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#Sclerodermas Reel by @sclerodermajourney_chelby - Thanking my family for participating in Rare Disease Day yesterday. This was lovely to see @rarediseasedayofficial #showyourstripes #sclerodermaawaren
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@sclerodermajourney_chelby
Thanking my family for participating in Rare Disease Day yesterday. This was lovely to see @rarediseasedayofficial #showyourstripes #sclerodermaawareness #sclerodermawarrior #helpfindacureforscleroderma
#Sclerodermas Reel by @themoexperience25 - #RareDiseaseDay #raredc2026 #themoexperience25 #RareButNotInvisible #sclerodermaawareness #EquityForRare
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@themoexperience25
#RareDiseaseDay #raredc2026 #themoexperience25 #RareButNotInvisible #sclerodermaawareness #EquityForRare
#Sclerodermas Reel by @road_back_foundation (verified account) - Is scleroderma a treatable infection?
The data from the Road Back Foundation patient community says this question must be asked.
In a review of 304 in
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@road_back_foundation
Is scleroderma a treatable infection? The data from the Road Back Foundation patient community says this question must be asked. In a review of 304 individuals diagnosed with systemic scleroderma who shared their outcomes on the RBF Patient Community Discussion Forum: • 221 patients (73%) reported remission • 82 patients (27%) reported noticeable improvement • Only 2 patients (<1%) reported no improvement Even more striking — among 97 scleroderma patients who reported being tested for Lyme disease: • 71 (73%) tested positive • 24 (25%) tested negative • Lyme testing is known to produce high false-negative rates These outcomes were reported by patients using antibiotic protocol therapy, a treatment approach first advanced by rheumatologist Dr. Thomas McPherson Brown and supported by decades of clinical experience. Yet today, most scleroderma patients are still placed on long-term immune-suppressing drugs — often without being screened for infectious triggers that may be driving the disease process. Before suppressing the immune system, shouldn’t we rule out infection? At Road Back Foundation, we believe: ✔️ Scleroderma should be evaluated as a potentially infection-driven illness ✔️ Patients deserve comprehensive screening before irreversible treatment decisions ✔️ First, do no harm must remain the guiding principle of care 📌 These data reflect real-world patient-reported outcomes from one of the largest scleroderma-focused communities in the world. 🔗 Learn more at RoadBack.org #Scleroderma #SystemicSclerosis #LymeDisease #LymeArthritis #InfectiousAutoimmunity #AntibioticProtocol #APTherapy #AutoimmuneDisease #RareDisease #PatientReportedOutcomes #MedicalFreedom #InformedConsent #ChronicIllness #Misdiagnosis #FunctionalMedicine #IntegrativeMedicine #RoadBackFoundation #FirstDoNoHarm
#Sclerodermas Reel by @sclerodermacan - Today on Rare Disease Day, we're talking about something that doesn't always get the spotlight - policy.
Policy might sound technical or political. Bu
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@sclerodermacan
Today on Rare Disease Day, we’re talking about something that doesn’t always get the spotlight — policy. Policy might sound technical or political. But for people living with rare diseases, policy is personal. It determines: • How long it takes to get diagnosed • Whether treatments are covered • If life-saving medications are affordable • How quickly new therapies are approved • Whether patients can access specialists close to home • How research is funded For rare diseases like systemic sclerosis, delays and gaps in the system don’t just create inconvenience — they compound disease burden. Diagnostic delays, limited drug access, and inconsistent coverage across provinces are not medical problems alone. They are policy problems. Good policy means: ✔ Faster diagnoses ✔ Fair and equitable drug access ✔ Investment in research ✔ Support for caregivers ✔ A stronger, more responsive health system On Rare Disease Day, we honour the strength of our community — and we reaffirm that advocacy matters. Because when policy improves, lives improve. #RareDiseaseDay #PolicyMatters #HealthEquity #RareDiseaseAdvocacy

✨ Guia de Descoberta #Sclerodermas

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🌟 Criadores em Destaque: @sclerodermacan, @sclerodermajourney_chelby, @road_back_foundation e outros lideram a comunidade

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💡 Posts top têm média de 439.5 visualizações (1.5x acima da média)

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🔥 #Sclerodermas mostra crescimento constante - publique consistentemente para construir presença

📹 Vídeos verticais de alta qualidade (9:16) funcionam melhor para #Sclerodermas - use boa iluminação e áudio claro

✍️ Legendas detalhadas com história funcionam bem - comprimento médio 809 caracteres

✨ Muitos criadores verificados estão ativos (25%) - estude o estilo de conteúdo deles

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Explorar Sclerodermas#linear scleroderma awareness month#morphea scleroderma#systemic scleroderma#scleroderma and autoimmune diseases#scleroderma awareness month#scleroderma morphea#scleroderma treatment options 2026#localized scleroderma