I need help in weaning of Omeprazole. I have been a 20Mg a day user since 2002 and the last 5 years have been hell. I am now at the point that I really need to get off this drug, whatever my GP is saying. Does anyone have any tips and suggestions on how they got off the pills. The daily symptoms I'm having is terrible.
View 31 RepliesMy LTHR had been scheduled for next week. During my pre op session last week the dr remarked that the pains down my left leg may be due to a spine issue, while the groin pain would almost certainly would be due to my bad left hip. He is suggesting that I see his spine colleague before he definitely goes ahead with the hip op.
My question to you hippies: before your hip op did you have pains down your leg(s) including ankle? And (this is the important bit) did the hip op get rid of the leg pains? I am thinking that if your answer is yes to both questions then maybe I should get a second opinion from another surgeon.
Having hysterectomy next tuesday. terrified.have no support at all as a bit of a recluse. i keep being told what i can and can't do after op by different medical staff so a bit confused as well. i'm 66.
View 37 RepliesI am due to have a LTHR on May 11. Just looking for a support group to join because I'm sure I will have post-op issues that are being or have been discussed here.
I do struggle with anxiety in certain situations and I am concerned about waking up intubated (hope I don't have to), the compression hose (getting them on and off and just the restrictive nature of them), and the risk of being on blood thinners for a month (although I prefer that risk over not taking blood thinners and having a higher risk for blood clots).
I am 47 and have had hip issues since I was in high school - though never diagnosed until two years ago, I had a femoral acetabular impingement that, with diagnosis, could have been repaired years ago and I wouldn't be in this situation now, more than likely. So, I'm frustrated that this has to happen now but the impingement has caused arthritis, which is now end stage bone on bone so I need to get this done to lessen my pain and increase my mobility.
If anyone could share some of their experiences and perhaps advise on when this nightmare is going to end I'd really appreciate it.
I’m 34, otherwise healthy, started Mirtazapine (in some sense against my instincts) about two years ago due to severe anxiety (no depression at all) and panic attacks. My Doctor prescribed Mirtazapine 30mg, to be tapered upwards from 7.5mg.
I remember the first few days I felt a weird sensation when swallowing (simply felt like uncoordinated swallowing, where the food/drink seemed to be going at the wrong velocity towards its target). However, after a while and increasing dosage this symptom vanished more or less.
Fast forward about a year and a half forward, and (apart from helping my IBS by making me numb) - the drug was totally useless anxiety-wise. I was still feeling very bad. True, I had not gotten many panic attacks, but I found that they were just transposed with a very generalized anxiety which I believe (self-diagnosed) had almost become a phobia: I became afraid of trying new things altogether from fear of having e.g., an allergic reaction (never had any of those ever in my life and never feared them before either). I had quit sports because I could not stand the sensations involving an increase in heart rate or blood flow. Done all of the tests and all is fine with my heart and everything else for that matter. It’s all in the head but the head controls your body and your mind.
The Mirtazapine just made me numb; I could feel less love to my fiancée (now wife!) and cared less about the world in general. Realizing that I had just become more anxious (if less panicky) the Doc upped the dosage to 45mg. What a disaster. More than a month afterwards I was just getting more and more anxious on a daily basis.
Eventually, AMA, I decided that going on Mirtazapine was the biggest mistake of my life. I started tapering, very VERY slowly. I think I went from 45 to 15mg with relative ease, taking more than two weeks at a time to decrease the dosage by 3-4mg at a time. Each time, I would feel great for 2 days, then start developing quite severe cramps and feel lousy for another week or so, then I’d get slightly better. Knowing that I am really ultrasensitive to any change in physiological parameters I tapered from 15mg to 3.75mg in a turtle’s pace: 3.75mg at a time, with more than a month (and even two sometimes) between each taper. I have a PhD in Chemistry so I know what I’m doing. Again, every time, after 2-3 victorious days where I’d feel like I’ve conquered mount Everest, I’d then feel lousy for 4-8 days; but then things would seem to be a bit better. Weirdly, at the lower doses of 7.5mg and 3.75mg I started again experiencing swallowing difficulties; I started choking on water and became very mindful of my swallowing dyscoordination. Still I felt altogether quite alright – and I believed that the remainder would be similar.
