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Newborn twins fight rare genetic disease, family says itll costs millions of dollars to save their lives Month Week [Video] New parents are fighting to save the lives of their… dlvr.it/T6Btx9

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After living with SMA for three decades, Kevin Schaefer has learned to live well with his disease, not fight against it. If you’re trying to do the same, these tips might help: bit.ly/3Wo41SK

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In his latest vlog, Michael Morale weighs in on if he thinks insurance companies will pay for a combination therapy using apitegromab.

Check out our SMA vlogs here: bit.ly/3RKFmWl

In his latest vlog, Michael Morale weighs in on if he thinks insurance companies will pay for a combination therapy using apitegromab.

Check out our SMA vlogs here: bit.ly/3RKFmWl 

#SpinalMuscularAtrophy #SMAAwareness #SMACommunity #SMALife #LivingWithSMA
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The world of accessibility has improved by leaps and bounds over the past several decades, but DeAnn Runge wonders if we might be slowing down. See why in our forums: bit.ly/3U33McV

The world of accessibility has improved by leaps and bounds over the past several decades, but DeAnn Runge wonders if we might be slowing down. See why in our forums: bit.ly/3U33McV 

#SpinalMuscularAtrophy #SMAAwareness #SMACommunity #SMALife #LivingWithSMA
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