Saturday, December 26, 2009

Re: [epilepsy] Help Me Understand

 

Money is another major issue for them.  They are without insurance and are in the process of getting community assistance so they didn't have money to get her blood work done.  My sister took her down last monday though to get her bloodwork done.

I know the dr's try different meds on her and seems they change so often?  Is that a normal thing or once you get on meds that maintain your blood levels you do ok on them?  I also read something about a certain "diet" kids get put on.  Does that help at all with adults?

Thanks!
Linda
 
 

________________________________
From: Millie Myers <mylmy@gogreencroft.net>
To: epilepsy@yahoogroups.com
Sent: Sat, December 26, 2009 1:24:29 PM
Subject: Re: [epilepsy] Help Me Understand

 
Linda,

When was her last blood test? Are her meds with in the levels they should be? Did she have a blood test after her sz? If not I suggest she get one.
Millie

----- Original Message -----
From: Linda Manchester
To: epilepsy@yahoogroup s.com
Sent: Saturday, December 26, 2009 11:12 AM
Subject: [epilepsy] Help Me Understand

I joined your group to educate myself. My 33 yrs old neice Libby is an inspiration to me. She is married to a very supportive man with a 1st and 3rd grader. My heart hurts because she had the surgery almost 2 yrs ago and it hasn't helped. Last week she had a seizure while walking to pickup her kids from school, feel off the sidewalk. That night she had another one at the top of her stairs and fell face first down the stairs.

We don't know if she is going to be able to take care of herself if she is alone. I've joined the group to educate myself and try to help my sister find support and encouragement for Libby. Libby is such an inspiration because she is so positive, has a wonderful sense of humor thru it all and is pressing on.

Thanks in advance for any advice, direction, websites, etc.

Merry Christmas
Linda

____________ _________ _________ __
From: Steve <stephenpales@ yahoo.com>
To: epilepsy@yahoogroup s.com
Sent: Sat, December 26, 2009 8:47:58 AM
Subject: [epilepsy] Re: Your post surgery memory efforts-

Hi Doris,

My surgery was 3 years ago. I feel my memory is worse BUT, I'm also 52 which is a time when memory can begin to not be the same. Also, what was felt by me in the months after a successful surgery in stopping seizures for me was a gain in self confidence!! ! I totally changed going from the quiet one living under a rock to talking allot. As my self confidence grew, I became more outgoing also. But, as I changed, my memory didn't improve. So all in all I changed so much but my memory not improving made me feel as though my memory got worse, though it didn't. I was so positive my memory got worse that I asked my Dr. if I could have a neuropsycological evaluation to compare pre and post tests. I had the test, and it showed there where no changes in me because of surgery. I mean no memory changes (smile). I've always had a poor memory since my epilepsy began in 1975. Add electrical activity and side effects of the meds. and my memory went to sleep (smile).
Plus a learning disability all my life. I swear its worse but its just that how much I changed deep within in positives ways made me feel as though my memory got worse! That's how it went for me. I'm still seizure free to this day, yea, seizures can come back but for me so far so good (big smile)! Doris, if you would like emailing me you can at stephenpales@ yahoo.com If you would like talking by voice on IM or phone, let me know. Take care, keep a smile on your face!

Steve

--- In epilepsy@yahoogroup s.com, "DorisY" <dorisellen@ ...> wrote:
>
> If you have had the surgery for epilepsy and experience current
> memory difficulty post surgery, your suggestions used for this
> would be appreciated.
> I am just super concerned about weather this is getting worse
> with time, and how much worse is it going to get.
> Thanks for your time and Happy New Year too.
> Doris
>

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