.  This not only helps out the list owner but, it makes
> messages much easier to read when they arrive in our inboxes.
>
> Yahoo! Groups Links
>
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>
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Re: [epilepsy] Re: brain surgery and driving.

 

Tammy,
   I'm sorry you were having so many seizures before your surgery, but my doctor and the meds. he put me since '80 have always kept at once in 3-4 wks. or what I thought was close to being controlled. I drove because of my not being aware if they were due to a seizure, but I wasn't fully aware of them. And felt at home in body shops. Since being on lacosamide since 6/08 with a different doctor, I still have one per 5-12 wks.. In Maryland 26wks. is required to legally drive. But, I'm thinking of buying a new one because I'm sick and tired of taking the bus since '98, and my public life having dropped all the way down.
Tim B.       

--- On Fri, 7/31/09, uniquepnk tds.net <Uniquepnk@tds.net> wrote:

From: uniquepnk tds.net <Uniquepnk@tds.net>
Subject: Re: [epilepsy] Re: brain surgery and driving.
To: epilepsy@yahoogroups.com
Date: Friday, July 31, 2009, 9:31 PM

 

Tim,

I had the surgery and I am glad I had it done, but it did not stop the
seizures completely. I don't see why you were driving if you were still
having seizures after the surgery. I went 9 months and thought I would get
to drive too, but then they started back. As long as there is a chance I am
going to have seizures I will not consider driving, even as much as I wanted
to years ago. It doesn't mean as much to me anymore, so as long as I am safe
and everybody around me, that is all that matters. I am not having 25
seizures a month, but since it is not near that many I am very happy about
having the surgery.I am sorry it did not stop yours or mine completely, but
that is just the way things are. Take care.

Tammy

On Thu, Jul 30, 2009 at 10:29 PM, TIMOTHY BALDWIN <tbb1@prodigy. net> wrote:

