SSRI history and one dose of expired ashwaganda has destroyed my life in a matter of months

Welcome to our community. Please fill in the following template as a way of introducing yourself, and helping others to understand your background and situation.

Where are you from (country)? US

How did you find this forum (Google search – if so, what search terms? Via link from a forum or website – if so, what page? Other?). PFS subreddit

What is your current age, height, weight? 41, 200lbs, 6’1"

What specific drug did you use (finasteride, dutasteride, saw palmetto, isotretinoin/Accutane, fluoxetine, sertraline, citalopram, leuprorelin, etc…)? 25 years of SSRI use for anxiety. Off for 1 year. Took a 400mg dose of expired ashwaganda April 15 (stupid I know, I didn’t think anything of it as I’d taken before no issues)

What dose did you take (eg. 1 mg/day, 1 mg every other day etc.)? Doses varied by med, but 400mg ashwaganda

What condition was being treated with the drug?
Anxiety/sleep

For how long did you take the drug (weeks/months/years)? 1 day

Date when you started the drug? 4/15/2025

Date when you quit the drug? 4/15/2025

Age when you quit? 41

How did you quit (cold turkey or taper off)? Cold turkey

How long into your usage did you notice the onset of side effects? Within 7 hours post dose

What side effects did you experience that have yet to resolve since discontinuation?

  • Severe global muscle weakness
  • Complete lack of muscle stamina, muscles tire within seconds and shake instantly with contraction
  • muscle atrophy
  • loss of tactile sensation across the entire body (touch feels dulled or less)
  • Extreme fatigue like my body just has no energy at all (especially in the morning)
  • Emotional Blunting/Adhedonia (can’t cry, laugh, get excited, like my brain has been fried)
  • Random muscle twitching all over my body
  • insomnia (3-4 hours a night even with aides)
  • burning hands and feet with tingling
  • burning sensation across my entire body
  • weird irregular heartbeat throughout the day even doing nothing
  • eye pain/dryness and some blurring
  • severe genital numbness/ED/shrinkage
  • inability to sweat
  • brain fog/hazy thought
  • memory/recall issues
  • issues with mental imagery
  • no hunger or thirst signals
  • no body odor
  • no sebum/oil production (extremely dry skin and hair)
  • cracking and popping joints everywhere

Check the boxes that apply. You can save your post first, then interactively check/uncheck the boxes by clicking on them. If your symptoms change, please update your list.

Sexual
[ ] Loss of Libido / Sex Drive
[X ] Erectile Dysfunction
[ ] Complete Impotence
[X ] Loss of Morning Erections
[ X] Loss of Spontaneous Erections
[X ] Loss of Nocturnal Erections
[ X] Watery Ejaculate
[X ] Reduced Ejaculate
[X ] Inability or Difficulty to Ejaculate / Orgasm
[ ] Reduced Sperm Count / Motility

Mental
[ X] Emotional Blunting / Emotionally Flat
[X ] Difficulty Focusing / Concentrating
[ ] Confusion
[X ] Memory Loss / Forgetfulness
[X ] Stumbling over Words / Losing Train of Thought
[ ] Slurring of Speech
[X ] Lack of Motivation / Feeling Passive / Complacency
[ X] Extreme Anxiety / Panic Attacks
[ ] Severe Depression / Melancholy
[X ] Suicidal Thoughts

Physical
[X ] Penile Tissue Changes (narrowing, shrinkage, wrinkled)
[X ] Penis curvature / rotation on axis
[ ] Testicular Pain
[X ] Testicular Shrinkage / Loss of Fullness
[X ] Genital numbness / sensitivity decrease
[ ] Weight Gain
[X ] Gynecomastia (male breasts)
[X ] Muscle Wastage
[X ] Muscle Weakness
[X ] Joint Pain
[X ] Dry / Dark Circles under eyes

Misc
[ ] Prostate pain
[ X] Persistent Fatigue / Exhaustion
[ ] Stomach Pains / Digestion Problems
[ ] Constipation / “Poo Pellets”
[X ] Vision - Acuity Decrease / Blurriness
[X ] Tinnitus (ringing or high pitched sound in ears)
[ ] Hearing loss
[ ] Increased hair loss
[X ] Frequent urination
[ ] Lowered body temperature

[ X] Other (please explain)
See full list of effects above

What (if any) treatments have you undertaken to recover from your side effects since discontinuation of the drug? Not much. I was in the hospital for 3 weeks, 1 week post crash, and doctors could see I was severely messed up. They did all kinds of blood tests and neuromuscular disease tests but nothing.

