Migraines everyday, all day, for 9 months. Help!!

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Remember your worst migraine. How much pain you were in and how you just couldn't do anything. That's how I am everyday.

Right so I'm a 20 year old female, I'm and student and work as a waitress part time.

So, I started with a headache on the 18th January this year, pain killers didn't touch it. Woke up the next day and still had a terrible headache.

I have a terrible headache all day, everyday, without fail. It's got to the point now that I'm stressed; fed up, hardly sleeping, can't concentrate at uni or any time really.

Please understand that the pain never goes, the headache never ends. I have literally had a migraine 24/7 for 9 months now.

I wear glasses (short sighted) but I know it's not my eyes causing the migraines.

I've cut out everything that's apparently supposed to aggravate headaches. Stop drinking caffeine, stop eating chocolate and cheese. No change in the headaches.

This continued for a week or two before I went to see my GP who referred me to a neurologist.

The first neurologist thought I had tension headaches caused by stress.

At this point, I wasn't stressed at all, not with uni or work, nothing. So I didn't quite understand this diagnosis.

Anyway he put me onto tablets called amitriptyline, which is an antidepressant, and told me to gradually increase my dosage up to 50mg a day. This didn't help at all, had horrible side affects.

I then saw another neurologist who diagnosed me with migraines, put me into Topamax, which are an anti epileptic drug meant to also treat migraines. I got my dose up to 100mg within 3 months and the side affects were horrible and didn't help at all.

I've had a CT scan, which was normal. Had an MRI scan, which was normal. I've also tried Imigran and some migraine medication that melts into your tongue, with no affect what so ever.

After trying all this, an idea was put forward that I could have raised intracranial hypertension, so yesterday I had a Lumbar Puncture. The pressure was at 19 and a half (apparently if its over 20 it's high), so it's not thought its that. The migraines were worse for a week after the lumbar puncture, I couldn't even sit up without being in agony and being sick. Spent a week in bed unable to move.

I've got another type of MRI scan booked for the end of this month that's apparently going to look at the veins/blood vessels in my head to see if there is a problem there.

I feel like I'm not being taken seriously now by doctors, because "there isn't anything to be worried about, like a tumour" as I'm always told! As much as I'm so very glad I don't have anything serious to be worried about, I hate spending everyday in so much pain that I can't function.

Please don't think I'm over reacting/attention seeking/whatever, but I am literally fed up and can't cope. I can't get a minute of relief, I'm constantly in pain (different variations of pain, but pain all the same). As I'm writing this I'm crying my eyes out because I haven't managed to sleep more than 3 hours a night in that past 4 days. I'm exhausted and depressed now. I've even told my GP that I am so depressed now, I have thought on more than one occasion of overdosing just to end this pain. And he literally turned me away saying he couldn't do anything. I feel so defeated.

If anyone has had this type of problem before or knows someone that has, please let me know.

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  • Posted

    Hello,

    I was reading through the discussion looking for some comfort in my brain injury and realized that this is kind of a little pain management support group. I'm sorry to hear, becky loise that you haven't found any treatment for your migraine.

    I'm 15, and about a 18 months ago i got a concussion in gym class. Ever since then, I have had terrible migraines, focus issues, vision problems, dizziness, vertigo, nausea, a whole range of symptoms. I've tried amitriptyline, topomax, aderol, concerta, frova, naproxen, D.H.E, atlas orthogonal, nerve blocks, and physical therapy, all unsuccesful. Where I used to be an all A honors student, I'm now pulling Ds in gen ed classes. My own father tells me that I'm using my injury as an excuse to slack on school work, my teachers lecture me about managing my time better, and my doctors tell me its because I'm not getting enough sleep. In the past year my depression has gone from feeling a little down to thinking about how many pills it takes to stop my heart, then back again. I'm not really looking for solutions, just support. Thank you for reading

  • Posted

    Hi Olivia,

    I can't relate to the brain injury, but I can relate to slipping in coursework and the depression. I've sat in front of my doctors plenty of times, crying my eyes out because I've got so fed up, I've thought about taking an OD.

    But honestly, no matter how bad the pain is, is isn't worth throwing your (life away, no matter how little a life it is. Don't listen to anyone about you not working hard enough, or using it as an excuse. No one knows how bad that pain/confusion/symptoms are, apart from you. And trust me, if they could take a walk in your shoes, then they would never say it again.

    I'm so sorry to hear your story though. If I had started with these migraines at 15, I don't know where I'd be now, or how I would cope.

