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What can I take for a headache if on warfarin?
What can I take for a headache if on warfarin? I haven't had a headache for ages and I know not to take ibuprofen
What can I take for a headache if on warfarin? I haven't had a headache for ages and I know not to take ibuprofen
Charts
in
Hughes Syndrome APS Forum
7 months ago
Migraine and visual hallucinations
I’ve suffered with migraines for many years since I was about 11 (I’m 35 now). Anyway as I’ve gotten older they’ve thankfully become less frequent and severe (though I take propranalol to prevent). I had an attack begin late last night with my usual blind spots and visual disturbance. It was bed time
I’ve suffered with migraines for many years since I was about 11 (I’m 35 now). Anyway as I’ve gotten older they’ve thankfully become less frequent and severe (though I take propranalol to prevent). I had an attack begin late last night with my usual blind spots and visual disturbance. It was bed time
PTNewbie
in
National Migraine Centre
7 months ago
Headaches
Hello. I've just been diagnosed after years of mysterious symptoms. I'm suffering with terrible headaches. I've been given tablets fir migraines but they don't touch it. Yoga and meditation aren't working. Has anybody any ideas please. They aren't the only thing that's bothering me but they are the most
Hello. I've just been diagnosed after years of mysterious symptoms. I'm suffering with terrible headaches. I've been given tablets fir migraines but they don't touch it. Yoga and meditation aren't working. Has anybody any ideas please. They aren't the only thing that's bothering me but they are the most
Championbaker
in
LUPUS UK
7 months ago
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viral meningitis
I was diagnosed with Viral Meningitis in2012.It's 2024 soon and i have migrains every day since along with everyday chills.Something is still wrong !!! My Neurologist said my Meninges,the coating around brain takes 15 years to heal,i have 3 more years to go !! I dont't believe that !! They are just
I was diagnosed with Viral Meningitis in2012.It's 2024 soon and i have migrains every day since along with everyday chills.Something is still wrong !!! My Neurologist said my Meninges,the coating around brain takes 15 years to heal,i have 3 more years to go !! I dont't believe that !! They are just
bekele
in
Meningitis Now
7 months ago
TLE and weakness
I have temporal lobe epilepsy, shrunken hippocampus and mesial temporal sclerosis, all on the right side of my brain. Would this the cause of weakness in my right leg?Also I've noticed lately, that this bitterly cold weather seems to affect my right side. Awaiting a report from a recent mri (19th Nov
I have temporal lobe epilepsy, shrunken hippocampus and mesial temporal sclerosis, all on the right side of my brain. Would this the cause of weakness in my right leg?Also I've noticed lately, that this bitterly cold weather seems to affect my right side. Awaiting a report from a recent mri (19th Nov
Dawn43
in
Epilepsy Action
7 months ago
I'm struggling
I said i was too fatigued, but didnt actually have a
migraine
. But because she still defines me as 'just a
chronic
Migraine
Sufferer '. I was having to justify my pain - both mentally and physically. Life is just unbelievably hard, and I don't like the new me.
I said i was too fatigued, but didnt actually have a
migraine
. But because she still defines me as 'just a
chronic
Migraine
Sufferer '. I was having to justify my pain - both mentally and physically. Life is just unbelievably hard, and I don't like the new me.
Kittycat2013
in
Neuro Support
10 months ago
Migraines
Hello lovely community, I was in hospital yesterday with a flare-up; we now think it was an atypical migraine. But it looked a lot like past episodes I have had. For the past few years I have had recurrent unexplained heart episodes, where my heart rate goes up and stays elevated for hours at a time
Hello lovely community, I was in hospital yesterday with a flare-up; we now think it was an atypical migraine. But it looked a lot like past episodes I have had. For the past few years I have had recurrent unexplained heart episodes, where my heart rate goes up and stays elevated for hours at a time
MusicalFurbaby
in
LUPUS UK
7 months ago
Visual disturbance
Went to the cinema yesterday and had this type of visual disturbance (left eye only) about half way through the film. It lasted about 15 mn and then disappeared. I got this photo from a website which suggests that it's a benign ocular migraine type thing. I did start getting this on and off a few months
Went to the cinema yesterday and had this type of visual disturbance (left eye only) about half way through the film. It lasted about 15 mn and then disappeared. I got this photo from a website which suggests that it's a benign ocular migraine type thing. I did start getting this on and off a few months
Dochaz
in
PMRGCAuk
8 months ago
advice
One year ago, my spasticity was so severe I took too many Baclofen tablets at the same time, that I almost died! Now I take 1 Tizanidine at bedtime. I also have a small notebook I keep next to all the muscle-relaxing pills and log in what I take to make sure I never overdose on muscle relaxing drugs
One year ago, my spasticity was so severe I took too many Baclofen tablets at the same time, that I almost died! Now I take 1 Tizanidine at bedtime. I also have a small notebook I keep next to all the muscle-relaxing pills and log in what I take to make sure I never overdose on muscle relaxing drugs
Online2020
in
My MSAA Community
8 months ago
Platelets increase
My mun was diagnosed with thrombocytosis around 3 yrs ago. She has been on Hydresan for these years but during the past two blood tests she had to take her platelets went up to 600 in the first one and the second one was 700..We will contact her doctor but is this something to worry about? Ever since
My mun was diagnosed with thrombocytosis around 3 yrs ago. She has been on Hydresan for these years but during the past two blood tests she had to take her platelets went up to 600 in the first one and the second one was 700..We will contact her doctor but is this something to worry about? Ever since
PHGR
in
MPN Voice
8 months ago
Post viral stuff!!
