Primary Biliary Cholangitis

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Primary Biliary Cholangitis
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I'm new here!

Hi, my name is Shirely Jo. I'm here because I'm concerned I may have another AI disease + it's alot to deal with!

#MightyTogether #MultipleSclerosis # Sjogrens Disease # Primary Biliary Cholangitis # Presently ruling out Autoimmune Skin Disease

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Migraine chronic pain insomnia. Need medical advocate

Good morning!
I'm checking in with my mighty people! I’ve been in migraine and awake for three days. I’ve been functioning like this for almost 15 years. My chronic pain prevents me from sleeping. Then everything gets worse from there. No sleep equals increased pain. I need some love and support today. I’m hurting so bad. It’s a horrible feeling. If I can get some rest, the pain will ease a bit. The cycle continues like Ground Hog Day in the movie. I am referred to return to the Mayo Clinic in Rochester, MN. Does anyone have contacts for support and housing in Rochester? I plan on moving there to get the care I so desperately need.
I’m open and willing to receive ALL suggestions! I genuinely need your strength!!! I’m hopeful the new tech at Mayo will help reduce my pain. Reducing bits and pieces would be life-changing for me.
I’m on my own with no medical care support. It has broken my heart not having anyone to care for me.

I appreciate your support!
I am so grateful for ALL of you!
Thank you so much for your support!!! 🤗🩷#PrimaryBiliaryCholangitis
#Headache #Migraine #RareDisease #misdiagosed #ChronicPain #MayoClinic #Insomnia #showmejeanie

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Join us on Rare Disease Day for a livestream discussing the social impact of rare disease!

In honor of Rare Disease Day, Mike Porath, Founder and CEO of The Mighty, Carli, a 26-year old woman living with fibrodysplasia ossificans progressiva (FOP), and Jeanine, a woman in her 50s living with primary biliary cholangitis (PBC), will dive into a live discussion speaking to their personal experiences related to the social and emotional impacts of rare disease on their lives.

Be sure to tune into this discussion on navigating the ins and outs of life, relationships, and rare disease from three experienced advocates by signing up here:

Sponsored by Ipsen.

#RareDisease #FibrodysplasiaOssificansProgressiva #PrimaryBiliaryCholangitis #RareDiseaseDay

Getting to the Heart of the Social Impact of Rare Disease | The Mighty

Virtual Event - Join Mighty founder Mike Porath as he talks with two patient advocates, Carli and Jeanine, who live with fibrodysplasia ossificans progressiva (FOP) and primary biliary cholangitis (PBC) to discuss navigating social impact and relationships while living with a rare disease.
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Join us on Rare Disease Day for a livestream discussing the social impact of rare disease!

In honor of Rare Disease Day, Mike Porath, Founder and CEO of The Mighty, Carli, a 26-year old woman living with fibrodysplasia ossificans progressiva (FOP), and Jeanine, a woman in her 50s living with primary biliary cholangitis (PBC), will dive into a live discussion speaking to their personal experiences related to the social and emotional impacts of rare disease on their lives.

Be sure to tune into this discussion on navigating the ins and outs of life, relationships, and rare disease from three experienced advocates by signing up here:

Sponsored by Ipsen.

#RareDisease #FibrodysplasiaOssificansProgressiva #PrimaryBiliaryCholangitis #RareDiseaseDay

Getting to the Heart of the Social Impact of Rare Disease | The Mighty

Virtual Event - Join Mighty founder Mike Porath as he talks with two patient advocates, Carli and Jeanine, who live with fibrodysplasia ossificans progressiva (FOP) and primary biliary cholangitis (PBC) to discuss navigating social impact and relationships while living with a rare disease.
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