    I hope you do find a solution, or at the least find a way to cope

    Here to talk to though!

  • Posted

    Hello becky, i have messaged you please see it.. As i really care for you and is suffering from almost the same situation...

    please see my msgs regularly and reply regularly..

    if you want to see my message see on the top right of the page and there us my messages..

    do reply to your well wisher.. Keep smiling.. smilesmilesmilesmile

  • Posted

    I know exactly how you feel. I had the same thing in August of 2001 (9 months) and about 2yrs ago, I had a Migraine for about 4 months. In 2001 they did everything including a medicine infusion. The only thing that did was cause me to miss a day of work and be really drowsy. None of the meds actually worked. I spend countless hours in the ER, hospital, and doctors office. They took so much blood from me, that my left arm, has built up scar tissue. One day it just went away. I didn't even realize it until my husband asked me how I felt. I had gotten so used to dealing with it, that I didn't even notice it was gone.

    Fast forward to 2012. I was in the ER was a Migraine and a PA gave me a prescription for Fiorinal #3. I had never heard of it before but I was happy to get my " Usual cocktail" of Diluaded and Phenergan. I took one

    of the pills and it worked. My Migraine was gone!! I was excited! All of the Percocet and Vicodin pills over the year didn't compare. But there is a catch to this drug; you can only take up to 6 within a 24hr period. If you take more you will get a rebound headache. That's worse than a Migraine. If u get one u have to stop taking ALL meds!!

    My advice, ask your doc for the meds. Take 1. Eliminate as much light as u can for 24 hours. Take the meds 4-6 hours. Sleep if u can.

    I pray this works for you. I'm doing this now because my employer decided to change the lighting and now I have a Migrane.

  • Posted

    I've never replied to a forum but this one seems good. I'm in USA. Migraines for ten years. My grandmother had them...they ARE heridatary. Went to head ache specialist once who took scans..normal...and prescribed me Lyrica which was so strong, I took the first small dose....woke up the next day in bed with closes on...and didnt remember...I take B2 and Feverfew, Magnesium, Butterbur and fish oil with flax seed....I wanted to try Topomax aka "Dopomax" (since it makes people stupid) but not really looking forward to that. I had a dr tell me they were tension and wanted to give me blood pressure meds....didnt go that route. I KNOW if I eat too much pizza two many days in a row (aka leftovers), I will end up sick...I think lack of sleep is a trigger, as is alcohol...but so is stress! So we seem to be doomed. I am non functional and throw up when I get a migraine...I've remember what normal headaches were like and hate it when people say" Sorry you have a headache"...it's like....no.....you don't get it.....I'm sick....feel like I'm gonna throw up...etc...not a headache...Something I DO find helps at times....is pulling my chin back....horizontally toward the direction of the back of my head....I also bend my arm....put my elbow and my body flat on the wall and then turn my head....away from the wall...if I do this quite often when amigraine comes on, it might shorten the life of the thing but sometimes I just wait it out....suffering...throwing up....waiting for it to be gone....but you cant eat when you have one and you cant sleep so that just makes them all the worse. These are wrecking my life. I have a part time job and an ebay business as there is no way I could hold a full time job as I'd be fired...I feel for the initial poster of this site who has had them since such a young age and for so many days in a row....I do know that people who have had these migraines that are much older, finally have them go away but I'm not gonna wait til I'm 80 years old! We all know the triggers....what we need is some help! some REAL help!!!. I don't mean to be insensitive to all the other posts but I had to vent....to people who get it....no one does unless you are one of us....I read through the posts quickly but do you all have any hopes for Co Q10???? Any success? I'm going to try it....Thank you for letting me vent and next post won't be so "me oriented"....just needed to vent. Thank you.
    • Posted

      Great comment! it wasn't a "me" "me" "me" thing! We are just expressing our frustration on trying to cope with life with so much pain to endure! Thank you for your advice on helping with these. I promise you one thing...I'm gonna try it because God knows I've tried evrything else!!!! Thank you for sharing! If you want to read my comment about mine it is below.
  • Posted

    Hi all

    Just managed to keep it together for 3 weeks! Had to. Dad in hospital delirius with water infection and caring for Mum who is almost wheelchair bound after strokes.

    Stress can bring my migraines on but anxiety can def keep them at bay! Go figure.

    Not sure if the B2 etc is working but the Candesartan at v low dose 2 mg is helping with my bp spikes which I know are triggers for me so don't rule out all the bp meds. I couldn't tolerate the beta blocker types but verapamil worked to some extent but candesartan has less side effects for me.

