Withdrawal symptoms of celebrex

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Hi, 23M here and I want to ask if this will help treat severe protracted withdrawal from ssris? I cold turkey stopped almost exactly 1 year ago and a lot of seriously debilitating symptoms have not gone away.
The anhedonia/emotional numbing and insomnia being the worst by far but other symptoms like sexual dysfunction and tinnitus have barely improved either. I’ve tried so many supplements from fish oil and shilajit to microdosing psilocybin. So far nothing has worked.
I’ve heard people say that cerebrolysin helped them greatly with alcohol withdrawal or stimulant abuse and I want to know this can help me too.

G'day guys. My name is Liam, I'm 23 and from New Zealand. I posted on this page about a year ago I'd say and asked for advice about my alcoholism. I was depressed and knew I was an alcoholic. I received a bunch of support it honestly blew me away. But I inevitably left with my tail between my legs because it all got a bit 'too real' all of a sudden.
My girlfriend at the time said she wouldn't accept my marriage proposal unless I had quit alcohol and that sobered be up quick. So I went to a few alcoholics anonymous meetings with her and decided after the third one it was time.
Long story short I'm currently four months sober and by the grace of God, I've had zero withdrawal symptoms after 4 years of being a 1-1.5 bottles of whiskey a day drinker! And a few weeks ago I finally popped the question, and she said yes!
So thank you to everyone for your prior support and help, it really means a lot. And for anyone wondering...yes, you CAN do it. You absolutely can. I no longer feel like alcohol is my oxygen (I know you know what I mean). And I know it's scary, but man, lean on God and ask for help, and He will help you.
Thanks again!

A week or so ago I posted explaining how I wanted to quit nicotine pouches and, as suggested by commenters, i bought my last every pot of them. As of today I am on my last two pouches, and I have been cutting down on them since my last post to ween myself off. When I run out, either today or tomorrow, that is it.
Does anyone have any tips to get through the first couple days of withdrawal symptoms and cravings?
Thanks in advance, and wish me luck :)

A brief background: my husband was diagnosed with ptsd after spending 6 weeks in a psychiatric/substance abuse program (in-patient). He is currently wrapping up an additional 2 months in an outpatient program. He has made a lot of progress and the changes are noticeable. He is on a list of meds, has regular appts with his psychiatrist, and of course, weekly therapy. However, lately, I’ve noticed some familiar behavior: slight withdrawal, had one drinking slip, took meds intended for one thing to reduce symptoms of anxiety. I am worried that once he finishes this outpatient program, he may revert back to maladaptive behaviors.
The biggest struggle we have is communication. He has not shared all of his trauma info with me, and I am not pushing him to share or even expecting him to share, but it’s a barrier for sure. He keeps his feelings to himself and doesn’t ask for help. This is very hard for me and I’m not sure it’s sustainable.
I guess my question is: how do I continue to be a support system when he won’t freely communicate? I wouldn’t say I’m walking on eggshells, but I definitely feel like I don’t know what might come next. (We are starting therapy together soon.)

I removed processed foods, added sugars and caffeine from my diet on April 9. Aside from some really tough withdrawal symptoms that have mostly subsided, I’ve gained mental clarity, calmness and unexpected weight loss. Over the past five weeks I am down 14 pounds. I’m 5’6” and originally weighed about 165. I weigh 151 this morning. I’ve been on diet treatment plans like Noom and tried food delivery options like HelloFresh. I even had a gym membership and worked out regularly and just could not lose weight. I work from home so it’s difficult to be as active as I used to be in the office. These 14 pounds have been sticking around with me for the past couple of years and I’ve been working so hard to get them off. It’s startling to me how the weight just melted off of me.
I eat lots of fruit as a natural source of sugar.
I hope this serves some encouragement to those of you who are on your health journey. I actually don’t wanna lose any more weight than I have. I sure hope the trend stops soon.

