Jump to content

Search the Community

Showing results for tags 'headache'.



More search options

  • Search By Tags

    Type tags separated by commas.
  • Search By Author

Content Type


Forums

  • Support
    • Read This First
    • Introductions and updates
    • Tapering
    • Symptoms and self-care
    • Finding meaning
    • Relationships and social life
  • Members only
  • Current events
    • Success stories: Recovery from withdrawal
    • Events, actions, controversies
    • In the media
    • From journals and scientific sources

Find results in...

Find results that contain...


Date Created

  • Start

    End


Last Updated

  • Start

    End


Filter by number of...

Found 10 results

  1. My story appears to be similar to many folks here on this forum. Reading all of these accounts has helped me accept my symptoms as a result of Zoloft, which has at least given me some piece of mind. Before I explain my timeline and struggle with getting off Zoloft, I want to bring to the forum’s attention something my psychiatrist informed me of which I have found no evidence of elsewhere. Hopefully someone can verify this. My psychiatrist explained the following: The FDA allows for a 30% upward or downward margin of error on Zoloft pills. He explained that a 50mg Sertraline (Zoloft) may have up to 65mg or as low as 38.5mg. Another example, a 25mg Sertraline may have have as much as 32.5mg and as low as 17.5mg. Can anyone validate this? If this is true, it is unimaginable. My story: I started 50mg of Zoloft in 2012 for general anxiety, social stress and general dissatisfaction. My psychiatrist at the time said “It was about as harmful as taking an aspirin.” In 2013 we increased my dose to 75mg. My psychiatrist retired in 2015 and I continued at 75mg through my general doctor’s refills. In 2018, I felt I was in a good place and tried to go cold turkey. After a couple of weeks of torture, I returned to 75mg. After learning that I should taper, and also feeling I was in a good place, I decided to reduce my dose to 50mg in July of 2019. Two weeks of intense symptoms ensued but by the end of the second week things became more manageable. I wanted to reduce the symptoms and requested (it took some convincing of my new psychiatrist) a liquid form of Sertraline in August. I reduced to 45mg but felt like I was not getting a consistent dose (sticking to the glass) and it was difficult to swallow even when mixed with water. My psychiatrist recommended that I switch to a 25mg pill + a half and a quarter of another 25mg pill bringing me to 42.5mg in September. I stayed at 42.5mg for September and October and was distracted by a series of sinus infections (antibiotics and 2 rounds of prednisone). Thinking I was ill from the infections, I did not realize most of my symptoms were Zoloft related. All of my symptoms were rationalized but my general doctors. Dizziness, light headed, extreme head pressure, headaches, persistent neck pain, fogginess, loss of appetite, ear pops and pings, jittery, imbalance, loss of equilibrium, flu-like symptoms and tingles in hands...doctors all rationalized them as symptoms of sinus/ear infection and the steroids. This went on for almost 2 months, while somehow I was still functioning. Until I called my psychiatrist last week and he informed me that it might be because we switched to a smaller pill which may have 30% less than is listed on the bottle. He prescribed the 50mg for me and within 2 days I felt somewhat improved, but noticed some brain zaps and the continuation of symptoms. My psychiatrist said that 50mg may not be enough to counteract a withdrawal and that we may need to go up to 75mg to stabilize. This past Sunday (10/27) I upped my dosage to 75mg. I am feeling some improvement, but still not feeling right: light headed, light sensitivity, headaches, fogginess, inconsistent appetite, ear pops and pings, jittery, imbalance and tingles in hands... So I am back where I started, 75mg, and hopefully stabilizing soon. Lots of information here from fellow “survivors” but I am scared. Shouldn’t I feel totally better? Could a couple months of enduring withdrawal make stabilizing more difficult? And most importantly, is the 30% margin of error that my psychiatrist shared with me true?? If so, we need to change that! Thank you for your time.
  2. Admin note: link to benzo forum thread - LaughingKat: Switch from Ativan to Klonopin Hello, everyone, and thank you for being here. Here's my story: In July 2017 I started a severe bout of anxiety, mostly health-related, that I never entirely got over, although I'm not having daily panic attacks anymore. I worked on it with talk therapy, which I continue, but in January 2018, I decided I needed pharmaceutical help and saw a psychiatrist who prescribed 10 mg of Celexa daily as well as Ativan as needed. Something similar had happened to me 20 years before, so I knew to be cautious about how much Ativan I took. The Celexa did help take the edge off my anxiety but the sexual side effects depressed me. In November 2018, having made some progress in therapy, I decided they were unacceptable and decreased the dose to 5 mg. I didn't consult the psychiatrist but I figured that since Celexa wasn't addictive like Ativan, it wouldn't matter. (Haha.) Actually I didn't feel any withdrawal effects until March 2019, which puzzles me. I started having ferocious headaches and intense neck and jaw tension, along with little painful "sparks" in my eyes every once in a while. I have never been a headachey person and I'd never felt anything like this before. They feel like electric knives going into my scalp. I thought it was just tension (my daughter had been in an auto accident and I was taking care of her while she recovered from injuries) but in early April 2019 I called the psychiatrist and told him about the headaches. He said the headaches were "likely" from the Celexa and since I was on "a baby dose" at that point I should stop taking them. It's been a month and I still have the headaches, neck and jaw tension, eye pain. Not every day but most days. At this point the psychiatrist says just don't worry about the headaches, they're not important or major. But they feel major to me! Sometimes I take ibuprofen and that helps. But I resist taking it. I've had up to 5 days without headaches and then when they come back I'm heartbroken and scared. But I'm grateful to have learned here on this site that SSRI withdrawal isn't always a straight line. Can anyone reassure me further, especially about the weird timeline of the headaches? Why did they start three months after I decreased the Celexa dose? And why do they continue a month after I stopped entirely? Has someone had a similar experience, similar symptoms with Celexa? I know several things in my story go against the good advice on this site. But I do not want to go back to taking Celexa, even a small dose. I vowed to myself I would never take a ssri again unless I was prepared to take it for the rest of my life. Thanks for listening.
  3. Nevertoolate

