Dr. Tracy Dixon-Salazar(@TracyDixonSalaz) 's Twitter Profileg
Dr. Tracy Dixon-Salazar

@TracyDixonSalaz

Mom. Rare Disease & LGS Advocate. Neuroscientist. The largest most neglected healthcare resource, worldwide, is the patient. Executive Director @LGS_Foundation

ID:1528566637

linkhttp://lgsfoundation.org calendar_today18-06-2013 18:52:25

5,2K Tweets

2,7K Followers

974 Following

Dr. Tracy Dixon-Salazar(@TracyDixonSalaz) 's Twitter Profile Photo

Miss Pouty Pants doesn't want to train for her walk today. Maybe tomorrow. You can still cheer her on, though. Or even donate to this amazing cause if your heart leads you to. Thank you, friends. LGS Foundation

lgsfoundation.salsalabs.org/2024walkforlgs…

Miss Pouty Pants doesn't want to train for her walk today. Maybe tomorrow. You can still cheer her on, though. Or even donate to this amazing cause if your heart leads you to. Thank you, friends. @LGS_Foundation #epilepsy #intellectualdisability #autisim lgsfoundation.salsalabs.org/2024walkforlgs…
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Dr. Tracy Dixon-Salazar(@TracyDixonSalaz) 's Twitter Profile Photo

Savannah is walking a mile for LGS Research in 10 days! She’s working hard. If you’d like to support her, please send her your well wishes. And you can even donate.

Go Savannah, go!

lgsfoundation.salsalabs.org/2024walkforlgs…

Savannah’s Walk ‘n’ Wheel for LGS Research

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LGS Foundation(@LGS_Foundation) 's Twitter Profile Photo

The financial resource toolkit, found on the LGS Learning and Resource Center, provides financial planning, medical financial assistance, and general financial assistance links for sites that we feel contain useful information for families.

👉 Learn more: lgsfoundation.org/financial-reso…

The financial resource toolkit, found on the LGS Learning and Resource Center, provides financial planning, medical financial assistance, and general financial assistance links for sites that we feel contain useful information for families. 👉 Learn more: lgsfoundation.org/financial-reso…
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LGS Foundation(@LGS_Foundation) 's Twitter Profile Photo

Meet Haley! Haley was first diagnosed with infantile spasms at birth. Then, other severe seizures started happening, which led to an LGS diagnosis at age 14. Her mom said that Haley is non-verbal and non-ambulatory, but her spirit is grand.

Meet Haley! Haley was first diagnosed with infantile spasms at birth. Then, other severe seizures started happening, which led to an LGS diagnosis at age 14. Her mom said that Haley is non-verbal and non-ambulatory, but her spirit is grand. #LennoxGastautSyndrome #Epilepsy
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LGS Foundation(@LGS_Foundation) 's Twitter Profile Photo

Meet Natalie 👋 She served as the President of the LGS Foundation’s Board of Directors from 2020-2023 and is now serving as the Past President. She and her family have dedicated much of their lives to bringing awareness to others about seizures and .

Meet Natalie 👋 She served as the President of the LGS Foundation’s Board of Directors from 2020-2023 and is now serving as the Past President. She and her family have dedicated much of their lives to bringing awareness to others about seizures and #LennoxGastautSyndrome.
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Epilepsy Sparks(@EpilepsySparks) 's Twitter Profile Photo

🎉🗣️ Check out the contents covered in today’s podcast 🎧📹 the amazing neurologist & researcher Linda Dalic 🤩 from Austin Health 🇦🇺👇! Linda explains things in such an easy-to-understand way!

Here's the Chapters 📖

〰️ Meet Linda ⚡🧠
〰️ Deep Brain Stimulation (DBS) for…

🎉🗣️ Check out the contents covered in today’s podcast 🎧📹 the amazing neurologist & researcher Linda Dalic 🤩 from @Austin_Health 🇦🇺👇! Linda explains things in such an easy-to-understand way! Here's the Chapters 📖 〰️ Meet Linda ⚡🧠 〰️ Deep Brain Stimulation (DBS) for…
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Torie Robinson 🇺🇦(@TorieRobinson10) 's Twitter Profile Photo

😀 I don’t know if you’ll be as excited about the results as I, but…(!) In this week’s podcast, neurologist Linda Dalic 🇦🇺 shares with us the huuuuge seizure reduction in people with the rare 🧠 Lennox Gastaut Syndrome (LGS) - as the result of Deep Brain Stimulation…

😀 I don’t know if you’ll be as excited about the results as I, but…(!) In this week’s podcast, neurologist Linda Dalic 🇦🇺 shares with us the huuuuge seizure reduction in people with the rare #epilepsy 🧠 Lennox Gastaut Syndrome (LGS) - as the result of Deep Brain Stimulation…
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LGS Foundation(@LGS_Foundation) 's Twitter Profile Photo

The 9th Annual Walk ‘n’ Wheel for LGS Research is just ONE MONTH away! 📆

Join us on Saturday, April 20, 2024:
📍Kannapolis, NC
📍Tampa, FL
📍Virtually

🚨Sign up today to secure your t-shirt – available for both in-person and virtual attendees!

🔗 lgsfoundation.org/walk-n-wheel-f…

The 9th Annual Walk ‘n’ Wheel for LGS Research is just ONE MONTH away! 📆 Join us on Saturday, April 20, 2024: 📍Kannapolis, NC 📍Tampa, FL 📍Virtually 🚨Sign up today to secure your t-shirt – available for both in-person and virtual attendees! 🔗 lgsfoundation.org/walk-n-wheel-f…
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Aaron Warren(@aaewarren) 's Twitter Profile Photo

it’s online! we show that larger lesion volume, germline variants in GATOR1 genes, and connectivity with the default-mode network drive earlier seizure onset 😮

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LGS Foundation(@LGS_Foundation) 's Twitter Profile Photo

Last month, Advocates for LGS participated in Rare Disease Week on Capitol Hill. While there, they learned of current legislation aimed at supporting initiatives impacting the community.

Click to read the full story
🔗lgsfoundation.org/rare-disease-w…

Last month, Advocates for LGS participated in Rare Disease Week on Capitol Hill. While there, they learned of current legislation aimed at supporting initiatives impacting the #RareDisease community. Click to read the full story 🔗lgsfoundation.org/rare-disease-w… #LennoxGastautSyndrome
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LGS Foundation(@LGS_Foundation) 's Twitter Profile Photo

Meet Andrea! Andrea had a typical childhood, until the age of seven, when she experienced her first seizure. She was diagnosed with epilepsy after undergoing some testing, and later, was diagnosed with Lennox-Gastaut Syndrome.

Meet Andrea! Andrea had a typical childhood, until the age of seven, when she experienced her first seizure. She was diagnosed with epilepsy after undergoing some testing, and later, was diagnosed with Lennox-Gastaut Syndrome. #LennoxGastautSyndrome #Epilepsy #RareDisease
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LGS Foundation(@LGS_Foundation) 's Twitter Profile Photo

We're dedicated to providing a comprehensive LGS Learning & Resource Center! Here, you can learn about things like treatments for seizures, which offers a list of FDA-approved treatments often used in those with LGS.

🔗lgsfoundation.org/treatments-for…

We're dedicated to providing a comprehensive LGS Learning & Resource Center! Here, you can learn about things like treatments for seizures, which offers a list of FDA-approved treatments often used in those with LGS. 🔗lgsfoundation.org/treatments-for…
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