All
Search
Images
Videos
Shorts
Maps
News
More
Shopping
Flights
Travel
Notebook
Report an inappropriate content
Please select one of the options below.
Not Relevant
Offensive
Adult
Child Sexual Abuse
Spina Bifida
Awareness
Angelman Syndrome
Awareness
Cancer
Awareness
Tourette Syndrome
Awareness
Ovarian Cancer
Awareness
Down Syndrome
Awareness
ADHD
Awareness
Microcephaly
Awareness
Parkinson's Disease
Awareness
Alzheimer's Disease
Awareness
Ataxia
Awareness
Scoliosis
Awareness
Parkinson's
Awareness
Fetal Alcohol Syndrome
Awareness
Cystic Fibrosis
Awareness
Epilepsy
Awareness
Asthma
Awareness
Traumatic Brain Injury
Awareness
Cerebral Palsy
Awareness
Multiple Sclerosis
Awareness
Length
All
Short (less than 5 minutes)
Medium (5-20 minutes)
Long (more than 20 minutes)
Date
All
Past 24 hours
Past week
Past month
Past year
Resolution
All
Lower than 360p
360p or higher
480p or higher
720p or higher
1080p or higher
Source
All
Dailymotion
Vimeo
Metacafe
Hulu
VEVO
Myspace
MTV
CBS
Fox
CNN
MSN
Price
All
Free
Paid
Clear filters
SafeSearch:
Moderate
Strict
Moderate (default)
Off
Filter
Spina Bifida
Awareness
Angelman Syndrome
Awareness
Cancer
Awareness
Tourette Syndrome
Awareness
Ovarian Cancer
Awareness
Down Syndrome
Awareness
ADHD
Awareness
Microcephaly
Awareness
Parkinson's Disease
Awareness
Alzheimer's Disease
Awareness
Ataxia
Awareness
Scoliosis
Awareness
Parkinson's
Awareness
Fetal Alcohol Syndrome
Awareness
Cystic Fibrosis
Awareness
Epilepsy
Awareness
Asthma
Awareness
Traumatic Brain Injury
Awareness
Cerebral Palsy
Awareness
Multiple Sclerosis
Awareness
Litchfield mom runs Boston Marathon for daughter with spinal muscular atrophy
1 month ago
wmur.com
4:40
Spinal Muscular Atrophy Awareness Month
9 months ago
wsaz.com
Spinal Muscular Atrophy (SMA) | Biogen
Apr 6, 2023
biogen.com
2:14
Meet a 16-year-old who's raising awareness about Spinal Muscular Atrophy
Aug 8, 2019
9news.com
1:48
August is Spinal Muscular Atrophy (SMA) Awareness Month, and on this occasion, we'll be sharing voices from the SMA community. Danielle shares her family’s journey - from her own late diagnosis to raising two young children also living with SMA. Her story is one of resilience, progress, and hope for a better future. #SMAAwarenessMonth #BreakingDownBarriers #spinalmuscularatrophy | Muscular Dystrophy Canada
1.2K views
9 months ago
Facebook
Muscular Dystrophy Canada
1:27
🧠 Understanding Spinal Muscular Atrophy (SMA)🧠 Spinal Muscular Atrophy is a genetic disorder that affects the motor neurons in the spinal cord, leading to muscle weakness and atrophy. Here’s what you need to know: What is SMA? - Definition: A group of inherited disorders characterized by the degeneration of motor neurons, which are vital for muscle control. - Symptoms: Includes muscle weakness, difficulty in movement, and in severe cases, respiratory issues. Who is at Risk? - Genetics:Individu
3.4K views
4 months ago
Facebook
Lorraine MY Physio
0:45
August is Spinal Muscular Atrophy Awareness month Learn more about what SMA is, the early symptoms Read lived experiences of persons with SMA on www.patientsengage.com Note that there is a support group for SMA in India as well: @Cure SMA India Cure SMA #SMAAwarenessMonth #spinalmuscularatrophy | PatientsEngage
265 views
Aug 25, 2024
Facebook
PatientsEngage
Living with Spinal Muscular Atrophy
Aug 9, 2024
citynews.ca
1:24
Spinal muscular atrophy (SMA) treatment has come a long way, from no options to three approved treatments and real hope. But access is still unequal across Canada. This SMA Awareness Month, we’re calling for fair treatment for every person with SMA. #SMAAwarenessMonth | Muscular Dystrophy Canada
1.1K views
9 months ago
Facebook
Muscular Dystrophy Canada
1:01