    Ways to cope with daily anxiety

    [A simple technique for headache, racing thoughts or anxiety] This is a very simple method I've found works for me. I hope it works for you too. Simply sit or lay down, close your eyes and massage 💆 your forehead firmly between the eyes in an anti clockwise direction. Continue as long as it takes.
  4. HI all, I am currently on day 11 of no zoloft. I was pretty much on zoloft since I turned 16 ( 20 years), I went on it for depression but I believe it created me to have anxiety. I have seen many psychiatrist and my GP and no one ever asked why I am on it still. It was not until I started doing some research of my own the last few weeks because I have been increasing tired and my memory is so bad. I found that the zoloft can cause memory loss and anxiety. Since being off zoloft I have noticed a huge increase in energy along with my anixety decreasing. Up until yesterday, I had little side effects. Starting yesterday (day 10 of no zoloft) I have the WORST headache that will not go away. I have tried ibuprofen, claritin, excedrin, magnesium fizz. Anyone else have a similar story? If so, when will these headaches stop??? OR can you suggest something that will help?
  5. Hi, I am 6 weeks into withdrawing from citalopram 20mg. I have taken it for 20 years. I initially halved the dose to 10mg for 4 weeks then 10mg every other day for 3 weeks now. I am experiencing severe, debilitating headache on an almost permanent basis. I think I've reduced the dose too quickly. After reading this site, I am thinking about reinstating 10mg daily. I see my doctor tomorrow. Any advice gratefully received. I feel terrible.
  6. SeattleKee

