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Old 10-31-2011, 10:06 PM   #1
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Tension or Cluster headache? Or brain aneurysm? Please help?!?

For almost six weeks I have been dealing with this tight dull ache pain in the back of my head lower left side. It can go from left side to the middle to the right side and both side of my neck and shoulder. But for the most part the dull ache stays on the left side near my left ear. My neck feels tight and from time to time I can feel a bit of weakness on my left arm. The entire back of my head feels very tender, sore, and bruised like feeling It just doesn't feel normal just sore.

I do feel some back upper pain and have had some headaches and some migrains but they are not the worse migrains of my life, I've had worse. I've felt some dizziness at times and have recently noticed my left eye feels a little sore but my eyes get a burning feeling I think its caused by my contacts. I have been stressing a lot due to moving, school, and everyday life, I have also had some trouble sleeping I wake up with a crank in my neck and just feel sleepy during the day. I was doing just fine and one night that tight feeling just suddenly happened and its been like this for weeks.

I have gone to the hospital 3 times and was told the first time it was headaches, 2nd time I was told it was or could be a hemmorage and that I would die, the 3rd time I was told they couldn't do anything because it wasn't an emergency but discharged me with a tension headache. I've taken a little bit of Ibuphron but it upset my stomach and didn't do much.

I do have bad posture, spend a lot of time on my computer, no fainting, no nausea, no vomiting, if ything I'm fine except for the neck and head pain,No hypertension the only issue I have is a nuerological disability that affects only the hands and feet. Its called CMT (Charco Maire Tooth diease) BUT PLEASE SOMEONE HELP ME FIQURE OUT WHAT COULD BE THE PROBLEM SO I CAN FIND OUT THE PROBLEM AND THANK YOU KINDLY TO THOSE WHO DO HELP ME
I also noticed there have been times when I turned my head to the left and it felt like my nerve in my neck snaped and it hurt for a few seconds but it all feels tight

 
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Old 11-03-2011, 01:01 PM   #2
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

I don't think it is a cluster headache because my friend gets them and it is very painful. You might go to your primary doctor or a neurologist to tell them what is going on. It sounds like tension, stress and migraine related headache. If I am stressed or tired, I tend to get migraines and there are medicines for those. Find ways to get a good night's sleep and try to create less stress and tension in your life. I know it isn't easy but there are ways. Best wishes.

 
Old 11-03-2011, 02:53 PM   #3
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

Thank you for replying back to me, I'm putting so much worrying and stress on myself thinking about what it could be that I just hope its just some sort of tension headache. I never had this problem before so I can't handle it the right way. But my main doctor was no help and I do need to see a nuero for this I hope I will soon.

 
Old 11-04-2011, 09:17 AM   #4
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

did anyone at the ER ever actually bother to simply do a contrasted MRI on your brain AND that c spine level? what made them even think that you had some type of actual rupture of vessels inside your brain and then SENT you home??? a bit insane to say the least there.

and ANY levels of ongoing stress and tension WILL tend to hit those muscles up there and in men, also usually wraps around the heads more often too? in women, we tend to carry our stress more often within our necks and upper shoulders/backs areas. when it comes to 'haed pain' there realistically can be many different types of real generators for them and reasons. and some can crossover to other areas too makijg the headache more deeper and more involved, esp the longer we have them. but there just also ARE 'symptomatic' headaches too that tell us something IS wrong. and this is where the testing comes in to better define the trigger(s).

the absolute ONLY way at this point that they even CAN potentially rule out or rule in anything IS with getting that very indepth look into both your brain and the c spine too. they can be very interconnected depending upon what YOUR underlying problems or generators just are.

as far as trying to rule out the possible aneurysm(and also include exclude other possibles), it also could usually be done with starting out with that definitely CONTRASTED type of MRI too. i had an annie back in 05 that i really was not haveing any 'big' symptoms from, not even one single headache either which really amazed me since most of the population and myself ALWAYS assumed that any type of aneurysm WOULD also generate automatic headpain(usually depends more upon actual location and size). but there are also many other types of vascular malformations that one can even be born with anywhere within the brain or like myself, in my actual spinal cord as well, tho much rareer in cord, more commonly found in brain.

