<?xml version="1.0" encoding="UTF-8"?><rss version="2.0"><channel><title>DMD Awareness</title><description>Independent, source-linked information about Duchenne Muscular Dystrophy (DMD): what it is, how it progresses, current treatments, and the access debate shaping families today.</description><link>https://dmdawareness.com/</link><item><title>Heart Care in Duchenne: Why Monitoring Starts Early</title><link>https://dmdawareness.com/blog/heart-care-duchenne/</link><guid isPermaLink="true">https://dmdawareness.com/blog/heart-care-duchenne/</guid><description>DMD cardiomyopathy is now the leading cause of death in Duchenne. Early heart monitoring and cardio-protective therapy are core to current standards of care.</description><pubDate>Wed, 20 May 2026 00:00:00 GMT</pubDate><category>cardiac</category><category>care</category><category>monitoring</category><category>standards-of-care</category></item><item><title>DMD Patient Advocacy History and Impact</title><link>https://dmdawareness.com/blog/dmd-patient-advocacy-history/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dmd-patient-advocacy-history/</guid><description>Dmd patient advocacy history shows how families shaped research priorities, drug review, care standards, and access debates.</description><pubDate>Mon, 11 May 2026 00:00:00 GMT</pubDate><category>advocacy</category><category>history</category><category>policy</category></item><item><title>Health Misinformation Rare Disease Therapy Debates</title><link>https://dmdawareness.com/blog/health-misinformation-rare-disease/</link><guid isPermaLink="true">https://dmdawareness.com/blog/health-misinformation-rare-disease/</guid><description>Health misinformation rare disease debates can distort uncertainty, trust, access, and family decision-making around emerging therapies.</description><pubDate>Mon, 04 May 2026 00:00:00 GMT</pubDate><category>misinformation</category><category>rare-disease</category><category>access</category></item><item><title>Newborn Screening for Duchenne: Pros and Limits</title><link>https://dmdawareness.com/blog/newborn-screening-duchenne/</link><guid isPermaLink="true">https://dmdawareness.com/blog/newborn-screening-duchenne/</guid><description>Newborn screening for Duchenne may support earlier care and counseling, but evidence, ethics, and treatment access remain unsettled.</description><pubDate>Mon, 27 Apr 2026 00:00:00 GMT</pubDate><category>screening</category><category>newborns</category><category>diagnosis</category></item><item><title>Duchenne Treatment Access Georgia: What Happened</title><link>https://dmdawareness.com/blog/georgia-dmd-access-case/</link><guid isPermaLink="true">https://dmdawareness.com/blog/georgia-dmd-access-case/</guid><description>Duchenne treatment access in Georgia: how evidence, cost, protests, and misinformation collided in a rare disease care debate.</description><pubDate>Mon, 20 Apr 2026 00:00:00 GMT</pubDate><category>georgia</category><category>access</category><category>misinformation</category></item><item><title>DMD Treatment Access by Country: Why It Varies</title><link>https://dmdawareness.com/blog/dmd-treatment-access-by-country/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dmd-treatment-access-by-country/</guid><description>Dmd treatment access by country varies through regulators, payers, health technology assessment, pricing, and local budgets.</description><pubDate>Mon, 13 Apr 2026 00:00:00 GMT</pubDate><category>access</category><category>policy</category><category>global</category></item><item><title>DMD Transition to Adulthood: Planning Ahead</title><link>https://dmdawareness.com/blog/dmd-transition-to-adulthood/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dmd-transition-to-adulthood/</guid><description>Dmd transition to adulthood covers adult care, independence, assistive technology, education, work, and identity.