I've been suffering from these for some time and they've recently become worse. I also had migraine headaches in my youth and now occasionally have silent migraines - aura, but no headache. I've recently been diagnosed with fibromyalgia and I understand that this type of headache is common with fibro. I wondered if others have suffered from this and what, if any, medication has been tried.
View 1 RepliesI've been suffering from this type of headache for some time and they've recently become worse. I also had migraine headaches in my youth and now occasionally have silent migraines - aura, but no headache. I've recently been diagnosed with fibromyalgia and I understand that this type of headache is common with fibro. I wondered if others have suffered from this and what, if any, medication has been tried.
View 1 RepliesMy partner gets this severe stabbing pain all over in his head whenever he's about to climax, then it's a severe headache and he can hardly move for several hours after ?
View 1 RepliesI can only eat very, very small amounts of fruit and vegetables--even organic ones, otherwise I get a headache 8 to 12 hours later. Does anyone else suffer from this condition? Is there anything that can be done to lessen the effect?
Cooking the fruit or veggies does nothing, and I am desperate to find a solution.
I don't know if im posting in the right place, but here it goes!! So this all started about a month ago, all I noticed was I was a bit more tired, no big deal I thought it was the change of season or something. I was like this for maybe a week before I woke up march 20th and felt very off. My normal routine is to go the gym in the morning, so I got myself up to get ready and realized I didn't think I could go, I felt very dizzy, lightheaded, pressure behind my eyes, stuffy nose, extremely heavy eyes, very fatigued, and a little spaced out. I drove to a walk in clinic by my house, they did routine blood work, checked my thyroid, checked for Epstein barr, and for mono, all negative. I did have a low grade fever if even that it was like 99.5. Now lets go back a few months...i have had a stuffy nose since November constantly blowing it with bloody discharge and i attributed it to the dry heat and the winter weather. I have also had many sinus infections in the past year. I didn't realize it until I thought about it. I also had a concussion, my third one back in August. Went to the ER and got a CT scan, everything was normal and they released me. 2 days later I went back to the ER, I was nauseas and it felt like my head was on fire and on CT scan they said I had inflamed nasal sinuses. Everything else was normal so they gave me antibiotics and i was released again. At that time I thought nothing of it and I got better in a few days. Now back to march 20th and the Dr. They knew of my previous sinus infection because I had went to them in December and they were surprised that since I saw them I was still stuffy, they gave me nasal spray and sent me home. A week later I still feel the same, exactly the same, maybe a little worse. I saw an allergist who tested me for allergies and of course everything was negative. I was so tired at work one day I had to lay down and close my eyes. Im just exhausted even after a full nights sleep and my eyes are so heavy. My headache lasted from march 20-27th and then subsided but still had all the other symptoms. Over that weekends I actually started feeling better everyday! I was sk happy and thought it was some sort of virus or something and it was going away. I still felt off but it started getting bad again April 3rd. This time it was all my symptoms but very exaggerated. Extreme fatigue, extremely heavy eyes, poor concentration, confusion, blurry vision in my right eye, spacing out, brain fog, sensitive to light, pressure behind my eyes, im forgetful, still a little stuffy but not nearly as bad, im a little pale and my headache is gone but my head still feels weird with weird pains that last a second. I went to my pcp on Monday and told him the whole story. He put me on a strong dose of antibiotics and some steroids. The next day I saw an optometrist and i am nearsighted and have an astigmatism in my right eye so i'm getting glasses. It was weird to me though because my vision just became blurry a few days before, unless i just didn't notice it before that and my eyes are always heavy, even as soon as I wake up which I think is weird. So the next day I saw my ENT and told him the whole story and he looked in my nose, flushed it, and took a sono of my sinuses and said my right paranasal sinus in very congested and I need a CT scan of my sinuses. I'm nervous about the CT scan because that will be the 5th CT scan I have had since my first in 2010 from my first concussion. I feel like that's a lot of radiation to my head and face i'm only 25 years old and I feel like that cant be the only reason I have all these symptoms. As soon as I got home from my ENT i noticed this painful hard lump next to my ear on my jaw. my dentist told me to come in and he said my TMJ joint was inflamed on my right side only and that it should go away in a few weeks, I do grind my teeth at night, but I think its weird that my right eye is now bad, my right paranasal sinus is very congested, and my right TMJ joint is inflamed! I see my neurologist. I have a neurologist in the first place because back in 2009 I had a what I thought was a vaccine reaction to the HPV vaccine. A few hours after I got it the room was spinning and I was so nauseous and weak. A week after that vaccine I was having trouble walking, tingling in my legs and arms, severe fatigue and weakness, severe headache. I got an MRI back then to rule out MS and did an EEG and an EMG all normal and after several months all the symptoms went away. So yesterday my neuro did a vertigo test which came back normal, now she wants me to get another MRI next week to rule out MS again and I'm terrified. I don't have any numbness or tingling or trouble walking but i'm so scared. My life was so normal and I was actually in the best place I've ever been in my life before this happened and now its all turning to ****. Im crying everyday because from the moment I wake up until the second I fall asleep I feel all the symptoms. They are getting worse, I am getting more frustrated, I am getting more scared that this is something serious because its not going away. Did this ever happen to someone else? Does anyone think this is really MS? I'm assuming my optometrist looked at my optic nerve and would have said something if it looked weird. I have also heard of silent migraines where u have all the symptoms of the migraines except the headache because I have also recently felt like im seeing flashing lights or its hard to explain but its like when im looking at a bright wall, its like I was just staring at static on a tv and then looked at the wall, except im always seeing it I find myself staring into space I have to like snap myself out of it. This whole experience is driving me crazy and i am so irritable and upset. I've also lost my appetite and i cant stop crying because this feeling wont go away it is affecting my life so negatively. I don't even know what to think i want to feel normal and I want my life back its affecting my job, my relationships with everyone, and myself and my happiness I want to do the things I used to. Im sorry for all the jumping around in the story and how long it is, I am very overwhelmed.