How wrong was I. I have come off it completely exactly two weeks ago. Again 2-3 days where I felt fine, then a few more days with cramps. Then, good old panic hit, with terrible anxiety that just keeps getting worse and worse. I feel terrible weakness, zero energy, I have withered due to loss of appetite (since when I eat my stomach just cramps a few hours later; actually not so bad since I had put on some weight during my time on Mirtazapine). I feel completely overwhelmed by the symptoms: every time there is something new. I feel weird tingling sensations and I have strange feelings of pressure in my stomach. I get dizzy a lot and then just feel weak. My muscles are sore without any reason. I was certain that these issues would resolve in a few days; Mirtazapine’s half-life is quite long and I know that receptors can take 2-3 weeks to get re-modulated (actually that’s why they always say that the beneficial effects of Mirtazapine will take around 2-3 weeks to become effective when you go on it). But I did not expect this gradual and horrible worsening of symptoms over the last 14 days. I have had to start treatment with Benzo’s (as needed, I try to avoid them but sometimes there’s just no way around it) and they seem to help in some instances, whereas in others they only seem to do a moderate/poor job at managing the symptoms. For the first time in my life yesterday I suffered from ED. Never happened to me before and despite a very supporting and loving wife, I felt that was yet another crushing blow. The weird thing is that all these things are not getting me depressed – just really anxious.
I can only hope that things will start to get better. I have no idea when these things would begin to get back on track. Doctors seem to be quite oblivious to my suffering, not really believing that withdrawal could be so powerful yet not finding ANYTHING else wrong. The situation is really frustrating.
One thing is clear to me: I’m never, EVER going back on this horrendous drug. It was a huge mistake beginning with it, and for all of you who need these kind of drugs: ask your GP or Psychiatrist what are the withdrawal difficulties expected for the medication. I know I sure wish I had asked it.
Chances are you are having your first colonoscopy too like me. I have decided to stop reading everyones stories about their colonoscopy experiences and to write about mine, mainly to stop myself freaking out. So hear goes, today I went to the hospital to collect my bowel prep, 'moviprep' pretty sure someone with a great sense of humour decided to call it that, good old bowel prep or perhaps 'bog hugger' might be more apt. Somehow I don't think a movie with the popcorn will ever be the same for me now. Anyway, spoke to a lovely nurse, who explained how to take the stuff, what I couldn't eat etc and about the procedure, and she didn't sugar coat it. So as I have to be at the hospital for 7.30am on Wednesday, I am allowed breakfast tomorrow before 9am. I can drink clear fluids all day. I have decided to stock up on energy drinks to take throughout the day, nurse said it was ok. I then start the moviprep between 5pm and 7pm, I have to mix a and b sachet in a litre of fluid and drink it, and drink 500ml of clear fluid after. Then I wait or maybe hug the loo, will let you know, loo permitting. Then the leaflet says rest for 2 hours, not sure if their interpretation of rest is the same as mine lol. Anyhow between 9pm and 11pm I have to mix another two sachets in 1 litre of water along with 500ml clear fluid to wash it down. It then says at 11pm or when you stop going to the toilet you can go to bed. MMMh. Well the nurse said as she went through the leaflet with me, "you might find you actually don't stop going to the loo". She then asked me if I had any worries. I said I was worried that I might poop my pants on the way to the hospital, (sorry a bit graphic, but do we all not feel that way). She did say some people do do, and suggested I wear a sanitary pad or the like. I also said I was worried it would hurt, whilst she didn't say it would or wouldn't, she said it could be very uncomfortable and for a few days afterwards too, but it affects everyone differently and that things settle once you get back eating and using the toilet normally again.
