PFS recovery is “not impossible. “ In June 2017 I fully recovered (except sleep) - Anonymous1968's post-PFS journal

Do you think the near starvation helped you (not trying to be insensitive or funny)? Did you do fasting/dieting protocols?

No, terrible idea, borne of desperation, caused horrific permanent health probs.

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The blood work revealed no diagnostic abnormalities. That leaves us with the possibility of the trial of intravenous methylprednisolone therapy as we had discussed in the office. This is something that could be done in Charlotte with the involvement of his physician. Specifically, we would be using this trial as not simply therapy but for diagnostic purposes. To accomplish that, a limited neurologic examination is appropriate prior to starting treatment to establish a baseline. At a minimum, standing and taking a few steps would be a good reference point since the imbalance was rather striking. This would be followed by five consecutive days of 1000 mg of intravenously administered methylprednisolone. It typically is administered over 90 minutes. At the end of the five days the exam is then repeated. If there is meaningful benefit and more than can be expected by chance or placebo effect, that would be interpreted as possible evidence of an autoinmune condition. In that case, I would like to be back in the loop to learn how things have gone, and I would then be happy to advise what to do beyond that. If there was rather striking improvement, the usual strategy we have done here is to continue the intravenous methylprednisolone once a week to complete 6 to 12 weeks of treatment. Beyond that, a decision must then be made how to extend immunosuppression but with modalities other than methylprednisolone. In that, case, I would then considerar involving colleagues from our Neuroimmunology group. I also advised a brief videotape of the before and after results in case we need to have objetive evidence of the degree of improvement.

Anybody else lost/regained emotionality/compassion?

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Yes from SSRI use. I have no emotions whatsoever. No happiness, no sadness, no love or empathy. Also no libido. And I can’t sleep naturally. It am taking high doses of benzos and Lyrica to sleep and that doesn’t always work so I have to pick and choose when to sleep. It’s awful and I can’t put myself through this much longer. Life was always tough for me but now it’s impossible. It is boring and meaningless now…

My full story is here:

https://forum.propeciahelp.com/t/methyl-steroids-and-or-time-luck-100-cured-my-sexual-probs/9416

In summary:

  • methyl steroids POSSIBLY 100% cured my PFS impotence/sexual dysfunction
  • I stopped sleeping normally in summer 2014 and stopped sleeping AT ALL Nov 2014-April 2015
  • I was able to zombie sleep 7-8 hrs a night until Dec 2016 by nightly taking both:
  • mirtazapine/remeron 30mg (prescribed off-label to promote REM sleep)
  • nortryptaline100mg
  • I stopped sleeping AT ALL from Dec 2016 for ONE YEAR (but basically was OK unbelievably)

In Dec 2017 my near prescribed Balsomra. It is ridiculously expensive ($15 a pill!) but my ins. covers it.

http://www.merck.com/product/usa/pi_circulars/b/belsomra/belsomra_pi.pdf

I have recently discovered that INTENSE late night exercise PLUS new sleep drug Balsomra currently puts me to “sleep/heavy rest” for 6+ hours.

I bike for 30+ minutes INTENSELY plus 25 pushups. So y’all can try it too.

Me tonight at 11:30pm:

Neurologist prescribed:

$15 a pill per night is a lot but at least it comes from a respected company so we know it’s safe!

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Ha true it’s a Merck drug!

But it is working for me, slept 5.5 hrs last night; 5.5 hours MORE than entire 2017!

Oh yeah most of you are thinking I’m lying or confused about not sleeping, but tis’ true. Iresearched it and there are two known semi-famous non-sleepers. One man was unfortunately shot in the head and the othersuffered brain fever. Both stopped sleeping forever without any adverse health detriment!

5 hours, that’s huge news! Congrats man, hopefully it lasts. And props to you for exercising, I stopped exercising when insomnia hit me, I tried a few times but it’s hard to keep a routine when you’re exhausted some days so I’m just gonna wait till it’s completely normal again lol.

Also anyone who thinks you’re lying is a tool.

So yep the “three trick pony” is actually working:

  • intense 30 minute workout at 10pm
  • Balsomra
  • reading serious book

I skipped exercising Friday night and paid the price! No sleep Friday night and PROFOUNDLY exhausted all day Saturday (just miserably lay in bed all day)!

Last night slept 5.5 hours again, after exercise etc.

Man there are so many morons and voodoo-hawking yahoos 'round here!

I’d like to:

Anyway I have some useful (!) and sane advice regarding sleeping:

I had the worst PFS insomnia, I nearly died in the first 2-3 years of that sleepless brain-fogged migrained hell but I started experimenting and reading stories here for tips and I was able to first restore my brain’s ability to reach REM sleep within weeks just using supplements like theanine and 5htp and then eventually regular quality sleep using no pharmas only glutathione capsules and fasting.

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Good news, intense late night exercise + Belsomra has consistently induced unconscious sleep (3-6 hours per night) for two weeks. Best sleep since Nov 2016!

Exercise alone does NOT work, as I discovered two nights ago when I temporarily ran out of Belsomra and did not sleep one second that night.

So it’s been a while since I updated but my situation is like this:

I regularly get 3-5 hours unconscious sleep every night. I take Belsomra and it apparently helps. Exercise positively helps. So that’s good.

But I have to take 2-4 1+ hour “rest naps” at random times every day. I feel profoundly exhausted and it slowly passes/subsides. Repeat endlessly.

Hmmmm…

In this case, I would check mitochondrial function and gluthatione levels.
For getting better MIT.function R alpha lipon acid and hydroperoxid.
Gluth.: supplementing reduced gluth.every day

I know you’re trying to be helpful, but your post is incomprehensible.

  • why would I get additional tests, after spending hundreds of thousands of dollars, including 6 MRIs
  • why these particular tests
  • what would these tests encourage me to purchase better than Balsomra, prescribed by a neurologist and supposedly the “cutting edge” of sleep pills

If you never regain sleep on your own, do you think you’ll be content using the drug and late night exercise method for the rest of your life?

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Are you talking to me? Talking to me? :slight_smile:

Hundreds of thousands of dollars?
Come on man, be realistic please.

You don’t need to do any tests. But don’t expect to get better just by doing nothing.
I am talking about being exhausted.
BTW those few tests don’t cost a thousand dollars. But could tell a lot.
MRI can show issues, but in most cases did not. But if so, nobody knows what to do.

And re sleep I was a similar case to yours. Couldn’t sleep the first 3 months.
Phosphatidylserin at 400mg and GABA. Walking in the morning! for 30 minutes.
Interm.fasting (irregular) helped better sleeping.
You can integrate those information or not - up to you.
When my gut issues were worst, so my sleep too. Just think about that. Gut - brain connection. Or research.

Good luck anyway.