If you have pre or post-drug blood tests, what hormonal changes have you encountered since discontinuing the drug (please post your test results in the “Blood Tests” section and link to them in your post)?

Anything not listed in the above questions you’d like to share about your experience?

Tell us your story, in your own words, about your usage and side effects experienced while on/off the drug.

I (41m in US) took a supplement that contained ashwaganda on a whim. It promised more restful and restorative sleep. I only took 400mg. Since then my decline has been rapid. To preface, I’ve been under a period of prolonged, chronic stress for the past 2.5 years, mostly driven failed Craniocervical fusions for my upper neck instability (ligaments are damaged and don’t hold my head on my neck without compression of brainstem). My last surgery was more successful. I was in the process of weaning off the neck brace (after 10 months) and strengthening my neck. I was improving. My kids were getting their dad back, my wife her husband. Then I took that pill. It was a Tuesday, April 15, 2025.

By Tuesday night I had genital numbness and severe ED. It freaked me out. I figured sleep on it and all will go away. The next day, I woke up with severe adhedonia and emotional blunting. I could feel absolutely no emotion, no joy, sadness, happiness, nothing. Hugging my wife and kids I felt nothing. Then came the brain fog, lack of mental imagery and what people call blank mind. Just attempting to imagine a past memory was next to impossible. By Wednesday evening, I started to notice other issues. I felt weak. I was standing in front of the bathroom mirror brushing my teeth and my wife noticed my left calf was twitching and tremoring. It was like it was trying to work but couldn’t. At this point, I was scared and started to seek out answers because all you hear is about how great ashwaganda is. Then I found this group and was horrified to hear I was not alone. As the days passed, the muscle weakness and fatigue became more severe. I went from sleeping 7-9 hours a night to maybe 1-3 hours. My physical therapist saw me later that week and noticed this strange global weakness across my muscle groups. She could tell something was wrong. I continued doing my home exercises and noticed doing neck exercises my strength appeared to just be gone. It didn’t make sense.

Fast forward to the next week and at my physical therapist appointment she noticed the weakness was even more severe. All the strength gains I’d gotten over 2 months had just disappeared. My muscles could contract, albeit weakly, but there was no stamina. Attempting to hold a contraction and my muscles just start shaking violently. She told me to see my doctor. My GP did all sorts of blood tests and they came back normal. She could see the same global muscle weakness. I still had all the other symptoms but this was my focus. The next day I woke up with extreme fatigue. I literally had no energy. I felt like I couldn’t even move to get outta bed. My wife had me call my doctor, they instructed me to go to the hospital.

I spent 3 weeks in the hospital. I told them about the onset of symptoms taking a supplement with ashwaganda, but was met with blank stares. They however, did see the weakness and are puzzled. They took more blood tests, antibody tests, and a number of autoimmune disease tests for neuromuscular disorders. They had know idea what is going on but have determined ash caused a severe shock to my central nervous system. It’s clear something in my brain was rewired and the signals being sent are no longer correct. While all of this is absolutely horrible, what is more terrifying is I’m losing muscle already. Just laying on a pillow, my neck muscles tremor and shake after a litte bit.