I am going to drink plenty of water and have a light diet of toast and eggs for lunch and some plain white rice and chicken tonight as although I wasn't advised to it seems it is better to avoid foods with any fibre in them. Probably have egg and toast for breakfast in the morning, then I am going to keep really busy till 5pm 'D' (for diarrhoea) Day as I am calling it.
I sincerely hope that I am sounding upbeat and chilled about this whole experience, that's my aim. In reality I am scared senseless, (poo less!!! - hopefully I will be by 11pm tomorrow night ha ha).
Because like everyone else not only is there the worry of the procedure there is the worry of what might be found.
I'm getting circumcised in 2 weeks time. Spare the 'don't do it' because I won't change my mind - sorry! haha. I'm 33 so have thought long and hard enough about it. Unless your in the same position, it's rather hard to understand but I have always felt like I should have been circumcised at birth.
What I was hoping for was to gain some before and after tips from those who have also had it done.
BEFORE
My doc said to not take any fish oil for a few days beforehand because this will increase the blood flow.
Can anyone comment of things which also should not or even should be taken which can decrease the blood flow? I regularly take vitamins, would it be best to cut these out also?
AFTER
Self dissolving stitches are used but I have read to take these out after 10 days to limit 'train track' scarring from appearing.
If there is any excess bleeding, cold compression should be used for 10 minutes every hour to stop.
Wear jocks to have the penis position upwards towards your heart to promote recovery.
Can anyone comment if it's a good idea to use anti scaring creams afterwards? I read Mederma and Vit-E Serum is quite good. Would you use anything directly after surgery, or only when the stitches are out?
So for those who have had it done, any tips or advice to help with a more successful recovery would AWESOME!
I've pondered my own need for a hip replacement. I'm sports mad and always have been, playing competitive squash for 20 years (probably the cause of my hip degeneration), followed by many years of rowing and subsequently cycling - which I still do with a passion. I was diagnosed with arthritis about 6 years ago (at 52) and have lived with it since then. Mine's been odd - I've never had the excruciating pain that most people seem to complain of - pain, yes - but bearable. My main issue has been with a gradual loss of range of movement. At this stage, I can barely tie a shoe on my right foot, putting a sock on is a nightmare - and cutting toe nails on that foot is pretty much impossible. But in the absence of severe pain and being still able to cycle with relatively little discomfort, I've never really known what to do about getting it fixed. That being said, I did decide to do something about it this year - and it looks as if I may actually be going in to get it done next week!! As I'm sure most of you did pre-op, I'm feeling pretty apprehensive - and still questioning whether I'm doing the right thing, even though I know I'm having many more 'bad days' and that the constant lack of a full quality of life is getting me down. So I guess I'm curious as to whether anyone has been in a similar position - and whether all you experienced hippies think I'm doing the right thing.
View 41 RepliesI started withdrawing from Mirtazapine back in Jan of this year, from 7.5mg. I got the liquid version and tapered down by 0.5ml (.75mg) initially every week, but had to stop that and start by dropping a day a week as I got withdrawals etc. I have been doing very well and was able to drop back to dropping it over 4-5 weeks. I got down to 0.1.5ml and the withdrawals kicked in, nausea, anxiety, sleep problems, cramps, etc etc. I stayed where I was for a few weeks but as things didn't really improve I continued to drop down to 0.1ml. During this time I have had some ok days and some awful days. Yesterday and today have been awful, dreadful low mood, very tired, anxiety and horrid nausea again.
My question is, initially I was going to go down to 0.5ml then taper off that to nothing, but the thought of another 3 months before being off it completely terrifies me. I am thinking about starting to taper off 1 night a week, over the next 7 weeks at the 0.1ml, but wonder if the withdrawals will be worse than ever!
id appreciate some advice. I have done the taper so ridiculously slowly, that I am now just fed up with the whole thing, and want to get back to normal again.
i was initially put on it as in Feb last year I had the flu, and was left with anxiety, my GP then prescribed Propranolol which gave me insomnia, and so it went on from there! The Mirt only made me sleep in the first week on being on it. I started it in June 2013, so been on it just over a year and have been withdrawing from it since Jan this year.