Brianna, an adult living with spinal muscular atrophy (SMA), wants movies and books to highlight the experiences of people with disabilities like her. Share Brianna’s story to help raise awareness about adults living with #SMA. | Genentech
82.8K views
Oct 3, 2019
Facebook
Genentech
5:56
Stars of new musical 'Most Likely Not To...' shine a light on spinal muscular atrophy
Feb 29, 2024
NBC News
1:18
Jesy Nelson discusses the incredible response to her post about Spinal Muscular Atrophy (SMA) and the impact raising awareness can have. | This Morning
72.1K views
4 months ago
Facebook
This Morning
1:09
We’re passionate about supporting the spinal muscular atrophy (SMA) community and helping people along their journey. New innovations in the past few years have redefined what it means to live with SMA. Hear what inspires and gives us hope as we close out SMA Awareness Month: | Biogen
18.2K views
Aug 31, 2022
Facebook
Biogen
West Michigan dad bikes 80 miles for Spinal Muscular Atrophy Awareness and Lori's Voice
Aug 13, 2021
fox17online.com
12:59
Spinraza High-Dose: The Treatment SMA Families Are Talking About | Victortheinspiration
10 views
3 weeks ago
YouTube
SMA Victor
5:55
#savemokshagna | Fighting Spinal Muscular Atrophy (SMA Type 1) | Awareness & Fundraiser@
316 views
1 month ago
YouTube
PHARMA LEARNING HUB
0:30
🚨 4 Month Baby Needs ₹16 Crore to Live 😢 | Save Ruthvika 💔🙏
8.8K views
4 weeks ago
YouTube
OC Square
0:46
Jesy's Heartwarming Moment: Baby's First Words!
43 views
2 weeks ago
YouTube
Gossip Glimpse
1:35
ITV News on Instagram: "Former Little Mix singer Jesy Nelson has said she feels she has a “duty of care” to raise awareness about the rare genetic condition her twins have been diagnosed with. The 34-year-old singer, who gave birth to twins Ocean Jade and Story Monroe Nelson-Foster prematurely in May with fiance Zion Foster, announced in a post on Sunday that the pair are unlikely to ever be able to walk after being diagnosed with SMA1 (spinal muscular atrophy). #itvnews #littlemix #jesynelson #
58.8K views
4 months ago
Instagram
itvnews
1:53
Sign the Petition for Spinal Muscular Atrophy Awareness
45.2K views
3 months ago
TikTok
nannyamies
1:19
Aashqeen on Instagram: "Why does one injection cost ₹17 crore? 😮 The reality behind the ₹17 crore SMA injection, also known as Zolgensma, the world’s most expensive medicine. . From why SMA (Spinal Muscular Atrophy) is so dangerous, to how gene therapy works, to why families in India are forced to raise ₹17 crore through crowdfunding. This video highlights the struggles of parents the harsh reality of rare disease treatment in India. . . . #sma #spinalmuscularatrophy #infotainment #reelkarofeel
1K views
6 months ago
Instagram
aashqeenplus
4:36
SMA Awareness: Supporting Spinal Muscular Atrophy Initiatives
1.5K views
4 months ago
TikTok
hannahlaidlerxo
0:52
Raising Awareness for Spinal Muscular Atrophy
1.8K views
4 months ago
TikTok
jesyangelic
Jesy Nelson Reveals Twins' Rare Diagnosis—What Parents Need To Know About Spinal Muscular Atrophy
4 months ago
parents.com
0:10
Understanding Spinal Muscular Atrophy and Awareness
7 months ago
TikTok
mrs_starling87
Tess Daly ♿️💋 | I don’t think I’ve ever done a dedicated video about my disability, so seeing as its Spinal Muscular Atrophy awareness month, now felt like... | Instagram
8 months ago
Instagram
1:58
Understanding Spinal Muscular Atrophy (SMA)
183.2K views
Jul 24, 2020
YouTube
Genentech
1:28
Measuring the SMA Experience: Laura’s Story
9.5K views
Jul 27, 2020
YouTube
Genentech
21:21
Meet Shane, live life to the fullest | My Last Days
3.7M views
Apr 8, 2013
YouTube
SoulPancake
1:44
Danyelle’s Story – Raising Two Children with Spinal Muscular Atrophy (SMA)
32.4K views
Dec 6, 2017
YouTube
Biogen
See more
More like this
Feedback