Chronic Pancreatitis Support | HealthUnlocked

Writing on behalf of my Mum. My Mum had her pancreas removed three years ago. She is still constantly feeling nauseous mostly after she has eaten. She tends to...

What I've noticed is there are 6 posts with not one comment. It's a strange support group. I can't as I no treatment for chronic pancreatitis including no...

well hello everyone, my story so far, after going back and forth to gps and hospital scans, back in 2002, i had the gallbladder and stones, removed, and bouts...

Hi I have joined on behalf of my wife who has chronic pancreatitis but is acute at this time She has just spent 7 days in hospital on pain relief but now...

Caring for your physical health is more than just exercise – it's also getting enough sleep, eating a balanced diet, and adding healthy habits to your routine!...

I have had stomach issues a long time. I recently found out that my chronic pancreatitis is severe, due to some specific tests that I took. My...

Living with pancreatitis can be challenging, but having a strong support system can make all the difference. Whether it's family, friends, healthcare...

Just wondered if anyone knows if being on Creon (PERT) means you're at the worst end of CP? I'm scared I really have PC but just haven't been able to get into...

I am trying to join a community but get this message - Request failed with status code 400 - Why?

After an appointment with a dietician I was tested for suspected EPI and my level was very low - 53. I have been prescribed Creon 25000 and taking those for...

I have been experiencing pancreatic pain for 6 mos now. Have been to the ED 5 times in that time period. I thought I knew what pain was with my lower back...

Hi there, Looking for support groups / networking groups of folks with type 3c diabetes. Long story short: - Necrotic Pancreatitis in 2022 - Hospitalized 4...

Everyone needs a good laugh, especially when dealing with the challenges of pancreatitis. Got a pancreas-related joke up your sleeve? Share your best...

Just wanted to say hey. Glad there's a support group for CP. Feel very alone in this. Pains no fun either. 🙂Sidney

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