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17307 results for "family therapy"
Researchers in Melbourne have successfully tested a breakthrough treatment for ARFID, a complex eating disorder affecting up to 2% of young people. The therapy combines family support with emotional coping skills to help teens overcome severe food avoidance.
Volunteer therapy dogs are providing emotional support to young patients and their families at Phoenix Children's Hospital. The four-legged visitors help ease anxiety and bring moments of joy during difficult hospital stays.
Nearly 30% of Americans are estranged from immediate family members, but experts say many rifts can be healed with the right approach. Gerontologists and aging specialists are sharing practical strategies to help families reconnect before it's too late.
When the Caraballos moved to Rhode Island, they worried their big family wouldn't fit in. Then their widowed neighbor showed up with a ladder and became part of the family. ##
A safer gene therapy for Duchenne muscular dystrophy just hit a major milestone, bringing hope to families facing this fatal muscle disease. The treatment could offer a better option than current therapies linked to serious side effects.
A mental health clinic in Bonn, Germany is pioneering a family-first approach to depression treatment that's helping loved ones stay healthy while supporting their partners. The breakthrough insight: teaching family members to set boundaries actually helps everyone heal faster.
Over 100 descendants of Jacob and Mary Wagner gathered in Arthur, Wisconsin, to mark a century of unbroken family reunions. Few American families can claim such a remarkable milestone of connection across generations.
The Lawson family made history when both parents and their two daughters walked across the graduation stage together at Miami-Dade College. Their journey from Jamaica to South Florida led to a milestone few families ever achieve.
Over 720 faith leaders across Britain are standing together to protect refugee families from being separated. Their letter to the Home Secretary warns that restricting family reunions could push desperate people toward dangerous smuggling networks.
A Kansas City hospital will multiply its capacity to deliver breakthrough cell and gene therapies that can cure diseases with a single treatment. The expansion promises to bring life-changing care closer to home for families across the Midwest.
A pharmaceutical company has brought new hope to families affected by a rare disease by resurrecting a gene therapy program that was once thought lost. The treatment offers a second chance for patients in a community that had faced devastating setbacks.
A therapist noticed runners open up more easily while moving, sparking a growing trend in outdoor therapy sessions. Walk-and-talk therapy combines mental health support with the proven benefits of nature and exercise.
A new gene therapy for Duchenne muscular dystrophy met its main goal in trials, bringing hope to families facing this devastating disease. The treatment successfully helped 28 of 30 patients produce a crucial muscle protein that could slow disease progression.
Pharmaceutical company Roche announced a new clinical trial that could bring a life-changing gene therapy for Duchenne muscular dystrophy to young patients across Europe. The move comes after extensive feedback from families and regulators who want to see this treatment option become available.
An eight-month-old infant in Israel became the first person to receive groundbreaking gene therapy that restores missing brain function, potentially saving children from a devastating form of epilepsy. The treatment represents years of research turning into real hope for families facing ultra-rare genetic diseases.
Families with rare diseases who once had to travel overseas and raise hundreds of thousands of dollars for life-saving treatments now have hope. Congress just introduced legislation that would let patients access personalized gene therapies without waiting for FDA approval.
The FDA just made it easier for life-saving gene therapies to reach patients with ultra-rare diseases who previously had few treatment options. The new pathway means families won't have to wait years for cures when the science shows real promise.
The FDA just approved the first gene therapy to treat genetic hearing loss, giving hope to dozens of families each year whose babies are born deaf. Even better? The company is making it free for all U.S. patients.
For the first time in years, doctors have a promising new weapon against one of the deadliest cancers. A targeted therapy that blocks specific gene mutations is bringing fresh hope to pancreatic cancer patients and their families.
A groundbreaking gene therapy called AMT-130 has slowed Huntington's disease progression by 75% in clinical trials, offering hope to families who've waited 154 years for effective treatment. The one-time treatment could preserve patients' ability to walk, speak, and connect with loved ones for years longer.
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