while this just 'could' be a ton of kind of 'backed up' and continued for many reasons tension and stress creating more muscular/tension/vascular type headaches for you, the fact that these seem to be mostly located way down in the more base of brain(tho could be the trap muscle too which DOES run partly up the back of our skulls) it DOES simply need better testing and defining the inner make up of your ongoing pain(this could just be a high upper c spine type of disc or other problem too). and as i said, right now to start with, just getting your own primary to simply refer you for that needed "contrasted MRI on brain and c spine" would be the ideal place to start the diagnostic process. it would either rule specific things in or out as potential generators/contributors of your symptoms anyways. then depending upon whats in the results would kind of dictate any of your next steps. but that 'baseline" testing needs to be finally done on you. if ANY oddities or suspiscous type of something should actually show up within any of the arteries within your brain at all, tho this is much less likely than other possibles, there is another scan that can look ONLY at all of your arteries within your brain called an MRA they can do too to REALLY see the full vascular structures within the brain where most major vascular malformations tend to create themselves. but this would be needed ONLY for best definition depending. but it IS there and availiable if needed, and so is the standard brain angiogram that is the BEST possible look one can get at all brain arteries done by an interventional neuroradiologist. but these are for AFTER just getting the inital scans rolling and only IF something should show. but looking at that c spine too seriously could be generating headpain. they are called 'cervicogenic headaches" when related to specific crappy stuff that just CAN be in our c spnes and the very close proximity to the head.

no one truely just ever 'knows' what is going on in any area of their own bodies til it either shows itslef on some type of scanning done, or 'presents' with some very destinctive types of symptoms "to IT". that most certainly has been both my sons and my own experiences here with alot of different things. some born with some 'aquired' but still there in us and not known about til 'scans'. just make CERTAIN with ANY testing that you get done or any that you already HAVE gotten done like at those hospials, that you ALWAYS obtain all of your very OWN copies of each and every testing result from ANY tests done on you so YOU simply have them for your own medical files you just keep on yourself at home. this also allows you the patient to also be able to read thru your own copies of all test results as well. this just helps you TONS and in many different ways or i would not be telling you to do this. trust me. but see what your primary can get done for you now. afterall, it IS your primarys overall job to help you in these types of situations and send you for 'appropriate to your symptoms' types of testing. esp with the 'unknowns', and NEEDING an actual diagnosis. good luck, but push for that brain and c spine with contrast at the very least right now.marcia
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3-22-01,herniated C-6-7
11-20-01,placement of hardware for failed fusion
9-22-03,removal of cavernous hemangioma that was inside spinal cord. Neuro damage to L hand L leg and R leg.

 
Old 11-04-2011, 10:33 AM   #5
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

Thank you feelbad for replying back to my post. I must say I am scared by what you wrote I didn't want to hear that it could be a brain aneurysm I just worry myself and think of all the things I have to go through. I thought and hoped it would be a simply tension headache due to stress. When I went to the hospital they did a normal CT scan and said there was no hemmorage the second time the doctor wanted me to do a spinal tap but I refused because of the risks it has. I have a nuerological disability that could be affected or made worse if I did that. My primary doctor is a really bad doctor he didn't even let me talk about my issues he just gave me a refferal and rushed me out. I am going to see if I can see a specialist but it is so tough with my schedule. I know with my back I do sit wrong I dont sit straight up But I've never had any history of truama or any injuries to my back or head so this is weird for me.

 
Old 11-04-2011, 07:51 PM   #6
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

I also do not think this sounds like cluster headaches. Have you ever read about myofascial pain syndrome and trigger points in the neck area? I was diagnosed with this and you have very similar symptoms. The weakness in your arms is likely from a nerve that is either irritated or pinched. With MPS, I have a lot of tenderness and tightness in my shoulders, neck, upper back mostly, and it goes into the base of my skull/back of head. At its worst, the pains would radiate up through the side of my head and could trigger a migraine. It was daily and hard to get through the day, and I would just have to rest every evening. Luckily I am noticing some improvement now that I'm doing some trigger point therapy! Definitely read about it to see if it sounds like a possibility. Maybe it is, or maybe something similar. You mentioned some kind of snapping feeling.. does your neck also pop or crackle often? My neck constantly makes sounds and I feel little pops. When the muscles are contracted so much and spasm, it can create joint stiffness and discomfort.