</description><pubDate>Mon, 06 Apr 2026 00:00:00 GMT</pubDate><category>adulthood</category><category>transition</category><category>care</category></item><item><title>Mental Health Duchenne Muscular Dystrophy Guide</title><link>https://dmdawareness.com/blog/mental-health-duchenne/</link><guid isPermaLink="true">https://dmdawareness.com/blog/mental-health-duchenne/</guid><description>Mental health in Duchenne muscular dystrophy care: patients, parents, siblings, anxiety, depression, behavior, and caregiver strain.</description><pubDate>Mon, 30 Mar 2026 00:00:00 GMT</pubDate><category>mental-health</category><category>families</category><category>care</category></item><item><title>School Accommodations Duchenne Families Can Discuss</title><link>https://dmdawareness.com/blog/school-accommodations-duchenne/</link><guid isPermaLink="true">https://dmdawareness.com/blog/school-accommodations-duchenne/</guid><description>School accommodations for Duchenne can cover access, fatigue, learning, emergency planning, mobility, and inclusion in everyday school life.</description><pubDate>Mon, 23 Mar 2026 00:00:00 GMT</pubDate><category>school</category><category>inclusion</category><category>children</category></item><item><title>DMD Standards of Care: What Good Care Includes</title><link>https://dmdawareness.com/blog/dmd-standards-of-care/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dmd-standards-of-care/</guid><description>Dmd standards of care include coordinated neuromuscular, heart, lung, rehab, bone, nutrition, and psychosocial support.</description><pubDate>Mon, 16 Mar 2026 00:00:00 GMT</pubDate><category>care</category><category>standards</category><category>families</category></item><item><title>DMD Clinical Trial: A Family Reading Guide</title><link>https://dmdawareness.com/blog/dmd-clinical-trial/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dmd-clinical-trial/</guid><description>Use this dmd clinical trial guide to understand phases, endpoints, eligibility, placebo, risks, and questions for a care team.</description><pubDate>Mon, 09 Mar 2026 00:00:00 GMT</pubDate><category>clinical-trials</category><category>research</category><category>families</category></item><item><title>DMD Treatment Cost: Why Prices Are So High</title><link>https://dmdawareness.com/blog/dmd-treatment-cost/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dmd-treatment-cost/</guid><description>Understand dmd treatment cost factors, including rare disease economics, manufacturing, evidence uncertainty, and payer decisions.</description><pubDate>Mon, 02 Mar 2026 00:00:00 GMT</pubDate><category>access</category><category>cost</category><category>policy</category></item><item><title>Gene Therapy Duchenne Muscular Dystrophy Update</title><link>https://dmdawareness.com/blog/gene-therapy-duchenne/</link><guid isPermaLink="true">https://dmdawareness.com/blog/gene-therapy-duchenne/</guid><description>Gene therapy for Duchenne muscular dystrophy, updated: micro-dystrophin, FDA approval, safety signals, and the unresolved questions ahead.</description><pubDate>Mon, 23 Feb 2026 00:00:00 GMT</pubDate><category>gene-therapy</category><category>treatments</category><category>safety</category></item><item><title>Exon Skipping Duchenne Therapies Explained</title><link>https://dmdawareness.com/blog/exon-skipping-duchenne/</link><guid isPermaLink="true">https://dmdawareness.com/blog/exon-skipping-duchenne/</guid><description>Exon skipping for Duchenne, explained: who may qualify, why approvals differ across jurisdictions, and why evidence debates continue.</description><pubDate>Mon, 16 Feb 2026 00:00:00 GMT</pubDate><category>treatments</category><category>exon-skipping</category><category>genetics</category></item><item><title>Corticosteroids in Duchenne Muscular Dystrophy</title><link>https://dmdawareness.com/blog/corticosteroids-duchenne/</link><guid isPermaLink="true">https://dmdawareness.com/blog/corticosteroids-duchenne/</guid><description>Corticosteroids in Duchenne muscular dystrophy: evidence on benefits, side effects, and the treatment questions families can bring to clinicians.