Menopause and Changes In Seizures
Prior to menopause I had been seizure free for 20 years. I have been on seizure medication since the age of six when I was diagnosed with epilepsy. At the age of 48 and premenopausal I started having seizures. Now ten years later post menopause I continue to have the seizures. Medication has not worked and hormone therapy has not worked. My seizures come almost every month and last for about 7-8 days and then they stop. I have tried different medications and even hormone replacement therapy and so far nothing has worked. I am wondering if there is anyone who has had or is having a similar experience dealing with a change in their seizure activity relating to premenopausal or menopausal. If so what have you tried, articles you may have read? My doctor is at a loss and has somewhat given up. I have read articles on Catamenial seizures however these do not apply to me. It's difficult to find any literature about this subject or possible solutions.
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Thank you for sharing your story. Sometimes we feel alone with our individual life journey with epilepsy. It helps to be reminded that we are not alone. I am so happy your wife has you by her side and that she is doing better. I will keep you both in my thoughts and prayers.
I would contact them, don't wait for them to contact you. I am a nurse and work in Internal Medicine and always tell patients to contact scheduling.
Hi Everybody,
There is a nice webinar about health in women with epilepsy. At the end of the webinar (48 minutes), it talks about menopause.
Here is the link:
Chris (@santosha)
Thank you for letting us know about this. I listened and it is not really helpful for women in menopause. The very end addresses how anti seizure medication affects bone density. It does not address changes in seizures after menopause. Information in this area does not seem to be adequately discussed anywhere. Most resources focus on seizures during menstrual cycles and pregnancy. This is my frustration.
As a post-menopausal female on an AED (Lamotrigine), who also has osteoporosis, I share your frustration. My seizures are rare, and seem to be stress induced. There is also what I believe to be a link to hormones. My first seizure was when I was in the early stages of puberty, my second at the being of perimenopause, and my third near the end of perimenopause.
Sadly, I have reached out to them a few times, and they keep telling me that they'll contact me.
Hi @juliehart4
Perhaps the 24/7 helpline of the Epilepsy Foundation could give you more information. Here is the link: https://www.epilepsy.com/247-helpline
I always got an answer from them when I reached the Epilepsy Foundation through e-mail (I am not in the US).
All my best to you!
Chris (@santosha)
Thanks Chris, I have done that and have not been given any helpful information on my particular situation. I have been battling this since perimenopause, over 15 years now. Four Neurologists , two specialists, I have also been to a level 4 epilepsy hospital and still no solutions. Additionally health insurance only allows you to do so much and then it’s out of pocket.
I am sorry to hear that @juliehart4. Have you tried to go to an epileptologist? Before finding my epileptologist, I went to many neurologists who could not provide me with some answers to my questions and treated me as a standard patient. And then I found this epileptologist, who has developed a customized treatment, considering all my issues, like being very sensible to medication, reversing medication action, my kind of epilepsy, etc. My epileptologist speaks directly to my gynecologist regarding all gynecological issues, working together with him.
I hope you find your way and answer to your questions. All the best!
Chris (@santosha)