I'm due to have Rectocele and cystocele repair. I had my last consultation with my surgeon back in August 2015 had my pre op assessment in September. I was told I would be in for surgery around December and I'm still waiting, I spoke to someone at the gynae waiting list team today and they said I'm not even on the list yet as they are so far behind. I completely understand that they are busy and their are woman out there a lot worse then me it's just that walking and lifting is becoming a real pain and I'm sick of taking co dydramol which blocks me up when I already struggle to go to the toilet for a bm.
Sorry for ranting I just wondered if anybody had any advice as I'm starting feel like I'm moaning all the time to my husband.
Well my date for my hysterectomy is in two days ( Wednesday) I'm absolutely petrified, I'm not sleeping and I feel so nervous.
Any advice from any of you lovely ladies would be so much appreciated right now. Because at this point in time I feel like running in the opposite direction.
So, I have my date! June! Excited and nervous all at the same time, I'm reading lots lately about swelling, pain and being off your feet longer than you thought. This IS a difficult surgery, and I know it's not going to be easy. Trying to put some positive vibes out, and remembering why you did this, is anyone brave enough to show off their tootsies? Maybe before and after? A lot to ask I know.
View 53 RepliesI'm 40 years old, mum to 2 girls 16 & 11. I just been diagnosed with psoriatic arthritis and I'm so scared and confused, I'm looking for people in the same boat to help me understand what I'm going through. I have suffered with scalp psoriasis for about 10 years. For about a year I had the odd pain here and there, but nothing I thought was worth going to the doctors about, but 6 months ago my knee started to hurt more regularly but I still put it down to getting old. One night I woke up in excruciating pain on my knee, could not move it at all, took a couple of hours with a bag of frozen peas to ease the pain and after taking painkillers the pain went and I carried on with my life. Just under 2 months ago that same pain came back but not just my knee, my shoulder, my elbow and my neck were affected too. I felt like I was paralysed by pain and had to be practically carried to the GP. That was the first time I ever heard of PA...I didn't even know it existed. My GP suspected it and sent me to loads of blood tests, and prescribed a load of tablets. A week later the pain was not easing so back to the GP and this time he gave me stronger co codamol and the pain started to get better. Another week and the blood tests results came back and showed inflammation, very low vit D and folic acid, so GP gave me supplements and decided to give me a 3 vial steroid injection, which he was hopeful could relieve me of pain for a month, while I was being referred to the rheumatologist. I was pain free for 3 days and then it came back with a vengeance. Back on the co codamol and naproxen but the pain was easing just a bit, I couldn't sleep as I any position made something hurt. GP asked for an urgent referral, but that got lost and despite me trying to get things moving, nothing was happening fast enough so I went private, got an appointment within 2 days and a diagnosis. I started methotrexate 2 weeks ago, which makes me very sick and diarrhoea for 3 days, then it settles. Still on co codamol for pain as I refused the steroids the rheumy wanted to prescribe. My life has been turned upside down, almost every day I wake up with different joints hurting. I feel like the pain is eating me away, it's so disheartening when I can't even prepare my child's lunch box because my hands won't allow it. I work through an agency and they are on the verge of getting rid of me because I have taken the odd day off when the pain is just too much. I have been on anti depressants for years and I feel my depression getting worse, I don't want to leave the house or see anyone because I feel so so low. Will it ever get better?
View 32 RepliesI am going in tomorrow to have my cyst and fibroid removed.could anyone tell me what happens once you get there.i have to go for 11 am an have been told I should go down by 2pm.
View 31 RepliesSo i've been on nortriptyline for over 4 years for chronic migraine. I'm 25 and have had migraines for years, they used to be constant everyday, when i waken up etc, my neurologist had me try all medication but i had no luck with beta blockers, topamax etc and my last chance was nortriptyline and if it didn't work, the next option was an injection into the base of my skull (which i didn't want) luckily the nortriptyline at 75 mg decreased the severity and frequency of my chronic daily migraines.. now i have other health problem undiagnosed yet, and very bad constipation problems and fluid in my abdomen with bad distention, i never thought until recently that the nortriptyline could have been causing this but from reading on the internet its possible.