 
Old 11-05-2011, 10:28 AM   #7
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

river, relax on the annie hon, i only mentioned this becasue you did, so i just wanted you to have THAT info too, along with everything else you asked about. i am in NO WAY saying this is what you have(i am NOT at all a doctor or 'diagnosing" you either, that needs to be done by the "right qualified" people and appropriate scans). anything IS just a 'possible' here when talking esp sudden onset headpain, thats all, K?

exactly how did this all 'present' to you six weeks ago?

as i mentioned above, this is more than likely the more common types of problems either within that c spine or as you mentioned, possible tension headaches. the real key here is going thru those deeper scans, esp on that upper c spine just to 'see' what may or may not be there as a contributor. you just ARE simply in the 'diagnostic phase" here so everything and anything needs testing and ruling out that just could generate your particular symptoms. that is how any doc actually arrives at any real diagnosis for their patients. looking at symptoms, sending for the most 'appropriate" types of testing FOR those symptoms and seeing what, if anything just may pop up on certain tests.

since they did a plain CT and did not see any actual 'bleeds' going on(new or even old ones that also would show well on plain CT), they are 'assuming" there is nothing up there(and there may be not). but, not using a contrast medium really does NOT look at the fuller larger arterial structures as well as with that contrast(among ALOT of other parts of the brain, they also cannot usually see ANY real potential bulges in arterial walls either since this ONLY uses what an x ray uses to gain pictures, radiation in 'slice' pics). while the arteries may have somewhat 'showen up' they just are not as clearly seen as with a contrasted MRI. all they were doing with that type of scan when they did it was 'only' really trying to rule out ANY either old bleeds or new ones, not alot else since this was merely a 'hunch' by an ER doc, since it really is not the ideal test to really 'see' all of the inner brain makeup and contrasted/highlighted vessels as an MRI with contrast would do. while a good CT really CAN see both old and new brain bleeds really well(they look for whats called 'hemosiderin staining' which is basically the iron deposit left behind from blood that for some reason just will NOT absorb back into only the "neural tissue" as it does in other areas of our body. like a bruise would. hemo S only shows up, as old or active 'bleeds' in the brain and the spinal cord in the form OF hemosiderin staining), but that is why CT is the 'go to' scan when any ER doc suspects this, its both fast and reliable FOR looking for bleeds. but a really good contrasted MRI done on BOTH that c spine and brain would give you and your docs a TON more potential info on the brain as a 'whole'. BUT river, keep in mind that actually having ANY form of vascular malformation such as aneurysm in your brain generating what you have going on is ONLY a VERY SMALL chance possible". the likelyhood of many other things actually more in your c spine is wayyy much higher.

i really do think considering your symptoms and already having another neurological type of condition too(which may or may not matter, but anything IS always possible when it comes to the human body and along with 'inherited/autosomal or recessive types of conditions too, of which i and my son have as well) that your c spine may hold the real true answers to your problem with the headpain. it is all in how you describe this and that area way down at the back of the head, which is where i TOO get some really nasty headpain from a bad C 2-3 area way up in my own c spine, amongst the other crap there. i have to actually use fioricet to help with those nasty suckers despite the LA narcotics and valium, among other meds i am also on for other muscle and pain crap. these particular headaches are very distictive in only my R side, but depending upon like soo many different 'possibles' one can simply have going on in their own spinal, from column to cord, your 'issue(s) could be simply more "centrally located", therefore just capable of setting off both sides with some level of ongoing inflammation to the nerves up there. it all really depends upon what just may be there and more important, where it is located within the spinal, meaning just what is 'it' impacting directly and indirectly. but ANY real levels of ongoing inflammation also would really set off those muscles up there too(kind of the old domino effect). this just occurs when our c spines have anything impacting nerves. as i mentioned before, there just ends up with this pretty constant 'firing" TO fascia/muscle from the inflammed source over and over again.

