MPN.network
MPN - Myeloproliferativeneoplasm network
Webcast - MPN Awareness Month September

1.-30.09.2023 •

September is the annual MPN Awareness Month. Thus, there are lots of different events and activities aiming to raise awareness of MPNs and supporting the belief that informing, connecting, and advocating for those who are affected is crucial for the well-being of patients.

We would like to give a brief overview of this year’s activities below.

Read more on Linkedin:
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#rarediseases #mpnawareness

Webcast MPN Breakfast 2023

On the occasion of the MPN Awareness Day which was celebrated on September 14 this year,  AOP Health was hosting its traditional MPN Breakfast – a panel discussion with international patient advocates, health care professionals and the CEO of AOP Health, Martin Steinhart. The event was focusing on the topic “Manager of your own Disease: Benefits & Challenges”.

Watch the webcast in 4 languages!

Webcasts - Young Patients Talks

Perspectives and hopes for the future from young patients living with an MPN

Externes Video

Beim abspielen dieses Videos werden durch den Drittanbieter YouTube (YouTube, LLC) auf Ihrem Endgerät Skripte geladen, Cookies gespeichert und personenbezogene Daten erfasst. Es erfolgt eine Datenübermittlung in die USA, welche über keinen EU-konformen Datenschutz verfügt.

Living with a rare disease like an MPN can feel isolating. Today, during MPN Awareness Month, we invite you to listen to Judit speak about her concerns & coping strategies for living with Myelofibrosis, a rare bone marrow cancer.

Judit emphasizes the importance of seeking support through young patients groups, and taking care of her physical and emotional well-being.

Externes Video

Beim abspielen dieses Videos werden durch den Drittanbieter YouTube (YouTube, LLC) auf Ihrem Endgerät Skripte geladen, Cookies gespeichert und personenbezogene Daten erfasst. Es erfolgt eine Datenübermittlung in die USA, welche über keinen EU-konformen Datenschutz verfügt.

Watch Carlota, a young MPN patient who received her diagnosis at age 16.

Carlota says that "Although the diagnosis is scary at first, there are people who can help us - experts, family and friends, that make it possible to live a normal life."

Hear what Carlota and young patients have to say about living with an MPN!

Externes Video

Beim abspielen dieses Videos werden durch den Drittanbieter YouTube (YouTube, LLC) auf Ihrem Endgerät Skripte geladen, Cookies gespeichert und personenbezogene Daten erfasst. Es erfolgt eine Datenübermittlung in die USA, welche über keinen EU-konformen Datenschutz verfügt.

Myeloproliferative Neoplasms (MPNs) are a group of chronic, rare diseases of the blood-forming cells in the bone marrow, which are considered blood cancers.

Hear what Paula G has to say about living with an MPN and her hopes for the future!

Externes Video

Beim abspielen dieses Videos werden durch den Drittanbieter YouTube (YouTube, LLC) auf Ihrem Endgerät Skripte geladen, Cookies gespeichert und personenbezogene Daten erfasst. Es erfolgt eine Datenübermittlung in die USA, welche über keinen EU-konformen Datenschutz verfügt.

Paula C, a young MPN patient, encourages others living with an MPN:

"Make the most of the moment and don't let the disease drag you down."

Living with a MPN diagnosis can be very challenging, especially if that diagnosis occurs in very young person. 

Listen to what Paula C talk about living with an MPN!

Externes Video

Beim abspielen dieses Videos werden durch den Drittanbieter YouTube (YouTube, LLC) auf Ihrem Endgerät Skripte geladen, Cookies gespeichert und personenbezogene Daten erfasst. Es erfolgt eine Datenübermittlung in die USA, welche über keinen EU-konformen Datenschutz verfügt.

MPN Awareness 2023 - Summary Young Patients

As Dr. Sobas, PhD, Wroclaw Medical University notes: "MPN is mainly a disease of elderly patients and the research is mostly dedicated to this group of patients. Not yet to younger patients." 

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