so I've been smoking weed for 3 years only evenings for getting better sleep first year wasn't a every night thing but from second year I was doing every night less than a gram and third year maximum a gram at night but I had to come off it 45 days ago cuz I was in panic mode after I changed my strains I couldn't get any sleep and I developed an obsession that I lost my ability to sleeping so i stopped weed I think situation got worsen i panicked went to ER 3 nights in a row didn't know that what was going on And I accept the fact that I'm just going through withdrawal symptoms Everything's was going fine for a week and than boom one night I got hit by intrusive thoughts out of nowhere and I got shocked get panicky since than I'm having anxiety and felt like I have no control of my thoughts at all racing 24/7 all negative first months was pure hell but going through second month feel little bit better when I'm with my gf or surrounded by family I feel quite good but when I'm alone it's coming back anyone experienced this before ?

what are your experiences?
I take citalopram around half a year now and overall am grateful. not saying the start was not hard, but it mostly has made a positive difference in my life and I feel I get my old life back, picked up old hobbies, am more able to be in crowded spaces, was slowly able to build some routines. my OCD did not recide, but is less powerful, I have less symptoms of anxiety on the physical side of things.
I still feel as if things still are slowly get better, so I am hopeful the slow but steady rise will continue. I am aware that it is a medication that might rob my body of certain nutrients, so I try to eat healthy sometimes lol. In the end it is a compromise. I am a bit scared of it stopping to work after some years or me getting off it and experiencing withdrawal. I might lower my dose at some point, but want to stay on it as long as possible. As I said, for me it is a compromise. I do not experience what others described of not feeling like themselves.
as a side note I am neurodivergent so it is a reality for me to live with some neurological differences due to brain development difference, so I am mostly referring to anxiety, OCD, depression, outlook.
I wonder how the experience and thought processes is for others that take it some months.

I'm asking out of pure curiousity. I started Methylphendate a few days ago, and I know a person can build a dependence on it, especially if you use it daily. So, if you're a long time user, have you ever experienced withdrawal?
If so, could you elaborate? How long had you been on it, how long were you off it before you started to expereince symptoms? How was it like? How'd you get it to end?
Thanks for the insight! I'm hoping I won't ever have to skip a dose, but who knows. I have ADHD, might forget to get a refill 😂

Hi so i’ve been using cetirizine for an itchy scalp from another skin condition it rlly helped for a long time but im tired of having to take it constantly. i used to take 10mg once every day then every other day and then once every 3 days because of seriously itchy symptoms recurring again but it wasn’t like before it was worse. at the point where i held off on my itchy symptoms on the third day without taking it id break out in hives. i continued usage for a little less than a year. i don’t want to depend on this anymore and i realized my story aligns with a lot of stories about withdrawal from cetirizine. i’m upset there are no warnings and now im miserable. i took a half a dose around 4 days ago now and im dealing with the itching by taking homeopathic allergy meds and homeopathic stress meds which are effective but i have to take maybe 3 per day w the situation now. when it flares up the itching is nightmarish i wish i was never recommended cetirizine. i want it to be out of my system and i don’t want to use it EVER AGAIN. however some ppl said they had to get back on it and taper down to deal w the symptoms and one person said once they tapered they didn’t have withdrawal. i want this to end for good as soon as possible and with as minimal suffering as possible pls give me advice. should i grit it out w the homeopathic remedies to soothe it a little or get back on cetirizine and taper off. don’t rec asking a dr bc they only recommend having it more often lol

Quitting smoking is a journey fraught with challenges. Understanding these obstacles and preparing to face them can significantly enhance your chances of success. Here are some common challenges and strategies to overcome them.

Common Quitting Challenges and Solutions

1. Nicotine Withdrawal Symptoms

• Symptoms: Includes cravings, irritability, headaches, and difficulty concentrating.
• Strategy: Use Tabex to ease withdrawal symptoms. This non-prescription medication helps reduce cravings by mimicking the effects of nicotine without the harmful impacts.

2. Habitual Smoking Triggers

• Triggers: Daily routines, social situations, or feelings that prompt smoking.
• Strategy: Identify your triggers and create a plan to avoid them or replace smoking with a healthier activity, such as walking or drinking water.

3. Emotional Dependence

• Issue: Many smokers use cigarettes as a way to cope with stress, anxiety, or depression.
• Strategy: Develop new coping mechanisms, such as exercise, meditation, or engaging in hobbies. Professional counseling can also be beneficial.