i did read up on your condition which was a bit confusing as to what can be impacted and that it also stated there can be 'varient' forms of this too. while it DOES mention that the peroneal nerves(the fibulas) are most involved, it also states that the muscle atrophy is from the 'neural nerves'. so i am wondering if that actual damage/loss stems AT where the "neural tissue"(cord/brain) is or further down the nerves(we ALL start out in utero in what is called the 'neural tube" and grow "out' from that base which then becomes our CNS or cord and brain)? from that i was reading it(the CMT) just sounded kind of contradictory in parts or really 'not right' in some ways? just what specifically IS impacted in YOU from this right now? but the thing with these types of conditions, who knows what took place way down to that chromosome level while you were forming. i only say this becasue i KNOW that it just IS possible for any inherited/autosomal dominant or recessive type of conditon to actually sometimes mutate itself into something different than it 'should" be? while your condition may NOT have anything at all to do with the other symptoms, it also just 'could be' at least playing some part in particular ways as well, depending. its just only a 'possible" here along with others. if you have never ever had your c spine down to that cord scanned, it just now NEEDS to be.

we had mutation occur with what i did not even know I had been born with as "autosomal dominant polycystic disease" that i passed on totally not knowing i had this to my youngest son. he unfortuently ended up with some totally insane and mutated form of this disease that caused his liver to start generating little fibers and not ANY of the actual charachteristic cysts, that eventually at age 12, placed him into liver failure. and we had had NO CLUE that he was even sick TIL age 12 either since children really can compensate sooo well with medical crap. this is also when we were told that either myself or my hubby had actually given him the initial catalyst of ADPKD. neither one of us thought it was 'me'. but after one ultrsound was done(all of us had this including our oldest son too) that showed MY major major devistation/destruction going on in both my liver and kidneys all these years by MAJORLY huge polyglobs of cysts, BUT still having perfect labs, we found out it ran on my moms side(my mom had no clue this was there either). i was already about 40 yrs old when i even found out i had had this my whole life, and so did my sister(she had no clue either), and in the same organs too(normal areas are usually 'just' kidneys so 'ours' mutated somewhat too). but what my son ended up with was sooo incredibly insane and sick, and a total mutation of the condition he inherited. thankfully he DID get his miracle of transplant and is alive today(Tx was in 2000) ONLY because of the kindness and giving of a family who just lost their child. very crazy and gutwreching experience. so trust me river, there just sometimes CAN be some forms/variants(and yours also DOES state the variants just ARE also possible too on top of what can occur natuarally at the DNA/chromosome levels) that can happen within any disease and this one actually states it as well. or there can be mutated versions too that as this goes thru the 'generations' of chromosomes, can also have even environmental factors change or affect it. i just wanted to throw that out there simply knowing how certain 'condition types" can be too.

if your primary is simply NOT doing just what ARE HIS actual 'jobs' for you as their patient, you DO have the option of firing them and finding another one who actually cares about their patients(finding out how others you know primarys just are with your friends or family really IS one of the very best ways of finding a 'good one' to start going to). it all depends upon how YOU feel this doc is actually 'doing' for you here overall, esp when trying to diagnose anything in their patients. if he IS referring you to others, thats a good thing. some docs, despite not having a flippin clue as to what is really the underlying problem in their own patients, have some sort of complex that wont allow them to simply send them off to the 'appropriate' types of specialists, or even do the best and appropriate types of needed testing to even FIND a potential reason/Dx for their patients. that type of primary no one wants to have. thankfully i have had an amazing one considering all my many ongoing referrals, tests needed and the sick surgeries i have had to have. i will hunt him down at home if he should up and retire on me, lol. i WOULD be sooo lost without him.

but DO really try and see about just getting that very basic contrasted brain and c spine MRI. that is just the best place to start given what your ongoing symptoms just are. this would just rule out alot and/or possibly rule that one thing IN as the potential culprit and generator. until you can simply get that done, you really cannot get anywhere here river, you just NEED some answers. it is just that 'starting point' for you right now. and by they way, do NOT allow any spinal taps at LEAST until that brain and c spine gets a good look over, and someone also explains an absolute "have to" NEED for one. i would not have allowed that either in THAT type of circumstance. it simply was and still IS WAY down on the list of what should be done FIRST. ya did the right thing there river. just start things going, and if you have to, keep pushing that doc til he simply DOES for you what he is supposed to do(that type of MRI WOULD pretty much be the 'standard protocal" given your ongoing symptomology). if he does not, then do try and find another much more hands on caring type primary who will work with you to actually get to the root of what your 'problem' actually is. good luck river, marcia
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3-22-01,herniated C-6-7
11-20-01,placement of hardware for failed fusion
9-22-03,removal of cavernous hemangioma that was inside spinal cord. Neuro damage to L hand L leg and R leg.