>
>
> Everyone,
> Its looks like allot of people have commented about how successful their
> operations were, that's different than me. In '96 my l. temporal lobe was
> mostly removed, before the surgery I was aware of a seizure occurring every
> 3-4 weeks, Others probably happened that I knew nothing of. After my
> unsuccessful surgery my seizure rate didn't change, and I continued
> to take the same amount of medicines. In '74 I had my first few seizure and
> was diagnosed. I continued to drive and totaled my five cars each
> were repaired at least as many times as possible. In '98 I finally quit
> driving I gave up with my ridicules good luck, my crashes were always alone
> without another car involved and the police always assumed that I'd fallen
> asleep. If someone else was involved who saw that my eyes were open and the
> cop may write that the accident was due to a seizure, If people in that
> car saw lawyers could look at my past medical records and decide that I
> shouldn't have been driving in the first place...
> Tim B.
>
> --- On Thu, 7/30/09, sept161999@aol. com <sept161999% 40aol.com> <
> sept161999@aol. com <sept161999% 40aol.com> > wrote:
>
> From: sept161999@aol. com <sept161999% 40aol.com> <sept161999@aol. com<sept161999% 40aol.com>
> >
> Subject: Re: [epilepsy] Re: brain surgery and driving.
> To: epilepsy@yahoogroup s.com <epilepsy%40yahoogr oups.com>
> Date: Thursday, July 30, 2009, 7:41 PM
>
>
>
> congrats.
> my doctors asked me before they discharged me from the hospital a few days
> after the surgery if theres anything they could do.
> i said "could you write me prescriptions for my medications" ?
> they looked at me like i was crazy.
> i guess they never saw someone who wanted medication even after surgery
> talk with your dr.
> hope everything goes good
> Brian
>
> In a message dated 7/30/2009 6:20:51 A.M. Pacific Daylight Time,
> tristinspike26@ yahoo.com writes:
>
> Brian,
> Oh, I already had the surgery (Nov 12, 08). It was a cinch! I know that
> surgery isn't a guarantee, but it's worked so far. You mentioned that I
> shouldn't think of it as a way to get off of my meds. Although I'm still on
>
> extreme dosages, I do plan to talk my neuro into decreasing my dosages at
> my next visit. I know I'll probably never be fully "sober," (lol) but I do
> think I could cut back a few hundered mg.
>
> Tristin :)
>
> --- On Thu, 7/30/09, _sept161999@ aol.sep_ (mailto:sept161999@ aol. com)
> <_sept161999@ aol.sep_ (mailto:sept161999@ aol. com) > wrote:
>
> From: _sept161999@ aol.sep_ (mailto:sept161999@ aol. com)
> <_sept161999@ aol.sep_ (mailto:sept161999@ aol. com) >
> Subject: Re: [epilepsy] Re: brain surgery and driving.
> To: _epilepsy@yahoogrou pepile_ (mailto:epilepsy@ yahoogroup s.com)
> Date: Thursday, July 30, 2009, 9:09 AM
>
> it's true that surgery is not for everyone but looking into it might not
>
> hurt. I had surgery. before surgery i would have an average 50 seizures
> per
>
> day from age 2 to age 29. now after surgery ive been seizure free a little
>
> more then 9 in a half years. Just remember if you want to have it done do
> a
>
> lot of homework into what you must do(testing) how things would be done.
>
> get references on doctors. BUT REMEMBER SURGERY IS NOT A GUARANTEE IT WILL
>
> STOP OR EVEN CONTROL SEIZURES. and also you might have to stay on
> medication
>
> so dont think of surgery as a way to also being able to stop medications.
>
> Brian
>
> In a message dated 7/30/2009 5:54:22 A.M. Pacific Daylight Time,
>
> tristinspike26@ yahoo.com writes:
>
> Well Birdman,
>
> I understand that surgery isn't always perfect, and it doesn't work for
>
> everyone. But I can't criticize it. It's worked for me, so far. I'm 8
>
> months seizure-free thanks to a left temporal lobectomy. I've waited a
> long
>
> time to get my driver's license, and driving I'm gonna do. I know there's
>
> the possibility of having another seizure, and I know to take precautions
>
> if/when I start feeling strange. I have to take advantage of this time
>
> because it may not last for long.
>
> Tristin :)
>
> --- On Thu, 7/30/09, korky106_a <_korky106_a@ yahoo.kor_
>
> (mailto:korky106_ (mailto:korky1> wrote:
>
> From: korky106_a <_korky106_a@ yahoo.kor_ (mailto:korky106_ _korky106_ a@y>
>
> Subject: [epilepsy] Re: brain surgery and driving.
>
> To: _epilepsy@yahoogrou pepile_ (mailto:epilepsy@ To: _epilepsy@yaho
>
> Date: Thursday, July 30, 2009, 1:56 AM
>
> I am well aware the desire for people to drive- I think it may be more for
>
> a person with seizures. i am 58- I have had seizures since I was 13- I was
>
> bit by a mosquito and given encephalitis- my brain became infected-
>
> swelled up to the point I went into a coma for 18 hrs. The drs did not
> expect me
>
> to come out of it and live. I have brain damage because of this and
>
> seizures- all kinds. I have had a right temporal lobectomy to remove what
> they
>
> thought was the damaged cells and take away my seizures. Well some time
> went
>
> by without seizures- I got my license and- away I drove feeling GREAT-
> well
>
> i have totalled my Honda Accord because I had a seizure- surgery is NOT
>
> always perfect- I found this out when I totaled my Taurus as a result of a
>
> seizure accident. OKEASE reconsider driving- I will NEVER try driving
> again. I
>
> am fortunate to be alive and to have not hurt anyone as a result of my
>
> driving- I can adjust to not driving- I could
>
> NEVER adjust to hurting a person because I chose to drive when I
>
> shouldn't- THINK TWICE- Thanks- Birdman--- In epilepsy@yahoogroup s.com,
>
> "tristinspike26" <tristinspike26@ ...> wrote:
>
> >
>
> > Hi all,
>
> > Tomorrow I'm kind of going to share my epilepsy surgery testimony with
>
> my friend's (Lisa's) neurologist. I'm totally tickled that she wants me to
>
> talk to her neurologist and tell him what surgery did for me. We're trying
>
> to get her referred to the Medical College of Georgia; where I had my
>
> surgery. Surgery worked so far for me. I hope and pray that my friend,
> Lisa,
>
> turns out to be a good candidate. Maybe surgery will work for her too. It
> makes
>
> me feel good knowing that my struggle with epilepsy and my surgery might
>
> inspire someone else (Lisa). Since I got my driver's license (for the past
>
> month) I've been driving Lisa around and helping her get to where she
> needs
>
> to go. I've been in her shoes. I know what it's like. It's just my way of
>
> paying it forward.
>
> >
>
> > Tristin :)
>
> >
>
> [Non-text portions of this message have been removed]
>
> ************ **Hot Deals at Dell on Popular Laptops perfect for Back to
>
> School
>
> (_http://pr.atwola. _ (http://pr.atwola. /) com/promoclk/ 100126575x122310
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> 2Fck%2F12309% 2D81939%2D1629% 2D9)
>
> [Non-text portions of this message have been removed]
>
> [Non-text portions of this message have been removed]
>
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> School
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> [Non-text portions of this message have been removed]
>
> [Non-text portions of this message have been removed]
>
>
>

