LGS Grupo de Esperanza - Reunión del grupo de apoyo de noviembr
2024-11-21 20:00 - 21:00 (America/New_York) | Virtual
Join us Thursday, November 21st at 8 pm ET
Nadie debería caminar solo en este sendero
El grupo de esperanza de LGS es un espacio seguro para reunirnos virtualmente y compartir nuestras historias.
Únase a las cuidadoras Bertha Guillén y Michele Torres cada mes mientras nos escuchamos, acompañamos y apoyamos mutuamente como madres y padres de niños con LGS.
Juntos somos más fuertes. Nadie debería caminar solo en este sendero. Todos son bienvenidos, ya sea que sea nuevo a LGS o tenga muchos años de experiencia. ¡Hay esperanza para nuestros niños!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Caregiver of Adults with LGS - Nov. Support Group Meeting
2024-11-25 20:00 - 21:00 (America/New_York) | Virtual
Join us Monday, November 25th at 8 pm ET
Living with LGS is a marathon, not a sprint.
Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great. Not only do the needs of the individual with LGS change in adulthood, but, so, too, do the needs of aging caregivers. We invite parents and caregivers of adults with LGS to join us for discussion and support as together we face the ever-changing challenges associated with LGS. (Parents of adolescents are also welcome to join the support group.)
Adult caregivers, Geraldine and Elizabeth host a monthly support group meetup to discuss the challenges associated with caring for an adult with Lennox-Gastaut Syndrome.

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

A New Musical: It's All Your Fault, Tyler Price!
2024-12-05 19:30 - 22:00 (America/Los_Angeles) | The Hudson Theatre, Santa Monica Boulevard, Los Angeles, CA, 90038, United States
Emmy winner Ben Decter (Lucifer) and Tony nominee Kristin Hanggi (Rock of Ages) have collaborated on a new musical, It’s All Your Fault, Tyler Price! The work will get a world premiere at the Hudson Theatre in Hollywood November 7-December 15. Opening night will be November 14th.
On December 5th, all proceeds will go directly to the LGS Foundation!
Click here to get your tickets now!
The musical follows a middle school kid who punches his bully, Tyler Price, defending his epileptic sister. His principal demands he explain himself to the entire school, which, naturally drives him to stage a musical.
“When my family was in crisis—my little girl, diagnosed with Lennox-Gastaut Syndrome, was having 100 seizures a day and we felt so isolated—I never imagined a musical would grow out of it. Writing these songs helped my family have difficult conversations and come together,” says Decter in a statement. “It’s All Your Fault, Tyler Price! is a fun, irreverent look at a family going through a really hard time—that everyone can relate to.”
“This musical is a true passion project for us. It’s about dealing with struggles in our families and how challenging it is to be seen by those closest to us,” adds Hanggi. “Through art, our characters learn to explore uncomfortable feelings—things that can be difficult to share or admit. We can’t wait for Los Angeles—where I’ve gotten the opportunity to launch other new musicals—to see our show!”
Sponsors and Community Partners for the upcoming production include Epilepsy Foundation, Epilepsy Foundation Los Angeles, the Lennox-Gastaut Syndrome (LGS) Foundation, The Children’s Ranch, and more.
Learn more about the amazing cast and show dates at TylerPriceMusical.com.
New Los Angeles Musical Highlights One Family’s Struggle to Live With Epilepsy and Lennox-Gastaut Syndrome

LGS Foundation @ AES
2024-12-06 - 2024-12-10 | THE LOS ANGELES CONVENTION CENTER, South Figueroa Street, Los Angeles, CA, 90015, United States
Join us at AES in Los Angeles, California
Are you attending the American Epilepsy Society Annual Meeting in December?
We invite you to stop by Booth N2148 in the Epilepsy Resource Area of the Exhibit Hall. Our team will be available from December 7 – 9, 2024 to support and assist with inquires.
Learn More

To learn more about the LGS Foundation’s Research Programs, visit our Finding the Cures, Together page.

Standing Together. Stronger Together. - January Support Group Meeting
2025-01-14 20:00 - 21:00 (America/New_York) | Virtual
Join us on Tuesday, January 14th at 8 pm ET.
Topic: Celebrating You in 2025!
LGS caregivers do not give themselves enough credit so let’s start the year off right. Let’s talk about you and all that you managed to pull off last year.
Maybe you advocated strongly at an IEP meeting. Maybe you started a new job. Maybe you got a massage or managed to finally shower every day. Let’s begin 2025 by pledging a strong commitment to honoring ourselves as caregivers, and so much more!

