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Found 8 results

  1. Hi all , I am 8 months off reinstated sertraline for a month ( by doc) and Aripropazole. History Its around 4 years back when i passed out my college and not get placed even after making to finals in many interviews .. that i decided to write competitive exam for PG. I had taken coaching but just before exam I came back and found myself unable to recall things. My brain is just like nothing in it. I found myself in despair and stopped studying. This fog is happening all the time since my engineering but I managed to get average marks sometimes and sometimes very good . There is more in back history but I ll get to it later. So, my parents took me to a psychiatrist ( family known) and he put me to Olanzapine and one more thing. He diganosed me bipolar2. I got about 10 pounds on it but its not help . Meanwhile after 4 months, with the help of a relative , I got intern in a company and I moved out with fog to a distant city. TThere in a hospital, they put me on floxetine and Amisulpride for 3 months . Then i moved to a private psychiatrist ... where it starts getting haywire . He stopped fluoxetine and Amisulpride . And put me on Venlafaxine and Seroquel... As i was interning, i get usual heat racing in between job times but my doctor convinced me to stay with it . 4 months and I just started feeling agitated due to stress. It happened that I slapped a senior on abusing me and there I left a job I never happened to get physical in my school or college .. but it happened. Doctor told me to scrap the prescription he wrote of raising Venlafaxine. And he put me paroxetine + Oxcarbazepine. In his words , it is best tolerable and has lesser side effects. I managed to get a job by my own and cracking first time. But this time there is lot of work and culture pressure. Its a startup with full of politics . Boss and his boss .. all keep on putting things. Let office aside, I started feeling some well .. overly casual ... excited .. raged .. Iits about 25 mg Paroxetine and 300/600 mg Oxcarbazepine. I had unusual violent acts .. had hit a school friend .. insomnia.. I decided to leave the paxil by asking the doctor . He said half in a week and then other half a week to off. Thats when it all started , i cannot sleep whole night and with day light i start getting a nap. I left going office with fear of state i was in . I cannot wake and even if I .. i was too tired and angry . Doctor then gave me Mirtazapine which didn't help . I resigned job telling muly boss about all and came back home. It was Nov,2015. I start getting yhese uncontrollable rage that I locked myself in a room. Parents took to a local shrink who put me on Venlafaxine+ Mirtazapine(CRF), lamotrigine, resperidal, Seroquel. The NEXT Day I woke up so fresh .. all calm like 12 yrs back .. i was smiling happy.. but it lasted only 4 hrs .. and i am doomed again . I took those meds 10 days and i decided to go off. Physical Damage. I got brain zaps as sounds with eye movement .. While on Paxil I got severe neck stiffness and movement pains - which came out as Osteophytes. Anger , heart race , memory, fog , chest pains , fatigue ... All I beared for 4 months. Reinstatement after 4 months. Father took me to another psych who put me on Sertraline+ Aripropazole+ Seroquel. I started having increases restless legs than before and the doctor asked me not to go over net. After 2 visits and when he said it wslas Aripropazole for restlessness all time.. and he is cutting it . I stopped all meds . Withdrawals in 8 months. All first symptoms with some new like utter sensitivity in teeth. It is while breathe in most of the teeth . Muscles gone from forearms .. My left hands gone ulnar neuropathy and i got surgery done when no hope lived. Right hand has stiffness too . MAnger I am living with .. I have stopped talking .. I have decided to go sit on my Shop but I was unable to understand the talk . In spite anger biuts and memory makes it difficult to adjust. I keep forgetting people faces .. important talks . So i stopped . Now I am muted all the time with burst inside . Read success stories and play CoC. This is the most I can write now.