    Still hoping for a cure but meantime cranio sacral therapy gives me most relief!

    Good luck all

    Hxx

  • Posted

    Update; I'm not feeling very pleased with myself. Six weeks have passed since stopping cocodamol and I'm still getting a lot of migraine headaches. I've also got a very bad cough which doesn't hurt. Looks like I'll now have to go cold turkey on triptans as well. Not sure if I can face it. Hope the pain clinic is helping you Becky:-\
    • Posted

      Hey there,

      sordy to hear that staying off pain meds hasn't been helping you! That's terrible, but the same for me really. I had a bad habit of taking them on the 'off chance' they helped but wouldn't, and now I haven't touched them in a long time unless really really in pain and haven't been able to take a sick day sad

      Hope things are better for you now though since posting this comment?

      ive now been put on different tablets, something called Zonegran, and again just feel so awful. Drowsy and nauseous.

  • Posted

    Hi Becky,

    As I was browsing the internet for a syptom unrelated to migraines I came across this discussion. I am sorry you have yet to find a way to relieve your migraines. I suffered from migraines for about 14 years (I still get them occassionally) but used to get them about 5-8 times a month. I tried almost every medication that you mentioned and either nothing helped or I had bad side effects. Honestly speaking, the only thing that has helped me was going vegan. The first 3 months after eating nothing but vegan foods I felt wonderful. I had no migraines, anxiety went away, dizziness, etc. Everyone is different so maybe you can give this a try. Alot of the food we eat contain ingredients that trigger migraines like MSG and tons of others. My weakness are chocolate, cheese (except mozarella), soy sauce, foods that contain sodium nitrate such as bacon, lunchmeat, etc. Now I just get migraines at the start of my menstrual cycle here and there but they are not as bad as they use to be. I hope this information helps you and some of you that are also having a hard time finding answers. If you have any other questions please feel free to contact me :-) 

    -Christina

    • Posted

      Thank you, shall definitely look into what I'm eating and if it could be causing the migraines smile glad yours are better! 
  • Posted

    Hi, Becky-Louise. So sorry to hear you are going thru all this. I know what it is like as I am going thru the same thing. It's a pain being a guinea pig isn't it? I am a spiritual person and believe in the whole body, mind, spirit concept. There is always an emotional component to our illness which manifest in physiological ways. I am working on all three areas to identify the root cause. I try not to let my headaches control my life and my focus although it is extremely difficult at times. I also prefer natural solutions after ruling out anything organic which it sounds like you pretty much have which is a big positive. One Johns Hopkins neurologist suggested a supplement called Migravent which is basically herbs and vitamin B2. I have pretty much eliminated most of my dietary triggers and now the main cause seems to be high blood pressure. I am slender, active, and have never had high blood pressure in the past. Don't know how old you are, but hormone regulation is huge in women who are under stress so am working on balancing those as well. Hope you are feeling much better. Remember, pain is fear leaving the body. There is absolutely nothing to be afraid of in life, not even death. So, press on and give thanks for all things and always, keep looking up!
  • Posted

    I am so sorry to hear of your suffering! I've had migraines off and on for the past year, not continuious like you. I've been trying pill after pill, supplement afer supplement, chiropractor, acupuncture, dietary restrictions, etc., etc., with nothing working. All clear on the MRI. Still, they've only gotten stronger and more frequent. Until I finally got blood tests, at my own suggestion (not sure why this didn't happen before the MRI). Showed I was quite deficient in Vitamin D. I started supplementing immediately, of course, and noticed a significant change within 24 hours. An online search revealed people who said they suffered for years—decades, even—and D ended up being the solution. It's not even been a week yet, so I'm still crossing my fingers that this continues to be my solution, but so far, so good. Perhaps you've done the blood tests already, and even tried D, but wanted to mention in case you hadn't. And to possibly help anyone else here. When I scoured the internet for solutions before learning of my own deficiency, I never saw Vitamin D listed as something that might help. It seems crazy after all the pain and drugs and doctors that for me it *may* be something so incredibly basic. Best of luck to you in finding relief!
    • Posted

      Thank you smile

      actually out of all the tests I've had done, blood tests hasn't been one of them, but I'm getting a blood test this week for a different problem so will ask my doctor to look out for that.

      you would think that would be one of the first things they would test. 

      Glad you've found an answer to your own migraines, and it was easy to sort out. All the best

       

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