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Rare Disease Connect Profile
Rare Disease Connect

@chronicallysass

Followers
271
Following
43
Media
115
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1K

Raising awareness for rare diseases #Stiffpersonsyndrome patient Living to be the healthiest I can be while keeping a good spirit, attitude and loving others ❤️

Nashville, TN
Joined August 2016
Don't wanna be here? Send us removal request.
@dazzle4rare
dazzle4rare
3 years
@colormystripes The lovely @chronicallysass is the Human who runs the FB page. She has been a #Dazzle4Rare OG & absolute awesome person!
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@chronicallysass
Rare Disease Connect
3 years
Do you remember when you joined Twitter? I do! #MyTwitterAnniversary
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@PatientWorthy
Patient Worthy
3 years
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@chronicallysass
Rare Disease Connect
3 years
Anxiety and depression, the unwanted accomplice to #raredisease and #chronicillness some days they take over and all I can do is try to sleep them away
@FibroFlutters
Flutters and Strutters (Formerly FibroFlutters)
3 years
#MentalHealth affects us all in different ways when living day to day with #rarediseases & #chronicillness. It doesn't matter whether you are male or female ➡ talking to others & knowing you are among people that also have #anxiety can really help. #Health #Dazzle4Rare
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@SeqComplete
SeqComplete
3 years
#RareDisease @iPainOfficial: '#Dazzle4Rare - is a cross-community of support for undiagnosed & rare disease awareness. Unlike most awareness events, this week is meant to enable #raredisease communities of all sizes to … https://t.co/XUgpZ8gbbQ, see more
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@dazzle4rare
dazzle4rare
3 years
United Advocacy Australia @unitedadvocacy unites with non-profit organizations around the globe, helping to raise awareness for many conditions. Let’s #Dazzle4Rare!
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@ncbrsfoundation
NCBRS Worldwide Foundation - Nicolaides Baraitser
3 years
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@dazzle4rare
dazzle4rare
3 years
Thank you to these beautiful faces. When you share my message about #RareDisease I reach your family & friends. When I share yours, I do the same. So, what do YOU want others to know about your NPO, advocacy, or personal experience during #Dazzle4Rare
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@amyholmanturner
StiffPersonSyndome
3 years
The United Porphyrias Association is committed to improving the quality of life of the porphyria patient community and is relentlessly focused on advancing disease awareness, research, and therapies in all the porphyrias. #Dazzle4Rare
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@aneinternationa
ANE International
3 years
This is why we #Dazzle4Rare. Destan's family bravely share their son's battle with #Covid19 associated #AcuteNecrotizingEncephalopathy "...it was like everything just went away... all the happiness, all the innocence... " https://t.co/kVFCCuikor @dazzle4rare #ANEawareness
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@ncbrsfoundation
NCBRS Worldwide Foundation - Nicolaides Baraitser
3 years
Today we are sharing about other organisations, advocates and more as part of #Dazzle4Rare2022... Make sure to follow our posts to learn more... 🧡💚💙 #Dazzle4Rare #WeAreRareFamily #NCBRS #NCBRSRare @dazzle4rare
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@unitedadvocacy
Judy-The United Advocate
3 years
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@RareBeacon
Beacon for Rare Diseases
3 years
#PatientGroups provide the emotional support after a #RareDiagnosis They provide the understanding & medical info needed to make informed decisions about one’s health Without patient groups, rare patients and their families would be left overwhelmed, isolated and misunderstood.
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@chronicallysass
Rare Disease Connect
3 years
Ugh 😔headlines like this give me serious Ick. There has to be a better way to bring attention to #RareDisease without further ostracizing an already underrepresented community #dazzle4rare #stiffpersonsyndrome
@GillianHSapia
Gillian Sapia RN
3 years
I hate articles that label #raredisease as “weird” or “strange” we aren’t a freak show. I hate this language because there is real person behind each dx #medicalminority #pavethewayfda
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@Ataxia_and_Me
Ataxia and Me CIO 1184030
3 years
today on #Dazzle4Rare its the 10th of August ... Ataxia is rare. #Friedreich’s #ataxia, which is the most common type of hereditary ataxia, affects approximately 1 in every 50,000 people. #kNOwATAXIA our #animations at https://t.co/ettiRxVuJv (by @SondraB_RareQoL
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@dazzle4rare
dazzle4rare
3 years
Want 2 make a difference 4 the #Gastroparesis community? Join us on FB https://t.co/CTQIUeJOdm or see https://t.co/DQV7qmGfTJ #Dazzle4Rare
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@FibroFlutters
Flutters and Strutters (Formerly FibroFlutters)
3 years
#MentalHealth affects us all in different ways when living day to day with #rarediseases & #chronicillness. It doesn't matter whether you are male or female ➡ talking to others & knowing you are among people that also have #anxiety can really help. #Health #Dazzle4Rare
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@chronicallysass
Rare Disease Connect
3 years
… but they never go away quite so easily and never for long. Being able to relate to others in the rare disease community makes having #stiffpersonsyndrome a little more tolerable…
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@chronicallysass
Rare Disease Connect
3 years
Anxiety and depression, the unwanted accomplice to #raredisease and #chronicillness some days they take over and all I can do is try to sleep them away
@FibroFlutters
Flutters and Strutters (Formerly FibroFlutters)
3 years
#MentalHealth affects us all in different ways when living day to day with #rarediseases & #chronicillness. It doesn't matter whether you are male or female ➡ talking to others & knowing you are among people that also have #anxiety can really help. #Health #Dazzle4Rare
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@FibroFlutters
Flutters and Strutters (Formerly FibroFlutters)
3 years
We are open to everyone #notjustpatients #Caregivers, + #healthprofessionals are welcome too! 🔵Help us to make this #mentalhealth community work for you 🔵Lets get a #raredisease women's group going to help fill the current void. #Dazzle4Rare #FibroFlutters #ZebraStrutters
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