  2. Hello, My name is Cathy and I live in Minnesota. I have a long history of depression, numerous meds, ECT, a study for VNS, a study for genotypes, etc. Typically I would get into more detail but it hurts too much to type. I started Nardil about 7-8 weeks ago and was on a steady 60 mg. dose for at least five weeks. Early on I started developing "carpal tunnel" type symptoms. I had done a short MAO trial in the late 80s and remembered when I was on one, I had almost had carpal tunnel surgery. I went off the MAO for other reasons and the symptoms all went away, prior to surgery fortunately. I later learned that Nardil depletes B6. When my symptoms started this time, I began adding in B6. I was not sleeping well, often up til 4 or 5 am unless I took Trazadone, in which case I would sleep until 4 or 5 pm. About two weeks ago, I started getting more fidgety, restless legs, etc (the insomnia was different from what I typically have--if I can't sleep it is usually because my brain will not shut off. This insomnia was as if my body did not want to go to sleep--tossing, turning, etc. My back and neck started becoming tighter too--I am a typical type A, first born, Taurus, former lawyer--so they are usually tight to begin with. This was worse. With insomnia, restlessness, etc. I stayed up and did a lot of housework, cleaning the basement, cleaning the garage, etc. Somewhere along the way, my shoulders, neck, arms, and hands developed excruciating pain. The hands were typical neuropathy symptoms. I could not drive or type. I used heat, ice, lots of Ibuprofen, Naproxen, Tylenol, and even some old celebrex. I did gentle stretches. I had chiropractic. Nothing helped. I went to urgent care and was given muscle relaxers (one that was safe with an MAO) and a referral to physical therapy. Those did not help either. All in all, I think the symptoms were due to pyridoxine depletion (my nerves were probably more prone to damage--recovered alcoholic who had footdrop--although the college incident makes me wonder if I am just low on B6 to start with), a lack of sleep (thus no healing), and the added movements and tension. I am still experiencing the neck and hand pain. It is a little better now, thus the typing. However, in the last few days, it has been to the point where I can't even move my fingers. I am now going off Nardil. I feel more depressed, angry, irritated, jumpy, fidgety, extremely restless, tired but not sleepy, and in general, bad all over. I am not sure when the use symptoms overlap with the withdrawal symptoms. Typically I do not have much for withdrawal symptoms, but this sucks. I did read the advice--keep it simple and stable and taper slowly. Right now I am about one step away from checking in to the hospital--but it is the weekend and the holiday on Monday. Plus once I get there, I will have wished I stayed home. Just looking for support and understanding. My fiancee (provided our relationship makes it thru this) does not really get depression or meds. He tries, but his understanding of it is limited. Thank you, Cathy
  3. I recently have been working on cleansing my system. i was on several pscyh drugs over the years but olanzapine was hell on steroids. i am on my third year of symptoms. the term 'mad as a hatter' comes from chronic mercury exposure while making hats. looking back on my insanity during withdrawal i have to consider my own mercury exposure and its role in my withdrawal symptoms. while discontinuing olanzapine, i developed verbal tics and jerking movements, similar to tourettes syndrome. there is an article on pubmed of a case from olanzapine withdrawal causing tics. ironically, olanzapine is used to treat tics. but eli lily pushes zyprexa on everyone including the elderly and children so thats no surprise. there also seems to be a link between mercury and tourettes and i have five 'silver fillings' in my mouth' and looking back i think my mental health problems began shortly after putting them in. some have been in for almost 20 years now. i don't do sugar or soft drinks anymore but a coke used to make me sick when i was peaking during withdrawal. i would imagine that the hfcs, carbonation, and aluminum from the can combined with acid hitting a mouth full of mercury sounds like a recipe for disaster. so no wonder it made me sick. i have been doing a cleanse and was getting good results for the most part. mostly was trying to deal with parasites and put some the EBV/CFS in its place that i got last summer. i realized too late that i was also mobilizing mercury without a binder in my gut. i was using acetyl cytseine (NAC) and MSM both sulfur based supplements. also organic vitamin c powder, b12 and glutathione. i was planning on removing metals at some point but havent done so. most of the supplements i take can mobilize mercury i realized as they are for detoxing. if you mobilize mercury without a binder you can redistribute it around tissues, organs and brain. so no good. you can get it out but sometimes organ damage can be very long lasting and even permanent. i kind of wish i wouldn't have flushed all that candida down the toilet now bc it was probably at least feeding on my mercury. itll grow back im sure lol. oh boy love how us amateurs have to figure this stuff out on our own. but i seem to have myriad problems happening that are uncharted territory for most steroid and antibiotic GPs. my point of all this is i think there might be a link between mercury exposure and severity of withdrawal. olanzapine isn't easy for anyone and any of them can be hard but withdrawal symptoms and mercury toxicity are almost exactly the same. together i would imagine to be quite synergistic. i have also noticed that my nerve pain has gotten more severe and my kidneys are a little tender in addition to my tics getting worse. but its only been a short time and my symptoms arent that much more severe. so i wonder how much my mercury exposure is preventing me from becoming fully well and exacerbating my withdrawal symptoms or visa versa. i am making plans to get them removed from a biological dentist because you don't want to use a regular dentist. so if you haven't started tapering or are stable and have fillings in you might want to get those out and do a several months long mercury cleanup. it may make your life a lot easier and prevent brain damage. i really have felt brain damaged but i continue to improve but i still have plenty of symptoms. i know im ready for the burning hot nerve pain to be over though and the tics and pretty much all of it to be over. still one more drug to quit to boot. Lord give me strength. anyhow i thought it might be an interesting link to consider in all of this withdrawal business. i would be pretty apprehensive about fish oil myself and never felt super great about taking it but thats just me personally. cheers and God bless.