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Re: [epilepsy] Question? License

 

Yes...I felt better to have one + never use it than deal with the other ID thing or have to get a new license if I get better.
Thanks for the encouragement.
Jen+shad-ow

Sent from my Verizon Wireless BlackBerry

-----Original Message-----
From: william.fisher602@comcast.net

Date: Sat, 1 Aug 2009 02:22:59
To: <epilepsy@yahoogroups.com>
Subject: Re: [epilepsy] Question?


When I had my first  seizure over 20 years ago at the age of 50 my doctor ask me to give uo driving but to keep mt license as a form of id because it had my picture on it. If I did not he would have the DMV pull it willfish57@yahoo.com

GOD BLESS you & keep you

----- Original Message -----
From: jenandshadow@yahoo.com
To: epilepsy@yahoogroups.com
Sent: Friday, July 31, 2009 7:12:40 PM GMT -05:00 US/Canada Eastern
Subject: Re: [epilepsy] Question?

 




Should I tell?
The questions I asked myself when informed of my seizures were?
1-If I choose to DRIVE how will I feel if one of these causes me to kill a child with my car?
2-Can I Live with myself knowing that I could have prevented this unnecessary child's life being snuffed out because I so wanted to go get myself a mocha? Etc...
3-Do I have to give up my license?
4-Can I just take time off from driving without giving up my license until I can tell if my seizures will lessen or get controlled?
5-What measures can I take to be sure I do not endanger myself or the innocent.

I still renewed my license this year, but (because my seizure dog would scream if I tried to drive during any portion of unsafe seizure state+ I kept a pillow+blankets+ food + water in my car + pulled over at my dogs first reaction, I did continue to drive for a few years with this safe policing for my safety+ the public) my doctors never yanked my license. Maybe you could only drive with someone who can alert to your seizures + take the wheel + pull you over=driving only on low traveled roads other than freeway where reaction time is critical+ stay out of neighborhoods. Have these safe supervisors evaluate how you are doing and verbally tell you-as my dog would-mom it's time to go home. I'd ask if we could make one more stop+ see if he RELAXED OR STRESSED at the thought. If he cried I would go straight home.
For the last two years I drove I stuck to off PEAK hours + less crowded or NON-STRESS FILLED DRIVER roads. I went and shopped at night and always lay down in the back + rested 'til the seizure + after affects passed + my dog let me drive.
The last year I only drove approximately four 25 mile round trips per month: go get mocha + to walmart + to grocery + for pleasure a 30-45 minute look at houses for sale. At 11 pm I'm sure many figured I was scouting neighborhoods to burglarize-because I would return + compare some new ones to old ones I loved.... Sorry I do have a point here...I never drove more than 10 minutes/5 miles from my home the last year. But I had 3 times when I didn't recognize so I could heed Shadow's alert + had a few wake up calls. Then I got rid of the car, lost 10 pounds fast + kept my license=still hoping my Seizures will be solved somehow.
Doc's may need to know if your human seizure alert dogs can't safely see you in time for them to help. Boy would I love to let you meet Shadow. We could start by driving around apartment+ he should alert. If there is any danger-You could definitely get a per scription for seizure alert dog. Mine does more than most. Do you know anyone with a seizure dog? Ask them if next time you have what your frind thinks is a seizure you can have him drive you over to be checked out. A good seizure dog is more accurate than any medical equipment to date~why? Because when we seize/ our body emits an odor only a dog can smell+some cats.
~jen+shadow~
Sent from my Verizon Wireless BlackBerry

-----Original Message-----
From: "tristinspike26" < tristinspike26@yahoo.com >

Date: Fri, 31 Jul 2009 22:00:45
To: < epilepsy@yahoogroups.com >
Subject: [epilepsy] Question?


