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SMA Disease
255 reactions · 38 shares | Trying to understand a rare disease like #SMA without meeting people living with it is just impossible. The phrase ‘you just don’t get it, until you get it’ comes to mind. Sangeeta, Former Roche Patient Advocacy Lead for Rare Diseases, reflects on her first encounter with a young man whose life with SMA was eye-opening for all of us. #SMAAwarenessMonth | Roche Careers | Facebook
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255 reactions · 38 shares | Trying to understand a rare disease like #SMA without meeting people living with it is just impossible. The phrase ‘you just don’t get it, until you get it’ comes to mind. Sangeeta, Former Roche Patient Advocacy Lead for Rare Diseases, reflects on her first encounter with a young man whose life with SMA was eye-opening for all of us. #SMAAwarenessMonth | Roche Careers | Facebook
FacebookRoche Careers
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10K reactions · 1.4K shares | Today, the Jangra family is seeing their world slip away right in front of their eyes. Their baby’s SMA diagnosis has shattered them. They need ₹17.50 crores to save their son’s life. Spiritual and motivational speaker Jaya Kishori Ji has joined these parents’ fight for their baby’s life and requests you to come to their rescue. Together, let’s save baby Kanav from the horrors of this baby-killer disease.: https://bit.ly/3wmn8hP | Impact Guru | Facebook
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10K reactions · 1.4K shares | Today, the Jangra family is seeing their world slip away right in front of their eyes. Their baby’s SMA diagnosis has shattered them. They need ₹17.50 crores to save their son’s life. Spiritual and motivational speaker Jaya Kishori Ji has joined these parents’ fight for their baby’s life and requests you to come to their rescue. Together, let’s save baby Kanav from the horrors of this baby-killer disease.: https://bit.ly/3wmn8hP | Impact Guru | Facebook
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2.3M views · 10K reactions | Jaya Kishori Ji the spiritual speaker has joined the fight for baby kanav's life and requests you to come to his rescue. Jangra family is seeing their world slip away right in front of their eyes. Their baby’s SMA diagnosis has shattered thier heart. They need ₹17.50 crores to save their son’s life.Let’s save baby Kanav together from the deadly disease. Donate Now : https://bit.ly/3X2kj05 | Impact Guru | Facebook
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2.3M views · 10K reactions | Jaya Kishori Ji the spiritual speaker has joined the fight for baby kanav's life and requests you to come to his rescue. Jangra family is seeing their world slip away right in front of their eyes. Their baby’s SMA diagnosis has shattered thier heart. They need ₹17.50 crores to save their son’s life.Let’s save baby Kanav together from the deadly disease. Donate Now : https://bit.ly/3X2kj05 | Impact Guru | Facebook
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26 reactions | Meet Lyza. Lyza is 22 years old and has been on an approved treatment for spinal muscular atrophy (SMA) for over 7 years. While current treatments have helped her, she’s eager for more. “And there's so many things left to do. There is always room for more.” What would more mean to you? Visit Life Takes Muscle to explore what muscle strength means to people living with SMA: https://bit.ly/3P51CaB #SMAAwareness #CureSMA #SMAStrong | Life Takes Muscle | Facebook
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