4. Social Pressure

• Pressure: Social situations where friends or family members smoke can increase the temptation to smoke.
• Strategy: Communicate your goals to your social circles and seek support from friends who encourage your quit attempt. Choose to spend time in smoke-free environments.

5. Fear of Weight Gain

• Concern: Many fear weight gain as a common side effect of quitting smoking.
• Strategy: Maintain a healthy diet and regular exercise routine. Focus on the overall health benefits of quitting rather than short-term weight changes.

6. Overcoming a Relapse

• Challenge: Slipping up and smoking a cigarette can feel like a failure.
• Strategy: Treat any relapse as a learning opportunity. Analyze what led to the relapse and strengthen your strategies to prevent future occurrences.

The Role of Tabex in Overcoming These Challenges

Tabex plays a crucial role in overcoming the challenges of quitting smoking by reducing physical dependency on nicotine, thereby allowing you to focus more on the psychological aspects of quitting. By diminishing the severity of withdrawal symptoms, Tabex makes it easier to stick to your quit plan.

Conclusion

Quitting smoking is undoubtedly challenging, but with the right strategies and support, including Tabex, you can overcome these hurdles. Each day smoke-free is a step towards a healthier life.

I've decided to come off mirtazapine the side effects are getting worse for me and I can't deal with them anymor,more depressed more anxiety detached restless and the list goes on plus its not a great med to be on with me having kidney disease I did not know this before I started it
I have been on it nearly 3 moths at 15mg my GP thinks it's OK to drop to 7.5 mg for couple of weeks then stop because I haven't been on it long and said its a low dose but that seems a bit quick to me
So anyone that is coming off and tapering or has already come off it what was your taper like ? and what doses were you on ?and for how long ?
Not looking for medical advice just other people experiences thanks
Also did you get any withdrawals and what sort of symptoms?