 
Old 11-05-2011, 04:06 PM   #8
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

@ Turrrra, I have never heard of MPS, but I was able to look it up and from what I was reading I would say I can relate to some of the symptoms. I can't of course be certain but I can only hope that its something simple. I still do have tenderness in my neck and shoulders and still have that dull ache pain on my left side that has never gone away. It stays there from the moment I get up to the moment I go back to sleep. Have you ever experience that? The feeling like something is there like say a ball of some sort of dull ache pain all day? My head feels so sore and tender I can't even touch my head oh I mean I can but it just feels like pressure.

I do have an appointment with a nuerologist on Nov 23 hopefully by then I won't feel it so much and hopefully I can just finally find out what is it and heal. How long did you feel your pain before finding out what you had?

 
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Old 11-05-2011, 10:32 PM   #9
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

I'm glad that you have an appointment soon! A neurologist might not look into muscle issues, but you can certainly ask. My neurologist mainly helped with giving me medications, but I had to go to different doctors for more help. Yes, the feelings you described are similar to me. It is just there from waking up and lasts through the full day. With me, it would get worse as the day went on. Then every evening, I had to just lay down because I didn't feel well enough to do much else. The feelings have been there since earlier spring of this year. I just recently got a diagnosis and started treatment, but at least I notice some improvement! My doctor told me that it could possibly go away on its own, but for many people, it takes time getting treatment to make it go away. Keep us updated of how your appointment goes!

 
Old 11-06-2011, 03:22 PM   #10
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

Gosh I truly feel for you and pray that your agony and worry will soon be relieved. I am surprised that the doctors have not been able to help. I know it is hard but try to relax, meditate. Have you ever tried fasting for a short while? Once you take the pressure off digesting food, the body is freed to concentrate energy on healing.
I hope you will be better soon, sorry that i cannot think what could be the cause except a lot of stress has built up in you.

 
Old 11-07-2011, 09:17 AM   #11
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Thank you Miss Milly, for your response I did not know about that digesting and healing part I should try that this week. Your prayer will be helpful sometimes that might be the best healing ever God hears are prayers may he hear yours for me. Thank you.


@ Turrra Really a neurologist wouldn't help much? I figured they would do a contrast MRI and that would help to see what it could be. Would a regular doctor be able to help me out, too? Especially with my back and neck?

Last night I had for some weird reason felt lightheaded so I took 1000mg of Tylenol and it didn't do much. Today I don't have a headache not a severe one just a slight light one for now but I still feel pain. I had another lady tell me that it could be a brain aneurysm and it only scares me more and stresses me out.

How may days, weeks, or months did you wait until you saw your doctor? I feel like I'm waiting way to long and I feel Nov 23 is even longer. This week will be 7 weeks but I just want it to go away and feel free from pain and to control it if its something simple or at least I hope its something simple.


Well, this all started during the evening I was doing fine, I just went to the movies and just sitting there I suddenly got a dull pain on my left side that just shot me. I tried to move my head but I got so nauseous and scared but it was just a sharp dull pain. And since that day it never went away.

How did you find out that you had an aneurysm or annie as you say? Especially since you didn't feel anything. Did you have hypertension or something? How did they treat you and cure you?

If I go to the neurologist should I mention doing a C spine test? What do they do? Do they just take a picture of my back or does it involve something else? I feel that this appointment is so far away.

With my disability I have CMT type 2 that is the one I believe that affects the inside of the nerve so I don't have it as bad as the people who have type 1. It can be tough to understand my doctor who I see every year for this is still trying to find new information about it and trying to help but its always the same information every year.

I'm so sorry to hear about your condition and the condition of your son as well. Sometimes I just don't understand what certain things happen to our bodies but I can only pray and hope that everything will be alright for you and your family. I will keep them in my prayers.

River

Last edited by Mod-S4; 11-13-2011 at 08:50 PM.

 
Old 11-07-2011, 08:36 PM   #12
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

I'm sorry, my response was a little confusing! I think the neurologist is still a good idea and a good place to start. I went to one first and they helped me out with medication and ruling out anything life threatening. They can get you the MRI to make sure everything looks okay. I talked to my general doctor about the neck and back of head discomfort and she recommended a physical therapist. I am sure that a neurologist or general doctor can refer you to a different kind of specialist if they think it's needed. Most of all, I think the MRI will be good so you don't have to worry!

