He practices in Encino California. If I was in the USA I would first ask him directly if his treatment has made a big impact in releiving PFS symptoms to his previous/current patients before being his patient. The link is below.
Also I have included a youtube link where just last month he was discussing it. Its a long video but go to 1.01 (one hour and one minute into to the video) and you will see
Does he have any evidence to back this up?
@Ronnie99, the fact that you were able to essentially fully recover for 6 months by just modifying hormone levels (indirectly) to me is quite clear evidence that we don’t suffer from brain injury.
You would have to contact him to ask for evidence etc.
Regarding my recovery for the 6 months my definition of a brain injury and Dr Gordons view is a dysfunction in the hormonal systems or neurosteroid systems.
I essesianlty beleive the glucorticoids get dysfuntioned but the key is what is causing this dysfunction, what precipitates that.
This study is what I beleive is the issue.
Start discussing it. There won’t be a cure until the community does something other than popping the same pills that haven’t worked for 15 years. It’s literally proven fool’s gold. Would be just as stupid to beat head against brick wall. Figure out a way to provide scientists more data and ability to get state funding and the cure will come. It’s really that simple.
What’s your proposed path forward? Be clear.
The idea isn’t for one person to show up with deliverance in one swoop.
The idea is that the community needs to start talking about the right things to start witnessing progress.
Here is one example of an idea: A letter to you, forum
I really beleive Dr Mark Gordon will get us close as possible to a cure or a huge improvement in symptoms, I just can access him as I live in Australia, this guy knows his stuff and as of the last few months has been focusing on Finasteride and its effects. Has someone been to him recently say the last 3-6 months ?
Why?
Me too.
Just the last few months?
He is a expert in TBI, and is one of the only doctors in the world to treat his patients differently in terms of testing a set of hormone markers in a panel he uses and then replenishing these hormones which are deficent or to high, and within a period of time lot of his patients feel better.
Regarding the last few months, He stated that he is seeing similar markers/hormones problems he was diagnosing with non finasteride users and finding the same issues in finasteride patients. So his method of treatment is similar except it is now with finasteride patients, so im confident in his approach.
Where abouts in Australia do you live ?
I see. You seem to know a fair bit about him.
I’m in Melbourne (Australia’s own little prison). Where are you?
Yes thats why I beleive he is the closest we can come to a cure or a huge improvement in our symptoms. I took Accutane and Finasteride but I beleive my symptoms came from when I took Accutane when I was 17 years old.
Im from Sydney…yes Melbourne will be doing good soon and easing some restrictions.
Did you take Accutane or finasteride, whats your symptoms ?
Ah. I took Finasteride. Low libido, emotional numbness, numbish genitals are my main complaints.
Here is a patient testimonial on Dr Gordons website regarding tratment on Post finasteride syndrome patient. Below is the screenshot.
Plz fill the survey bro. 
A lot of these PFS doctors do virtual appointments so you could probably set one up with Dr Gordon to be treated. For what it’s worth, another user on here said he went to him and he was extremely expensive and offered the same sort of treatment as other well-known PFS doctors like Jacobs and Goldstein. Not sure how long ago he went to him though and maybe he’s refined his treatment method since then.
how can I fill in the survey as im using a Ipad ?
I contacted him, but he said its impossible to treat international patients because of the blood tests needed etc.
Yes I seen another user tried him some years back, with some success, though I think your right in now his treatment would be different as he stated in a recent post in september that he is focusing now on Finasteride Syndrome and he is seeing similar similarities in his testing biomarkers from his current TBI (Traumatic Brain Injury) patients who suffered symptoms from blast trauma, conscussion etc and he says the only difference really is that we have a chemical induced injury rather than a blunt forced, and the similarites in the hormones/neurosteroids are similar. I really hope a few people see him and report back to us here from there experience with him.
Guys, be careful spending money on doctors for PFS. Until we get research done, they’re just as blind as any of the rest of us as to what PFS is. The easiest way in the world for unscrupulous people to make money is by selling hope to desperate people suffering from currently incurable conditions.
@vkg1, just because somebody doesn’t know the exact underlying cause doesn’t mean they are unable to provide treatment for it.
How did this guy recover? What he used?
John Cleave. (I found his Facebook and contacted him, i will report back if he replies.)