How I keep weight on me and do back-to-back fasting?
When I do back-to-back extended fasts I go into a fasted state into a feasting state. I rapidly gain weight back from water weight, body density, muscle strength, etc. I break the fasts in different ways. Though, I prefer to break it healthy or with fruits or vegetables. Sometimes I break it with conventional foods like snacks or a microwavable vegan meal. It also depends on the fast as well. If it was a pure dry fast the whole way through then I'm breaking mostly on fruits then later some vegetables. I find it easy to gain weight back. I tend to feast on different foods. A lot of vegetables with some favorite snack foods like chips and one carby meal. Along with more snack foods like packages of cashews and some sweet snacks with not too much sugar in them.
Then my feasting window may go longer than I would like it. Then I'll move to eating pizza and plant-based burgers, potato wedges etc. So, just a lot of carbs and snacks.
The snacks really add a lot of calories very quickly. At the moment I am probably around 184lbs. After ended those back to back fasts I was probably about 181lbs. Before the start of those fasts I estimated I weighed around 195lbs. During the breaks and refeed periods I get back to working out. Full body workouts, machines weights and leg workout and cardio at the track. Carbs plus working out adds a lot of weight rapidly. Usually, after working out I start eating and I eat all night long. I'm eating something once I finish the meal, I am then snacking for the rest of the night. Along with lots of water. That adds a lot of water weight as well. All of which comes off in the first 2 days of the next fast.
Now, doing back-to-back extended fastings ultimately is reducing my weight as my overall net fat loss continues to trend downward despite feasting on refeeds. Because it's a lot of fasting. More fasting then eating basically. According to a friend 145lbs would be my weight at very low body fat percentage at 3-4% body fat levels. So, with that figure I can estimate I'm carrying about 40lbs of fat including water weight and body density, food contents. Without the dramatic weight loss in the beginning of the fast then probably around 25lbs of pure fat at this very moment. Although, at this moment my goal is not to keep lots of weight on me. I will allow my weight to trend downward to a normal body weight of 170lbs. If I wanted to keep weight then eating and feasting a lot more on carbs would do it.
How I maintained weight by living off almost exclusively an 80-90% vegetable diet along with back-to-back dry fasting for nearly an entire year of 2018?
I lived on this diet for nearly 3 years from 2017-2020. Yes, this diet really has a lot of benefits. First, there were no messy bowel movements. There was no smell. No stinky smell. Nothing. It's a diet filled with a lot of fiber. And there's very little concentration of any macronutrients. I received a lot of some nutrients but, it was slow absorption because of the large amount of fiber in the diet. I allowed myself to eat only 10g of sugar in a snack food. I barely had any conventional sugar. Sometimes, wheat bread or some variation of breads I ate outside of eating vegetables. That was as worst as my diet was during those 3 years. No meats. No cheese, no dairy, no eggs. Just vegetabes with a small amount of fruit. These vegetable mostly consisted of steamed or boiled cruciferous vegetables such as cauliflower, broccoli, brussel sprouts, and carrots, potatoes. Leafy greens, tomatoes, cucumbers, pickles, olives, string beans and salads with no sauces. Every now and then I might eat a very expensive small personal vegan pizza made out of cauliflower, vegan cheese and vegetables.
With a diet like that you would think it would be hard to maintain weight. Initially, I lost weight. Once I reached around 170-175lbs in back to back fastings. During my eating I normally feasted a few hours a day on these foods. I counted the calories and I always reached 2000 or more calories in eating. During two back to back water fasts is where I lost most of my weight from 195lbs to 178lbs. The water fasts were 13 days then followed by a 9 day fast.
Every other fasts were hard and soft dry. I was doing on average 2 extended dry fasts a month of 5-9 days then followed by 5-9 days of eating during the whole year of 2018. I feasted as much as I could every day. I probably gained 2-3lbs or more fat back.
With that diet there was very little detoxing during the first 7 days. Most of life just felt physically normal in the first 6 days of dry fasting. My body was highly adapted to it and it was as easy as driving. I never struggled with any detox, pain symptoms, fatigue, withdrawal effects. nothing. Only going to 7 days did I began to release a lot of toxins and things started dying when hitting that wall. The second crises. I never really broke through it.
I eventually reached around 168 - 170lbs. Like I said, your weight eventually trends downward with all of the fasting even though I feasted on buffets of foods. If you're naturally underweight then you would probably want to add a lot of water weight on a healthy diet or a conventional healthy carb diet through feasting. Along with weight training adding muscle seems to traps more weight on the body as well. Most people deal with being overweight in that case stick to high water content vegetables, workouts and 1 carb meal along with an abundance of vegetables and water to refeed in back to back extended dry fasts.

I posted a little while ago about my experience with seizures specifically ones that occurred due to the withdrawal symptoms of alcoholism. I have now been sober for a few years but I still experience crippling anxiety about having another combined with poor sleep (insomnia). Sometimes while falling asleep at night I will have the almost extreme moments of anxiety where I’m almost about to fall asleep but all of a sudden out of nowhere my head feels like it’s exploding. It’s not painful but it’s like a very aggressive feeling of panic and my vision changes and gets very blurry. I am wondering if these are panic attacks or partial seizures or if anyone else has experienced this before?

