Benzo withdrawal 14 months off, still suffering with cognitive impairment
#181
Posted 20 May 2016 - 01:01 PM
Here are some tips if you ever decide to try again
WARNING : DO NOT USE GINKGO UNLESS YOU ARE OFF BENZOS > 30 DAYS
http://www.benzobudd...p?topic=94005.0
Cured Oct 2013. My success story:
http://www.benzobudd...p?topic=92537.0
Ginkgo supplements :
Ginkgo extract 24% flavone glycosides and 6 % terpene lactones ones 60 mg 7am and 7pm when cycled on.
I only needed this for 12 weeks. Brand I used - GinkgoGold
Tips :
1) Dose every 12 hours (critical)
2) Stop Ginkgo 1 week after 4 weeks
3) No herbs, alcohol, relax teas, meds impacting gaba or weed
4) Be prepared for significant increase in sxs for the first few weeks.
Suggestions, opinions and/or advice provided by the author of this post should not be regarded as medical advice; nor should it substitute for professional medical care. Consult your doctor before making any changes to your medication.
#182
Posted 27 May 2016 - 11:19 PM
Anybody have success switching from a benzo to benzo-analogue etizolam, and then tapering off of that?
How about pregabalin, gabapentin, phenibut, baclofen - as substitutes for benzos until off of benzos?
And then phenobarbital at the end to be off everything PAWS free.
Anyone have protracted withdrawal syndrome after tapering off of etizolam or phenibut? I believe it is unique only to benzos. I did not have PAWS with phenibut or etizolam myself.
I have been my own guinea pig, and I think I have found success. Although, I am not completely done yet. I will share if it ultimately proves successful in preventing any sort of PAWS after years of benzo use. My plan is hinted at in details above.
I haven't had a regular benzodiazepine in months and am fine. This, after 8 years prescribed alprazolam or clonazopam daily.
Edited by PowerfulP, 27 May 2016 - 11:30 PM.
#183
Posted 28 May 2016 - 01:31 AM
I haven't had a regular benzodiazepine in months and am fine. This, after 8 years prescribed alprazolam or clonazopam daily.
consider yourself lucky
#184
Posted 28 May 2016 - 02:09 AM
I haven't had a regular benzodiazepine in months and am fine. This, after 8 years prescribed alprazolam or clonazopam daily.
consider yourself lucky
Well....after 2.5 years of trial and error and lots of PAWS.
#185
Posted 28 May 2016 - 08:20 AM
I haven't had a regular benzodiazepine in months and am fine. This, after 8 years prescribed alprazolam or clonazopam daily.
consider yourself lucky
Well....after 2.5 years of trial and error and lots of PAWS.
Also Tianeptine and Memantine were in my stable. I will be outlining my process in detail soon enough, when I am absolutely finished and certain.
Flumazenil definitely has a place for preventing PAWS. I believe an inverse agonist called α5IA may ultimately prove to be much better at preventing PAWS altogether. I am a chemical researcher and have a doctorate but Sigma-Aldrich is the only vendor, and I'm not part of an organization that can purchase from there. Here's some relevant links.
First, the wikipedia entry - https://en.wikipedia.org/wiki/Α5IA
Second, only vendor I have found http://www.sigmaaldr...S&focus=product
http://www.wikiwand.com/en/Α5IA
An Inverse Agonist Selective for α5 Subunit-Containing GABAA Receptors Enhances Cognition
http://jpet.aspetjou...jpet;316/3/1335
#186
Posted 28 May 2016 - 12:06 PM
I think sigma aldrich could sell you something for one person businnes activity. Especialy if you have doctorate.
#187
Posted 17 June 2016 - 06:20 AM
I think sigma aldrich could sell you something for one person businnes activity. Especialy if you have doctorate.
I did try, but I'm often a one-man operation, but I do have a nice lab exceeding all requirements. I think they disliked I was not a company.
