Tech Tip: Export Limitation with the SMA Data Manager M - Sunny. SMA Corporate Blog
9:11
sma-sunny.com
Tech Tip: Export Limitation with the SMA Data Manager M - Sunny. SMA Corporate Blog
In this tech tip video, we demonstrate the required equipment and configuration needed to set up export limitation, including net zero export.
Mar 24, 2021
SMA Disease
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
0:37
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
FacebookImpact Guru
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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
1:14
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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2.2M views · 189K reactions | Ridhay Avinash Boliyar*, is battling a rare disease called *Spinal Muscular Atrophy Type 1 (SMA 1)*, for which we require funds amounting to approximately *₹9 crores*. We are hopeful that your love and support will help us overcome this challenging phase. Please contribute wholeheartedly, spread the word and keep Ridhay in your prayers❤️ #humanity #sharethelove #hussainmansuri | Hussain Mansuri | Facebook
1:18
2.2M views · 189K reactions | Ridhay Avinash Boliyar*, is battling a rare disease called *Spinal Muscular Atrophy Type 1 (SMA 1)*, for which we require funds amounting to approximately *₹9 crores*. We are hopeful that your love and support will help us overcome this challenging phase. Please contribute wholeheartedly, spread the word and keep Ridhay in your prayers❤️ #humanity #sharethelove #hussainmansuri | Hussain Mansuri | Facebook
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