I don't know why but I waited about 3 months before seeing a doctor about the discomfort and pain. I guess I kept hoping it would go away on its own! I did see the neurologist before this, but it was for my migraines and I didn't have any of the neck or back of head symptoms at that time. Honestly, I felt like if it was something extremely serious, I would have been getting much worse very quickly. From what I hear, a regular aneurysm (not ruptured) often goes unnoticed. Some people find them in their MRI and the doctors just closely monitor them with regular scans if the person hasn't had any trouble. I doubt that this would be the case for you based on your symptoms. That also wouldn't really have the neck area involved.

I would check every now and then to see if they might have a cancellation so you can get in earlier. That way you don't have that anxiety from waiting! I also find that when I am very concerned about something and tell them, they can sometimes move up your appointment.

 
Old 11-08-2011, 04:32 PM   #13
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

It's ok we all tend to get confused. I should of started with a nuerologist first instead of the emergency room, no one there could help me nor my own primary doctor. I'm not sure if the nuerologist can help me with my neck and back pain but it wouldn't hurt to mention it. I'm going to mention doing all sorts of MRI's and contrasts just to be safe.

Wow! 3 months, brave of you to wait that long, but your probably not like me... worrying everyday about it, but I was somewhat the same. I just keep hoping its nothing bad and that it would eventually go away. I just don't want to wait 3 months but waiting for 2 weeks feels like its going to be 3 months. I hear that some people don't even have any symptoms when its not ruptured but how do they know they have one? I honesty want to say I don't have the textbook symptoms of an anyursem or at least
that I know of.

Have you ever noticed any changes with your eyes? I sometimes get a burning feeling like I've been wearing my contacts for 24 hours without using eye drops. But I will for sure call tomorrow to see if they by any chance have anything ahead of time hopefully they do.

 
Old 11-08-2011, 05:15 PM   #14
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Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

It doesn't hurt to ask! Oh yeah ER's are not always helpful. I have heard that some people have gotten some good help from the ER on this board, but I've heard other stories where if the person is not dying, you have to wait hours and they dismiss you so quickly. Your neurologist can order an MRI with and without contrast of your brain. Although I only got x-rays of my jaw and neck, of course getting an MRI is another option for you. If your insurance covers them, I would get whichever scans they offer just to ease your mind! They were going to be very expensive for me even with my insurance.

I think I do worry less than the average person about my own health, but I've been a bit more of a worrier lately. I don't worry that I'm in danger, but I worry that I'll be in pain for a long time and that it will affect my quality of life. I try to do things I enjoy to keep myself distracted Many people find out about a non-ruptured aneurysm from getting an MRI for something else. I've heard this about a few different things that can be going on in the head!

Yes, I do get symptoms in my eyes. My doctor told me that eye burning or dryness can be related to neck issues because of the nerves that are involved. Same with ears, sinuses, and the jaw. I've noticed that sometimes my eyes feel a bit shaky, like they are shifting back and forth, but not sure if that can be related!

Good luck with the appointment. Hope an earlier one comes up for you if none are available now, ask if they can keep you in mind if one gets canceled anytime after, since you are feeling very anxious.

 
Old 11-09-2011, 09:38 AM   #15
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riverphx2 HB User
Re: Tension or Cluster headache? Or brain aneurysm? Please help?!?

That's my case at the hospital I'm the one that does not have a life threatening issue (Thank God) so I wait and get discharged fast. So I say in my case they're not so helpful if your not having a serious issue.

Yeah, I just want to do what is best, whatever needs to be done to find out the issue. I'm getting more headaches now than often but its funny cause I have three wisdom teeth that need to come out. One is impacted on top of a nerve but its not on the side that is near the head pain. But thats something different.

Oh, that's me I always think of something is wrong its very wrong like I think I might die or it could be something very bad like cancer or something. I'm a huge hypochondriac It wasn't so bad as it is now but I sure hate it. I can keep myself distracted for a while but I end up thinking about it the next minute.

Yeah, I kept thinking the same about the eye issue, its right in the back so maybe whatever is causing the issue is just making my eyes feel dry and burning at times. But I need had the shaky eyes but I should explain that to the doctor as well.

I will for sure keep you updated once I get my appointment, having been able to get anything sooner but will keep trying.

 
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