SAN
DIEGO, July 8, 2024 /PRNewswire/ -- On
July 12, 2024, the LGS Foundation
will kick off its 9th International Family & Professional
Conference in Phoenix, Arizona.
The highly anticipated, 3-day hybrid conference unites global
leaders, healthcare professionals, family leaders, and advocates in
the fight against Lennox-Gastaut Syndrome (LGS). This
groundbreaking event will be a nexus for cutting-edge research,
innovative therapies, and community support initiatives.
LGS, a rare and severe form of epilepsy, presents complex
challenges for patients and caregivers worldwide. However, through
collaborative efforts, the landscape of treatment and care is
rapidly evolving. The conference serves as a platform to accelerate
progress and drive tangible change.
Participants can expect a diverse program featuring keynote
presentations, panel discussions, interactive workshops, and poster
sessions. Renowned experts will share the latest advancements in
LGS research, spanning genetics, neurology, pharmacology, and
holistic care approaches. Moreover, the conference will spotlight
patient stories, fostering empathy and understanding among
attendees.
"Making connections, especially in person, is so important for
our journey. It really does make it a little easier knowing we
aren't alone." - Lesa McLeod, LGS
Caregiver
Key themes of this years conference include:
- Innovative Therapies: Exploring novel treatment
modalities and pharmaceutical developments to enhance seizure
management and quality of life.
- Multidisciplinary Care: Emphasizing the importance
of collaborative care models.
- Community Empowerment: Amplifying the voices of
patients, caregivers, and advocates to drive policy change,
increase awareness, and reduce stigma.
"The LGS Foundation's Family & Professional Conference is
truly a highlight for those impacted by LGS," said Karen Groff, President of the Board of Directors
at the LGS Foundation and mom to a son with LGS. "We learn about
scientific updates, treatment options, and available programs and
resources. We laugh. We cry. We have fun. Most importantly
connections are made with other caregivers who understand this
difficult journey. We become a community of advocacy, hope, and
support that will one day find the cures for LGS."
"Attending the LGS conference is good for the mind, body, spirit
and soul." - Keshia Crum
For more information, visit the LGS Foundation's website.
About the LGS Foundation
The Lennox-Gastaut Syndrome
(LGS) Foundation is a nonprofit organization dedicated to improving
the lives of individuals impacted by LGS. It educates the public
about LGS, supports families living with the condition, and drives
research to find the cures.
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SOURCE Lennox-Gastaut Syndrome (LGS) Foundation