My immediate danger is now this. If my neck muscles continue to weaken and atrophy, my neck hardware will take on the load and will fail. I don’t know if it will even be possible to strengthen my neck again with what is happening. If that happens, I will become bedridden. I’m not ready to go guys. Several of you have messaged me and provided guidance. I’ve looked at the research studies on PFS/PSSD. I’ve perused countless groups for guidance. I was already in the process of fixing my gut before all this happened and am now aggressively looking into FMT. My family, my wife’s family have all thrown out their supplements containing ashwaganda. My wife and 2 girls visited me in the hospital. It was sad. It’s hard not to think of what will happen to me in the future or what I likely am going to miss out on. I’m trying to stay positive but reading all these stories and experiences shows me that this poison destroys people.

I’m not sure how much time I have left. I’m not ready to go nor am I ready to face what is likely to come. It’s crazy. I only took 400mg. That said, in thinking about my own history and learning about PFS/PSSD, this result may have been inevitable. You see, ever since I was 14 I’ve been on some sort of anti-depressant med for anxiety. It’s all I’ve ever known. For the past year or so I’ve taken nothing because my surgeon said SSRIs/SNRIs are horrible for bone health and disrupt fusion. All those years of use clearly destroyed my gut and changed my brain. Ashwaganda was just the trigger to push it all over the edge. Anyway, if you’ve gotten this far, thank you for reading. Right now, as I sit here in a hospital bed awaiting my fate by this poison, I’m hurting a lot. Everything I was trying to get back in life just gone. I will probably not get to see my girls drive, graduate from school, or go to college. I’m sad even though I can’t really feel it. I wish there was a faster and clear cut treatment. I fear the next few months are going to be tortuous for me and even then I don’t know how long I’ll last.

Update 6-6-2025: Unfortunately, absolutely no changes. I seem to be getting worse. The sleep deprivation is taking a toll and nothing seems to help. I regret taking that capsule every single day. I still don’t understand how it could completely destroy a person like it has me. New symptoms have cropped up. I no longer can sweat. My skin is dry and produces no sebum. My hair is dry and brittle with no more oil. Little brown spots have started appearing everywhere on my skin. My muscles still shake violently with contraction. For now, I’m trying to figure out sleep and then pushing for more testing, but my doctors are not listening. I know it’s only been a few months, but right now, it appears I have a severe form of PFS/PSSD. I’m at a loss for words. And my hardware has loosened, so I’m now in danger of catastrophic failure. My surgeon has me back in a full brace but that too will accelerate further atrophy. He fully acknowledges that I’ve experienced some sort of extreme neuroendocrine injury, autonomic dysfunction, and HPA Axis dysfunction. Right now, I’m bedridden mostly, in a holding pattern because my surgeon is away in Europe for 1 month. Separately, we are weighing the risks. In my current state, surgery could kill me especially all the necessary medicines which could overwhelm my fragile CNS. However, if we wait, my hardware could fail further causing brainstem or spinal cord injury. And all the while, I am slowly losing my wife and kids. The mental pain is unimaginable.

Lastly the real kicker and yes, I am a complete idiot. You see I’d taken this supplement before with no issues, 2 years ago. Like an idiot, I didn’t even think to look at the expiration date, just popped them like I used to. Well, turns out it was expired by 2 years and the psychoactive compounds in ashwaganda can degrade into more dangerous and potently destructive compounds. People can get PFS like symptoms from fresh ashwaganda. What I took was a nuclear bomb and explains my severe reaction. I understand if I receive no sympathy for this stupid mistake and it’s ironic, when I told docs at the hospital this, instead of checking for Neurotoxicity was just told, oh, it probably just lost some potency. Quite the contrary. It destroyed my brain, my body, and my life. I’m staying strong everyday even as I deteriorate further. I am not looking forward to being permanently bedridden for what life I have left but my surgeon told me, unfortunately, it is a realistic possibility, given all my circumstances.

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I’m very sorry to hear all of that. I know I can’t offer anything that will truly help, but it might ease it a little knowing that there’s already two big research projects underway, and that you may at least find some comfort in this forum and on the reddit page run by this forum’s admins. I wish you all the best.

