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Event Series Event Series: Parent Support Group

Parent Support Group

September 17, 2025 @ 7:00 pm - 8:00 pm

Free

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
September 17, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
May 15
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
May 20, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
May 17, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
December 17, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
July 17
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
July 15, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
July 19, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
March 18, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
August 21
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
August 19, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
August 16, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
June 17, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
October 16
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
October 21, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
October 18, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
September 16, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
November 20
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
November 18, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
November 15, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
December 16, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
January 15, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
January 20, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
March 17, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
February 19, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
February 17, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
June 16, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
April 16, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
April 21, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
September 15, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
May 21, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
May 19, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
December 15, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
July 16, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
July 21, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
March 20
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
March 15, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
August 20, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
August 18, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
June 19
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
June 21, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
October 15, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
October 20, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
September 18
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
September 20, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
November 19, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
November 17, 2027
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
December 18
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
January 17
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
January 21, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
January 19, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
March 19, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
February 21
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
February 18, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
February 16, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
June 18, 2025
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
April 17
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
April 15, 2026
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom

One of the best resources for the parent of a child with epilepsy are the experiences of other parents. This group welcomes parents and caregivers of young children, adults, and every age in between.

Hi! We are Matt and Lisa Daly. Our journey with the Epilepsy Foundation began when our 23 year old daughter, Caela, was diagnosed with epilepsy in 2019. At the time, she was a junior in college in Florida. We knew what epilepsy was, but had no idea what to do, where to turn or how to get help.  That’s when our family’s epilepsy journey began.  The Epilepsy Foundation helps us in our journey and assists us as we navigate this new world.  The support group has wonderful parents/guardians.  It is a time when we can ask questions, share our thoughts, challenges as well as our triumphs.

To this day, our daughter is drug-resistant.  So our journey for treatment and a cure continues.  As parents who are educators in public school districts, we feel blessed to have resources to turn to and help point us in the right direction as we continue to find what is going to work best for Caela.

To Register Email amy@epilepsyct.com.

Details

Date:
April 19, 2028
Time:
7:00 pm - 8:00 pm
Series:
Cost:
Free
Event Category:

Venue

Zoom