    SeattleKee

    I began tapering escitalopram six weeks ago (December 2017). I did so in conjunction with advice from my physician, a naturopath. I was at 20 mg. I began by reducing to 15 mg twice a week and 20 mg the remainder of the week. The sequence, then, was reduction to 15 mg three times weekly, reduction to 15 mg every other day. Then 15 mg daily. I then moved from 15 mg to 10 mg twice a week, then 10 mg every other day, then 10 mg daily. I have been at 10 mg. for about two weeks. I am now experiencing withdrawal symptoms. These symptoms include a sharp headache along the medial line between the right and left hemispheres of the brain. The intensity of the headache fluctuates, but, even at minimum, I am aware it is there. I also experience slight periodic nausea, never to point of vomiting, some irritability and a certain edginess or low level anxiety. In addition, I am noticing in increase in hypervigilance and self-critical thinking. All symptoms have been tolerable, if uncomfortable. My history with antidepressants is a long one. I started in 1982 when prescribed lithium carbonate for depression. Later, in the late 1980s, I moved to prozac. In the early 2000s I began taking Lexapro. I am choosing to taper and end medication as the stressors exasperating previous depressive episodes have been resolved for some time. I wish to be medication free in order to evaluate my psychological and emotional state in that condition. Secondarily, as I live in a state the has legalized THC and CBD. I am interested in using these for symptom relief and would like to hear from others who have tried these for self-medication. My physician is aware and supports this as a potential for symptom relief. Thank you.
  7. Hello Everyone, I am very glad to have found this forum. As you will see in my signature, I am a 28 year old female with a long history for Sertraline use. I began taking Sertraline at age 15 for severe OCD/anxiety and have been on it ever since then. At one point, probably around 18 or so, I maxed out at 200 mg/day of Sertraline and stayed on that does to about age 25. Around age 25 I was able to taper from 200 mg to 100 mg successfully without really any symptoms of withdrawl that I can recall. I have worked extremely hard to overcome my illness, and am finally at a point in life where I feel I have amassed enough tools through therapy and support to try to come off of Sertraline completely, especially because we would like to have children within the next 5 years. With the support of my doctor, I am tapering down to 75 mg from 100 mg. It has been about a week and a half since I began the reduced dose and the past few days I have experienced very serious dizziness, headaches, nausea, and fatigue. I have joined this forum with hopes that someone may be able to provide me with tips for dealing with these uncomfortable symptoms. It is so bad that I really should not be driving and had to stay home from work today. My understanding is that pain relievers such as advil and aleve can make SSRIs less effective, so I don't want to take any pain relievers for the headache if it will make the situation worse. I am determined to get off of this medication though it seems it will be a difficult journey. *I would just like to mention that perhaps there is one confounding factor in my situation - I began Gabapentin about 3 weeks ago to help with numbness/tingling in my forearm from cubital tunnel neuropathies. I know this is also a neuro drug, so I figured I would mention it as well. Any tips, support, or encouragement that you can provide would be a huge help! Thank you in advanced! Mademoiselle
  8. cheery