This monthly support group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

LGS Grupo de Esperanza
2025-01-16 20:00 - 21:00 (America/New_York) | Virtual
Join us Thursday, January 16th at 8 pm ET
Nadie debería caminar solo en este sendero
El grupo de esperanza de LGS es un espacio seguro para reunirnos virtualmente y compartir nuestras historias.
Únase a las cuidadoras Bertha Guillén y Michele Torres cada mes mientras nos escuchamos, acompañamos y apoyamos mutuamente como madres y padres de niños con LGS.
Juntos somos más fuertes. Nadie debería caminar solo en este sendero. Todos son bienvenidos, ya sea que sea nuevo a LGS o tenga muchos años de experiencia. ¡Hay esperanza para nuestros niños!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Dad to Dad - January Support Group Meeting
2025-01-21 20:00 - 21:00 (America/New_York) | Virtual
Join us Tuesday, January 21st at 8 pm ET
Hosted by dads, for dads.
Join our exclusive support group for male caregivers and Dads as we talk, share, and offer encouragement to each other along this LGS journey. Bring your favorite beverage and carve out some time for just you!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Caregiver of Adults with LGS - January Support Group Meeting
2025-01-27 20:00 - 21:00 (America/New_York) | Virtual
Join us Monday, January 27th at 8 pm ET
Living with LGS is a marathon, not a sprint.
Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great. Not only do the needs of the individual with LGS change in adulthood, but, so, too, do the needs of aging caregivers. We invite parents and caregivers of adults with LGS to join us for discussion and support as together we face the ever-changing challenges associated with LGS. (Parents of adolescents are also welcome to join the support group.)
Adult caregivers, Geraldine and Elizabeth host a monthly support group meetup to discuss the challenges associated with caring for an adult with Lennox-Gastaut Syndrome.

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Standing Together. Stronger Together. - February Support Group Meeting
2025-02-11 20:00 - 21:00 (America/New_York) | Virtual
Join us on Tuesday, February 11th at 8 pm ET.
Topic: It’s All About Love!
We shed a lot of tears as caregivers. Because we love so deeply and fight for our loved ones so fiercely. It isn’t always a heartbreaking love. There’s joy as well. With Valentine’s Day just around the corner, can we stop for a moment and celebrate LOVE?

This monthly support group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Dad to Dad - February Support Group Meeting
2025-02-18 20:00 - 21:00 (America/New_York) | Virtual
Join us Tuesday, February 18th at 8 pm ET
Hosted by dads, for dads.
Join our exclusive support group for male caregivers and Dads as we talk, share, and offer encouragement to each other along this LGS journey. Bring your favorite beverage and carve out some time for just you!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

LGS Grupo de Esperanza
2025-02-20 20:00 - 21:00 (America/New_York) | Virtual
Join us Thursday, February 20th at 8 pm ET
Nadie debería caminar solo en este sendero
El grupo de esperanza de LGS es un espacio seguro para reunirnos virtualmente y compartir nuestras historias.
Únase a las cuidadoras Bertha Guillén y Michele Torres cada mes mientras nos escuchamos, acompañamos y apoyamos mutuamente como madres y padres de niños con LGS.
Juntos somos más fuertes. Nadie debería caminar solo en este sendero. Todos son bienvenidos, ya sea que sea nuevo a LGS o tenga muchos años de experiencia. ¡Hay esperanza para nuestros niños!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Caregiver of Adults with LGS – February Support Group Meeting
2025-02-24 20:00 - 21:00 (America/New_York) | Virtual
Join us Monday, February 24th at 8 pm ET
Living with LGS is a marathon, not a sprint.
Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great. Not only do the needs of the individual with LGS change in adulthood, but, so, too, do the needs of aging caregivers. We invite parents and caregivers of adults with LGS to join us for discussion and support as together we face the ever-changing challenges associated with LGS. (Parents of adolescents are also welcome to join the support group.)
Adult caregivers, Geraldine and Elizabeth host a monthly support group meetup to discuss the challenges associated with caring for an adult with Lennox-Gastaut Syndrome.

