Finally found some hope

Some months ago I went to a doctor and he couldn’t help me but recommended me to visit a group of doctors who are specialised in andrology and treating difficult cases. So I went there, and I met with one of the doctors. My main problem is muscle loss (along with no libido,etc.), so I explained him my situation and all my story. Not only did he listen carefully to everything I said, but he told me he had heard some doctors talk about PFS. He explained me that this group (Fundació Puigvert), mixes medical consultancy with research. They try experimental treatments in people who do not respond to other treatments, and they do research with the patient.

The doctor who recommended me this team (who, btw, was not related to them) told me they had made many discoveries with patients that couldn’t find no solution to their problem. The first doctor I met in Fundació Puigvert told me they would do every step to try to end up with a solution. They also told me I am the first PFS case they have visited (finasteride is not common in Spain).

Unfortunately, my mutual insurance company does not cover visits with this foundation, and I am not in a good economical situation, so I won’t be able to continue this process in the next months, since I think a large number of medical tests will be needed. I will try to save some money and maybe in 9 or 10 months I will go there again.

I have made a google search of Fundació Puigvert, and they have made some impressive achievements. So if anyone wants to try something, I recommend visiting them, as they have also been the most receptive people I have met regarding PFS until now. They are based in Barcelona, and they are easy to find via Google (at least searching from Spain). Probably for Americans this is not an option, but for Europeans, flying to Barcelona is usually very cheap.

If anyone visits them, please let me know how it goes.

Estaría bien saber qué opinan. Y comentarlo un poco.

Aunque sólo sirva para que haya más conocimiento en España de esto.

Fantastic. Good to get more doctors looking into this. Just be skeptical when it comes to paying a fortune for these guys. I paid Jacobs $650 just to get a prescription for clomid. We need docs with brain scanning super equipment and molecular imagining/routing devices. Otherwise the new docs are way behind us already regarding what works and what doesn’t

Hola Kan soy español tambien
Muchas gracias por el post, Te han dicho algun producto para tomar o pasos a seguir??

Hello kan I am spanish too
Thank you for your post
Did they tell you to take any product or follow some steps?

No, sólo comentaron que el primer paso sería analizar la parte endocrinológica para asegurar que el problema no es hormonal.

No, they only said the first step would be to analyze the endocrinological part to be sure that the problem is not hormone related.

Gracias, Te han dicho que hormonas se analizan? Son conscientes del problema? Han tenido/solucionado algun caso como el tuyo/nuestro?
Yo he ido a dos dermas y todos recomiendan finas y cuando a uno le conte mis efectos secundarios me dijo que esperase que se pasarian solos.
Creo que es imposible que solo un 2% este afectado…

Thank you. Did they tell you what hormones to analyze? Are they aware of this problem? Did they have/solve any case such as ours/yours?
Ive visited two dermatologist and they all recommend to take Finasteride. I told one of them about my side effects and he told me to wait for them to dissapear
I think it is impossible that only the 2% is affected…

Well lets see its been almost 10 years and my nuts are still shrunk from finasteride… still waiting for those sides to disappear.

This week they have appeared in the news for having done the first all-robotic kidney transplant in Europe.

europe.newsweek.com/europes-firs … ona-330479