UK Members

Science PFS Research
#1

Hi,

I would like to round up together all the members of the forum that are UK based and try to get together to do something about:

  1. Litigation (the aim would be to re-invest any settlement in research)
  2. Working with NHS and NICE to set up some group study that will officially look into PFS
  3. Raise capital/ funding for research through donation and charity events (I have few ideas around this)

Please let me know or pm if you are willing to help
thanks

#2

Sergio, you already know I’m 100% behind what you are trying to do after our conversations.

Lets hope we can get others from the UK onboard too. Fully appreciate what your trying to achieve.

Speak soon

#3

Sergio,

I see your post is from earlier this year and I am a new member as of today - but I would be very intested in helping.

Bryan

#4

I am from the UK (London). I am going to see a sleep specialist today for my results. I have prepared all my notes. I am hoping that Propecia’s effects on sleep will pique his interest.

#5

I’m in!

jamielondon what specialist did you see?

#6

I’ll join any efforts on this as well.

#7

Could we pull data from all the members on this site who are based in the UK and create a UK contact list? If there are 3000 members and 500 are from the UK let’s say, we could really co-ordinate effectively, for the purposes of litigation and raising the profile of PFS to UK based doctors and the NHS in general.

#8

Dr Williams at Nuffield Sleep Centre- did nothing for me. I am being sent to another specialist regarding sleep.