#188
Posted 23 June 2016 - 05:32 AM
#189
Posted 15 January 2017 - 09:21 PM
I think the peptide BPC-157 is extremely interesting when it comes to "curing" PAWS. Here's a quote from Metabolic Alchemy--
"A novel gastric pentadecapeptide BPC 157 with different beneficial activities and anticonvulsant effect interacting with GABAergic system could improve diazepam efficacy coadministered (10 microg/kg, 10 ng/kg i.p.) with diazepam (5.0 mg/kg i.p.) twice daily for 10 days, since diazepam chronic medication would otherwise predispose for diazepam- tolerance/withdrawal development (shorter latency to convulsion after convulsant). In diazepam chronically treated mice, it attenuated diazepam tolerance (provoked by later acute administration of diazepam together with convulsant) and postponed physical dependence/withdrawal effects (provoked by later administration of isoniazid). In tolerance assay, at 42 h after the end of conditioning regimen, shorter preconvulsive latencies than in healthy (non-diazepam conditioned) mice following isoniazid (800 mg/kg i.p.) (as hallmark of tolerance) were observed if diazepam (5.0 mg/kg i.p.) was again given acutely to mice previously conditioned with diazepam alone (use of picrotoxin 3.0 mg/kg i.p., as convulsant, with acute application of diazepam in previously diazepam conditioned mice did not lead to tolerance hallmark). This was completely avoided in diazepam+BPC 157 10 microg or diazepam+BPC 157 10 ng chronically treated animals. In physical dependence assay (isoniazid challenge assessed at 6, 14, 42 and 72 h after conditioning medication), when compared to diazepam non-conditioned healthy mice, in diazepam conditioned mice residual anticonvulsive activity was not present already at the earliest post-conditioning interval (i.e., not different latency to isoniazid-convulsions), whereas shorter preconvulsive latencies (as physical dependence/withdrawal hallmark) were noted in diazepam conditioned mice following isoniazid challenge at 42 h and at 72 h after end of conditioning treatment. In diazepam+BPC 157 10 microg- conditioned mice, a residual anticonvulsive activity (i.e., longer latency to isoniazid convulsion) was noted at 6 h post-conditioning, whereas shorter preconvulsive latencies appeared only at 72 h-post-conditioning period. In conclusion, taken together these data (lack of tolerance development (tolerance studies), prolonged residual anticonvulsive activity, and postponed physical dependence/withdrawal hallmark in diazepam+BPC 157 chronically treated mice) with common benzodiazepines tolerance/withdrawal knowledge, it could be speculated that BPC 157 acts favoring the natural homeostasis of the GABA receptor complex as well as enhancing the GABAergic transmission, and having a mechanism at least partly different from those involved in diazepam tolerance/withdrawal, it may be likely used in further therapy of diazepam tolerance and withdrawal."
Bumping this. I've seen some interesting anecdotal reports on this substance on Reddit. Wondering if anybody has tried this for cognitive or mental health issues?
Where can i buy this bpc? I would give it a chance.
Peptides Warehouse has it. There is talk about it on Reddit
#190
Posted 17 January 2017 - 04:58 PM
Flumazenil?
#191
Posted 10 August 2017 - 10:06 AM
The PAWS I mostly have are belly bloating (benzo-belly), face tension and face tinglings; sometimes muscle jerks.
Everytime I take something GABA-ergic the withdrawals come back and I am sick of it.
Has anybody has had succes (faster receptor healing) using GABA-A antagonists?
You have ginkgo, muira puama, kudzu root...
I will now try high doses of ginkgo and see if there is improvement.
#192
Posted 10 August 2017 - 12:52 PM
Writing computer programs is mentally such a delicate job, that even the time you take a shit dan set off your concentration. If you dump in strong psychotropics, like benzos or antidepressants, it stirrs the pot so much that you are entirely thrown out of your high fidelity comfort zone.
Following weeks and month of pressure to perform in a job regardless, your mind taxes your bodily resources so much to overcome the disturbance, that you figuratively learn to run around with all your faculties overclocked 24/7 as your default mental state.
This is not really a result of drug use or withdrawal, its a result of your psyche trying to accomplish something its not fit for.
