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MitoAction

MitoAction

Support, Education, Outreach and Advocacy for Children and Adults Living with Mitochondrial Disease

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Caroline Pereira Duraes

Sep 25, 2019

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Kearns Sayre Syndrome (KSS)

Caroline was a brave and happy little girl who liked to laugh and made others laugh. She had a positive impact on all who knew her. Even though severely ill for many years she never complained. She was often surrounded by her books and enjoyed time spent looking through them. But most of all she loved coloring, sometimes for hours at a time; her favorite colors were purple, pink and yellow. We miss her so much and are thinking about her every day!

Love Candido (dad), Anita (mom), and Gabriel (brother)

Upcoming
Events

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Oct 5
6:00 pm - 7:00 pm Event Series

CPEO & Me

Oct 6
12:00 pm - 1:00 pm

Expert Series: Ultra-Rare Mitochondrial Diseases: Development Challenges and Opportunities

Oct 6
1:15 pm - 2:15 pm

Weekly Support Call

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Expert
Series

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Upcoming Presentations

Oct 6
12:00 pm - 1:00 pm

Expert Series: Ultra-Rare Mitochondrial Diseases: Development Challenges and Opportunities

Nov 1
7:00 pm - 8:00 pm

Expert Series: LCHADD Retinopathy Update: Moving Toward a Treatment

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Last Presentation

Episode 2: Wondering Wednesdays: Ask the Genetic Counselor (February 22, 2023)
Presented August 28, 2023

P.O. Box 310
Novi, MI 48376
(888) 648-6228
info@mitoaction.org

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