    Cheery Here

    Hello! I am SO grateful to have found this site. What a wonderful place and great form of support! I had never taken antidepressants but was prescribed escitalopram after a tragedy I experienced. I started last August and had terrible side effects. So lethargic, jaw clenching, hair loss, tooth pain, swallowing issues to name a few. I believe now I tapered far too quickly. On the advice of a friend I simply cut the pills in half during a two week period and was done. I had some brain zaps and dizziness for the first few weeks and then felt fine. After about two months I started experiencing new symptoms each day. Started with weakness in one arm that got to the point my wrist would just flop over. Then horrible ear pain. Then numbness, tingling, burning, twitching, muscle aches, joint pain all over. Electric shocks through my body were horrible also. Tender spots on my scalp really freaked me out. I had NO idea until I found this site these were withdrawal symptoms. I thought something was terribly wrong with me. I had gone to the doctor and had every test and they were all perfect. He said I was stressed which I am not. I just returned from vacation so very relaxed. The symptoms have started to subside thank goodness but now 6 months out I am having terrible sinus pain and sinus headaches that have lasted for days. My sinuses will also get inflamed when irritated but certain things but it is never consistent. Sometimes it's food, sometimes perfume, sometimes the cold weather. This is all so depressing. I just want to feel normal again. I have literally tried every over the counter drug for my sinus headaches and nothing works. I have bought a million supplements and nothing seems to help either. Some bring my nerve symptoms right back to the forefront. It is still mind-blowing to me that a drug I was on for such a short period of time could do all this. Has anyone else had these sinus headaches and found something that has helped reduce the pain? How long should I expect all this to last? Thanks for your responses and reading my story.
  9. Hello- I am taking 37.5 mg of venlafaxine. I have been on it since March 2015 for treatment of migraines caused by a concussion. My doctor said I could try going off now (no migraines since May) because we want to start trying to conceive again. I could tell that withdrawal wouldn't be easy from a dizzy/vertigo feeling and headaches I get when I take a dose a bit late. I also had a hard time starting the drug- not sleeping for 3 days and lost 7 pounds. I started taking it every 36 hours, but was feeling quite groggy, no attention span. I found this forum and saw that is never recommended to increase time between doses, which makes sense given the short half life. So I called my dr and pharmacist several times until I finally received a prescription for tablets. I started though by tapering the beads of drug. For the past couple days I removed 6 of the 36 beads. This is more like 26%... But I am giving it a try for now. I am wondering about the 4 week period between tapers. Is this a conservative timespan meant to apply to all drugs? For something with a short half life, such as venlafaxine would symptoms really appear 2-3 weeks later? I was thinking I would taper 20% every 2-3 weeks and then drop by 3 mg when I hit 12 mg. But even at this rate it would take a minimum of 22 weeks to wean off. That's almost as long as I've been on it! Any advice from someone who weaned off the lowest dose and how it went for them? The dose is so small, I'm hoping that a 'larger' drop of 6 mg or so would not be so impactful. Why is it important for the drops to keep becoming smaller? I can't imagine, but this plan with a typical dose of 100 mg or more would take years! As a note I do take a fair amount of supplements that I've found to help with my headaches.. These are Mg, B2, vit E, omega 3, and Co Q10.
  10. Hi, I found this forum when I was looking for information on tapering off of Effexor. I've been on Effexor about six or seven years and stopped taking it after a brief taper three weeks ago. I first started taking antidepressants after the birth of my son sixteen years ago. After a prolonged labor, C-Section, and spinal tap that went too high, I was intubated and sustained a throat injury. I could not lie down because that would cause me to cough. I can remember trying to sleep with a cough drop in my mouth to keep me from coughing. I basically didn't sleep for about three months and sank into a depression. Prozac was a wonder drug and gave me an amazing amount of energy. Eventually the drug stopped working, and I tried Celexa which didn't work before trying Effexor. On Effexor, I was pretty happy. I felt like I developed strong coping skills including exercise, and mindfulness. I started to train to be a life coach, and I was pretty much on top of the world and believed that if we try hard enough and have good enough coping skills we can manage our emotions. My psychiatrist started being pulled away into management duties, and the office cancelled several of my appointments. Finally, he was pulled into management full, time. I also became really annoyed with the clinic, and their, "it can take seven to ten days to authorize a refill" policy. Once I went an entire weekend without Effexor and became severely debilitated, and I was thinking that I would prefer not to have to deal with that. I mentioned this to my GP, who supported my desire to get off, and wrote me a six week taping prescription which I started August 15th. Taping from 150 milligrams August 15th: 75 milligrams for two weeks Sept. 1: 27.5 milligrams for two weeks The last two weeks I was supposed to go every other day at 37.5, but I had read that would just put me on a roller coaster, so I just decided to stop. I can see that this may not have been a good choice. I think tapering all the way to 27.5 milligrams was not too bad. I experienced some dizziness and crankiness but it was manageable. Here's how it's been since then: Week one and two: The worst symptom was the feeling that my brain was sloshing around in my head with every step I took. For about three days, I was filled with rage. I wanted to get away from my husband and two teenagers because I was so irritable. I thought about going to a hotel or flying to NYC to see a friend, but I didn't do any of that. I have also had chills and nausea and hot flashes. If I had been expected to perform anything at a high level, it would have been nearly impossible. Three weeks in to this, I find that I am having crying spells. I have never had crying spells, and I have never felt as off-balance as I do now. I'm trying to figure out what my next step should be. Should I stick it out since I'm almost a month in, or do I go back on Effexor? I just finished Theresa Borchard's book, and I found it quite disturbing. She describes trying all the alternative therapies and ultimately finding a traditional drug cocktail that works. It's a great book, but I wonder if I have a brain like hers, or if I can get through the withdrawal to be the person I thought I could be, or if my serotonin is now so depleted I'll have to stay on these drugs for life.
×
×
  • Create New...

Important Information

Terms of Use Privacy Policy