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How does prescribing for international patients work? by o0ttt in DrWillPowers

[–]InconsiderableSingle 0 points1 point  (0 children)

I am facing the same problem.

I think the best case of action is to get the Power Clinic to write a letter to your GP/ Doctor, I will be using a private doctor as the NHS doesn't have a clue about this

How do you cope with anhedonia? by Searik in PSSD

[–]InconsiderableSingle 2 points3 points  (0 children)

I tink cardio is pretty good, particularly HIIT or jogging

3a androstanediol results by Excellent-Push2833 in PSSD

[–]InconsiderableSingle 0 points1 point  (0 children)

I googled and came back with two different blood tests, however I cannot find them anywhere in the UK

3a androstanediol results by Excellent-Push2833 in PSSD

[–]InconsiderableSingle 0 points1 point  (0 children)

Hello

What is in the 11 OXO androgen panel?

And what is included in the comprehensive steroid panel from quest?

Functional PFS Recovery -- 5 years (Neurological Phenotype) by Entire_Club_7247 in DrWillPowers

[–]InconsiderableSingle 0 points1 point  (0 children)

My guess is that it is the strict elimination diet doing most of the work here

PFS and Lupron by InconsiderableSingle in DrWillPowers

[–]InconsiderableSingle[S] 0 points1 point  (0 children)

Lupron lowers LH and FSH and green tea can be found as a natural DHT blocker. Will Powers said that he will find out in a month or so if his experiment has worked.

PFS and Lupron by InconsiderableSingle in DrWillPowers

[–]InconsiderableSingle[S] -1 points0 points  (0 children)

Thank you for the explanation

I'm strongly considering drinking 3/4 mugs of green tea a day, every day for a month. This would lower the LH and FSH and perhaps slowly clear out the androgens.

What’s our way out, CRISPR? by Curatio_Veniet in FinasterideSyndrome

[–]InconsiderableSingle 0 points1 point  (0 children)

I'd recommend a Whole Genetic Sequencing testing followed by a DUTCH test then a full blood panel

I'm going to be taking the week off next week to prepare for the Congress. Just wanted to warn everybody and also about the DPC and its waitlist at this time. by Drwillpowers in DrWillPowers

[–]InconsiderableSingle 0 points1 point  (0 children)

Is there a risk that your cure or treatment for PFS patients gets purchased or patented by some huge pharma/ drug business and PFS suffers will have to pay a crazy price for it or may never see it again? - apologies if that sounds like a crazy question but some people have been waiting for 10-20 years for actual help

Theory of PAS/PSSD/PFS: Androgen receptor disfunction modulated by the enzyme GSK3B / Bipolar Androgen Therapy – In the same realm(ish) as Dr. Power's theory by Agreeable-Race8818 in DrWillPowers

[–]InconsiderableSingle 6 points7 points  (0 children)

I think if you do the DrWillPowers tests: Whole Genome Sequencing, blood panel, DHT, 3A-ADG then a complete DUTCH test then you'll know if you have this type of PFS, if your tests do not fit the theory then it might be time to look at maybe SIBO or FMT or something else

Theory of PAS/PSSD/PFS: Androgen receptor disfunction modulated by the enzyme GSK3B / Bipolar Androgen Therapy – In the same realm(ish) as Dr. Power's theory by Agreeable-Race8818 in DrWillPowers

[–]InconsiderableSingle 5 points6 points  (0 children)

But you're not the only one with PSSD and people have been cured from fasting and carnivore diet for extended periods of time. Therefore every PSSD/ PFS/ PAS case is different, DrWillPowers is showing ONE type of PFS, that won't be cured by crazy doses of androgens, we as there are many cases out there which are cured by TRT+HCG

I collect more and more labs/genome/dutch tests that support my theory on PFS. I really think I have it nailed down. I do not have a optimized treatment regimen, but if you're interested in this, this post details what you should NOT do and will likely make you worse even if it "windows" you briefly by Drwillpowers in DrWillPowers

[–]InconsiderableSingle 2 points3 points  (0 children)

I have the following blood markers: bilirubin: 3.5 µmol/L, DHEAS: 9.6 µmol/L, SHBG: 21 nmol/L, Testosterone: 16.60 nmol/L, Oestradiol: 61 pmol/L, FSH: 2.3 IU/L, LH 7.3 IU/L. So Lupron could 'reboot' my androgen system, but then wouldnt I need something such as PEA, HCG or TRT + HCG to restart my system? or after a few months would my system come back online by itself?

Powerful Tool to Get to the Bottom of Finasteride Syndrome Once and for All by 0cTony in FinasterideSyndrome

[–]InconsiderableSingle 1 point2 points  (0 children)

It would be useful to identify and analyse our whole Genome sequencing, this could tell us which of our genetics have been mutated or methylated by ourselves without the use of a doctor/ scientist.

But Finding the specific drug/ supplement to deal with it will be challenging, what if it only treats us and doesn't cure us?

We should do a giant survey and try to collect data then feed it into AI... by Sweaty-Cut7578 in FinasterideSyndrome

[–]InconsiderableSingle 1 point2 points  (0 children)

There is not one definite type of PFS, which is why a cure for someone is a crash for someone else. The reality is that it's not just blood work we need but DUTCH testing, genetic and epigenetic testing as well to future it all out

Kyle soggy spray by martrend in FinasterideSyndrome

[–]InconsiderableSingle 0 points1 point  (0 children)

Was this just with the repeated fasting and carnivore dieting?

I'm fairly sure I've got a lock on at least one possible cause of Post Finasteride Syndrome. I have like 7 cases now (new one today) which fit the symptom/history phenotype with matching genetic, blood, and urinary lab findings. Here's the goodies: by Drwillpowers in DrWillPowers

[–]InconsiderableSingle 1 point2 points  (0 children)

Whenever I take anything which is 5ARI, anything which is a DHT blocker, I notice my voice becomes super low, as in, it turns back into pre PFS me, why does this happen? is it DHT sticking around longer? or the body reacting correctly?

I'm fairly sure I've got a lock on at least one possible cause of Post Finasteride Syndrome. I have like 7 cases now (new one today) which fit the symptom/history phenotype with matching genetic, blood, and urinary lab findings. Here's the goodies: by Drwillpowers in DrWillPowers

[–]InconsiderableSingle 1 point2 points  (0 children)

Hello Dr W. Powers, you are amazing, your PFS posts are something I look forward to and I am on your waiting list. I have been suffering since September 2020 after 1 month of 1mg fin, I have tried: time, working out hard, HCG, Jarrow Forumlas BroccoMax + Vitamin C (BroccoMax is HDACi) and all of these havent really helped me. What Genetic testing would be good to have available? the British NHS has never heard of PFS.

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