Thank you. Honestly, I’m still in disbelief. April 14 I was fine. Finally turning a corner after Craniocervical fusion hell. Getting stronger. I went on several dates with my wife the prior weekend. She was so happy. April 15, a nuclear bomb went off in my body. I just had no idea ashwaganda could degrade into something so toxic but at the same time it was incredibly stupid not to even think about the expiration. I’m sure it had oxidized horribly after a few years, so who knows what I even really took. My guess is ashwaganda root extract on steroids. For now I’m dealing with the fallout. The hardest part will be losing my wife and kids. I can’t stop it from happening. She is an amazing woman. For 3 years I’ve been in Craniocervical fusion hell. First 2 fusions failed, 1 hardware failure in a month and the other lack of bone fusion. This third one was better, partial fusion. I had a chance to get my life back with neck strengthening. It literally feels like destiny came crashing in and said NOPE. I’d never even heard of ashwagandha until Nov 2022 from a doc. I used to take it for anxiety and sleep. The same bottle. Pretty much seems like I’m an honorary darwin award, but still, no one else can believe the damage either. Like every doc played it off saying, nah, it’d just lose potency. Well, AI and some research shows otherwise. I basically ingested a neurotoxin with all the lovely negative ashwaganda side effects compounded to the extreme. So yeah, I’m probably going to need the support from all of you. No one else around me understands and many don’t really care. Oh that’s so awful…and they move on. That said, I did find one person through reddit who experienced the same exact symptoms I listed from also expired ashwaganda. Like exactly the same. However, he’s a biochemical engineer and toxicologist so started a protocol right away to negate all the oxidative stress, glutamate surge, NMDA receptor, Gaba hit, serotonin hit and glutathione depletion. He’s still recovering but his fast action gave him a chance. I’m doing the protocol now but honestly don’t have much faith but I have nothing else. Basically microdosed antioxidant, vitamin, and neurosteroid support to try to help the body repair and gently get systems back online vs all the brute forcing high doses of random stuff that you see people doing and crashing. Ultimately, I really have no idea what it did to my body, but my symptoms match PFS to a T. So yeah, I’m still here fighting, but admittedly I’m tired, I’m exhausted. Even my surgeon knows I’ve got major neuroendocrine disruption and excitoxicity which has given him pause to even try to fix my hardware which is now coming loose because my muscles just don’t work and my neck was already severely atrophied so the load is in the hardware. So back in a collar causing more atrophy. I’m not ready for the world of hurt that is coming. Watching my family slip away and missing out everyday is enough mental pain to add to everything else. And of course, I can’t even feel the emotions. I’m hurting and crying deeply inside but I can’t even shed a damn tear. This shit sucks.

Yeah, it seems like basically any drug that affects the endocrine system can cause this. We see it from Saw Palmetto, Accutane, SSRIs and other stuff. Usually it happens from Finasteride because it’s a much stronger and more potent drug than anything else.
It’s tough but the only thing I can recommend that I know will not cause any negative effects is time. It doesn’t help everyone but most people do have some ease of symptoms with time and some even get a degree of recovery where they don’t even think about this condition, even people who have got hit hard by this for a while.

Very sorry to hear of your struggles. It’s wild the situation some of us find ourselves in after seemingly innocent things. You’ve been through a lot, but you’re super early on. Don’t give up hope.

I think you have developed an autoimmune disease. You have 90% of my symptoms apart from the fact that I sweat estrogen and that I produce sebum and earwax but they are not indicative of anything. In my opinion, the problem should not be addressed on the hormonal profile and on the history of Aswanafanda. By the way, expired or not, only one tablet hurt me too. Taking T stimulants like Mucuna, creatine, zinc, vitamin D I’m only worse. This leads me to think that SSRIs and finasteride can cause an autoimmune reaction in some predisposed subjects in my case aggravated by the Covid vaccine in 2021 then contracted in 2022 and 2023 with devastating symptoms. T causes neuro steroid production as SSRIs increase neuro steroids and this increases the activity of these antibodies that attach purified proteins to the production of neuro steroids. There are some guys who have studied this and have been tested for these antibodies called antibodies against GPCR proteins. You can’t find workers who make them only in Germany for Europe they cost a lot of money (multiple packages cost more than 2/3 thousand euros). Any treatment is based on plant immunoglobulins and immunosuppressive treatments. I find myself very much in what you wrote. Think about it and let me know