  4. Serotonin Toxicity vs. Serotonin Discontinuation Syndrome: I have had very severe chronic serotonin toxicity. Neuralgia and neuropathy developed over a 4 years period to include the entire right side of my body. Level 8-10 pain daily for 12 weeks before anyone figured it out. Given injectable IMITREX to" help" -- wrong, made it worse, could have killed me! The toxicity started wrecking my ANS: sweats, chills, loosing 1/2 - 2 lbs daily for months, high fevers, low fevers, high blood pressure, migraines, vertigo, bowel issues, at points inability to walk or voluntarily move my body. Basically, hell. The pain was so severe that I would dissociate — once for 3 whole days. Are there any resources here or elsewhere that offer in depth information about Serotonin Toxicity? The toxicity was caused by receiving TMS treatments. Transcranial Magnetic Stimulation. I had one round of 36 treatments 4 years ago, got me out of depression and "coincidentally" a developed neuraligia/neuropathy at the same time. Again had TMS this past December - February. The doctor who treated me is a leading researcher, psychiatrist, runs a program training other docs to give TMS treatments and I mean it -- a really a lovely woman, smart, and compassionate -- told me when I was asking if the TMS was giving me muscles spasms and increased nerve pain, "That's an issue for your neurologist." Previously she had also told me that one of the ways that TMS works, is it increases the effect of serotonin based medications. She didn't see Serotonin Syndrome sitting in front of her and asking her "What's going on here?" Today the pharmacist told me that TMS reduced the blood/brain barrier. WARNING: TMS + Venlafaxine caused serotonin toxicity for me, be cautious! Another smart compassionate and more curious woman and — my psychiatrist figured it out after I delivered her all the puzzle pieces I had been collecting. She told me to immediately stop the Imitrex and start a taper of Venalfaxine. VERY SLOWLY, though she didn't give me specifics on what slowly meant. I came up with what I thought was slow taper, and half way through had to double the length. I tapered Venlafaxine in 3 months from 225 to 0. I had taken it for 10+ years. Psych meds for 25 years. I had to, because it was quite literally killing me. But now of course, I'm ten days off and I'm feeling pretty sick: Parkinson-like movement symptoms being the chief concerning symptoms, especially when combined with the vertigo. I take a few moments to "Get going" when I want to move. And then I lurch around for another 10 seconds until my body remembers how to walk. I have the bruises to prove it! At times, just standing still my whole body shakes like a tree in the wind. I keep dropping things and have no strength in my hands. Can someone inform me what this is? Is this part of Discontinuation Syndrome? Its kinda freaking me out. I also have the usual! discontinuation symptoms! ringing ears, painful eyes, weird noises in my head, muscle twitches, nausea, diarrhea, brain fog, EMOTIONAL!, Over energized and completely fatigued. Visual disturbances. Muscle and joint pain almost everywhere. Swollen hands. Itching skin so bad I thought I was having anaphylaxis and went to the ER two days ago. Surprised I could remember all my symptoms, cause really the brain fog + zero memory issue makes it so this post took me several days to write, in several 1 hour sessions. I used to write semi-professionally. So this is actually a symptom as well. Last night, I had about 2-3 hours of uncontrollable rage (self directed violence) that was provoked by sensory overload. Embarrassing, terrifying. Is this part of Discontinuation Syndrome? I know the best remedy for "discontinuation syndrome" is reinstatement. I tried 3 mg prozac. Got nerve pain from head to toe within 4 hours (a symptom of Serotonin Toxicity). BUT, on the flip side the next day a started feeling better. My psychiatrist is going to look at all the possible SSRI and SNRIs to see which one might be possible in a micro dose. I spoke to my psychiatrist today and she suggested 20 mg non-extended release venlafaxine twice a day, with a a slower taper. I need to figure out what a slower taper would look like. I read 10% decrease per month? Is that correct? Any resources, advice on that? BUT, the thing is, I don't think any boosting of serotonin is a good idea for me right now given how extremely ill I got from serotonin toxicity. AND YET, my "discontinuation" is fairly severe, so I’ve decided to go back on. I’m choosing nerve damage because I don’t want to risk long term discontinuation syndrome. I will get myself ready to be in pain. What's worse: body wide neuropathy (nerve damage) in both