Donate now for the #GivingTuesday double match to #EndThePain! Donate here: https://hope.pachyonychia.org/donate_paypal/ | Pachyonychia Congenita Project
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FacebookPachyonychia Congenita Project
PC Project exists so people like our PC friend here doesn’t have to manage on their own for years without a diagnosis. #EndThePain #GeneticTesting #Pachyonychia #RareDisease #PPKs #pEDDs | Pachyonychia Congenita Project
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PC Project exists so people like our PC friend here doesn’t have to manage on their own for years without a diagnosis. #EndThePain #GeneticTesting #Pachyonychia #RareDisease #PPKs #pEDDs | Pachyonychia Congenita Project
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FacebookPachyonychia Congenita Project
Jurre (11) heeft Pachyonychia Congenita, een zeldzame genetische aandoening van de huid. Hij vertelt Raïsha hoe hij daarmee omgaat: 'Tot mijn puberteit wordt het steeds erger.' #JZHMH | BNNVARA
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Jurre (11) heeft Pachyonychia Congenita, een zeldzame genetische aandoening van de huid. Hij vertelt Raïsha hoe hij daarmee omgaat: 'Tot mijn puberteit wordt het steeds erger.' #JZHMH | BNNVARA
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FacebookBNNVARA
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Sandra Lee, MD, FAAD on Instagram: "🧬 Thick, painful nails? Calluses that just won’t quit? 👀 I don't think this is a nail fungus, I think this is Pachyonychia Congenita — a rare genetic condition that affects the nails and skin.⁠ ⁠ 💡 Pro tip: While you can’t prevent a genetic condition like this, keeping thickened skin moisturized and treated with urea or lactic acid can make a big difference in comfort and confidence.👣💅⁠ ⁠ #DrPimplePopper #SkinSchool #PachyonychiaCongenita #DermDeepDive #K
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