Fundraising gathers momentum, matching donations and new YouTube content
Latest updates from the PFS Network team
Almost a month since announcing our latest awareness campaign and plans for research at The Institute for Human Genetics at the University Medical Center Schleswig-Holstein in 2022, we’re pleased to bring you some important updates.
We have been blown away by the generosity of Post-Finasteride Syndrome patients and their families since announcing our latest research project.
In a little over three weeks, we’ve reached €35,000 of our €80,000 target. To all who have contributed, we are deeply appreciative.
With our fundraising target well within reach, we’re encouraging our mailing list to please consider setting up a monthly recurring donation on our donate page.
If each of the 103 subscribers to our mailing list set up a recurring donation of €100, the study would be fully funded in 4 months. That means groundbreaking new research to further our understanding of Post-Finasteride Syndrome could begin in March 2022.
To help reach our target faster, the PFS Network team are increasing our personal commitment. Over the next month our team will match all donations made, up to €5000.
For example, if we receive €5000 in donations by December 25th, we will personally contribute an additional €5000. If we receive €4000, we will contribute an additional €4000.
We are pleased to announce that PFS Network is now a registered charity on GoFundMe. That means any patient or their family in the United States, United Kingdom, Australia or New Zealand can set up a fundraiser on GoFundMe and nominate PFS Network as your charity of choice.
We strongly encourage any patients with supportive family & friends to run a small fundraiser to maximise the impact of your contribution.
To simplify this process and make it easy for patients, our team have created a template for patients to set up their own personal GoFundMe campaign. This includes a video from the PFS Network team explaining our upcoming study, a templated message for the campaign, and an instruction guide on how to set it up.
We are very pleased several patients have reached out already to set up their own campaign. If you are interested in running your own fundraiser, please get in touch and we’ll be happy to help you set it up.
New YouTube video
Please check out our YouTube channel, subscribe and like this important video.
If you have any questions about upcoming research, or anything else, please get in touch: email@example.com.
PFS Network team