What you need is a long long vacation on a farm, away from your life. Month maybe, half a year.
Trust me that if you keep grinding your teeth off with this idea that you can somrhow rectify this problem with some utterly pseudoscietific BS about your neurotransmitters and drugs, its only going to tear you apart further.
On another note: try some kind of "homeopathy". Take miniscule quantities of benzos again and see how you CNS re-recognizes the "poison". It might very well result in some kind of rectification. I am talking 1/10th a tablet or so. I have personally experienced this a few times.
Well, I read your original post an let me tell you, that you got it all wrong. There is no way to be convincing about this, and no medical study can fudge the proper conclusion into that direction either.
Writing computer programs is mentally such a delicate job, that even the time you take a shit dan set off your concentration. If you dump in strong psychotropics, like benzos or antidepressants, it stirrs the pot so much that you are entirely thrown out of your high fidelity comfort zone.
Following weeks and month of pressure to perform in a job regardless, your mind taxes your bodily resources so much to overcome the disturbance, that you figuratively learn to run around with all your faculties overclocked 24/7 as your default mental state.
This is not really a result of drug use or withdrawal, its a result of your psyche trying to accomplish something its not fit for.
What you need is a long long vacation on a farm, away from your life. Month maybe, half a year.
Trust me that if you keep grinding your teeth off with this idea that you can somrhow rectify this problem with some utterly pseudoscietific BS about your neurotransmitters and drugs, its only going to tear you apart further.
On another note: try some kind of "homeopathy". Take miniscule quantities of benzos again and see how you CNS re-recognizes the "poison". It might very well result in some kind of rectification. I am talking 1/10th a tablet or so. I have personally experienced this a few times.
#193
Posted 14 August 2017 - 01:21 AM
The PAWS I mostly have are belly bloating (benzo-belly), face tension and face tinglings; sometimes muscle jerks.
Everytime I take something GABA-ergic the withdrawals come back and I am sick of it.
Has anybody has had succes (faster receptor healing) using GABA-A antagonists?
You have ginkgo, muira puama, kudzu root...
I will now try high doses of ginkgo and see if there is improvement.
I personally have found seroquel works well. It is not perfect, and it won't help with a lot of the physical problems you're describing, but it helps you sleep and reduces anxiety significantly. The major side effects are fatigue, which gets better, and weight gain, which for me is quite noticeable. It does negatively impact cognition to a degree, but that may also be withdrawal related. What I like about it is that you can skip days or even a week, which I have done.
It works fast, so I would suggest trying it for 2 weeks at say 25mg per day, and see how you feel. You can order it from India, but I have been using a head doc.
#194
Posted 14 August 2017 - 10:27 AM
I realize I haven't posted in my own topic since quite a while. There has been some development.
At some point the whole thing turned into a classic case of CFS - fatigue, low energy - mental and physical. The primary symptoms of benzo withdrawal (anxiety, sleep troubles) have long gone.
Last year, at the beginning of summer, I had the opportunity to meet a top doctor, who lives as a foreigner in my country. This was great, since health care in my country is primitive and various doctors' visits in 5 years had brought me nowhere (the usual ignorance and BS: "it is in your head", "it is psychological", "you are imagining this", "you should rest more"). Because of his extreme knowledge and experience, he managed to put a proper functional diagnosis (and not the usual "psychosomatic origin" crap), which all the ignorants failed to do during all those years. He looked at some common blood work (where all was within the ref. ranges !), asked me a few questions and said "Boy, you have a condition called leaky gut. Your GI tract is poisoning you and that is the reason why your cells can't produce energy in a proper way". Finally I had a proper diagnosis, and not the usual undetermined BS !
That was a real surprise to me, since all in all I didn't have any GI symptoms, but he said that leaky gut can go on asymptomatic in terms of GI issues. Indeed, my research since has confirmed this may rather be true. He gave me various recommendations and I have been trying some things since then with variable success - cleansing enemas, diet probiotics, supplements. There have been moments where I felt almost like my old self, full with energy. My guess is those were the moments when my gut lining got in a better shape (tight junction closing up) and toxins were no longer leaking into my bloodstream. However it didn't last. My guess is there is some notorious bad bacteria, which I can't fully exterminate without resorting to antibiotics. There is a partial success, but it appears to grow again and the released LPS (lipopolysaccharides) are damaging my gut lining, restarting the vicious cycle.
