It acts as an anti-depressant. Many PFS guys are depressed, so I don’t see any reason why they would oppose it’s use.
Docs may not be using it on us because it’s use would be off-label. It’s only approved by the FDA in post partum depression.
Docs can use medication for off label use without difficulty. Goldstein himself has tried a few medications used for depression and other health issues to try to treat PFS. Its just the logistics of having to be monitored in a hospital for a 60 hr IV infusion which complicates this situation. You would pretty much have to pay out of pocket for everything I imagine.
Could we get some people to try this, instead of all the stuff people are using nowadays that were proven to be useless? I’m willing to donate for it.
I too would be interested to see if it improves people, but we have to ask, is this a good use of tens of thousands of dollars?
In a best case scenario it will improve the single person who undertook it (lacking statistical significance as it’s a single person). Few others will be able to afford the treatment at this stage.
Worst case scenario it won’t even benefit that individual, and the money will be blown. This money would be better channelled into further research into the condition.
At least we’ll have an immediate result, instead of having to wait for 5+ years as often happens with studies. Also, maybe there are some who have the money to have it done themselves?
I dont see how this could possibly be a one time use.
Just wait the phase III guys
That shit that is sold online is no garbage I have tried myself and it works exactly as is supposed to work and you obviously didnt tried the correct brand of tribulus.
Keep this thread about Zulresso please.
are you willing to try it? I’ll donate as wwll
I would if I could, I don’t live in the US unfortunately.
Supposedly you can buy 217 for much less
One person? That’s a false statement.
Then why are you still here Belikewater?
Allopregnanolone also has strong anti-inflammatory properties by decreasing TNFa. Melcangi found high levels of TNFa in PFS (can’t remember if it was humans or rat models).
I just made the test to see if I could get more allopregnenalonone effects with it, it worked but its not the cure obviously, but had a completly reversal of symptoms while on it, lots of emotions came back strongly.
Seriously? Does anybody even believe these bullshit claims anymore? If you had a complete reversal of symptoms then you have a treatment in your hands, why don’t you simply keep using it and get on with your life?
These bs improvement claims are extremely harmful to this community I think. At best it’s a waste of our money and time, and at worst it harms you further and you end up worse than before.
Having spent 5-10 years on this forum, I think that people who make these claims either have serious mental health problems, or are trying to deceive people into buying useless crap.
Not wishing to rain on anyone’s parade when I say this, but given the record this forum has of finding “cures” that don’t work for anyone else or work for a few people and then stop working on subsequent use, what are you going to do if you pool 30k on one person getting a treatment that works for them? Will you all then get your own 30k for the same treatment? What if it doesn’t work for the guinea pig? Does that mean it won’t work for anyone else?
Like I said, I’m not trying to rain on anyone’s parade, but I’ll just say the previous Mercangi research cost less than it will cost to treat one person with this drug. It’s possible that once we have some more leads, it might be better to fund something like that instead.
I didnt say it stayed, but somehow very big improvement and reversal on symptoms while on it, also I was doing glycine and little corticoids at that time, so maybe I reduced inflamattion by a lot.