Let’s not lose momentum – Im-patient’s must go onwards to keep achieving results!
We want your support to ensure that we can run another im-patient event in Barcelona, which is where the idea was first forged – and where there will be quite a large #pharma audience of around 1300 people. I am of course referring to the Annual 17th Barcelona eyeforpharma Conference, which is on 12th-14th March 2019.
I hope you agree that we need to take advantage of such an opportunity!
Go here now to fill in your details and make sure you’re part of it:
And finally, this is vital if our movement is to grow –
Please do encourage others to join.
It’s time to get your patient voice heard, there are many, many good ideas out there that are in your networks, but aren’t in mine, so please can you share this post to reach as many people as possible.
Your ideas may help to change how the pharma-patient relationship grows.
Only, if these ideas are ‘heard’ do we have a chance to make them a reality!
Read what eyeforpharma Chairman Paul Simms had to say about the Im-patient events that happened in October.
An impatient truth
- Published on November 8, 2018
Check the eyeforpharma Patient Policy which is how myself and Sonia get to go and participate in their events.
We are not employed by eyeforpharma
eyeforpharma: Patient Policy By Paul Simms, Chairman, eyeforpharma. Updated August 2017
17th Annual eyeforpharma Barcelona (Commercial, Digital & Patients)
Mar 12, 2019 to Mar 14, 2019 Barcelona
Where Pharma Becomes The Solution
Why not check it out via this link >>>
Many thanks for taking the time to read
Wishing you all wellness
Carole, CEO FibroFlutters / Co-Founder Fibro Flutters Sunderland
Advocating for a Multi-Disciplinary approach to all aspects of medical healthcare. With a model approach using all the ‘stakeholders’ I’ve designed a patient’s perspective of what patient-centred care, patient-included, patient-involved, patient-centric should look like and involve, that’s everyone by the way!
You all need to pitch in!!
FibroFlutters – Support Group for people with Fibromyalgia, Chronic Pain, EDS/Hypermobility, Mental health, Chronic fatigue/Me, Rare & others offering friendship, support & advice in Sunderland, NE UK and offering online support via our social media network across the globe.
PLEASE NOTE: We are not medical professionals nor claim to be, and remember that you should always consult your doctor about any health problems and not use Dr Google, or rely on information that you may read online through 3rd parties.
Please can you read our ‘Disclaimer’ & ‘Privacy’ notes and if you have a problem we are always open to discussion, just e-mail Carole
MANY THANKS in advance for your understanding –
from the administrator – fibrofly73
Many thanks for reading our posts and helping to share the news that other folks like you write, or, find.
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