New approach to Treating Drug-Resistant Epilepsy

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Profile picture for Dan Noyes @dannoyes

Thank you so much for sharing because I am reaching that point where they've tried six different AE drugs with little success. I will share this with my Mayo team to get their feedback.

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@dannoyes
Hi Dan,
Looking back at our discussion about this new approach, I've been wondering if you had a chance to bring it up with your Mayo doctor. I'd love to hear what he or she thought!
Chris

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Profile picture for Dan Noyes @dannoyes

Thank you so much for sharing because I am reaching that point where they've tried six different AE drugs with little success. I will share this with my Mayo team to get their feedback.

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@dannoyes, yes, it becomes difficult when drugs do not work. Thanks for sharing. I wanted to know that, is this treatment sucessfully implemented and approved?

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Can drug resistant epilepsy be treated...or is there any role of stem cell transplant in epilepsy??

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My great respect for Mayo Clinic. Most especially for its Neurology Department. I thank the Lord for all their graciousness and kindness to not just me, but more people who have been, are and can be blessed with their exceptional care!

I wish you all better... Just like I wish for myself.

Thank you Mayo Clinic for continuing your hard work and gaining knowledge to help those of us with this incomparable (to other) disease(s).

Sincerely,

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@laura1961
You are very welcome. You will find that you have a family here so always know that you're not alone. We may not have all the answers but we'll always help any way we can.
Kerry

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Profile picture for keeg1010 @keeg1010

@laura1961
I completely agree with Chris. It can be extremely frustrating and overwhelming when you feel like the doctors aren't helping. My advice is to never give up. Keep fighting until you find the doctor who understands and is knowledgeable about what you're going through and knows how to help. We were very lucky to be able to get in with Mayo Clinic. They have been wonderful and are very thorough. My son also has the diagnosis of Mesial Temporal Sclerosis and didn't start having seizures until adulthood. We have been through so many doctors, I've lost count. However, once you find the one, your life will change and your stress will decrease. I'm glad you found this group. Everyone here is very helpful, encouraging, and dedicated. You have friends here that are on your side. I wish you luck and as always, feel free to reach out if you have questions.
Take care,
Kerry

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@keeg1010 Thank you so much for the encouragement I really appreciate you and other members understanding where I am coming from regarding the TBI

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Profile picture for Chris Gautier, Volunteer Mentor @santosha

@laura1961
Hi Laura
I completely understand that feeling of wanting to give up on doctors. But as I shared in my post, I'm so glad I kept searching until I found the right doctor to truly care for me. It made all the difference.
Several members of our group have been treated at Mayo Clinic and might be able to share their experiences with you: @dannoyes, @keeg1010, @royanthony, @tchandos, @absentsenior, and @patrassi. Feel free to reach out to them if you'd like to hear their perspectives.
Since you're in Australia, it would be wonderful to find a good epileptologist closer to home. Mayo Clinic might also be able to refer you to a specialist in Australia.
Please, keep persisting!
Chris

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@santosha Thank you for those links I have seen the 1st member but will take a further look at the others too.

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Profile picture for Chris Gautier, Volunteer Mentor @santosha

@laura1961
Hi Laura,
Cure Epilepsy is excellent and very trustworthy, worth exploring. They have a podcast called "Seizing Life" that I really enjoy:
- Welcome to Seizing Life
Cure Epilepsy
https://www.cureepilepsy.org/seizing-life/welcome-to-seizing-life/
Mayo Clinic also has dedicated epilepsy content you might find helpful:
- Epilepsy
Mayo Clinic
https://www.mayoclinic.org/diseases-conditions/epilepsy/symptoms-causes/syc-20350093
Besides the Epilepsy Foundation, both are great resources as you navigate your journey.
Chris

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@santosha Yes I have watched Seizing Life thank you & had a look at the Mayo Clinic page too

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Profile picture for Chris Gautier, Volunteer Mentor @santosha

@laura1961
Good morning, Laura!
Thank you so much for sharing those extra details—it really helps me understand your epilepsy journey better.
When we have secondarily generalized seizures (which include drop seizures, also known as atonic seizures), we may not always remember the focal seizures that happened right before. This has already happened to me when I had tonic-clonic seizures!
A complete diet change can be very overwhelming. I took it slowly, making one change at a time so I could see what actually helped reduce my seizures. I started by cutting out gluten—which was challenging enough on its own!—and that alone reduced my seizures by about 60%. Later, I stopped eating carbs at dinner. All that was done with my doctor's supervision.
Keeping a daily diary when I was trying to identify and better manage my seizure triggers based on the Andrews-Reiter approach — https://www.andrewsreiter.com/ — was incredibly worthwhile and taught me so much about what worked and what didn't.
Since hormonal changes are a well-known trigger for women (these are called catamenial seizures), my doctor worked with my gynecologist to find a solution. They suggested I take birth control pills continuously for 5-6 months without breaks to stop my periods during these months. This has also helped reduce my seizures. This worked for me since I'm not yet in menopause.
The key for me was making these changes gradually, one at a time. If my doctor had recommended everything at once, I probably would have felt too overwhelmed to stick with it. Taking it step by step made it manageable and helped me understand what was actually making a difference.
I really hope you find a specialized epilepsy doctor soon who will give you the thoughtful care you deserve. Keeping my fingers crossed for you!
Chris

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@santosha You are so lucky to have found such a knowledgeable Dr, they are not all like that looking into our hormones.

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@laura1961
I completely agree with Chris. It can be extremely frustrating and overwhelming when you feel like the doctors aren't helping. My advice is to never give up. Keep fighting until you find the doctor who understands and is knowledgeable about what you're going through and knows how to help. We were very lucky to be able to get in with Mayo Clinic. They have been wonderful and are very thorough. My son also has the diagnosis of Mesial Temporal Sclerosis and didn't start having seizures until adulthood. We have been through so many doctors, I've lost count. However, once you find the one, your life will change and your stress will decrease. I'm glad you found this group. Everyone here is very helpful, encouraging, and dedicated. You have friends here that are on your side. I wish you luck and as always, feel free to reach out if you have questions.
Take care,
Kerry

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