Charles River Laboratories’ Post

As the parent of a child with FOXG1 Syndrome, Nasha Fitter is leading the charge to find a treatment for her daughter and other children with ultra-rare diseases. Learn more about the FOXG1 Research Foundation and how it wants to “give kids the life they deserve” in the season five finale of Vital Science. https://okt.to/h8Lldt

As the parent of a child with FOXG1 Syndrome, Nasha Fitter is leading the charge to find a treatment for her daughter and other children with ultra-rare diseases. Learn more about the FOXG1 Research Foundation and how it wants to “give kids the life they deserve” in the season five finale of Vital Science. https://okt.to/j9hqQf

As the parent of a child with FOXG1 Syndrome, Nasha Fitter is leading the charge to find a treatment for her daughter and other children with ultra-rare diseases. Learn more about the FOXG1 Research Foundation and how it wants to “give kids the life they deserve” in the season five finale of Vital Science. https://okt.to/wctyqn

As the parent of a child with FOXG1 Syndrome, Nasha Fitter is leading the charge to find a treatment for her daughter and other children with ultra-rare diseases. Learn more about the FOXG1 Research Foundation and how it wants to “give kids the life they deserve” in the season five finale of Vital Science. https://okt.to/nsybvz

As the parent of a child with FOXG1 Syndrome, Nasha Fitter is leading the charge to find a treatment for her daughter and other children with ultra-rare diseases. Learn more about the FOXG1 Research Foundation and how it wants to “give kids the life they deserve” in the season five finale of Vital Science. https://okt.to/zT28ID

As the parent of a child with FOXG1 Syndrome, Nasha Fitter is leading the charge to find a treatment for her daughter and other children with ultra-rare diseases. Learn more about the FOXG1 Research Foundation and how it wants to “give kids the life they deserve” in the season five finale of Vital Science. https://okt.to/07ymLw

Did you know that there are about 300 million people worldwide who have a RARE Disease? A rare disease or disorder is a condition that affects fewer than 200,000 individuals. There are currently more than 10,000 rare disorders that have been found (NORD, 2024). As TR professionals, part of our role is to raise awareness and to learn more about the people we may work with.  This year, we have a SUPER RARE Disease day, as we can celebrate it on February 29 - the rarest day of the year! Learn more about Rare Disease Day and Rare conditions below: https://lnkd.in/gmy43MXj https://lnkd.in/gk6hbAF

March is Autoimmune Awareness Month! Let's join hands to raise awareness and make a difference for those battling autoimmune disease. Together, we can: 1) Increase understanding 2) Advance research 3) Create hope for those living with autoimmune conditions. Educate yourself about autoimmune disease and explore ways you can contribute to a brighter future! Take the first step to get my FREE 7-Day Educational Email Course, and learn how to reverse and prevent autoimmune disease 👉https://lnkd.in/debzk2T4 #AutoimmuneDoctor #ChronicIllness #AutoimmuneFree #AutoimmunePrevention #AutoimmuneAwareness #RaiseAwareness #HopeForTomorrow #AutoimmuneAwarenessMonth

March is Autoimmune Awareness Month! Let's join hands to raise awareness and make a difference for those battling autoimmune disease. Together, we can: 1) Increase understanding 2) Advance research 3) Create hope for those living with autoimmune conditions. Educate yourself about autoimmune disease and explore ways you can contribute to a brighter future! Take the first step to get my FREE 7-Day Educational Email Course, and learn how to reverse and prevent autoimmune disease 👉https://lnkd.in/dmCiJ_s4 #AutoimmuneDoctor #ChronicIllness #AutoimmuneFree #AutoimmunePrevention #AutoimmuneAwareness #RaiseAwareness #HopeForTomorrow #AutoimmuneAwarenessMonth

The RARE Revolution Magazine has a new book series on Amazon! They say "Our series, Sibling Stories, helps siblings learn more about rare diseases. Although the series is about Angelman syndrome, it applies to many rare diseases." @Rare Sibling Stories #RareDisease #SiblingStories #AngelmanSyndrome