What is the benzodiazepine connection ? I may have come to a revelation when researching H Pylori infection. It is indeed a gram-negative bacteria, which releases LPS upon death. However, that pathogenic mechanism of action seems to be ignored and people are more focused on the more familiar mechanism of action, where in order to protect itself, H Pylori lowers stomach acidity (through production of an enzyme - urease). The body tries to compensate by increasing acid production, but this causes stomach / deudenum ulcers. Those are a clear sign of a H Pylori infections. I myself don't have those, but from the info I have read it appears a H Pylori infection can indeed go on asymptomatic (no GI symptoms, but a whole myriad of other issues throughout the body, because of the leaky gut). I looked at the treatment, the so called "tripple therapy". In addition to two different antibiotics it includes a PPI (proton-pump inhibitor). A PPI lowers stomach acidity, thus causing H Pylori to somehow - as I understand - "lower it's guard", so that the antibiotics have a stronger effect. I wonder: could the benzos 6 years have acted as PPI somehow, indirectly maybe ? As allosteric modulators they are controlling the opening of the Cl- ion channels. Perhaps they have lowered my stomach acidity, opening the gates for a full-blown - though hidden - H Pylori infection, triggering the whole disaster. I am going to discuss this with that doctor and will do a test for H Pylori this week. There is a bit of hope that the whole thing could be resolved with a 2-weeks course of antibiotics after 6 years of suffering.
So I am wondering: how many of you fellow post-benzo sufferers may have a leaky gut without even suspecting it ?
Edited by Kompota, 14 August 2017 - 10:30 AM.
#195
Posted 15 August 2017 - 04:41 PM
I am not saying that there aren't at least some practices from the whole fringe business that can do some good, like eating grinded papaya seeds until you puke an shit the demons out of your body. But overall its just plain esotheric and conversely other practices just do as much harm. Like eating antibiotics frequently.
#196
Posted 15 August 2017 - 04:50 PM
#197
Posted 06 October 2019 - 01:53 PM
