"Being an athlete, I knew this pain wasn’t normal. My first doctor dismissed it as bursitis, but a second opinion revealed cancer.” — Thomas Goode
We recognize Minority Cancer Awareness Month and the importance of early and accurate diagnosis. #IMFMPOWER
https://t.co/s9vDMAUlY8
Domestic travel. 8+ hours wasted in total due to all sorts of delays including 2+ hours waiting for luggage! Please get your act together @TorontoPearson@AirCanada
We know there is power in numbers, and this #RareDiseaseDay we are celebrating by sharing the voices, faces and experiences of the community to empower and connect others facing similar journeys. #RareDiseaseDay#RAREis
Did you know that approximately 160,000 new #myeloma cases are diagnosed each year? During #BloodCancerAwarenessMonth, we ask you to share the knowledge, advice, and discoveries you've made along your journey to elevate your voices. Will you help us? #kNOwMyeloma
Ce n’est pas facile d’expliquer le cancer aux enfants. Pour vous aider, nous avons conçu un livre de conte gratuit. Lisez-le et partagez-le gratuitement https://t.co/ET9028Ff4R
May is #AsianHeritageMonth.
At Amgen Canada, we’re using this time to celebrate #diversity, #inclusion and belonging while shining a light on our employee resource group, the Amgen Asian Association (AAA).
Toronto Video Of Year Contender ( man beats man with SNAKE)
Yes, you read that right, buddy is attacking another man in Toronto @ Dundas and Manning, it is believed with a snake….peak Toronto.
#Toronto
Celebrating all the incredible #OntarioDoctors, who continue to deliver the best possible care to their patients even amidst challenging times. #ThankYou for all that you do to keep our communities safe and healthy. #DoctorsDay#NationalPhysiciansDay
When Jack Aiello was diagnosed with myeloma in 1995, patients had a 2-3 year life expectancy. Today, when a doctor sees a standard-risk patient, they expect to see them 10 years from now. Jack credits the collaboration in the #myeloma field for this progress. #25Voices#MMRF25
Quand un membre de la famille reçoit un diagnostic de #myélomemultiple, on se demande souvent comment l’annoncer aux enfants. C’est difficile, mais nécessaire.
Nous avons donc créé une histoire à cette fin: https://t.co/nKyeAf8LQe
When a family member is diagnosed with #multiplemyeloma we often face the question of what to tell our children. Talking to a child about a loved one’s diagnosis isn’t always easy, but it is necessary.
We created a story to help: https://t.co/BFSRoJuhcB
The work towards achieving health equity from trials to treatment demands diverse input from industry. This #InternationalWomensDay, we recognize that the representation of women in the workplace, especially in leadership positions, is critical to innovation and success.
March is Multiple myeloma awareness month. Help increase awareness for this 2nd most common blood cancer that remains incurable, for now.
Spread the word. Like. Share. Repost.
Learn more at https://t.co/BGXeyCV17k
#MAM2023#myelomaawarenesscanada
It often takes more than 3 visits with a physician before being diagnosed.
This Myeloma Awareness Month, stop this devastating cancer from cutting short the lives of those we love.
Like. Share. Repost.
Head to https://t.co/BGXeyCV17k
#MAM2023#myelomaawarenesscanada
This week, CDC’s campus is illuminated in #RareDiseaseDay colors in honor of the #RareDisease community.
💚 💙 💗 💜
Today is Rare Disease Day, which raises awareness for the 7,000+ rare diseases that affect over 25 million Americans. https://t.co/DCseBMhhof @RareDiseases@NIH