View 3 RepliesAt the age of 79 I became aware that the pads on the balls of both feet felt tight and a bit puffy and hardish. Then gradually I experienced a sensation in my toes which I can describe as tingly. This area of both feet became susceptible to cold and required contact with heat pads to feel more comfortable. No pain is experienced. Walking seems to alleviate the tingling sensation. After a visit to a G.P. Raynauds Syndrome was confirmed and keeping the feet warm at all times was advised.
Although I live in a well heated bungalow I take heat-pads to bed at night.
In the morning my toes feel quite warm and look rather pinkish red. This condition doesn't affect my normal activities in any way after a year of beginning. 8)
My daughter is taking hydrocortisone for primary Addison's due to Pheochromocytoma. Does anybody know if she should be taking something to help prevent osteoporosis??
View 1 RepliesI just wondered if anyone has any idea how common it is to have primary hyperparathyroidism?
View 5 RepliesI've been diagnosed with hyperparathyroidism on Thursday 5th of November, I was wondering if anybody has had natural treatment for this please?
In the meantime I'm going ahead with being put on the waiting list for an operation, I have my ultrasound scan tomorrow, Tuesday the 24th of November .
It would be good to hear from those members who have used natural treatment for primary hyperparathyroidism and to find out how you are getting on now please ?
I have had "M.E. " for 19 years , I'm being treated naturally, this helps with my weight and also some of the other symptoms , however I'm still not well enough to work and need help at home etc
After a very painful kidney stone problem and thus being told I have Bilateral kidney stones; I have just been diagnosed with Primary hyperparathyroidism. The docs want to operate to remove the faulty gland(s) but I am very concerned about the procedure in the UK which does not seem to include the mini op or MIRP operation. Has anyone had this type of surgery in UK(either mini or other) and what were your experiences? I am wondering if I should travel to Florida for it?? I also have low vit D and they want me to take vit d supplements. I think this is dangerous to elevate my calcium level even more?
View 2 RepliesI kissed and had sex with a female partner with unknown std status 6 weeks ago I have not had any symptoms but I'm scared il have a recurrent outbreak. The sex was protected. What are the chances that I had an asymptomatic outbreak and it's only a matter of time for a recurrence to happen. I'm still terrified please help
View 3 RepliesI'm 27y,male,weight 44kg. I've started to have headache after having a very tough semester at college 2 months back and it become worse 2 weeks back when i visited a neurologist who diagnosed me with "tension headache".
He prescribed me a cortisone injection in addition to 9 days of prednisolone (3 days 60mg, 3 days 40mg, 3 days 20mg).
The tension headache has gone, however, I still have headache on the sides of my head and behind my eyes, some pressure in my ears sometimes.
During my prednisolone course,I had severe depression, mood changes, anxiety (i couldn't sleep), sweating & lose of appetite. (I didn't have any history with these weird side effects)
Now, it's day 6 after stopping the prednisolone and i still have some depression/worried but i think i'm getting better day after the other.
My questions:
1. How long does it take for Prednisolone to clear out from my system?
2. Since tension headache has gone, why am I'm still having headache (sides of head,behind eyes & sometimes pressure in ears).
I have recently been diagnosed as having hyperparathyroidism and I am currently on the waiting list to have two nodules removed. On reading up on the condition sickness is a symptom but for some reason my consultant wouldn't say that my continued sickness for the last 18 months is being caused by my overactive glands. I am getting desperate now so is there anyone on the Forum who is suffering / suffered the same problem and after having the op felt human again ?.
View 5 RepliesDo you think that Sjogrens caused my pbc(primary biliary cirrhosis)? or maybe its just the autoimmune system and I happen to have both?
