Dr. Brenda Harris MD

Recommended Articles

• Breakthrough Research on Facioscapulohumeral Muscular Dystrophy

  A study which was recently published in the Natural Communications journal, outlines a major breakthrough in research around facioscapulohumeral muscular dystrophy, also known as FSHD.The study was performed by the University of Minnesota Medical School. Researchers at the university inserted the...

• Teen with Spinal Muscular Atrophy Being Kept Alive with Spinraza

  Many researchers and medical professionals today are constantly striving to better the opportunities for those diagnosed with a variety of diseases and conditions.  As time has progressed, these treatments have improved in their effectiveness, especially as those in the medical world begin to...

• A Great Resource for Muscular Dystrophy Patients and Caregivers

  There is a group of diseases which fall into the ‘neuromuscular disorders’ category and that are characterized by symptoms which, either directly or indirectly, impair the functioning of the muscles. The direct effect would be via the pathology of the voluntary muscle itself, while the indirect...

• Infant Botulism: Causes and Treatment

  What is infant botulism?Infant botulism is a serious illness in babies when they ingest Clostridium botulinum, a type of bacteria that produce harmful toxins in the body. The illness causes breathing problems and muscle weakness. However, this condition is quite rare. Each year, less than 100 infant...

• Was the Backlash Justified? 60 Minutes Portrayal of Max Whelan, a 12-Year-Old Boy with Severe Non-Verbal Autism

  12-year-old Max Whelan has severe non-verbal autism and an undiagnosed intellectual disability, which makes him prone to unpredictable violent behavior and destructive meltdowns. “He is unpredictable. One minute he will be aggressive, hitting and punching anything he can reach, and the next he...

• Duchenne Muscular Dystrophy Therapy Receives Rare Pediatric Disease Designation

  Duchenne Muscular Dystrophy is characterized by progressive muscle degeneration paired with weakness.  This is caused by the lack of dystrophin.  This protein is the key to muscles staying strong and uninjured.  This disorder is typically found when a person is very young, as early as three years...