Migraine After Exercise - Aura (zig - Zag Lines)
Jun 4, 2016
I've been suffering from post exercise migraines for 12 years (since I was 11). Every time when I have muscle tension, I get a headache or migraine with aura (zig - zag lines). It all started when I was 11 and started to play tennis. After one year I stopped training and after that migraines were less frequent. But now, even if I walk, I have headache. I noticed that magnesium helps to reduce the pain, but migraines are still present.
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Was diagnosed last year as having migraine with aura. started off with numbness all down my neck and left arm, confusion at times and the very odd headache. woke one morning and thought i was having a stroke... i was confused , completely numb and disoriented. went to A&E and was admitted for 5 days of tests and scans.
i had a MRI brain scan, MRI neck scan, CT brain scan, chest x rays, neck Xrays and every imaginable blood test you could imagine. all negative and clear, except for neck MRI showing a slight bulge in the c6/c7 disc but not impinging on any nerves.
so after seeing the neurologist i was sent home with the diagnosis of migraine with aura and given a 6 month prescription for amitriptyline.
after researching the amitriptyline i decided not to take it , as i didn't feel that the rare headaches i was getting were bad and as i have a young child with some medical issues i needed to be alert at night in case he needed me.
since june i was being suffering with a constant headache, on my left side, and when its bad it goes right in behind my eyes and across my forehead. it was coming and going but its been constant for the last few days and im wondering if this is really migraine.im also suffering from regular panic attack lately . does migraine last persistently for days or weeks, should the aura symptoms not disappear when there is no headache.... i am so scared that there is something else going on even though all tests were clear.... thinking of going to GP and maybe trying the amitriptyline but from researching it seems that preventative medication is hit or miss and usually comes with side effects.....
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I have been reading over the time on this site some scared and desperate lovely ladies in need of reassurance. I know because i have been there and i just want to reach out a reassuring hand and say it probably is the start of menopause, of course get it checked out but don't feel you are alone and going mad! Here is some of my awful symptoms!
Nausea
Anxiety
Panic attacks
Gastritis
Food cravings
Earache
Headaches
Migraine auras
Leg cramps
Nose and gum bleeds
Acne
Hot sweats
Brain fog
Heavy clotty periods
Irregular periods
Eye twitches
Mood swings
Sensitive teeth
Brittle nails
Watery eyes
Dry eyes
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I've had migraines throughout my life. Mine really peeked in my early 40s going through peri menopause they would be 3 days long. Now the painful migraines have gotten so much better and shorter. I also use Imitrex as needed.
I would also get an Ocular Migraine (visual disturbances such a bright zig zag lines, vibrating bright lines in vision) about every 4-5 years. They were checked out the first time and the doc said they were not harmful.
Recently my dog decided to put me on Atenolol to prevent migraines. After 3 days of being on them I started to have the Ocular Migraines every single day now! I've never had that happen. The Atenolol has stopped the painful migraines completely but I don't think I can handle something like an LSD trip every single day. This doesn't seem right. My doc doesn't think it's causing it but suggested I go off of it to see.
Anyone else with Ocular migraines?
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I've had migraines a good chunk of my life and I haven't had one in roughly 9 months but I have been experiencing almost like mini migraines? in that I experience pain very similar to a migraine but without the aura or having to lie down or take it seriously. I guess these could be tension headaches, but I'm not sure? I've also been experience other symptoms, including: ear pain, sensitivity to light/sound, ringing in the ears, and various pains all over my body. these symptoms can happen with a migraine but lately they've been constant and if not, happening often enough that I'm noticing. I've had a brain scan and nothing. I don't think it's ever been like this before and I'm curious as to what it could be? As in, a starting point. I do have migraine medication but all it does is put me to sleep, it doesn't help with the pain. Not sure if that matters.
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It all started a few months ago when I noticed blood on my toilet paper. It was just a few spots. Then I started to notice these random red lines and also orange lines on my toilet paper. Then ii also started to notice these black specks and spots on my toilet paper. That was two months ago and these symptoms are still concurrent. Lately though I find that my bowel activities are strange. Ive been having to a lot more lately, Diarrhea, Constipation diarrhea.
And also last week my poop was completely green, and this morning my stool has these weird yellow round things in it. I know it wasn't corn as I haven't eaten that in a few months. The blood is usually bright red and sometimes its more of a dark maroon color. A few months ago I also had a weird a cold that made me have blood in my throat when i would clear my throat but it went away. I have also had shortness of breath and abdominal pains once in awhile.
I went to the doctor and they said that they will send me for a ultrasound but what are chances that this cancer?