View 3 RepliesI have just been diagnosed with pleurisy yesterday after an horrendous weekend of stabbing pains, in my ribs and back, but not particularly in my chest. It came on suddenly last thursday night in bed without any warning and was accompanied by fever symptoms similar to flu ie boiling hot one minute and freezing the next. I had flu about 6 weeks ago, got rid of it and it recurred again in the shape of a chesty cough which causes a crushing feeling in my chest and ribs. The doctor prescribed me strong antibiotics and was told to take paracetamol for the pain which has shifted all over my ribs and back, not staying in one place. He also ruled out a water infection whilst I was there. I still have a fever and can't do much more than rest as I'm tired much of the time but manage to keep my pain down to a minimum by dosing up with codeine/paracetamol every four hours, even managing to get some sleep last night. I hope this info helps someone else in the same predicament.
View 1 Repliescan any 1 help me, im a 23yr old female and have had flu like symptoms for last 4 days, high temp congested nose and dry cough, but now this cough has turned into a chesty cough and everytime i cough i am getting a stabbing pain in my chest, have not been drs yet as it's weekend and don't want to waste any 1s time, not sure if this is a bad luck or related to symptoms above but i'm also experiencing terrible pain in my lower right abdomen groin into my back, kidney pain, can this be related to the flu like symptoms or something totally different.
View 1 RepliesI have had the typical sciatica for years on and off nothing debilitating so I am familiar w/the pain in the buttocks and moved down the leg etc but this is different so if anyone has had this please let me know I'm so confused...a month ago I actually went to ER w/pain behind my thigh that felt like I was being stabbed...then it would stop and come back 10-12 seconds later lasting about 2-3 seconds and VERY painful did this consistently for 6 hrs and disappeared as fast as it came! GONE for 1 month until this past Sat started again altho not as constant ..until the past hr I have had it every 30 seconds and I cannot fig out what causes it ...or what it is ..the ER gave me Valium and my reg Dr said take magnesium altho my levels were within range. I almost feels like I was tasered or stabbed (have really never experienced either but seems like that's what it would feel like) so do you think this could be sciatica?
View 1 RepliesI was diagnosed back in May 2014 with diverticular disease because I had a sharp pain in my lower left abdomen but recently I have had a pain in my lower right abdomen and am waiting to go for another colonoscopy. has anyone else experienced this with diverticular disease as the doctor doesn't think the pain is caused by my diverticular am worried as it feels like a stabbing pain.
View 3 RepliesI started last week noticing shooting leg and butt pain went to Chiropractor and seemed fine.
Then about 2 days ago went into bad wicked leg cramp(left side of body)and very bad stabbing back pain .
went to dr who says it's pinched she has me on cyclobenzaprine aka Flexeril hcl 10 mg 2 per day I took it at 4pm and Tramadol hcl 50i took at 6pm mg every 6 hrs have done that today plus bath/heat pad , icy hot spray, mineral ice and cold ice pack, everything I've done seems to make it worst or just not help . The heat and cold treatments seem to make it worst and aggravate the pain into cramp like symptoms
Wondering how normal that is have tossed out back before and muscle relaxers put me to sleep and make it go away this isn't even helping. I find laying painful standing walking are near in possible and extremely painful to the point it makes me want to cry literately like a throbbing stabbing pain ,sitting seems to be better then laying but not buy much.
unsure how to describe this part but when walking what little bit I do back has a odd pop sensation and leg and back starts to spasm to the point i can't put weight on leg or move.
Wondering if anyone has any home treatments or advice.
As i find this can't be normal after that many pills to feel still worse then when I went to the doctor. i'm in central time so pills are still hrs away from me taking more
Secondly, I'm here because I'm concerned about chest pain I've been having for the past 3 days, even though my PCP examined me and sent me home with instructions to get rest, fluids, and take extra iron tabs for the next couple days (I appeared anemic but my level was in the normal range).
So when the pain began it was sharp stabbing accompanied by hot flashes and nausea and lightheadedness. Since then, it has been a consistent, sometimes worse sometimes better, feeling like someone is pressing on or squeezing my chest, and today the pain was radiating into my left arm, and both hands were tingling. I also have off and on indigestion, lightheadedness, and constantly feel like I CAN'T BREATHE despite no congestion or any cold symptoms or anything.
The other thing is, I've been absolutely exhausted since this began. Like, I can barely walk to the bathroom and back. And have taken 5 hour naps every day since Thursday and otherwise have barely left the couch.
I just don't think I can go on like this another day, but I don't know what else to do! My resting EKG was normal. Although my PCP did say I would benefit from an echo because I have a preexisting diastolic murmur.
Hello I have tarsal tunnel syndrome which was diagnosed by a nerve conduction test. I go back to see my foot and ankle surgeon in three weeks
Does anyone else have this syndrome? If so how was it treated. So far all i know is mine is caused by bruising and possibly a fracture of an old injury.
The stabbing pain i get is at times is unbearable lasts only for a few seconds its like someone has stabbed me in the foot with a hot sharp blade and electrocuted at the same time. Also have tingling in my feet muscle spasms leading up to my knee all the time but more noticeable with online in bed at night.