It’s a situation very similar to a very slow ALS but you don’t have to go to a surgeon it won’t help you. For me you are out of the way when you think of the Aswanafanda tablet for me the dramatic problems have created them for you 22 years of SSRI as brain narrowing and inability to properly process neuro transmitters. It is useless to think about something else is the shortage of neuro transmitters but they are missing because the brain is no longer able to process them and therefore they are discarded. All attempts to stimulate production cause serious accidents and worsening of conditions. Neuronal plasticity should be reactivated but 10 years of life are not enough to achieve this. Let me know what you think

Anyone who has like you and me modified the brain’s ability to properly process neurotransmitters is no longer a patient of gym protocols, diet or supplements and any hormones. We turned off some areas of the brain because SSRIs and finasterides do it. When you suspend the system turns on again but the wires are those of 25 years ago oxidized, do you understand?? We are passing the super fiber on the 80s copper wires that the system burns. This produces oxidative stress that leads to pain, extreme muscle loss, weakness and everything you’ve written. The problem is in the head that no longer has the space and strength to resist the DHT and the consequent load of the neurotransmitter. I’ll ask you a question, have you ever suffered from recurrent migraines?? I did a lot and it was the sign that my head was struggling, I never explained it to myself, now I understand …

The possible solution goes through the reconstruction of neuronal plasticity and the ability of the brain to support an adequate production of neuro steroids which in this case is cut because it is considered superfluous the brain defends itself by turning off the source of inflammation if the neurotransmitters produce stress and inflammation the brain reacts trying to turn them off with the cut of these activities and from there the physical symptoms to fall … They are my theories evidence of scientific foundation take them for what they are.

Know that I did MRI with contrast to the skull and marrow, CT total body, 2 EMG with nerve conduction test, numerous blood tests without finding anything. There are three or four of us in this forum to be so I am very similar to your condition unfortunately but there is no cure the only thing I can tell you is to stay away from any stimulant (tea, coffee, zinc, vit. d, Mucuna, weights, creatine …) it worsens the load on your brain that is not able to hold as the Aswanaganda tablet gave you proof that increased your T and therefore the DHT that no longer has room in our brains to work safely without doing damage and producing beneficial effects. I’m close to you. Good luck and write to me but above all tell your surgeon who didn’t understand anything about what you have and possibly try with a good neurologist even if even there it will be difficult to find something useful

I’m not but the issue is my neck. My atrophy is severe from immobilization for 10 months. Only 1 month of rehab and boom, hit with this. My muscles don’t work. I can’t strengthen them and now my hardware is failing. My surgeon says I’m at risk of catastrophic failure but realizes surgery in my condition is incredibly risky. So unfortunately, time isn’t really on my side! My fusion is only partial so there is instability at C1, C2, C3, C4. And now the muscles I need to strengthen I can’t. Until they turn on, atrophy will continue. This alone will leave me bedridden. I’m still in shock. And my guess is this crap has hosed bone metabolism so future fusion is bleak. I already had issues growing bone before. If my neck was normal, then sure time. Even now though I’m mostly bedridden because of this. Sorry, I’m in shock.Screenshot_20240803-123012|230x500

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I am so truly sorry you’re going through this. That was a harrowing read. Please read my experience with sodium butyrate. Its nearly took me out but I did recover from it.

I also took ashawganda for over a year and I feel it has accelerated my decline. Crashwaganda.

You are in my thoughts my friend. Please reach out at anytime you are not alone!

What are you eating these days?

I feel very alone. Only my brother and my Mom are starting to understand the severity of my condition. I’ve started a document to tell my life story so that someday my girls, only 7 and 8 now, will know a little more about their dad and what I’ve gone through. Everyday is torture.