CNS and ANS? Or Parkinsons like movement issues, vertigo, fits of rage, and the risk of long term discontinuation syndrome? OR??? Is there something I can do about discontinuation that will not raise Serotonin? I'm pretty freaked out by realizing I'm in between two really horrible things, and I do not know with certainty what to do. Please make any responses concise and focused on the above question. I've got major information processing issues. (In the end it took me several hours to write this post. I tried to keep it focused. THANK YOU! -------------- What I am doing: EXERCISE I am making myself go out and do gardening every day. Hard physical labor. Somehow this works for me. Can't explain it. I don't question it, though it is making my muscles sore from the work out. Figure I’m regaining the strength I lost with 4 years of nerve pain. Most days I use foam rollers and yoga therapy (my profession) to soften the rocks in my muscles. And ice baths (fabulous for my nerve pain and muscle spasms and migraines) DIET: I drink lots of water and coconut water, lemon, mint. Basic diet for past 5 months: DO EAT: above ground vegetables, meats, fish, eggs, seeds, nuts, water. DON'T EAT: grains, no fruits, no dairy, no root vegetables (EXCEPT gratefully purple potatoes, parsnips and turnips :-) ! RECENT DIET ADJUSTMENTS Reinstated coffee and it seems to help me move a bit more smoothly. :-). Added Rice and bananas as foods I can eat when I'm still horribly nauseous and ravenous simultaneously. HERBAL TINCTURES: burdock, kava, lobelia, turmeric, white willow, and valerian. CURRENT DAILY MEDS: Felodopine for High blood pressure Oxcarbazepine for nerve pain Naproxen (Aleve) as an antidepressant (anti-inflammatories do help) Levothyrozine (hypothyroid) Levothyronine (hypothyroid) Singular for asthma Medical Marijuana — PCP, neurologic and psychiatrist all endorse this. Cannabis (oral infusion in cocoanut oil 2-3 times a day and vaping) Helps with the nerve pain, anxiety and depression. Total game changer for allowing me to be physically active and do things I enjoy and need to do to feel like I’m actually living — i.e. gardinging, socializing. Question: is cannabis seroternergic? Anyone know? PRN MEDS * Valium 5 mg PRN for muscle spasms, and at this point for the anxiety, irritability. Usually take 0-4 each day, depending on how bad things are. I chart it every day. Aware it is addictive. * Bendydryl (two OTC pills) with Promethazine suppository for neurological pain and nausea. Works OK for pain. * Low dose Ketamine nasal spray when the neurological pain is beyond bearing (to stay out of the ER) I’m finding that a single dose really puts the brakes on the discontinuation syndrome and have been using it that way. Previous does for nerve pain were 4-16 depending on the severity of the pain. CURRENT SUPPLEMENTS: Methylated B vitamins (I lack 1 of the genetic pairs for methylation) Vitamin D 5000 iu. for depression Alpha lipoid acid for neurological issues N Acetyl Cystine for neurological issues Reservatrol for neurological issues CoQ10 for neurological issues PAST: 10+ years venlafaxine ER 25 years psych meds. First ten years took almost all of the possibly relevant ones. Side effects and ineffectiveness. Starting 2 years ago I started slowly weaning off meds. I've gone from 14 meds to 7. Diagnoses: PTSD Major Depression Anxiety Sleep disorder "Post Lyme Disease" An auto-immune system problem? Migraines (Serotonin toxicity?) Neuralgia and neuropathy through out the right side of my body Yours truly, UrbanFeral -------------------- Med / discontinuation history. 2002? to 2016 Venlafaxine ER. First antidepressant that worked. Alas due to combination with TMS (transcranial Magnetic Stimulation) I developed chronic serotonin syndrome, extremely ill since January 2016. Tapered over 3 months from 225 to 0. (too fast!) It was easy till I got to the 37.5, and then discontinuation kicked in. As of 6/20/16 going back on 20 mg non-extended release, twice a day and beginning a slower taper. 2012-2016. One at a time, slowly I eliminated medications from 14 to 7. DX Plaquenil which had been treating post Lyme non-specific autoimmune disorder. Safely got off it over a 4 month period. DX Spironolactone for heart arrhythmias and high blood pressure. No issue getting off it. Lunesta for insomnia, tapered off over a 4-5 month period. Ativan - stopped taking it when I started taking Valium this year to control severe muscle spasms. Cannot remember what else I got stopped taking. 1992-2002, over 20 different medications tried alone or in combination that were either ineffective or had bad side effects. I'm going to work on a complete list. It's going to be real piece of work.