So im considering weaning off to see if my bowel problems go away and the fluid water retention, has anyone any suggestions on how to wean off this?
Withdrawal symptoms?
I know its possible that my terrible migraines could come back but i want to take a chance.
So I am a breastfeeding mom. My son is 5 and 1/2 months old. I introduced formula for supplementation when he was about 4 and 1/2 months old. When I got pregnant I set a goal of exclusively breastfeeding for 6 months. I only introduced formula due to the fact that my son ate alllll the time and when I would pump I was barely getting an ounce. So he only got formula like before bedtime and when we we're out and about. Now when I pump i get like 5 ounces. Now I am trying to only breastfeed in the morning when he first wakes up and at bedtime. But the reason for this post is because I am trying to find ways to wean my son from breast feeding. I know that it's a process and I don't want to just take it away completely I enjoy the bonding time and the comfort I can give him from it.
View 6 RepliesI took Propranolol 60 mg sustained release for a brief time, then reduced to 20 mg 2x per day. Bad side effects, low pulse rate, bradycardia and irregular heart beats, weaned off the stuff over weeks. Now been off it for about 2 plus weeks and still have a low pulse rate of only 60 with low blood pressure particularly while standing. Often feel faint with the low heart rate and BP. How long does it take for the body to readjust after getting off this med or is the bradycardia permanent. I had no problems before this drug and had bp around 140/80. now goes very low and sometimes high at night while lying down. Very scary stuff, I'm afraid it will never go back to normal.
View 1 RepliesMarch 25th I made the decision to leave the entertainment industry and get sober. Since then I have slipped up and drank only 3 times and have no desire to sip a drink again... It always makes me feel worse/horribly depressed. It just brings me to a dark place. I have been taking Xanax for the past 7 years because it helped me deal with my job... Being in the spotlight... Having no privacy... And it also helped me deal with a very mentally abusive Husband who also happened to be an actor and active cocaine addict. I am proud to say that I filed for divorce and finally got away from a very toxic lifestyle that I felt was leading to my death.
I am weening off Xanax... I am down to 3 mg a day (I was taking up to 10 mg a day... Maybe more at my worst point) and I am under a doctor's supervision.
All of this is just so hard. My whole life is changing and I know it is changing for the better in regards to my health but this is so hard. Divorce, massive job/.lifestyle change, moving out of la, searching for a job and going through all my savings fast. It is SO SO hard not to get caught up in fear right now. I have been SUPER depressed and overwhelmed and I have been letting my depression and anxiety get the best of me lately. I'm feeling really defeated lately and super overwhelmed.
I've only been on lyrica for 6 days now. Im finding the 75mg dose to strong 1 a day is what i am taking.I was wondering if the capsule can be split in half so i take half of that per day .then was wondering how long does it take to wean off completely if i decide to come off completely off the lyrica. And is it safe to take half of the 75mg has i've noticed that dose is not listed on the patient sheet etc.
View 31 RepliesI have just joined as I believe I may be becoming dependant. Currently I take between 3-6 nurofen plus a day. It began with my job which is very stressful at times. O would get constant headaches at work and found this was the only thing which helped. I never take anymore than 3-6 as I'm so worried about my liver and kidneys. I've decided to wean myself off, whether I go cold turkey is another thing. So today I haven't taken any nurofen plus. This morning I had hot and cold sweats slightly as well as a bit of a runny nose but they seemed to disappear as the day went on (the sweats mainly). But the headache has been with me most of the day but just a very dull ache. I took some ibuprofen before to ease it as I read this will help with the initial withdrawal headaches. Does anyone hAve any idea how long these headaches will last for while I wean myself off?? =
View 5 RepliesI don't know all the reasons why Doctors won't just tell a patient the truth about dependency, but, my best guess is fear of the unknown. In my opinion they are scared of Lawsuits. Scared of what this person may do. If you are trying to stop taking Oxycodone like I was in 2011 then you probably felt like no one was giving you a roadmap to success. You felt like you had somehow acquired a PHD in chemistry and the medical field with all of the knowledge you had obtained through the internet. You asked and pleaded for help to stop taking these drugs. I read everything. I felt as if no one cared. I felt like my doctors were pawning me off to pain management doctors and no one was simply saying the obvious...Stop taking them! That is it.
