• Home
  • What is CE?
  • For Patients
  • For Clinicians
  • About
  • My Story
  • More
    • Home
    • What is CE?
    • For Patients
    • For Clinicians
    • About
    • My Story
  • Home
  • What is CE?
  • For Patients
  • For Clinicians
  • About
  • My Story

FOR PATIENTS

Catamenial Epilepsy can take years to diagnose and can take just as long to find a medication that works. 


Why? Because you have to wait multiple cycles to judge the effectiveness of the medication. 


Then, when you think you've figured it out, your body and hormones change over time. 

Let's Work together

A key element of successful treatment is finding a knowledgeable and compassionate provider.  


However, they are extremely hard to find. In fact, I myself am searching for an expert right now since my neurologist retired.


Let's help each other out!

  • Do you have a provider that you love? 
  • Is there a hospital, practice, or university that has helped you with your journey?
  • Are there resources that made a difference in your life?


PLEASE EMAIL catamenialepilepsy@gmail.com AND I'LL START A LIST! 


As suggestions come in, I will add them to this page so everyone can benefit and have options for doctors and second opinions. 


This page could bring hope to thousands of women. I look forward to receiving suggestions!


  • What is CE?
  • For Patients
  • For Clinicians
  • About
  • My Story
  • Contact

Catamenial Epilepsy Foundation

Copyright © 2024 Catamenial Epilepsy Foundation - All Rights Reserved.

Powered by GoDaddy

This website uses cookies.

We use cookies to analyze website traffic and optimize your website experience. By accepting our use of cookies, your data will be aggregated with all other user data.

Accept