  5. Has anyone had neuropathy type symptoms? Mine are pretty severe: skin tingling, skin burning, limbs feel 'electrified', mouth and throat tingling, pulsating muscles, buzzing all over body, burning hands, numbing sensations... it makes me want to just rip my skin off! Is it normal to have this as part of WD? I feel like these symptoms are the WORST and have been ongoing since I CT'd. It makes me feel suicidal but of course I would never want to commit such a thing.
  6. I started tapering from Prozac, 40 mg and Elavil 40 mg in Oct. 2015. I did not know if I could do it. One of my motivations was 3 years of chronic pelvic pain which started while I was on medication. Then all through 2016 I got sick. I spent 2016 in bed, mostly too tired to do very much and the withdrawal from the drugs was one of mostly forgetting to take the medications as I felt sick and had pains and distress, malaise, flu like symptoms In Nov. 2015 I got very dizzy. In Jan. 2016 I noticed that I had electric zaps up and down my spine and inner trembling. I became so weak in August of 2016, I could barely do anything. It felt like I had infections but I never had fever. By Dec. 2016 I had severe pelvic and groin pain. I could barely sit in Jan and Feb 2017. During all this time I felt ill, but not depressed. Today, I started to feel clinical depression coming on. I have seen a neurologist who discounted my symptoms of neuropathy. I notice that anything can trip the inner trembling and inner electric zap feelings on. In the past and recently there were no explanations of gynecological pain (all tests normal) or abdominal pain ( had 2 colonoscopies). I could put up with all the symptoms - but now 17 months after I started - I am really depressed. My nervous system seems to be hyper and reacts to everything with very subtle neuropathic symptoms which the neurologist discounted. I thought about reinstating prozac but I am scared. I was on antidepressants for 20 years and could not discontinue any of them before. This is the first time I made it - but I think I have peripheral neuropathy and I may not be able to reinstate to any antidepressants. I am still seeing my psych doc thinking that I should go back. But would it be safe?
  7. Hi there, all through my withdrawal my right ear has felt blocked,although is actually isnt so my doc says, but since last October i feel like my ears have both become a lot worse, constant pressure/pain in both. Today it is driving me insane as the pain is in my ears, head,jaw and gums. Ok so iv had allergies all my life ie hay fever and cat allergies but can never remember it affecting my ears like this so im not sure if seasonal allergies are to blame, but then again it was snowing this winter and they were bad then too. This comes and goes but seems to be pretty persistent for the last 9 months now and it isn't shifting. Does anyone else suffer badly with their ears? i know the blocked feeling is common in withdrawal but not sure if many have the pressure?
  8. Hi, I came off of luvox (fluvoxamine) almost cold turkey in August 2013. I was on it for 4 years at a dose of 150mg. Earlier also I had tried to very slowly (over the period of a year) come off it but it gave me peripheral neuropathy and TMJ once I was off it completely. I went back on it last year because I felt my OCD symptoms have increased. Now again I have quit it but almost cold turkey (on August 1st, 2013). It has been 3.5 months now that I am off it. I thought that my withdrawals lasted for about three weeks of quitting it and that I was successfully able to get rid of them. But two months after being off of luvox I started experiencing extreme sensitivity to hot and cold. This gradually worsened to enormous tooth ache and redness in gums by the end of three months. I got a root canal done after that. My pain kept jumping throughout my whole mouth. My dentist said that my teeth look okay. I have started a thread here earlier (http://survivingantidepressants.org/index.php?/topic/5185-sever-pain-in-teeth-and-gums/) because I didn't know that as a new member I should have posted here. Yesterday I tried one of the supplement from "the road back". It seems that it has helped me with the teeth ache. The TMJ and stuffy feeling in face and limbs is still there. Before yesterday it was impossible for me to live without at least 1200mg of ibuprofen per day for the last 25 days. For many days I even took 3000mg. There is too much facial pain and it is difficulty lying down because the symptoms get worse when I lie down. I think luvox caused me teeth grinding and also damaged my peripheral nerves because of which I am experiencing tooth decay and teeth ache because the roots of my teeth are getting damaged and I am also having pain and tenderness in my joints and limbs. Do you recommend that i should go back on luvox and withdraw gradually? Or is it too long now that 3.5 months have passed? I would really appreciate your advice. Thanks