Recent Posts

Pages: [1] 2 3 ... 10
1
No scrub, I haven't but I'll probably try donepezil and see how effective it is.
2

I am hoping that the effectiveness grows with the contiuous use of Mestenon. Overall the symptoms are decreased about 30 %.

Good luck in refining your method.   30% is already much better than nothing, though.

Thank you Quantum and yes Mestenon is definitely the way forward but I feel like it's not enough. I feel like I need more medications to treat different things like inflammation or better way to keep the dosage high enough.
3
Does enebody of you hawe posibility to wisit hi colege educated funtcional medicine dr? They hawe different aproach from test labs and looking for the root couse of deseeses and they look in human body like a whole conected, not like separate organs and treat only symptomes.
http://www.nordiclabs.com/NLPage.aspx?id=317
4
Hi everyone,
So I just tried Orgasm on 60mg Mestenon; I took 60 mg at ~5pm then I took another another tablet at 7:30pm just in case, because Mestenon has a 3 hours range of effectiveness. I also want to add that I already took Mestenon 60mg yesterday and the day before.

Anyways at Orgasm I didn't feel much symptoms but at about 30 minutes symptoms started to pile and become very severe. At the start I didn't think I had symptoms but they slowly piled up to be heavy nausea, brainfog, disconnection and speech problems. On the speech problems at like 10 minutes I barely felt a problem saying anything but as time passed and I kept talking I started noticing a growing difficulty.

Overall though, orgasm usually cripples me into a zombie like state where I can barely say anything or think of anything. This time however, while still symptoms crept slowly afterwards, I feel like I'm not completely crippled. It was kinda similiar in a way to my Sam-e experience but this time I guess it was a much more noticeable of a difference.
I'll update you on my state tomorrow and see how my situation goes.

I am hoping that the effectiveness grows with the contiuous use of Mestenon. Overall the symptoms are decreased about 30 % which is unfortunately not as successful as emornazim's and scrub's.

Have you tried any other cholinesterase inhibitors? I had success with Pyridostigmine, but i'm very curious about taking Donepezil or Galantamine, especially Donepezil because it's half life is very long.
5
Support and Miscellaneous / Re: Suggestions
« Last post by Hopeoneday on Today at 12:37:06 AM »
This tread name must be changed if you ask me.
Two most important things for us-1. Our symptomes in and out of pois, 2. medical test results. (and compare them in anodher tread(allredy exist since recently).
6
Support and Miscellaneous / Re: Suggestions
« Last post by Quantum on June 17, 2018, 07:33:52 PM »
Yes good idea, i opened tread to put there symptomes in detail nobody responde.
I think that treads like this sugestion must be sticky. But this is on mods.
If mods make tread sticky all people will respond.

Hi Dizzy and HOD,

Similar threads already exist on the forum.  A big one can be found at http://poiscenter.com/forums/index.php?topic=81.100

However, after a time, those threads tend to turn into conversations thread, or are forgotten, or are not found by newcomers....   the one above is a sticky, is well in evidence at the top of the Lifestyle Diary forum board, is titled "POIS Summaries and Histories", but nevertheless, it is rarely referred to or posted in....the proof being that you both never saw it.   

Just to say that it is very hard to keep any thread "alive" for a long time.
7
At least 2 members have reported higher than normal levels of 17-alpha-OH-progesterone ( members Crushgrapes and Investigator).  See this thread: http://poiscenter.com/forums/index.php?topic=2532.msg21904#msg21904 .

( note:  I have not been tested for 17-OHP, so I am not reporting about myself, here)
8

I am hoping that the effectiveness grows with the contiuous use of Mestenon. Overall the symptoms are decreased about 30 %.

I am glad to hear this, Nas.  You often shared that you have found absolutely nothing so far to relieve your POIS, but not true anymore.  You seem to respond to cholinergic support.   It may be now a question of refining your method ( dosage, timing of dose, cholinergic add on like lecithin, etc....)

Good luck in refining your method.   30% is already much better than nothing, though.
9
Thanks everyone for chiming in with your thoughts.

I've researched this a lot and it came to the conclusion that some people are more sensitive than others to mercury fillings. however, keeping them over the long run can cause issues even if not related to POIS.

For that reason, I have found a holistic dentist certified by the IAOMT (International Association of Oral Medicine and Tocxicology) to have mine removed.

That didn't end my POIS at all but I'm still glad that I don't have to think about it anymore.

Cheers
10
Auto-Immune Causes and Treatments / Re: Vagus Nerve Stimulation
« Last post by Hopeoneday on June 17, 2018, 05:39:54 PM »
Thanks fernard, i remeber i times whot help me in big is heital hernia masage(puling gently stomach down when is empty), heital can twich wagus in esopagus walve.
Pages: [1] 2 3 ... 10