I’ve looked into sodium butyrate but I’m scared it will accelerate my decline. As far as food, mostly keto type diet and I take digestive enzymes. I’m pretty sure this has destabilized my digestion and I’m no longer get nutrients properly. I feel sick after eating and am sure it’s to do with poor gut motility. I force myself to eat but like many, I have no signals for hunger or thirst. Everything is just gone. I tolerate low dose vitamin E, Vit D, L theanine, bioquercertin, ALA, vit B to try to offset the oxidative damage that has occurred. I also sip Remag in water throughout the day to help reduce excitoxicity, help mitochondria heal, improve gaba and calm nerves. I’ve only been doing this for a week but will continue as long as I can. I use taurine, melatonin at night. It’s not ideal but gets me to 4 hours of sleep or so vs the 2 I was getting. I take 2.5mg each of DHEA and pregnenolone in the morning to try to nudge neurosteroid biosynthesis back online (everyone does extremely high doses of everything which is why in most cases it makes them worse. Our systems cannot handle it, so trying microdoses.). So I’m trying to slowly heal the oxidative damage and support all these messed up systems in hopes they can come back online. It might be a futile effort but it’s better than nothing. But yes, small doses of everything. I read far too much about people taking standard doses or high doses and I know our fragile systems cannot handle it but using microdosing approach based on a doctor in Lebanon who has had success treating people with post drug syndromes (not PFS per say, but PAS, Floxed, Lion’s Mane, etc).

It might be helpful to show others this presentation that PFSNetwork made:

as well as this research publication:

May help with people who deny this condition. The studies were done on people who took Finasteride but as previously mentioned all these drugs seem to cause the same syndrome.

Thanks. I’ve sent this and similar to my wife and family. They respond with, you didn’t take finesteride, even though I tell them ashwaganda can have similar effects. Ultimately, I am struggling considerably. I manage to get up out of bed a few times a day in a CTO brace but I know, this will be short lived. My options now are, I can attempt to walk about in the brace but still risk further hardware destabilization or deteriorate in the bed even if sitting up supported. There are no good options here. I wish my muscles would just turn on and start working again.

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I would honestly ditch those supplements. Some have been known to make others worse and could be contributing. Of course take this advice with your own discretion. But I know some supplements have made others much worse myself included

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Understandable. I’ve read about it everywhere. People crashing from everything. For now, everything is microdosed except taurine and remag. Taurine has helped me more than anything else especially regarding the nerve stuff. If I’d previously been a healthy person and got hit, I’d probably take that advice and for the first month, I was off everything. But given my situation with my neck, I have to try this. It’s a sound protocol for reducing oxidative stress, rebalancing glutamate and gaba and at least trying to reduce what is obvious excitoxicity. Now whether it’ll work, I don’t know. I have the experience of two people who’ve followed this same protocol, albeit both were healthy, before taking expired ashwaganda in a similar dose as me. But like anything, everyone’s biology is different. I truly wish I was in a wait it out type scenario. I’m just very close to catastrophic hardware failure and neck collapse. It’s not an exaggeration, it’s the insane reality for me. My surgeon requested additional MRI and CT scans early July to track progress. I’m reaching a situation where this is becoming a life threatening emergency but also my surgeon realizes that in my state anesthesia, IV antibiotics, pain meds, all the normal stuff they use for such a surgery could worsen this condition exponentially or possibly kill me because my CNS just could take the shock of it all, let alone clear the stuff. So yeah, this situation is like staring at turd sandwiches, neither is good but I’ll have to eat on of them at some point soon. And it is just insane. Yes, it was very stupid of me to pop a two year old supplement without thinking, but also, I don’t think anyone would remotely think it could do something like it has done to my body. Like my friends have said, they take old vitamins and medicine all the time. Most of the time, it’s not a big deal or you might feel a little sick. One friend threw out her 1.5 year old ashwaganda bottle. She told me, she was literally thinking of taking it again until this happened. Just stupidity and very bad luck I guess. I’m really trying. For now, it’s doing this protocol and deep breathing literally all day to stave off what all of you can imagine is an extreme stress response which makes all of this worse. It’s human. My life is destroyed and now I have to face a reality where my time with my kids and wife is very much short lived. Sure I might live for years but in a bed permanently, so not really living. I’m just glad there’s a place to share and express what I’m going through with a community that understands to a certain extent. I’m also struggling with past rumination. I know I can’t change it but it’s hard. April 14 making breakfast for the kids, helping out with chores around the house, doing all my rehab exercises, helping my 7 year old with Math, and going to my 8 year old tennis game. To now, mostly bedridden with an extremely uncertain future and a family that knows something is wrong but still haven’t quite grasped how dire the reality of my situation is. It’s not even life in slow motion, it’s like barely surviving moment to moment and life is literally passing by.