I'm just sat here wondering......because I don't have the energy to do anything else!!!!....whether or not I have a post viral flare! Is that even a thing? My 4 month old grandson has had bronchiolitis and our little superspreader very kindly passed on some version of the virus to his parents and me.
I'm just sat here wondering......because I don't have the energy to do anything else!!!!....whether or not I have a post viral flare! Is that even a thing? My 4 month old grandson has had bronchiolitis and our little superspreader very kindly passed on some version of the virus to his parents and me.
altywhite
in
PMRGCAuk
8 months ago
headache instead of a seizure?
Hi so i am 20 years old and i have had mild epilepsy since i was very young, i can’t remember exactly when i was diagnosed. i haven’t had a seizure in about 7 years but i’m not sure if that is because it is quite easy to avoid my trigger(fast flashing lights) or if i have grown out of the epilepsy. today
Hi so i am 20 years old and i have had mild epilepsy since i was very young, i can’t remember exactly when i was diagnosed. i haven’t had a seizure in about 7 years but i’m not sure if that is because it is quite easy to avoid my trigger(fast flashing lights) or if i have grown out of the epilepsy. today
noodleygirl
in
Epilepsy Action
8 months ago
The Migraine Journey!
Hello Community Fam, hooray it's Friday. I wanted to know if anyone is currently taking Nurtec for migraines. I had to titrate off of Topiramate -due to my Kidney Stone nightmare in January. I tried Qulipta initially, but had an unfavorable reaction (i.e. nausea, shaking) and discontinued use.. My migraines
Hello Community Fam, hooray it's Friday. I wanted to know if anyone is currently taking Nurtec for migraines. I had to titrate off of Topiramate -due to my Kidney Stone nightmare in January. I tried Qulipta initially, but had an unfavorable reaction (i.e. nausea, shaking) and discontinued use.. My migraines
GratefulNeeC
in
My MSAA Community
8 months ago
Migraines, headaches, and relationship to b12
I feel like I spend half my life with a headache these days 😭 There’s definitely migraine with prodrome/aura, which I suspect would be there to some degree without the PA as it’s so hormonal. Then there’s tension headaches, bad posture headaches, and a weird sort of one that feels like a sinus pressure
I feel like I spend half my life with a headache these days 😭 There’s definitely migraine with prodrome/aura, which I suspect would be there to some degree without the PA as it’s so hormonal. Then there’s tension headaches, bad posture headaches, and a weird sort of one that feels like a sinus pressure
MindfulSquirrel
in
Pernicious Anaemia Society
8 months ago
Propanolol Tolerance
I have mixed tremor (PD plus ET). For my tremor, I find that CD/LD plus propanolol works really well to manage my tremor symptoms. At least that was true until last week when I suddenly stopped getting any effect from the propanolol. No reduction in tremor and no lowering of BP as I have come to expect
I have mixed tremor (PD plus ET). For my tremor, I find that CD/LD plus propanolol works really well to manage my tremor symptoms. At least that was true until last week when I suddenly stopped getting any effect from the propanolol. No reduction in tremor and no lowering of BP as I have come to expect
scotta
in
Cure Parkinson's
8 months ago
major headache
Hi all got yet another migraine well out of it, symptoms seem much worse at this time of year, recently started getting dizziness, does anyone else get this plus cold hands and feet Hoping to rescue my day, love to all my fellow sufferers x
Hi all got yet another migraine well out of it, symptoms seem much worse at this time of year, recently started getting dizziness, does anyone else get this plus cold hands and feet Hoping to rescue my day, love to all my fellow sufferers x
missvenus
in
Fibromyalgia Action UK
8 months ago
root canals
hi all , I have been on the W and W program. My blood dis-order was discovered in 2019. I referred to it as a blood disorder as they still haven’t taken a bone marrow sample to confirm that it’s truly CLL. I am curious if anyone in the group has tried removing any old root canals to see if it
hi all , I have been on the W and W program. My blood dis-order was discovered in 2019. I referred to it as a blood disorder as they still haven’t taken a bone marrow sample to confirm that it’s truly CLL. I am curious if anyone in the group has tried removing any old root canals to see if it
Jrugg
in
CLL Support
2 days ago
Puzzled
Hi folks! Hope we're all travelling well. Can I tap into your collective wisdom and experience? I've just come back from my regular check up with the CLL specialist. My ALC has gone from 29 to 53 in 6 months, or 91% of the blood count. Before then, it was steadily rising, but dropping at intervals. The
Hi folks! Hope we're all travelling well. Can I tap into your collective wisdom and experience? I've just come back from my regular check up with the CLL specialist. My ALC has gone from 29 to 53 in 6 months, or 91% of the blood count. Before then, it was steadily rising, but dropping at intervals. The
Guffy
in
CLL Support
4 days ago
Migraine
Does anyone have the aura but not the headache , I've had migraine all my life but now just the aura and no headache at least not very often, doctors just wanted me to have epilepsy meds or go to a dark room any advice ?.
Does anyone have the aura but not the headache , I've had migraine all my life but now just the aura and no headache at least not very often, doctors just wanted me to have epilepsy meds or go to a dark room any advice ?.
RacingGirl3
in
IBS Network
8 months ago
Feeling Very Stuck
Hi, I'm really hoping someone can help, I'm a
chronic
migraine
sufferer and I feel like I'm at a dead end. Apologies in advance for the long message! I've been having migraines for the last ten years, over the past five years my migraine episodes have increased in intensity and frequency.
Hi, I'm really hoping someone can help, I'm a
chronic
migraine
sufferer and I feel like I'm at a dead end. Apologies in advance for the long message! I've been having migraines for the last ten years, over the past five years my migraine episodes have increased in intensity and frequency.
Ellie252
in
National Migraine Centre
1 year ago
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