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16K reactions · 1.2K comments | This is the story of how I was diagnosed with the terminal disease ALS at 25. #als #alsawareness #amyotrophiclateralsclerosis #mnd #motorneuronedisease #lougehrigsdisease #endals #raredisease #rarediseaseawareness #terminal #awareness #advocacy #education #disabled #disability | Mikey Stone | Facebook
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16K reactions · 1.2K comments | This is the story of how I was diag…
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How can we shorten the critical 12-14 month diagnostic delay in ALS? It starts in primary care by recognizing the key "red flag" symptoms: painless, progressive limb weakness, or progressive speech and swallowing issues with an unremarkable brain MRI. Spotting these signs early gets patients to a specialist faster. Learn to identify the key symptoms ➡️ https://www.facebook.com/events/1820767442204692 #CME #ALS #Neurology | Medscape
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How can we shorten the critical 12-14 month diagnostic delay in ALS…
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A delayed #ALS diagnosis can mean missed opportunities for treatment and loss of potential benefits. The thinkALS tool was created to combat this problem. Learn more on Connecting ALS: https://bit.ly/DiagnosisPod | The ALS Association
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16 reactions | Explore the #ALS journey – from early signs like muscle weakness to the challenges in mobility and speech , and the advanced phase with muscle atrophy and #paralysis . While there's no cure, the promise of #regenerativemedicine lights the path to better treatments. Stay informed and hopeful. #ALSawareness #lougehrigsdisease #MND | Advancells: Stem Cell Lab and Research | Facebook
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Can you spot the signs and symptoms of ALS? We'll tell you what to look out for. #ALSAware #ALSAwarenessMonth | The ALS Association
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Andrew Ross | My Own ALS Diagnosis | Educating on ALS/MND I want to share my own experience of getting diagnosed with ALS, as a follow-up to doctor... | Instagram
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