So since January I started experiencing awful visual issues, I had an MRI, CT & blood work & all came back clear, since then I started developing twitching after taking amitriptyline and I just assumed it was a withdrawal or simply BFS. In 2/3 months I have had muscle atrophy in my back, thighs, calves and I’m certain my tongue has became weaker and so has my neck - I have no swallowing issues but my swallowing feels odd and my speech perceived by myself feels slow and not right at all.
I have seen countless neurologists in this time and they have all sent me back with a clean bill of health even though I have had 1 EMG which showed ‘chronic neuropathic changes mainly distantly’ and therefore a Neuromusculur neurologist diagnosed me with bfs & anxiety.
I know for a fact I have probably one of the worst progressive types of ALS you could get especially at such a young age - the atrophy was noticed by an NHS doctor who has sent me for another EMG in 3 months? But I have a private EMG on the 16th of this month. I’m absolutely terrified I have no understanding to how this could of happened, if all started after I took some mirtazapine to help with insomnia and I believe this has triggered something although there is 0 literature of this ever occurring and that’s why I can’t believe this happening to me.
I’m here to see reassurance even though I’m certain I’m dying and loosing everything so rapidly - I believe I have JALS or bulbar onset due to the changes in my face & throat etc… the one thing I can’t understand is how multiple parts of my body seem to be loosing muscle at the same time, I have read that ALS starts in one and moves up to the next etc but for me it seems like it’s everywhere.
I don’t know to be honest I don’t really know I didn’t want to post this at all but I just maybe might find someone on here that is experiencing disgusting symptoms, had a bag EMG and still came out the other side. I don’t believe I will, my family & girlfriend currently think I’m completely fine due to the reassurance from all the doctors and even the Neurologist who read the EMG still diagnosed me with BFS?
The EMG was on 2nd of April and at that point I knew my legs were smaller but it wasn’t extremely extremely noticeable - the EMG had no active neuropathic changes as PSW and FIBS were normal, it was just + AMP, + DUR and - INT PAT with seen fasiculations.
Overall I’m lost and i know it’s known that vision isn’t affected by ALS but I read reports and I legit match the symptoms such as reduced eye tracking, impaired VOR. I just feel like the most unlucky person on this planet like how can I have all these visual symptoms and horrible physical symptoms at such a young age just after taking some anti depressants to helps with insomnia.
I really need some support guys and I want to truly believe I’ll be okay but as of right now nothing can sway my mind and I’m dreading the 16th for what it will show, I’m going to honestly just walk in and say ‘I believe I have bulbar onset als just please start on my face and work your way down’
I just can’t believe that I’m completely fine when everything in my body is changing and has changed so quickly. I can still ride my bike, I can still run, walk fine and do any activity I want. (Other than football probably because of my vision) but I can’t do them well. I used to be able to run 5k without any aches in my body but now my feet hurt and so do my legs and I’m just a complete mess.
Much love and I hope people on this forum can comfort me with reassurance :(