My boyfriend, Jamey, claims that I had a seizure today. He said we were talking, and I suddenly paused and started making moaning noises. He said I was unresponsive and was pinching myself. I find this hard to believe... I don't even remember having an aura. Should I tell my neurologist about this and risk losing my driver's license? I mean... I just bought a car last week! I already swore Jamey to secrecy, and I'm surely not going to tell any of my family. They will totally freak out! After 8 1/2 months of being seizure-free, I have a seizure? This can't be right. I guess you could say I'm in denial. If another one happens, I'll tell someone, but until then, I think I'm going to keep this to myself.


Tristin



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Re: [epilepsy] Question?

 

When I had my first  seizure over 20 years ago at the age of 50 my doctor ask me to give uo driving but to keep mt license as a form of id because it had my picture on it. If I did not he would have the DMV pull it willfish57@yahoo.com

GOD BLESS you & keep you

----- Original Message -----
From: jenandshadow@yahoo.com
To: epilepsy@yahoogroups.com
Sent: Friday, July 31, 2009 7:12:40 PM GMT -05:00 US/Canada Eastern
Subject: Re: [epilepsy] Question?

 

Should I tell?
The questions I asked myself when informed of my seizures were?
1-If I choose to DRIVE how will I feel if one of these causes me to kill a child with my car?
2-Can I Live with myself knowing that I could have prevented this unnecessary child's life being snuffed out because I so wanted to go get myself a mocha? Etc...
3-Do I have to give up my license?
4-Can I just take time off from driving without giving up my license until I can tell if my seizures will lessen or get controlled?
5-What measures can I take to be sure I do not endanger myself or the innocent.

I still renewed my license this year, but (because my seizure dog would scream if I tried to drive during any portion of unsafe seizure state+ I kept a pillow+blankets+ food + water in my car + pulled over at my dogs first reaction, I did continue to drive for a few years with this safe policing for my safety+ the public) my doctors never yanked my license. Maybe you could only drive with someone who can alert to your seizures + take the wheel + pull you over=driving only on low traveled roads other than freeway where reaction time is critical+ stay out of neighborhoods. Have these safe supervisors evaluate how you are doing and verbally tell you-as my dog would-mom it's time to go home. I'd ask if we could make one more stop+ see if he RELAXED OR STRESSED at the thought. If he cried I would go straight home.
For the last two years I drove I stuck to off PEAK hours + less crowded or NON-STRESS FILLED DRIVER roads. I went and shopped at night and always lay down in the back + rested 'til the seizure + after affects passed + my dog let me drive.
The last year I only drove approximately four 25 mile round trips per month: go get mocha + to walmart + to grocery + for pleasure a 30-45 minute look at houses for sale. At 11 pm I'm sure many figured I was scouting neighborhoods to burglarize-because I would return + compare some new ones to old ones I loved.... Sorry I do have a point here...I never drove more than 10 minutes/5 miles from my home the last year. But I had 3 times when I didn't recognize so I could heed Shadow's alert + had a few wake up calls. Then I got rid of the car, lost 10 pounds fast + kept my license=still hoping my Seizures will be solved somehow.
Doc's may need to know if your human seizure alert dogs can't safely see you in time for them to help. Boy would I love to let you meet Shadow. We could start by driving around apartment+ he should alert. If there is any danger-You could definitely get a per scription for seizure alert dog. Mine does more than most. Do you know anyone with a seizure dog? Ask them if next time you have what your frind thinks is a seizure you can have him drive you over to be checked out. A good seizure dog is more accurate than any medical equipment to date~why? Because when we seize/ our body emits an odor only a dog can smell+some cats.
~jen+shadow~
Sent from my Verizon Wireless BlackBerry

-----Original Message-----
From: "tristinspike26" < tristinspike26@yahoo.com >

Date: Fri, 31 Jul 2009 22:00:45
To: < epilepsy@yahoogroups.com >
Subject: [epilepsy] Question?

My boyfriend, Jamey, claims that I had a seizure today. He said we were talking, and I suddenly paused and started making moaning noises. He said I was unresponsive and was pinching myself. I find this hard to believe... I don't even remember having an aura. Should I tell my neurologist about this and risk losing my driver's license? I mean... I just bought a car last week! I already swore Jamey to secrecy, and I'm surely not going to tell any of my family. They will totally freak out! After 8 1/2 months of being seizure-free, I have a seizure? This can't be right. I guess you could say I'm in denial. If another one happens, I'll tell someone, but until then, I think I'm going to keep this to myself.

Tristin

------------------------------------

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