"Graves' Disease by the Numbers" and "Hashimoto's Disease by the Numbers": Huge thanks to Claudia E. Guillén López, MD (Twitter/X: @claudiaegl92) for these excellent resources!
Graves'? Disease & Thyroid Foundation的动态
最相关的动态
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May is #LupusAwarenessMonth! DYK that over 5 million people live with this disease worldwide? Learn MORE at MORE: www.morethanlupus.com #LearnMoreatMore #MoreThanLupus #LAM24 #LupusAwareness
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product led as a cure to the feature factory disease? just one of the many benefits Shahzad Shaikh and I discuss in our deep dive on PLG and how to apply as you move up (or down) market read the recap and watch the full episode on my newsletter (linked below in comments)
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?? What is #hemophilia, and what does it mean to live with it? Learn more about this rare disease and discover how the WFH supports those with hemophilia: https://bit.ly/3VB5DHZ #BleedingDisorders #RareDisease
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The countdown to #RareDiseaseDay is on, but for those living with a #RareDisease, every day is Rare Disease Day. To learn more about how you can support the rare disease community, visit RareDiseaseDay.com.
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Navigating a rare disease is challenging but you should never feel alone in your journey. #krabbeconnect can help connect you to a mentor. Learn more at - https://lnkd.in/gYSBgZWq
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This statistic is tragic and frustrating, and one of the reasons Rare Disease Week is so important. With legislators gathered in Washington this week, we need every member of our community to stand up and be counted. Click the link below to sign and submit a pre-written letter to your legislator(s), then share this post to your feed. Click this link to get started and watch the tutorial on this page for full instructions: https://ow.ly/T8LN50QHXII #RareDC2024 #BattenAdvocatesForACure #BattenDisease #RareDisease
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What do you wish people understood about rare disease? ?? Share your story in the comments below for a chance to win 'Thriving Rare' by Becky Tilley, an inspirational rare disease read.? ? Let's get the conversation started!? ? -? ? #raredisease #rarediseases #rarediseasemonth #rarediseaseawareness #rarediseaseadvocacy #spoonies #spooniesupport #spooniestrong #zebrastrong #KnowRare
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World Psoriasis Day 2024 is coming on October 29th, and this year's theme is "Psoriatic Disease and the Family." Let's recognize the impact psoriatic disease has on both patients and their loved ones and work together to support and care for each other. ?? Download the campaign resources on the website: https://lnkd.in/dEkJzBQ7 #psoriaticfamily #WPD2024 #WorldPsoriasisDay2024
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This #huntingtonsdiseaseawarenessmonth we are asking people to take 5 minutes to learn about the disease Sufferers wished that people were more aware and empathetic towards #huntingtonsdisease Take 5 mins and help us build a more #compassionatecommunity Visit https://lnkd.in/dKaFnvUy #learnin5 #huntingtonsInthefamily #huntingtonsin5minutes
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Independent Consultant
9 个月Sadly my 11 year old granddaughter has thyroid cancer and Hashimoto was discovered in her lymph nodes too.