SMA Stole My Lifelong Dream: Having and Raising a Child
As a woman with SMA, the part I struggle with is accepting I have been cheated of the opportunity to carry a life inside me.
As a woman with SMA, the part I struggle with is accepting I have been cheated of the opportunity to carry a life inside me.
Living with spinal muscular atrophy (SMA), routine is something I greatly appreciate.
I’m immensely grateful for the opportunity to receive medication for my rare disease, spinal muscular atrophy (SMA).
Something I look forward to every summer is swimming. Being in a pool has many health benefits for people with spinal muscular atrophy (SMA).
As the years go by, I’m learning how living with spinal muscular atrophy (SMA) is an ongoing education.
When living with spinal muscular atrophy (SMA), Spring allergies can mimic the common cold and cause protracted health issues.
I find myself with new aches and pains as I blow out my candles each year of my life with spinal muscular atrophy (SMA).
You would assume in 2022 there would be a feasible way for those of us dependent on our wheelchairs to fly on a plane. However, that isn’t the case.
If less generic equipment was handed out for those with rare disabilities, it would help reduce other unnecessary costs.
Prior to a change during my bout with COVID-19, my medication, Evrysdi® (risdiplam) for spinal muscular atrophy (SMA), was fully covered by my insurance.