I'm going to list all my symptoms.:
Blood on toilet paper once in a while. (Brighjt red and sometimes dark maroon...)
Black Specks/Spots on toilet paper once in a while.
Orange little lines, and also little red lines on toilet paper...
Frequent diarrhea/Runny stool.
Green Stool all day yesterday.
Today = Stool has yellow round things in it, looks like corn.
Abdominal pain sometimes,
Shortness of breath
Fatigue a lot of the time
Blood when clearing throat a few months ago but it never happened again.
I also went for a blood test when i had shortness of breathe a few months ago and they din't find anything.
Is it colon cancer?
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I never suffered from migraine attacks until I was in my mid-40's.
They seemed to be linked to the beginning of hormonal changes related to the start of menopause. I would get a pain over my left eye (usually, though right occasionally), with a feeling of nausea and sometimes slight numb feeling on the side of my face. I would turn quite a pale white colour, and also feel very tired, yawning a lot. I would take medication, migraleve tablets and lay down in a darkened room. Usually, I would recover within 24 hours, though I would feel 'worn out' for a few days after the attack.
Since I have discovered by self analysis, that citrus fruits, especially orange juice (which I no longer drink), chocolate and strong coffee all seem to be triggers, which I try to avoid.
For the last five years, I have been clear of migraines, but have now started to get them again. I have passed the menopause but have had a lot of stress in my life recently, so I wonder if this is the cause of the recurrence? My last attack was quite different from the others I have experienced, in that I was feeling fine (though had been really tired the day before for no apparent reason) when I suddenly developed black zigzag lines across my left eye (very frightening at first). These went on for about 10 minutes and then slowly I developed a severe migraine, though this was not over one particular eye, but both. I had feelings of nausea and also felt cold at times. I took Migraleve pink and yellow but the headache is still persisting the next day. I wonder why I developed these other symptoms of visual disturbance. Can stress really do this to your body?!
PS I know there is a family history of migraine.
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I had classic migraines through my teenage years which stopped for a couple of years before continuing at on average one every couple of months with the odd instance of a back to back cluster of 3-10 at once. They were always the same 20 minute aura then axe in the head pain and repeated vomiting for 6 hours followed by a 24hr hangover. Over the years I have tried all preventers with only Epilim and Topiramate working for 18 months. I built up tolerance to Epilim and Topiramate gave me side effects that ended in a blood disorder so cannot take either any more. Beta blockers and antidepressants never worked and Lisinopril was also a short lived waste of time. The only triptan that ever worked was Maxalt rizatriptan but again it lost its effect after 6 months. Something weird has now happened and I wonder if others have had this? I am now 36 and in the last 6 months my migraines have totally changed. I still get the aura but if I take Express Nurofen and an anti sickness tablet straight away or use a heat pack on the back of the neck no pain or sickness comes just 6 hours of extreme tiredness. I always used to throw up any tablets so this is a miracle however the frequency has stepped up to between 5 and 20 a month so it is really impacting on my life. I have had an MRI and all is normal. I have also tried supplements and alternative therapies with no success. Botox and nerve blockers are the next suggestion but will they treat this scenario if there is no pain? Will it stop the aura too and prevent the whole episode? Help!
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I think I have Oral Lichen Planus but I can't get a doctor to confirm it. I have had mouth sores in my cheek area since 2009 and now my gums are very red and inflamed and have been told that I have white lines on my inside cheek area. When I go to a dentist to have my teeth cleaned, I am always turned away because they don't like the looks of my mouth sores. In 2013 I had doctor swab my mouth and send for testing and also did blood work but was told nothing showed up. I think she was looking for bacterial infection. In the mean time, I continue with a very sore mouth.
I have a hard time eating anything because the sores are next to my bottom back teeth so eating irritates the sores a lot at night I sometimes bite the area with sores due to swelling so they pretty much never heal.
I recently went to a new dentist and she too wouldn't work on my teeth but she gave me details as to her concerns and told me to get checked for an Auto Immune disorder. I have since been to a doctor and had blood taken to check for that and then they sent me to ENT. He mentioned Oral Lichen Planus which was the first time I have heard of it. He wants to do a biopsy and then he mentioned a steroid rinse.
I also researched OLP and I have all the symptoms listed so I just don't understand how going to doctors since 2010 about the mouth sores, no one can figure it out? Am I finally heading in the right directions for diagnosis? I scares me that it has been left un treated for 5 years when I read that sometimes those with OPL can lead to mouth cancer.