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Standing Together. Stronger Together. - March Support Group Meeting
2025-03-11 19:00 - 21:00 (America/New_York) | Virtual
Join us on Tuesday, March 11th at 7 pm ET.
Topic: PTSD & the Impact of LGS on the Caregivers
Many LGS caregivers have expressed feeling traumatized from witnessing ongoing seizures and their effects on their loved ones.
Please join us for a special 2-hour support group that will begin with a recorded presentation from a trauma expert and mother of a child with catastrophic seizures. We’ll follow this talk with our support group and discussion.

This monthly support group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Dad to Dad - March Support Group Meeting
2025-03-18 20:00 - 21:00 (America/New_York) | Virtual
Join us Tuesday, March 18th at 8 pm ET
Hosted by dads, for dads.
Join our exclusive support group for male caregivers and Dads as we talk, share, and offer encouragement to each other along this LGS journey. Bring your favorite beverage and carve out some time for just you!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

LGS Grupo de Esperanza
2025-03-20 20:00 - 21:00 (America/New_York) | Virtual
Join us Thursday, March 20th at 8 pm ET
Nadie debería caminar solo en este sendero
El grupo de esperanza de LGS es un espacio seguro para reunirnos virtualmente y compartir nuestras historias.
Únase a las cuidadoras Bertha Guillén y Michele Torres cada mes mientras nos escuchamos, acompañamos y apoyamos mutuamente como madres y padres de niños con LGS.
Juntos somos más fuertes. Nadie debería caminar solo en este sendero. Todos son bienvenidos, ya sea que sea nuevo a LGS o tenga muchos años de experiencia. ¡Hay esperanza para nuestros niños!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Caregiver of Adults with LGS – March Support Group Meeting
2025-03-24 20:00 - 21:00 (America/New_York) | Virtual
Join us Monday, March 24th at 8 pm ET
Living with LGS is a marathon, not a sprint.
Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great. Not only do the needs of the individual with LGS change in adulthood, but, so, too, do the needs of aging caregivers. We invite parents and caregivers of adults with LGS to join us for discussion and support as together we face the ever-changing challenges associated with LGS. (Parents of adolescents are also welcome to join the support group.)
Adult caregivers, Geraldine and Elizabeth host a monthly support group meetup to discuss the challenges associated with caring for an adult with Lennox-Gastaut Syndrome.

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Standing Together. Stronger Together. - April Support Group Meeting
2025-04-08 20:00 - 21:00 (America/New_York) | Virtual
Join us on Tuesday, April 8th at 8 pm ET.
Topic: Spring is finally here. A time of new beginnings!
This has been a difficult winter for the LGS community. A lot of grief, a lot of new families, and as always, a lot of seizures. During these times, it’s more important than ever to connect with others. Join us! If you need to talk, we’ll always listen.

This monthly support group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Dad to Dad - April Support Group Meeting
2025-04-15 20:00 - 21:00 (America/New_York) | Virtual
Join us Tuesday, April 15th at 8 pm ET
Hosted by dads, for dads.
Join our exclusive support group for male caregivers and Dads as we talk, share, and offer encouragement to each other along this LGS journey. Bring your favorite beverage and carve out some time for just you!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

LGS Grupo de Esperanza - Reunión del Grupo de Apoyo de abril
2025-04-24 20:00 - 21:00 (America/New_York) | Virtual
Únase a nosotros el jueves 24 de abril a las 8 pm ET
Nadie debería caminar solo en este sendero
El grupo de esperanza de LGS es un espacio seguro para reunirnos virtualmente y compartir nuestras historias.
Únase a las cuidadoras Bertha Guillén y Michele Torres cada mes mientras nos escuchamos, acompañamos y apoyamos mutuamente como madres y padres de niños con LGS.
Juntos somos más fuertes. Nadie debería caminar solo en este sendero. Todos son bienvenidos, ya sea que sea nuevo a LGS o tenga muchos años de experiencia. ¡Hay esperanza para nuestros niños!

Este grupo mensual está disponible para familias LGS que son miembros de la Comunidad de apoyo a cuidadores en línea de la Fundación LGS.
Para unirse a nuestra comunidad en línea y obtener información de inicio de sesión, visite nuestro grupo en www.facebook.com/groups/lgsfoundation

10th Annual Walk ‘n’ Wheel for LGS Research
2025-04-26
Save the Date & Join us for Our
10th Annual Walk ‘n’ Wheel for LGS Research!
Saturday, April 26, 2025
This year, we are making LGS research history by uniting leading experts to create formal recommendations that will establish a standard of care for Lennox-Gastaut Syndrome (LGS). This consensus opinion will optimize treatment, provide a clear roadmap for patients, and serve as a vital stepping stone in LGS research.
This year’s 10th Annual Walk ‘n’ Wheel for LGS Research is more crucial than ever. Together, we are making huge strides toward a breakthrough and shaping the future of LGS treatments!