Thank you everyone for your thoughtful responses. Everyone brings some level of comfort. It’s nice to know that complete strangers care.

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And now it appears my body isn’t digesting food well. I honestly can’t believe what is happening to me in such short order.

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Still in massive disbelief. I know others have sadly gone through this but losing my wife and kids is hard man. 3 months ago my life was full of promise. After 3 years of surgeries, I finally had a chance to get my life back and boom, gone with a single dose. I just can’t wrap my head around it. Completely bedridden in less than 2 months. And now, I have to worry about bed sores while still dealing with all of these symptoms.

That said, last night, I think I got maybe 5 hours of sleep or so. I don’t know for sure but when I awoke it was at least light out. I never check my phone for time so I don’t increase the sleep anxiety. But still, getting a little more rest is something. First time in 2.5 months. I’m praying that I can at least continue to get this. My life as I knew it may be gone and my neck will unfortunately never recover, at least getting sleep back would be something to make this bedridden experience less of a hell. Sorry all. I’m just speechless. What I took must have been massively toxic. Now for some deep breathing. This anxiety about everything and the loss of my future is insane.

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Unfortunately was just a fluke. Back to 3-4 hours. I will regret taking those 2 pills for whatever time I have left. It was so stupid to take it without looking at the expiration date, but also how could it be so toxic and damaging. Sorry all, I am massively grieving and what’s worse is my upper neck is shifting and starting to cause brainstem compression symptoms. This doesn’t seem real at all. Like 3 months ago, cooking, cleaning, chores, rehab, and spending time with my wife and kids. Now I’m in a bed watching my body waste away. This feels like fate or destiny in some way. Like my fusion wasn’t complete and mostly failed where it mattered most, so I faced an uphill battle with rehab already. Taking that stuff just put a stop to it all. I don’t want to off myself because of my kids but I don’t want to live this level of suffering. Surgery won’t fix this, likely weaken me and probably cause an insane crash. Doing nothing will result in brainstem damage and further deterioration. I’m not ready guys to experience even more suffering man. I wish I could just go peacefully. 2.5 months. 2 tiny expired capsules.

Yeah. I totally agree with you. The issue for me is my fusion is unstable and with all the load on the hardware and loosening I’m in danger of catastrophic failure which could result in a spinal cord and/or brainstem injury. I may not have a choice but to go under the knife again just to save my life. It will 100% likely make my current condition much worse and render me bedridden anyway. There are no good options for me. If my muscles worked right, I’d be back to strengthening but as you know, in this state my body cannot strengthen nor build muscle. As you pointed out with no weights, doing anything like it will only serve to increase atrophy because the body cannot repair muscles normally, so instead attempting to strengthen will destroy muscle fibers further because there is no repair process happening. It’s insane. Every single day I regret taking that stuff. Like every single moment of every single day. I can’t change it and it hurts man. Imagine something like this and now I’m losing my wife of 13 years and my two young daughters. And I know the stress all of this has put me under is making this 1000 times worse but I can’t calm it down. Deep breathing for hours etc. does very little. I was already and lifelong anxiety sufferer, so getting this syndrome is literally the worst thing that could happen to me.