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I'm a 24 year old guy. Not a virgin (not sure if relevant) and I have a white lump / or white clot along the lines of my penile raphe. I've had it since I was a teen and I've noticed that it's getting bigger over the years. I'm worried and fear that it might endanger my health in the future.
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Is it good to east before you start working out? What to eat which will give you extra energy. Share here
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What types of exercises are okay. I'm only 5 weeks now, but would like to continue to exercise. Are there any lifting restrictions.
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I am 7 months and I want to exercise besides walking because I walk all the time so I'm looking for two. I don't want to hurt my baby so what can I do?
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Anyone know any safe exercises I can do? I'm only like 5 weeks but my 1st is 10 months and I haven't lost all the weight from my 1st pregnancy. I gained a lot.
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After a mild episode of unstable angina I had a single stent inserted in 2010. Since then I take the usual quartet of ramipril (2.5 mg), bisoprolol (2.5 mg), aspirin and simvastatin. I started Phase 4 rehab in January 2011 and now go to the Gym 2/3 times a week. The man aerobic component is a 20 minute row. I was advised not to allow my heart rate to exceed 75% of [220 -73 (my age) -30 = ] 97 but as I became fitter the average HR during rowing is 105 and the peak 111-113.
I feel fine, have never experienced any cardiac symptoms and the HR drops below 80 within 60 secs of stopping.
Am I taking a big risk? If not are there guidelines on HR during exercise for people like me?
I also have Parkinson's (no tremor) and exercise is very helpful in maintaining lung function and muscular tone so I have two reasons for exercising!
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Do you have to walk or exercise for you to go into labor because I really just stay inside most of the time.The only moving I do is clean.
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I got diagnosed today by a dermatologist after ten days of suffering and wrong diagnoses by GPs. He gave me some Elocon to apply but did say that steroids usually have little/no affect and keep using calamine. He also gave me Atarax 25mg tablets as I told him I have been taking double doses of Piriton antihistamine at night to help me sleep and stop me itching with no effect. He said that I should also moisturise with E45 on top of any topical treatment.
He did however say something that contradicts a lot that I see on the internet. He said I can continue to take baths, saunas and exercise as this does not affect the condition. The internet is full of warnings against this.
Has anyone had it and continued to exercise? I have become a real gym bunny for once and don't want to stop training til this thing goes.
Thanks for advice re head and shoulders. I just applied some in the shower and then went for 4mins on the sunbed. I am fair skinned and burn easily but seem fine from it. ! I am desperate for this thing to go and have bought an immune-boosting multivitamin.
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I had my nose cauterized not even 3 hours ago, it was the left side and I have the right side due in two weeks. Since I got home I've been researching what I can expect etc and I've read a few articles that suggest avoiding exercise for the next week or two? Is this necessary? I go to the gym 6 days a week and do a mixture of long runs, short and intense interval runs, weights and core work. When can this be resumed? I also train in boxing however I was fully expecting to have to put this on hold for however long it takes for my nose to heal but when will I be able to carry on with this and get hit without risking undoing what the doctor has done to my nose? On a separate note, my nose is quite sore, its extremely runny and I feel like I have a cold, when can I expect to feel like my normal self?
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I was doing exercise on Xanax and after 3 months my body fell apart. Heart hurt w/ palpitations, could no longer digest properly, breathing became difficult and labored throughout the night and day. Esophagus problems. Saw MANY doctors, no one could help me! I thought I was dying. I found the cause to be 0.25MG of Xanax! I thought I was going to die with all of the symptoms my body was displaying. Cost me $40,000 dollars for all the specialists I went to see. No one could help me. When I got off Xanax my body slowly came back. Do yourself a favor and stay away from XANAX. This is a very dangerous drug!
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I have Sciatica with a lot of bulges and other misc. sundries, and am being supervised by an orthopedist. With his blessings I am being treated by an acupuncturist with quite good results. Recently, the acupuncturist told me that I can no longer do "exercise " walks which I used to do for 35 minutes/ day at a hard pace because the disks between the lumbar vertebra are very narrow to non-existent. She says casual walking is fine, but that doesn't offer much exercise. She is suggesting that I find something else. Was wondering what else is there. I don't swim; she is thinking about a commercial health club . Any thoughts? Any possibilities she could be wrong on this? She has seen the MRI report.
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I'm 4 weeks in after a stapedectomy. Got advice to avoid lifting but also as much exercise as possible for the next month still (except for walking). Any ideas on what other mild exercise I could do? Anyone had difficulties with exercise after stapedectomy/ or want to tell how did it go with it afterwards and what kinds of exercise they did/do?
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