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Balancing Your SMA-Affected Child’s Nutrition

Posted: July 1st, 2011 | By: Staff | No Comments
Friday, July 1st, 2011
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Do you have questions about your SMA-affected child’s diet, nutrition and growth? Ms. Erin Seffrood, a Pediatric Clinical Nutritionist at the University of Wisconsin/American Family Children’s Hospital, has helpful advice for parents on how to balance dietary needs with physical development.

Ms. Seffrood offers an informative overview of the ‘elemental diet’ (also known as the ‘amino acid diet’), discusses its unique origin, and explains the need for more scientific research:

Ms. Seffrood addresses concerns parents have about their SMA-affected child’s weight and discusses the concept of ‘ideal weight’ in relation to monitoring a child’s growth:

Ms. Seffrood offers detailed insight on the use of growth charts for SMA-affected children, and explains the importance of personal observation and first-hand monitoring when considering the child’s growth:

Ms. Seffrood shares useful information on how to manage an SMA-affected child’s caloric intake and advises on which important aspects must be considered when monitoring the individual’s diet:

If you have questions or concerns about the information provided here, please contact FightSMA.

(Special thanks to Rich Bailey and Metro Video Productions.)

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Categories : Spinal Muscular Atrophy Science and Research, Spinal Muscular Atrophy Videos
 

Is SMA Keeping You or Your Child from a Good Night’s Sleep? Our Pediatric Specialists Offer Insight and Solutions

Posted: June 30th, 2011 | By: Staff | No Comments
Thursday, June 30th, 2011
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As SMA-affected families know all too well, SMA can harshly diminish both the caregiver’s and the patient’s ability to achieve quality rest. However, in the midst of the numerous other medical challenges that SMA often presents, the treatment of reduced sleep quality has had the potential to be an overlooked topic. At our recent Annual Conference in Washington, D.C., our panel of medical experts offered recommendations and support for caregivers who wish to improve their own or their loved one’s overall sleep health.


Pediatric Orthopedist Dr. Craig P. Eberson of Hasbro Children’s Hospital discusses the sleep issues associated with the SMA-affected and their caregivers, and shares his ideas for improving an individual’s physical comfort at bedtime:


Dr. Nanci Yuan, a Pediatric Pulmonologist and Board-Certified Sleep Medicine Physician at the Lucile Salter Packard Children’s Hospital at Stanford, notes that the current lack of education about SMA-related sleeping issues naturally inhibits diagnosis and treatment for these problems. Here, she offers her insight on respiratory problems in relation to sleep, and also addresses the severe role that poor sleep quality plays in the health of the SMA-affected and their caregivers:


Dr. Carolina Tesi-Rocha, a Pediatric Neurologist at Children’s National Medical Center, and Dr. Sandra Reyna, Co-Director of the Pediatric Motor Disorders Research Program at the University of Utah, discuss the multi-faceted reasons that the SMA-affected are likely to experience sleeping difficulties. They offer several recommendations for caregivers who may be struggling with sleep disorders of their own:


If you have questions or concerns about the information provided here, please contact FightSMA.

(Special thanks to Rich Bailey and Metro Video Productions.)

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Categories : FightSMA Articles, Spinal Muscular Atrophy Science and Research
 

Inspiration from Jake and Allie: A Story of Two Very Special Fighter Kids

Posted: June 29th, 2011 | By: Staff | 5 Comments
Wednesday, June 29th, 2011
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Little Allie (Jake's twin sister)

One of our young friends, Jake Brenner of New York, was recently charged with developing and completing an ‘Interpersonal Project’ for his school.  Jake, who lost his twin sister, Allie, to SMA when they were both nearly a year old, made it his goal that he would educate his school and community about this devastating disease. Going above the call and duty of the assignment, he also decided to raise money for an SMA cure by selling our blue FightSMA wristbands throughout his school and neighborhood.  Jake put a lot of time and special effort into this pursuit, and from these sales, he was able to raise quite a wonderful donation sum for SMA research.  All in all, his entire project was a marvelous success, and he received an ‘A+’ on the assignment from his teacher.

Jake, hard at work in his neighborhood

Jake recently turned thirteen, as would have Allie, and we are deeply humbled that he has chosen to honor her memory through this gracious contribution. Jake is such an incredibly well-spoken young fellow, so we’ll let him tell you more about it in his own words:

“On May 9, 1998, I wasn’t born alone. My twin sister Allie was also born that day. After about nine months of a happy life, we discovered that she had type 1 of Spinal Muscular Atrophy, the uncured and fatal disease that slowly saps away your muscle strength (to put it in simple terms.) On April 21, 1999, Allie lost her fight against the disease, less than a month from turning one. After learning this story, I knew I had to help, and this was the perfect opportunity.

