I have the exact problem for a few minutes then it is gone , not all the time. I think I would start tracking it - oh no help from the doctor I think we are all but cases..but I am scared.
i ate eggs friday and this happened to me for the first time.....and i ate chicken yesterday and it happened again....so weird.....i mean i have never had that kind of pain...i thought my head was going to explode.....but.....both times i had let the food sit out ....i wonder if it's food poisoning?
same here...sure wish we could find an answer....i've been up all night....
i had the same thing ,after a MRI ,my skull was thicking and putting pressure in my spinal cord,so i had a peace of my skull removed,and i no longer have a head ach when i have a bowel movement.i had this done 5 years ago
Did your coworker ever get to the bottom of this?
THIS means you have a tumor and it starts with this so you need to get it removed
I have this problem too; last night I had it so bad and I took 2 alka seltzers and 2 tylenols and after 30 or 45 minutes the pain was almost gone.
This is exactly what is going on with me..I am 47...what should I do
REALLY HATE WHEN PEOPLE SAY THEIR HEADACHES ARE WORSE THAN SOMEBODY'S ELSE'S. I ALSO HAVE HEADACHES FROM BOWL MOVEMENTS AND I ALSO HAVE BAD HEADACHES FROM CANCER BUT NOT ONCE WILL I TELL A PERSON MINES ARE WORSE JUST BECAUSE I HAVE A CANCEROUS BRAIN TUMOR WITH SWELLING BECAUSE THATS RIDICULOUS. MY HEADACHES AREN'T CONSISTENT AND THEY COME AND GO.
IT BREAKS MY HEART TO SEE YOU ALL SUFFER SO MUCH MY PAIN IS DEFINITELY NOTHING COMPARED TO U ALL. IM PRAYING FOR YOU ALL. PRAYING FOR YOUR HEALING AND THAT YOU GET ANSWERS..PLEASE EMAIL ME IF U EVER NEED TO TALK AT: ***this post is edited by moderator *** *** posting of private e-mails is not allowed*** *** all questions should be discussed on our website *** Please read our Terms of Use
You might want to check out vasovagel, postprandial hypotension, and POTS.
I have had this issue for years. I think it has to do with constellation. I have a difficult time going to the bathroom for years. I changed my diet, started drinking a lot of water all day, and stop eating chocolate, that would do it for sure. After a while I was no longer straining when using the bathroom, so no no more headache. Hope this helps some people.
I realize this is a year later but you said you were going to follow up with a kidney and vascular specialist. Just curious about your outcome! Thanks!
I’m a 47yr old female. I began having this problem a few weeks ago. I’ve had 4 episodes, each progressively worse. The last one was so severe I was unable to get out of the bathroom or call for help. Spent 10 minutes laying on the bathroom floor unable to do more than whimper. After getting help to get to bed and thevosin easing enough so I could speak, I had my blood pressure checked. It was 158/90. I’m normally around 90/60-100/70. I’m curios as to how high the pressure was during the height of the attack if it was still that high on the downside.
I also have a family history of Chiari Malformation, although I’ve never been checked for it. I also have a personal history of low back injury (herniated and bulging discs) and a history with migraines. The closest headaches I’ve had to compare to these headaches were:
1-a low pressure headache (low cerebral spinal fluid) due to a spinal fluid leak following accidental spinal cord puncture during sympathetic nerve blocks.
2-a cluster migraine that accompanied congestive heart failure caused by pre-eclampsia.
In each of those instances I had sudden onset pounding headache that felt like someone was hitting me in the head with an ax. The pain, just as with these new episodes, was so severe you just know you’re going to die because there is no way anyone could possibly survive that amount of pain in their head/brain. The difference is, with both of those, there was a known cause and treatment. The frustrating part of these is no known cause, no treatment or sure relief let alone cure. I’ve been on multiple sites in numerous groups each with the same symptoms and none with a clear diagnosis.
I also have a family history of Chiari Malformation, although I’ve never been checked for it. I also have a personal history of low back injury (herniated and bulging discs) and a history with migraines. The closest headaches I’ve had to compare to these headaches were:
1-a low pressure headache (low cerebral spinal fluid) due to a spinal fluid leak following accidental spinal cord puncture during sympathetic nerve blocks.
2-a cluster migraine that accompanied congestive heart failure caused by pre-eclampsia.
In each of those instances I had sudden onset pounding headache that felt like someone was hitting me in the head with an ax. The pain, just as with these new episodes, was so severe you just know you’re going to die because there is no way anyone could possibly survive that amount of pain in their head/brain. The difference is, with both of those, there was a known cause and treatment. The frustrating part of these is no known cause, no treatment or sure relief let alone cure. I’ve been on multiple sites in numerous groups each with the same symptoms and none with a clear diagnosis.
Same.
I have had Crohns over 30 years. I'm 48.
the past month my bowels have been soft and I get an immediate headache right after. I had my stools tested with my gastroenterologist at the clinic and was positive for c-diff which is a virus and they also said the looser the stools the more dehydrated you are even if you think your not.
I have had Crohns over 30 years. I'm 48.
the past month my bowels have been soft and I get an immediate headache right after. I had my stools tested with my gastroenterologist at the clinic and was positive for c-diff which is a virus and they also said the looser the stools the more dehydrated you are even if you think your not.
Im acribtokerd hnave s. Maybe its an allerfy thing?
Also look int psuedoaneurysms, chiari malformation, and subarachnoid Hemmorages
Also look int psuedoaneurysms, chiari malformation, and subarachnoid Hemmorages