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#rarediseaseawarenessmonth
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On behalf of the APS Foundation of America, Inc. (APSFA), we stand in solidarity with the millions of individuals and families worldwide observing Rare Disease Day.

#ShowYourStripes #RareDiseaseAwarenessMonth #AntiphospholipidSyndrome

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Donate Today

Support the 1 in 2000 Americans living with Antiphospholipid Syndrome, a rare autoimmune clotting disorder.

You can donate at apsfa.org/donate. We need to find a better treatments or a cure.

#ShowYourStripes #AntiphospholipidSyndrome #RareDiseaseAwarenessMonth

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Did you know?

Currently, there are more than 10,000 rare diseases identified.

#ShowYourStripes #RareDiseaseAwarenessMonth

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Did you know?

Any disease affecting fewer than 200,000 people in the US is considered rare.

#ShowYourStripes #RareDiseaseAwarenessMonth

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support networks, connecting patients and families facing similar challenges, which fosters a community of support and shared resources.

#RareDisease #RareDiseases #RareDiseaseAwarenessMonth #February #FeburaryIsRareDiseaseAwarenessMonth

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More than 30 Million Americans live with a rare disease. That's 1 in 10 of us.

#ShowYourStipes #rarediseaseawarenessmonth

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rare don"
care
February
Rare Disease
Awareness
Month
(RAREDISEASEMONTH | FEBRUARY2026 )
SRNA
connect. care. cure.™

rare don" care February Rare Disease Awareness Month (RAREDISEASEMONTH | FEBRUARY2026 ) SRNA connect. care. cure.™

Siegel Rare Neuroimmune
Association - The non-profit advocating for those those with ADEM, AFM, MOGAD, NMOSD, ON, and TM!

Having a rare disease is not easy. It is so much more than just a diagnosis. Finding support is difficult because not many people share the same diagnosis. The unanswered questions. The lack of experts close by. The psychological and emotional challenges. And the list goes on. Over 300 million people worldwide live with a rare disease.
28 February is Rare Disease Day, and since 2020, we at SRNA have decided to make the whole month of February
"SRNA's Rare Disease Month" because awareness of rare diseases should not be limited to just one day of the year.
We will be sharing stories, resources, facts, and helpful tips during the entire month of February.
Join us this month to share facts, your personal story, and raise awareness about your rare disorder!

Siegel Rare Neuroimmune Association - The non-profit advocating for those those with ADEM, AFM, MOGAD, NMOSD, ON, and TM! Having a rare disease is not easy. It is so much more than just a diagnosis. Finding support is difficult because not many people share the same diagnosis. The unanswered questions. The lack of experts close by. The psychological and emotional challenges. And the list goes on. Over 300 million people worldwide live with a rare disease. 28 February is Rare Disease Day, and since 2020, we at SRNA have decided to make the whole month of February "SRNA's Rare Disease Month" because awareness of rare diseases should not be limited to just one day of the year. We will be sharing stories, resources, facts, and helpful tips during the entire month of February. Join us this month to share facts, your personal story, and raise awareness about your rare disorder!

Goedemorgen! ✨ 28 februari is #RareDiseaseDay, maar heel februari is SRNA’s #RareDiseaseAwarenessMonth, omdat bewustwording van zeldzame ziekten niet beperkt mag zijn tot slechts één dag van het jaar. ❤️‍🔥💪

#ADEM #AFM #MOGAD #NMOSD #ON #TM &

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#rarediseaseawarenessmonth #antiphospholipidsyndrome

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#hisShirt (his) #manicpixiedreamgirl #PastMeWasBestMe #greenhairdontcare #rarediseaseawarenessmonth #crpsawareness #gastroparesisawareness #showyourstripes

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Happy #BlackHistoryMonth and #RareDiseaseAwarenessMonth ❤️
Rare Disease Day happens annually the last day of February as it's the rarest day of the year 🥹 #disability #chronicillness #marginalized #dei #AntisynthetaseSyndrome

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