10:00am – 2:00pm ET

10:30am – 2:00pm ET

Help Support LGS Research – Get Involved Now!
Lo

Orlando, FL - LGS Walk & Wheel Color Run
2025-04-26 09:00 - 11:00 (America/New_York) | Waterleigh Phase 2 Amenity Field, 10697 Atwater Bay Drive, Winter Garden, FL, 34787, United States
🎨 LGS Walk & Wheel Color Run – Supporting Jacob’s Journey 🎨Join us for a morning of color, fun, and community spirit as we run (or walk or wheel!) to support the LGS Foundation and Jacob’s Journey.
🗓 Date: April 26⏰ Time: 9 AM – 11 AM💵 Entry Fee: $5 (All proceeds go to the LGS Foundation)
Get ready to get colorful for a great cause! Bring your friends, wear white, and let’s make a difference together!
Donate to Support Our Fundraising Efforts

SF Bay, CA Local Walk 'n' Wheel for LGS Research
2025-04-26 11:00 - 13:00 (America/Los_Angeles) | Buri Buri Park, 200 Arroyo Dr, South San Francisco, CA, 94080, United States
Calling All SF Bay Area Families!
Join us on April 26, 2025, at Buri Buri Park in South San Francisco, CA, as we Step Together for a Breakthrough.
Come join us for the SF Bay Area Local Walk ‘n’ Wheel for LGS Research—a fun and meaningful event where families, friends, and community members come together in support of those living with Lennox-Gastaut Syndrome (LGS). Whether you walk, roll, or cheer from the sidelines, we’ll unite side by side to show our strength, love, and commitment to making a difference.
This event is all about building connections, sharing experiences, and supporting one another. It’s a chance to meet others who understand the journey of living with LGS, find encouragement, and be inspired by the power of community.
Let’s walk together, celebrate our shared hope, and raise awareness for research that can make a real impact in the lives of those affected by LGS. We hope you’ll join us for this uplifting, community-driven event and help us step closer to a breakthrough!
This event is free to all LGS community members, donations are appreciated. We can’t wait to see you there!

Donate to Support Our Fundraising Efforts

Eubank, KY Local Walk 'n' Wheel for LGS Research
2025-04-26 11:00 - 13:30 (America/New_York) | Eubank Community Park, Bulldog Street, Eubank, KY, 42567, United States
Join us on April 26, 2025, at Eubank Community Park as We Step Together for a Breakthrough.
We’re excited to invite you to Tyler’s Walk on Wheels, a special event supporting the Lennox-Gastaut Syndrome (LGS) Foundation. This cause means so much to us because it’s personal – our son Tyler has LGS, and while he’s doing well with amazing doctors and care, we’re determined to help fund the research that could lead to better treatments and, ultimately, a cure.
All proceeds from the event will go directly to LGS research. We’ll have raffles, door prizes, t-shirts, and music to make it a fun, meaningful day. Most importantly, we’ll be walking together, showing support for Tyler and all families affected by LGS.
Your presence would mean the world to us as we continue the fight for a cure. Thank you for being part of this journey with us.
This event is free to all LGS community members, donations are appreciated. We can’t wait to see you there!
Donate to Support Our Fundraising Efforts
Register to Attend Tyler’s Walk

Colorado Springs, CO Local Walk 'n' Wheel for LGS Research
2025-04-26 11:00 - 15:00 (America/Phoenix) | Bear Creek Regional Park, 2002 Creek Crossing Street, Colorado Springs, CO, 80905, United States
Calling All Colorado Families!
Join us on April 26, 2025, at Bear Creek Regional Park as we Step Together for a Breakthrough.
This special event is an opportunity for families and friends to come together in support of those living with Lennox-Gastaut Syndrome (LGS). Whether you walk or roll, we’ll unite side by side to show our strength and solidarity.
It’s a time to connect with others who are navigating the same journey, to find support and inspiration, and to build a stronger community. We’ll take a walk around the park, then enjoy delicious food, uplifting music, and great company.
Let’s create new friendships, share our stories, and leave with smiles on our faces and hearts full of hope. Together, we make a difference.
This event is free to all LGS community members. We can’t wait to see you there!
Donate to support our fundraising efforts
Register to Attend