</description><pubDate>Mon, 09 Feb 2026 00:00:00 GMT</pubDate><category>treatments</category><category>steroids</category><category>care</category></item><item><title>DMD Diagnosis: From Suspicion to Confirmation</title><link>https://dmdawareness.com/blog/dmd-diagnosis-pathway/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dmd-diagnosis-pathway/</guid><description>Understand the dmd diagnosis pathway, from early symptoms and CK testing to genetic confirmation and specialist follow-up.</description><pubDate>Mon, 02 Feb 2026 00:00:00 GMT</pubDate><category>diagnosis</category><category>testing</category><category>genetics</category></item><item><title>Early Signs of Duchenne Muscular Dystrophy</title><link>https://dmdawareness.com/blog/early-signs-duchenne/</link><guid isPermaLink="true">https://dmdawareness.com/blog/early-signs-duchenne/</guid><description>Early signs of Duchenne muscular dystrophy include delayed walking, frequent falls, calf enlargement, and when to ask a clinician about testing.</description><pubDate>Mon, 26 Jan 2026 00:00:00 GMT</pubDate><category>symptoms</category><category>diagnosis</category><category>children</category></item><item><title>DMD Carrier Mother: What to Know</title><link>https://dmdawareness.com/blog/dmd-carrier-mothers/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dmd-carrier-mothers/</guid><description>A dmd carrier mother may need genetic counseling, family testing, and cardiac follow-up. Learn the questions to raise with clinicians.</description><pubDate>Mon, 19 Jan 2026 00:00:00 GMT</pubDate><category>carriers</category><category>genetics</category><category>heart</category></item><item><title>The Dystrophin Gene Explained Simply</title><link>https://dmdawareness.com/blog/dystrophin-gene-explained/</link><guid isPermaLink="true">https://dmdawareness.com/blog/dystrophin-gene-explained/</guid><description>This dystrophin gene explained guide covers what dystrophin does, how mutations disrupt muscle, and why results shape DMD care.</description><pubDate>Mon, 12 Jan 2026 00:00:00 GMT</pubDate><category>dmd</category><category>genetics</category><category>dystrophin</category></item><item><title>Duchenne vs Becker Muscular Dystrophy</title><link>https://dmdawareness.com/blog/duchenne-vs-becker/</link><guid isPermaLink="true">https://dmdawareness.com/blog/duchenne-vs-becker/</guid><description>Duchenne versus Becker muscular dystrophy in plain English: the shared gene, the different severity, and the diagnosis questions families ask.</description><pubDate>Mon, 05 Jan 2026 00:00:00 GMT</pubDate><category>dmd</category><category>becker</category><category>genetics</category></item><item><title>What Is Duchenne Muscular Dystrophy?</title><link>https://dmdawareness.com/blog/what-is-duchenne-muscular-dystrophy/</link><guid isPermaLink="true">https://dmdawareness.com/blog/what-is-duchenne-muscular-dystrophy/</guid><description>What is Duchenne muscular dystrophy? Why it affects muscle, how symptoms appear, and what families can ask their care team next.</description><pubDate>Mon, 29 Dec 2025 00:00:00 GMT</pubDate><category>dmd</category><category>basics</category><category>genetics</category></item><item><title>Welcome to DMD Awareness</title><link>https://dmdawareness.com/blog/welcome/</link><guid isPermaLink="true">https://dmdawareness.com/blog/welcome/</guid><description>Why this site exists, what we publish, and the editorial principles behind it.</description><pubDate>Sat, 15 Nov 2025 00:00:00 GMT</pubDate><category>meta</category><category>editorial</category></item><item><title>Two Mothers, Two Realities</title><link>https://dmdawareness.com/articles/two-mothers-two-realities/</link><guid isPermaLink="true">https://dmdawareness.com/articles/two-mothers-two-realities/</guid><description>A reported piece on Duchenne Muscular Dystrophy, access to treatment, and the role information plays in deciding who receives care in time.</description><pubDate>Sat, 01 Nov 2025 00:00:00 GMT</pubDate><category>access</category><category>families</category><category>georgia</category><category>misinformation</category></item></channel></rss>