PFS Research Association e.V.
@ResearchPfs
The PFS Research Association e.V. is a patient-organized charity to accelerate the research of the Post-Finasteride Syndrome. Join us today!
ID:1396839730914992137
https://www.pfsresearch.org 24-05-2021 14:47:41
22 تغريدات
103 متابعون
9 التالية
PFS patient story #8 - Roman: pfs-research-association.medium.com/pfs-patient-st….
This one highlights once more that PFS is much more than just sexual symptoms. The neurological and physical symptoms and changes that PFS patients suffer from is what turns this disease truly into a living hell.
Going forward, we will share patient stories of PFS patients on a regular basis to illustrate the suffering patients endure and to highlight how important it is to find research-led treatment for those affected.
Find the first story here:
pfs-research-association.medium.com/pfs-patient-st…
(2/2) EVERYBODY is asked to retweet and make this go viral. 📢
We need public awareness and more research about the prevalence, etiology and therapy options for PSSD. More information can be found here:
pssdnetwork.org
#SSRI #InformedConsent #psychiatry #mentalhealth
(1/2) Please be aware of the risk to end up with Post SSRI Sexual Dysfunction after the use of a SSRI #antidepressant .
Next to the persistent loss of one's sexuality, which is very distressing itself, patients suffer from severe emotional blunting. This can be life ruining.
The PFS Research Association is raising money for its first project: 'Targeting Androgen Signalling For Mitochondria Protection In PFS' by George Barreto Ph.D..
Dr. G. Barreto a neuroscientist from the University of Limerick.
Let's raise15k Euros! Donate & Share: pfsresearch.org/donate