Understanding Pediatric Low-Grade Glioma Types & Treatments

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Pediatric low-grade gliomas (pLGG) are the most common type of brain tumor in children, with around 1700 cases diagnosed each year. Although these tumors grow and spread more slowly than high-grade tumors, half of the children who undergo surgery will end up relapsing and require additional treatments.
If your child has been diagnosed with pLGG, having a better understanding of this disease can help you make informed decisions about your child’s journey from diagnosis through survivorship. In our most recent webinar supported by Day One Biopharmaceuticals, Dr. Tab Cooney, the Medical Director of Day One Biopharmaceuticals, and the Pediatric Brain Tumor Foundation came together to educate the community about common types of pLGGs and treatments and have an opportunity to ask questions.
Learn more about upcoming webinars and view recordings of past webinars at curethekids.or....
#EndChildhoodCancer #plgg #childhoodcancer
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No one should have to face a child's brain tumor diagnosis alone. The Pediatric Brain Tumor Foundation is here for you with resources and programs to navigate every stage of the journey. If you or a family you know needs help, contact our Family Support team today at familysupport@curethekids.org and 800-253-6530.

Опубликовано:

5 окт 2024

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Комментарии : 5

@Na-ow7zg 3 месяца назад

Very interesting presentation. I’m suffering from this tumor in left since 2017, and sonic last year I feel weakness in leg in right side and also headache,dizziness, memory issues, speech issues sometimes. I from Saudi Arabia and I’m 42 years age.

@teneicepermission7143 Год назад

Thank you for the feedback about neuropsychological testing. I never thought to have my child tested or even myself. But I understand why it is helpful.

@teneicepermission7143 Год назад

Good Stuff.

@erikschlemmer9466 6 месяцев назад

Thank you for this information, my son has a low grade glioma located on his medulla and some along the pons located only on the right side. He has hearing loss on that side and a hemifacial spasm.

@PediatricBrainTumorFoundation 6 месяцев назад

Thank you for taking the time to watch this webinar and share about your son. If you’re ever in need of support to help you on your journey, we’re here to help. You can reach our Family Support team anytime at FamilySupport@curethekids.org, and we offer additional resources and information at curethekids.org/support-for-families.