I'm a 38 y/o female.
I was diagnosed with asthma as a kid.
Current meds Soprobec 200 two puffs AM, two puffs PM, ventolin as needed.
I moved into this flat in 2022, was fine before I moved and to begin with, then I developed worsening asthma symptoms as the months went on. I spent ages trying to fathom out the possible cause. I found no sign of mold or anything like that. then found out tobacco smoke from the man downstairs was coming into mine, it's been so bad on a couple of occasions my bathroom has 'fogged up' with smoke. I have tried everything, including having the council works department out to see if we could seal up any gaps etc, nope, no way of stopping it. He seems to vanish for long periods of time, leaving his flat empty. During these periods, my asthma symptoms vanish completely.
In response to my worsening asthma symptoms, in Jan 2024 the asthma nurses at my surgery decided to increase my ICS dose of Beclomethasone from 400mg a day to 800mg a day. Now I have high functioning Autism on top of all this, I am far from dumb or stupid, but anything to do with numbers seems to go over my head a lot of the time, even though I am better at maths now, amounts of things can still flummox me.
NOBODY told me this was considered a moderate to high dose and I should be carrying a steroid warning card, nobody, not once. I wrongly guessed it was only a few mg more than the soprobec 100 I was on. The Soprobec 100 was two puffs am, two puffs pm.
Now, since I have been on the Soprobec 200 at 800mg a day, I have developed some extreme and very disruptive possible side effects.
All possible other causes of these symptoms just got ruled out in a complete bloodwork which included diabetes, hypercalcemia, thyroid and iron deficiency, which are all possible causes of the things I have listed below, all tests have come back requiring no further action.
These are:
EXTREME, unquenchable thirst. I am drinking easily over four liters of water per day. I am also waking up several times a night for a drink, and if I go out I must carry water with me otherwise the thirst is VERY distressing. I feel dehydrated on a 'cellular level', like it doesn't matter how much I drink, I feel thirsty WHILE drinking water!.
Fatigue so bad I can hardly get up out of my chair most days and I am asleep by 9pm, where before I would like to chill with my dog watching a film or something till about 12pm. I have gone from waking literal miles through local fields and woodland with my dog, to barely being able to take her on the local park which is only across the road. I hardly ever go out, and if I do, I suffer immensely as my muscles start aching. I live upstairs and I am struggling getting up the stairs.
It feels as if I have lost all muscle tone all over my body. I no longer feel safe walking my dog as she is med size mastiff cross who is quite strong, she has almost pulled me over at times and I cannot even lift my kitchen bin bag or the laundry basket, I have NEVER had this problem before.
I have lost my appetite and have to force myself to eat every meal, often taking hours rather than minutes.
Episodes of vaginal thrush, something I have NOT had for YEARS, started when I went on this high dose of ICS.
My once 'perfect' periods are now very heavy and irregular.
I feel more angry than before. I had to seriously check my anger levels in my adult years, and developed a much more patient and stoical outlook to life, which brought my stress levels down massively. Since I went on this inhaler I have been snapping at people again, including my own family :(
Tingling hands. This can come on anytime, never had it before the inhaler.
A terrible hoarse voice and it feels like my voice is getting deeper and I am starting to sound 'male' other people have noticed this too.
Profuse sweating on my hands and feet. My hands DRIP with sweat, to the point I hide them from people. Never happened before this inhaler.
Salt and red meat cravings. I am not a big fan of either, and due to heart problems in the family I keep my salt intake low. Other day I just felt compelled to walk into the local coop and buy pork loins and a pack of beef biltong, things I haven't eaten in many moons. I recall saying to myself 'this is SO out of character for you'.
Episodes of nausea, two episodes of vomiting in the morning over two months (not preggers before anyone asks lol) which were not related to anything I had eaten.
Dizzy spells and almost fainting, usually happens if I push myself to do even basic stuff like household chores, which I usually enjoy doing.
I know these are listed as 'rare' side effects, but unusual thirst, tiredness and weakness is mentioned both in the patient info leaflet with the inhaler, and in various other information regarding side effects, such as this article: https://www.mayoclinic.org/drugs-supplements/corticosteroid-inhalation-route/side-effects/drg-20070533?p=1
I take the inhaler via a spacer, my technique is good, I've been doing this whole asthma game all my life, so I am pretty ofay with it all now lol.
I have had a battle over this inhaler with my GP and other asthma services as well. They just do NOT believe ICS can have systemic side effects, in contradiction to what the drug manufacturers say on the leaflet. I think I am going to have to go back to the GP and stand up for myself, which is not something I am good at at all, and present them with this information leaflet, which actually tells you to consult your doctor if you develop any of them!.
Would it be worth asking to try the same dose, as I do not want to risk withdrawal, I have experienced this before from ICS, but on a different steroid with a different inhaler?.
Is there any more bloodwork I could ask for, perhaps adrenal function or cortisol levels?.
I am at a loss, I need to control my asthma, but I also need to be able to live!.
Thank you for taking time to read this, I hope everyone is well and your asthma leaves you alone to enjoy the summer!. :)

Hi folks, my brother is 1 week into withdrawal from meth, and he’s developed a severe cough. It’s so bad that he has a hard time having a conversation. Is this a common withdrawal symptom, particularly among folks with asthma? Any tips on how to help alleviate the cough? He does have and has been using his asthma pump but the coughing persists. Any tips in general on easing the withdrawal symptoms?
I’ve tried to get him to reach out to any of the many local orgs that offer support / counselling / etc. but he insists on going this alone. I’m worried that the discomfort he’s experiencing will weaken his resolve. Any advice on this or in general would be very much appreciated!
In case this might help to know, he said he’s been a daily user of 1 to 2 puffs a day for the past 2 years.

I'm still struggling to find anyone to get me something that isn't effexor to take, but in the meantime guess her managed to miss her dose!? This sad potato! I'm so tired of this, I managed to not add it to my pill case but I put everything else in so it took me all day to realize I didn't take it. I've taken it but does anyone have any tips for handling the withdrawal symptoms while my pills get to work?

"Yes, some psychiatric drugs can cause permanent damage, but this is not a guaranteed outcome for everyone who takes them. The risk of permanent damage depends on various factors, such as:

1. Type of medication: Some medications, like antipsychotics, can have a higher risk of permanent side effects, such as tardive dyskinesia (involuntary movements).
2. Dosage and duration: Taking high doses for extended periods can increase the risk of permanent damage.
3. Individual susceptibility: Some people may be more prone to experiencing permanent side effects due to their genetic makeup or medical history.