我意識到我已經有一段時間沒有發表自己的主題了。有了一些發展。
在某種程度上,整個事情變成了CFS的經典案例-疲勞,低能量-身心。苯並撤退的主要症狀(焦慮,睡眠障礙)早已消失。
去年夏天初,我有機會見到了一位在國外居住的高級醫生。真是太好了,因為我國的醫療保健很原始,而且五年來各種醫生的拜訪使我無處可去(通常的無知和BS:“在你的腦海中”,“在心理上”,“你在想像這個”,“您應該多休息一下”)。由於他非常的知識和經驗,他設法進行了適當的功能診斷(而不是通常的“心身起源”廢話),這些年來所有無知者都沒有這樣做。他查看了一些常見的血液檢查(所有血液都在參考範圍內!),問了我幾個問題,然後說:“男孩,您有一種狀況稱為腸漏。
令我驚訝的是,因為我總體上沒有任何胃腸道症狀,但他說,就胃腸道問題而言,滲漏的腸道可能無症狀。確實,此後我的研究已經證實這可能是正確的。他給了我各種各樣的建議,從那以後我一直在嘗試一些成功的方法-清潔灌腸劑,飲食益生菌,補充劑。曾經有一段時間,我感到自己幾乎像我的舊自我,充滿了活力。我的猜測是那些時候我的腸壁形狀變好(緊密的連接處閉合)並且毒素不再洩漏到我的血液中。但是它並沒有持續。我的猜測是存在一些臭名昭著的壞細菌,如果不使用抗生素,我將無法完全消滅這些細菌。部分成功,
什麼是苯並二氮雜connection連接?在研究幽門螺桿菌感染時,我可能會發現一個啟示。它確實是革蘭氏陰性細菌,會在死亡時釋放LPS。但是,這種致病作用機制似乎被忽略了,人們更加專注於更為熟悉的作用機制,即為了保護自身,幽門螺桿菌會降低胃酸度(通過產生酶-脲酶)。人體試圖通過增加酸的產生來補償,但這會引起胃/小腸潰瘍。這些是幽門螺桿菌感染的明顯跡象。我自己沒有這些,但是從我閱讀的信息中看來,幽門螺桿菌感染確實可以繼續無症狀(無胃腸道症狀,但由於腸道漏水,整個身體還有許多其他問題)。我看了看治療,所謂的“ 除兩種不同的抗生素外,它還包括PPI(質子泵抑製劑)。PPI降低胃酸度,從而導致幽門螺桿菌-據我所知-“降低警惕”,因此抗生素具有更強的作用。我想知道:苯並6年是否可以間接地充當PPI?作為變構調節劑,它們控制Cl-離子通道的打開。也許他們降低了我的胃酸度,打開了一次幽門螺桿菌感染(儘管隱藏)的大門,引發了整個災難。我將與那個醫生討論這個問題,本週將對H Pylori進行檢查。充滿希望的是,經過6年的苦難,使用2週療程的抗生素可以解決整個問題。除兩種不同的抗生素外,它還包括PPI(質子泵抑製劑)。PPI降低胃酸度,從而導致幽門螺桿菌-據我所知-“降低警惕”,因此抗生素具有更強的作用。我想知道:苯並6年是否可以間接地充當PPI?作為變構調節劑,它們控制Cl-離子通道的打開。也許他們降低了我的胃酸度,打開了一次幽門螺桿菌感染(儘管隱藏)的大門,引發了整個災難。我將與那個醫生討論這個問題,本週將對H Pylori進行檢查。充滿希望的是,經過6年的苦難,使用2週療程的抗生素可以解決整個問題。因此,據我所知,幽門螺桿菌在某種程度上“降低了警惕”,從而使抗生素具有更強的作用。我想知道:苯並6年是否可以間接地充當PPI?作為變構調節劑,它們控制Cl-離子通道的打開。也許他們降低了我的胃酸度,打開了一次幽門螺桿菌感染(儘管隱藏)的大門,引發了整個災難。我將與那個醫生討論這個問題,本週將對H Pylori進行檢查。充滿希望的是,經過6年的苦難,使用2週療程的抗生素可以解決整個問題。因此,據我所知,幽門螺桿菌在某種程度上“降低了警惕”,從而使抗生素具有更強的作用。我想知道:苯並6年是否可以間接地充當PPI?作為變構調節劑,它們控制Cl-離子通道的打開。也許他們降低了我的胃酸度,打開了一次幽門螺桿菌感染(儘管隱藏)的大門,引發了整個災難。我將與那個醫生討論這個問題,本週將對H Pylori進行檢查。充滿希望的是,經過6年的苦難,使用2週療程的抗生素可以解決整個問題。間接地吧?作為變構調節劑,它們控制Cl-離子通道的打開。也許他們降低了我的胃酸度,打開了一次幽門螺桿菌感染(儘管隱藏)的大門,引發了整個災難。我將與那個醫生討論這個問題,本週將對H Pylori進行檢查。充滿希望的是,經過6年的苦難,使用2週療程的抗生素可以解決整個問題。間接地吧?作為變構調節劑,它們控制Cl-離子通道的打開。也許他們降低了我的胃酸度,打開了一次幽門螺桿菌感染(儘管隱藏)的大門,引發了整個災難。我將與那個醫生討論這個問題,本週將對H Pylori進行檢查。充滿希望的是,經過6年的苦難,使用2週療程的抗生素可以解決整個問題。
因此,我想知道:你們中有多少苯並二苯並二苯醚病患者的腸胃漏水甚至沒有懷疑?
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Have you fully recovered from benzodiazepine withdrawal? 100%?
Also tagged with one or more of these keywords: benzodiazepine, withdrawal, cognitive, impairment
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