I suffered a back injury, had spinal fusion, was given Oxycodone during recovery and was taking them for a year. As I felt my back injury and recovery or healing process of that surgery was over. I started weaning off the meds. Lowering my dosages. I did everything any normal person would do. I asked doctors, everyone, how? How to I stop taking this drug? The back injury and surgery was no longer my issue, the issue now was this feeling that I was a drug addict and it had to stop, in order to fully heal. In retrospect I would have gladly suffered the pains of the surgery, because, that was to be expected. After surgery it is going to hurt. You can expect to be in pain from that. What I didn't expect was becoming dependant on the drugs and being shunned by my own doctors who prescribed me the medications. Surgeons perform surgery. Mine didn't have any concerns with anything afterwards. I tried slowly weaning off the meds. I felt like c**p! I learned as much as I could from every media I could. I asked everyone How to stop taking these drugs. I asked all the questions one would ask? Will I die if I just stop taking them, How do I stop taking them? Is there someone who can give me a list of what to take and slowly taper them off of me? Nothing worked! Nothing....worked. After reading everyone's experiences and seeing everyone go through the same things I had been going through. I came across one post...one person...simply said "You people are stupid"....Stop taking the drugs. This was on a site where I had been reviewing probably fifty cases of people begging for relief, begging for answers on how to slowly wean off these meds. No one wants to feel pain. It's that simple, but, here's the reality....It's going to suck! You will feel terrible. Go to CVS and buy some circulatory leggings ( stocking to help bad circulation) They are tight fitting socks that go up to your crotch, put them on! Find your favorite pillow or large stuffed animal and get in bed, have plenty of Gatorade, pedialyte, anything to replenish the fluids and vitamins, you are going to need to keep drinking these fluids as much as possible! Tell your family to bear with you and forgive anything they hear come from your room. I screamed, I cursed, I cried and after a couple of days the worst was over. It was two Hard days. It was a hard week following, but the days get better, the weeks get better and the good news is...You will no longer be dependant or addicted to this ridiculous drug. I'm not a Doctor. I don't claim to be a drug Guru. I was a patient suffering from an injury and thrown away. My recovery process was just as important to me as my surgery. That was not the sentiment my surgeon shared. he performed surgery, that's his job and that's how he saw it. Oh , you're having difficulty with the medications? well here is a doctor who specializes in that, go away! The pain management doctor wanted to substitute my addiction, dependancy? (whatever) with other drugs? Methadone, you name it, and told me he was there to give me whatever I wanted for as long as I wanted. I can call that guy right now and get drugs if I wanted! Stop taking them! That's no life. The pains you are experiencing on a daily basis regardless of whatever injury or illness you have are increased by these pain medications. They tell your brain this doesn't hurt ...but, now you have this pain...these doctors have no idea, what you are going through. They will give you drugs, they will perform surgeries, but, they are not going to hold your hand and suffer with you, this horrible suffering... you are going to have to overcome. Check with your doctors first, tell them your plan, get their opinions and make a choice.
Ask your doctor this one question...Am I going to die if I quit taking these medications right now?
Once the drugs were no longer in my system (and I mean months, If not a year to fully regain my sanity of overcoming this) I was able to get my life back.
Do not flush your meds in the toilet! I do not want to drink from my tap water and worry about ingesting your meds. Empty the contents of your prescription bottles in the trash can and then dispense of the bottles themselves. I finally threw all my drugs away about a year AFTER I completely withdrew from my addiction...I was not in my right frame of mind to part with them. I honestly kept them as a backup to end my suffering, but, one day the clouds separated and my eyes were finally opened enough and were clear enough, not to need them anymore.