D Badiuk ACROMEGALY

President/Founder/Director of the Vancouver Acromegaly Support Group. Ambassador of Canada for Acromegaly. President and Founder of Acromegaly Canada.

[D Badiuk ACROMEGALY @dbadiuk16]

https://t.co/KNAEFvHYwl

[AcromegalyCanada @AcromegalyCAN]

What does Acromegaly Awareness Day mean to the acromegaly community? From celebration to recognition to contemplation, our members share their thoughts.

#AcromegalyAwarenessDay #Acromegaly #PituitaryDisease #RareDisease

[Pfizer Canada @PfizerCA]

Today is #AcromegalyAwarenessDay. Pfizer is proud to support @AcromegalyCAN on its interactive, online resource that walks visitors through daily life with acromegaly. For more information: https://t.co/eJE3omjgGh.

#RareDisease #WorldAcromegalyDay

[AcromegalyCanada @AcromegalyCAN]

Acromegaly Awareness Day is coming up on Wednesday, November 1. Help to raise awareness by sharing your story or feel free to use our graphics. ⤵️

#AcromegalyAwarenessDay

https://t.co/ocTfebZhkC

[AcromegalyCanada @AcromegalyCAN]

It's #AcromegalyAwarenessDay. #Acromegaly is caused by excess production of growth hormone in adults, usually due to a tumour on the #pituitary gland.

Join us today in sharing resources to raise awareness + reduce the time to get diagnosed.

[D Badiuk ACROMEGALY @dbadiuk16]

Acromegaly Awareness Day https://t.co/QI9FLMmi0d
For more images to post for acromegaly awareness day please go to acromegaly canada website and look under acromegaly awareness tab. Help spread the word about acromegaly, a disease that goes undetected for 5-10 years.

[AcromegalyCanada @AcromegalyCAN]

🏃‍♀️🚴‍♂️👨‍🦽🏊 Away we go! Our #ACROMOVE2023 cross-Canada fundraiser is underway. Huge thanks to all who are participating! We'd love to see your photos of your activities and medals--tag us and use #ACROMOVE.

If you'd like to donate directly, please visit https://t.co/nqE48ZpnRP.

[AcromegalyCanada @AcromegalyCAN]

🎉 Registration for #ACROMOVE is officially open! 🎉

Sign up today for our annual, cross-Canada fundraiser, happening July 22-23.

All donations will support #acromegaly and #gigantism awareness and advocacy efforts.

Details and registration: https://t.co/RsJs45wlIQ

[Niki Karavitaki @Karavitaki_Niki]

Results on the natural history of non-functioning pituitary microadenomas now out! Large study from the UK NFPA consortium with valuable data for our clinical practice. Many thanks to all collaborators! https://t.co/dMPsD1Qw58
@IMSR_UoB @BHPComms @ESEndocrinology @TheEndoSociety

[Recordati Rare Diseases @RecordatiD]

Cushing’s syndrome symptoms can be so different from person-to-person. “Every single Cushing’s patient has a history. Every single patient suffers in a different way.”

Find out more: https://t.co/2b5gYCUnMv
Video: https://t.co/fNZH2GY2Pz

#ThisCushing #CushingAwarenessDay

[AcromegalyCanada @AcromegalyCAN]

📣 Registration is open! 📣

Tickets are available for this year's Acromegaly Canada National Conference. Join us September 22-24 in Ottawa, Ontario, as we discuss all things #acromegaly and #gigantism.

✨Details + an early bird bonus⤵️

#AcroCon23

https://t.co/fHRyFUiMfN

[AcromegalyCanada @AcromegalyCAN]

Many #RareDiseases go undetected for years. Awareness is key to an earlier diagnosis.

#Acromegaly is caused by an excess production of growth hormone in adults, usually due to a tumour on the #pituitary gland.

Learn more: https://t.co/mhcYrJ4xxN

#RareDiseaseDay2023

[AcromegalyCanada @AcromegalyCAN]

A #RareDisease diagnosis can be scary and lonely...for patients and their loved ones. Support groups are a safe space to discuss day-to-day life, share fears, and celebrate successes.

Find #acromegaly support groups:
https://t.co/GkyJ0ZtoEI

#RareDiseaseDay2023 #RareDiseaseDay

[AcromegalyCanada @AcromegalyCAN]

A #RareDisease can affect every part of your life. Explore what daily life is like for people with #acromegaly with our interactive, online resource.

Visit https://t.co/pSuZDGCos5.

Bonus: we've just added new features!

#RareDiseaseDay2023 #RareDiseaseDay

[D Badiuk ACROMEGALY @dbadiuk16]

@AcroVan @AcromegalyCAN @Neurology @Endocrinology

[D Badiuk ACROMEGALY @dbadiuk16]

Live-talk, session 22 – Dr. Sylvia Asa discusses her groundbreaking work in endocrine pathology - Pituitary World News https://t.co/RSbWFjIuqa

[D Badiuk ACROMEGALY @dbadiuk16]

Live-talk, session 22 – Dr. Sylvia Asa discusses her groundbreaking work in endocrine pathology - Pituitary World News https://t.co/RSbWFjIuqa

[AcromegalyCanada @AcromegalyCAN]

Save the date! The 2023 Acromegaly Canada National Conference will take place September 22 to 24 in Ottawa, Ontario. Stay tuned for details and the link to register!

#Acromegaly #Gigantism #RareDisease #Pituitary #Endocrinology

[AcromegalyCanada @AcromegalyCAN]

🆕 Recordings from this year's Acromegaly Canada Conference are now available! Gain insights from leading medical professionals and patient advocates. Let's keep acromegaly awareness going well past #AcromegalyAwarenessDay.

https://t.co/gGjVr1KFhK

[D Badiuk ACROMEGALY @dbadiuk16]

https://t.co/q8yjf0n5pq

[D Badiuk ACROMEGALY @dbadiuk16]

https://t.co/6jwWYYy15C