“Thousands of infants die each year from SMA.  1 in 25 adults carry the SMA gene, and if both adults have the gene, their baby has a one in four chance of getting this uncured disease. Plus, most Americans have never heard of this disease. This is a major problem that together we can fix by finding a cure for SMA. I decided to raise awareness of SMA, make a flyer, and help my dad with his company by making an online donation site for SMA.

“To raise awareness of SMA, I told a lot of people my story and all about the disease. I also handed out pamphlets and postcards to my neighborhood telling them about the disease and telling them that I will be selling wristbands next week. After this, I made a flyer about selling the wristbands and about this disease. I put this flyer up at school and distributed them around my neighborhood. Finally, this week I helped my dad build an online donation site for SMA.

“I did so much better than I ever thought I would do! I called FightSMA and told them the amount of money I raised. They were ecstatic.  My money is going to researching for a cure, and about a month ago they had a breakthrough and the charity will need this money to help fund this research. I have learned a lot from this project. I learned that doing charity work, even a little, can go a long way. I learned that with my hard work, I am helping find a cure and save infants’ lives.  And I will definitely continue raising money until we find a cure.”

We are so overwhelmed with appreciation for all Jake’s hard work and accomplishments, and we are incredibly moved by the beauty of his actions.  We know that his whole family is very proud of him, too.

If you’re like Jake, and you would like to contribute to SMA awareness and education in your area, or if you are interested in learning more about what you can do support our research for a cure, please contact FightSMA.)

(Special thanks to the Brenner family.)

Comments (5)
Categories : Fighter Kids, FighterMom News, FightSMA Articles, FightSMA News, Spinal Muscular Atrophy Families and Friends
 

Applications Invited for New SMA Study

Posted: June 15th, 2011 | By: Staff | No Comments
Wednesday, June 15th, 2011
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The National Institutes of Health (NIH) has recently posted a funding opportunity announcement (FOA), issued by NINDS, to invite applications for a study of candidate biomarkers in Spinal Muscular Atrophy (SMA). According to the documentation:

The study will be done using the NeuroNEXT infrastructure (as established in response to RFA-NS-11-009, RFA-NS-11-010, RFA-NS-11-008) along with ad hoc clinical sites as appropriate.

This is a milestone-driven cooperative agreement program involving participation of NIH staff in the development of the project plan and monitoring of research progress.

The date for earliest submission is August 1, and applications are due by September 1  at 5pm.  For more information, follow this link.

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Categories : Spinal Muscular Atrophy Science and Research
 

Children’s Hospital in Boston Working on a New Approach to SMA Treatment

Posted: June 7th, 2011 | By: Staff | No Comments
Tuesday, June 7th, 2011
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Researchers at Children’s Hospital are looking into a new direction that they hope will eventually lead to a treatment for spinal muscular atrophy.  According to a news release published by the hospital:

The new findings reveal that loss of the SMA gene – and resulting depletion of a protein called SMN – makes nerve fibers from the spinal cord unable to navigate toward and form synapses (connections) with the muscles they’re meant to control. But they also demonstrate that this problem could be reversed in a zebrafish model of the disease.

To figure out the function of the SMN protein, the researchers, led by Mustafa Sahin, MD, PhD, and Judith Steen, PhD, of Children’s F.M. Kirby Neurobiology Center, began by asking what SMN interacts with. They used mass spectrometry, a technique from proteomics, to see what proteins SMN binds to.

One protein, called HuD, was a strong hit. The team also showed that SMN and HuD are found together in the nerve fibers (axons) that branch from motor neurons, and that both bind to RNAs that seem to regulate the production of another protein, neuritin (also called cpg15).

Sahin then collaborated with Christine Beattie, PhD, (The Ohio State University) who had developed a zebrafish model of this disease. When the SMN protein was blocked in zebrafish embryos, the axons were clearly abnormal. “They branch in the wrong directions and don’t really reach the right muscle,” says Sahin. “We thought this could be due to neuritin loss and asked, ‘can we put back neuritin and make the axons normal?’”

When they stimulated production of neuritin artificially – by injecting neuritin RNA into zebrafish embryos — the axons branched normally from the spinal cord and made normal connections to muscle.

Read the entire news release here.

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Categories : Spinal Muscular Atrophy Science and Research
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