Possible permanent damage from psychiatric drugs includes:

1. Tardive dyskinesia (antipsychotics)
2. Neuroleptic malignant syndrome (antipsychotics)
3. Parkinsonism (antipsychotics)
4. Sexual dysfunction (antidepressants, particularly SSRIs)
5. Cognitive impairment (benzodiazepines, particularly long-term use)
6. Dependence and withdrawal symptoms (benzodiazepines, antidepressants)

It's essential to work closely with a healthcare professional to weigh the benefits and risks of psychiatric medications and monitor for potential side effects. If you're concerned about permanent damage, don't hesitate to discuss your concerns with your doctor."

I keep hearing that it’s a high risk to combine some herbal supplements (which actually address symptoms) with some of my prescriptions (which are ineffective). So, I’m opting for the supplements and tapering off the rx. I’ve taken counsel from my doc regarding this. And 2 that I am weaning from, I’ve heard the withdrawal can cause neuropsych issues that were previously non-existent. Anyone have this experience with with either Wellbutrin or Effexor? Especially weaning this combo? Any advice?
May the psychiatric profession be cursed. Took me one year of messing around with herbs to resolve what they failed to for 30 years.

This isn’t really a mom post but I feel better posting here than in a doctor sub, as they can be pretty rude. Would really love some insight if any of you had this happen and what it was?
For the past few years I have felt crappy most days than few. Lately this past year it’s been a nightmare. In may 2023 I had a random cyst that’s been deep under my skin rupture and it turned out to be an extremely rare type of staph and an unidentified other type of bacteria. I was on 2 antibiotics before I was sent to the hospital. I was then admitted and on 3 iv antibiotics and it kept getting worse and I kept having reactions to literally every antibiotic. They ended up having to cut a gold ball sized hole to clear the junk out and I was in patients 14 days and had a nurse come daily for 3 months to my house. Then in December I caught Covid and was admitted four days and in February flu b and admitted another 7 days because my body was going ape shit. High BP High HR High Temp and no meds helped. Now I have more cysts than ever and have literally waited a year to get into a derm. All my bloodwork is perfect minus low iron. I’m so over how I feel. I’m nauseated 24/7, tired all the time, get boughts of high heart rates for days on end (135-147) (normal ecg minus tachycardia) feel like I’m going to pass out, dissociate all the time, horrible memory, periods are all out of wack, smell burning all the time or rubber, itch all over, bad constipation or diarrhea, a crawling and burning sensation in my skin, my face is always red, I feel malnutritioned even though I’m 214 and haven’t lost weight. I eat healthy 80/100 and am active at work. I drink a ton of water, watch my sugar and dairy and grains. I don’t do drugs, I do smoke ciggs sometimes, but I feel like I’m stuck in flight or fight. I can’t sleep, and when I do sleep I’m either up every hour or out for 12. I have dark circles under my eyes and my teeth are basically rotting and can’t find a dentist who will take my insurance. Literally every blood test I’ve had is fine! I’m to the point I cry every night and at work because it’s too hard on my body. I’m a single mom and this job is the only one I have and I can’t find anything remote or anything that pays better. I don’t know what to do. I’m seriously depressed and anxious 24/7. Has anyone had any of these symptoms? Even in the hospital the doctor kept saying it sounded like withdrawal but I’m literally on no drugs that would cost me to withdraw. I take Ativan maybe once a week if I’m having a panic attack only. My doctor is at a loss.
To add, when I do eat I immediately want to vomit but don’t and even water fills my stomach yet I’m still over weight. I’m starting to think it’s all inflammation.

I am a male, 30 years old, about 140lbs, not on any medications.
I recently (11 days ago) quit cannabis after long term chronic use, I had been generally getting better until tonight where I had some plain white rice and plain steak, about an hour later I began to feel some light nausea, chills, lightheadedness and suddenly began to cry seemingly out of the blue, I understand this is likely due to the withdrawals but I'm already nearly two weeks in and this is the first time things played out like this, I'm wondering what could have caused it, I read white rice can raise serotonin, could that have been the cause? It seems my other symptoms line up with that, and if so is there anything I can do right now to feel better?
Thank you for your time.