Caregiver of Adults with LGS - April Support Group Meeting
2025-04-28 20:00 - 21:00 (America/New_York) | Virtual
Join us Monday, April 28th at 8 pm ET
Living with LGS is a marathon, not a sprint.
Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great. Not only do the needs of the individual with LGS change in adulthood, but, so, too, do the needs of aging caregivers. We invite parents and caregivers of adults with LGS to join us for discussion and support as together we face the ever-changing challenges associated with LGS. (Parents of adolescents are also welcome to join the support group.)
Adult caregivers, Geraldine and Elizabeth host a monthly support group meetup to discuss the challenges associated with caring for an adult with Lennox-Gastaut Syndrome.

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Standing Together. Stronger Together. - May Support Group Meeting
2025-05-13 20:00 - 21:00 (America/New_York) | Virtual
Join us on Tuesday, May 13th at 8 pm ET.
Topic: Your Favorite Things!
What’s that thing that you need to get through the day? Is it your morning coffee? The 10-minute afternoon nap? The fully-charged iPad that will keep your loved one occupied so you can drink that coffee, or quietly close your eyes?
It’s always the little things in life that can be the BIGGEST things in life. We always hear “I don’t know how you do it”.
Join us and let us know, how do you do it?!

This monthly support group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

LGS Grupo de Esperanza - Reunión del Grupo de Apoyo de Mayo
2025-05-15 20:00 - 21:00 (America/New_York) | Virtual
Únase a nosotros el jueves 15 de mayo a las 8 pm ET
Nadie debería caminar solo en este sendero
El grupo de esperanza de LGS es un espacio seguro para reunirnos virtualmente y compartir nuestras historias.
Únase a las cuidadoras Bertha Guillén y Michele Torres cada mes mientras nos escuchamos, acompañamos y apoyamos mutuamente como madres y padres de niños con LGS.
Juntos somos más fuertes. Nadie debería caminar solo en este sendero. Todos son bienvenidos, ya sea que sea nuevo a LGS o tenga muchos años de experiencia. ¡Hay esperanza para nuestros niños!

Este grupo mensual está disponible para familias LGS que son miembros de la Comunidad de apoyo a cuidadores en línea de la Fundación LGS.
Para unirse a nuestra comunidad en línea y obtener información de inicio de sesión, visite nuestro grupo en www.facebook.com/groups/lgsfoundation

Caregiver of Adults with LGS - May Support Group Meeting
2025-05-19 20:00 - 21:00 (America/New_York) | Virtual
Join us Monday, May 19th at 8 pm ET
Living with LGS is a marathon, not a sprint.
Caring for an adult with LGS can be every bit as demanding as caring for a child with LGS, and the need for support is great. Not only do the needs of the individual with LGS change in adulthood, but, so, too, do the needs of aging caregivers. We invite parents and caregivers of adults with LGS to join us for discussion and support as together we face the ever-changing challenges associated with LGS. (Parents of adolescents are also welcome to join the support group.)
Adult caregivers, Geraldine and Elizabeth host a monthly support group meetup to discuss the challenges associated with caring for an adult with Lennox-Gastaut Syndrome.

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Dad to Dad - May Support Group Meeting
2025-05-20 20:00 - 21:00 (America/New_York) | Virtual
Join us Tuesday, May 20th at 8 pm ET
Hosted by dads, for dads.
Join our exclusive support group for male caregivers and Dads as we talk, share, and offer encouragement to each other along this LGS journey. Bring your favorite beverage and carve out some time for just you!

This monthly group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation

Standing Together. Stronger Together. - June Support Group Meeting
2025-06-10 20:00 - 21:00 (America/New_York) | Virtual
Join us on Tuesday, June 10th at 8 pm ET.
Topic: Managing the Business of LGS!
LGS is tough. Navigating all of the ‘systems’ shouldn’t have to be. But it is!!. It can often feel like you’re running a small business. Appointments, insurance denials, specialists, therapists, day programs, IEPs!! And who manages it all? YOU! Join all of the other ‘small business owners’ also known as ‘LGS Caregivers’, and let’s talk about it. Share your strategies, tips, and self-care ideas for when it gets to be too much!

This monthly support group is available to LGS families who are members of the LGS Foundation Online Caregiver Support Community.
To join our online community and for login information, please visit our group at www.facebook.com/groups/lgsfoundation
