Hi Does anyone experience upper right/ middle intermittent throb 24 hours after having a drink. Just a pint of cider or two glasses of wine can do it. Normal lft and low ggt, fatty liver diagnosed couple of years ago, only had odd drink since thanks
View 2 RepliesI have been diagnosed recently with this as an adult. I am a little confused as my pain is in my upper abdomen, right in the middle, about 2 inches above my belly button and below the ribs. Anyone else get pain here?
View 1 RepliesI know this is a strange one, but my wife and I have both been wondering about it lately. I have been married to the same gal for 20 plus years. We have always had a great sex life with no real problems. Strangely for years, when I ejaculate, it sometimes shot out a little, maybe in inch away from the penis, then the rest of it, flowed out. Now strangely at age 50, when I have sex with my wife, I feel my testicles throb, and they get like super tight, or such, and my ejaculation is so powerful and intense it makes me holler. It doesn't hurt or anything, but my gosh it shoots. We always love the good ol 'doggie style' position, and the other day when I was about to lose it, I pulled out, and my god it shot like 4 large loads, clear up to the back of her neck and upper back. Then my penis twitches and stays kind of hard for a lot longer afterwards. This has never happened when I was even younger... is this normal as we age? Is it ok...
View 1 RepliesI've been experiencing an intermittent vibration from the region of my heart for the last 5 months. It can occur at anytime but usually when I am at rest or sleeping. I also get PACs and tachycardia in the afternoons which occurs whenever I am standing or walking (approximately 110 bpm). Sometimes the vibration is triggered by a PAC.
I have done the following tests
- 24 hour ecg (normal)
- Echocardiogram (normal)
- Blood test to check electrolytes and thyroid (normal)
I am 31 years old and Male. I am currently taking medication for hypertension but have been assured this is not a side effect of the med.
I was wondering if anyone has experienced any kind of pain like this:
For the past couple years or so I have had this intermittent type of pain (it usually happens about a couple times a week, for instance it happened in the beginning of the week for at least two consecutive days and not at all today; each episode usually consists of a series of acute attacks, maybe several of them in a row, and then they would just stop). This would happen in several areas: mainly now my thighs and legs (almost always the back of them, though a couple times it has been along the front); sometimes it is in the arms too; for a little while it was in the back (though it hasn't happened there for a while now).
I'm not sure how to describe the pain (I wish there was some sort of questionnaire I could find that might help me in that area); it's definitely not severe, but then I'm known to have a high tolerance for pain. I would say it is more sharp than dull and it seems to be a kind of stabbing pain though maybe not exactly shooting, though I guess it could be thought of that way (I don't know that it's radiating either--I can't see how it can be radiating anywhere; it seems, if I am remembering correctly, it is moving along the length of some specific area; that doesn't seem like it would fit the description of radiating). It is definitely not tingling or numbness (except when it happens in the arms--then there is a definite weakness that results after it in which I have less of an ability to grasp anything with much strength).
I'm just curious as to what can be causing this, or maybe it's just normal when you age, though I wouldn't consider myself to be too old at just 33.
Well, if anyone has any ideas I would appreciate hearing them. I would say for sure the pain in the arms sounds like some sort of nerve pain but I'm not sure about the other areas. I went to the doctor once about it, but he wasn't able to help much, just called it "fibromyalgia" which is basically what they say when they don't know what it is. For a while I was sure it was nerve pain but then I keep hearing how nerve pain is more of a tingling, numbness or loss of sensation more than actual pain; and then the doctor calls it fibromyalgia which from what I gather is thought to be muscle pain. I do not participate in any rigorous exercises, just walks for a mile or more a few times a week so it shouldn't be due to any sort of injury.
Is it just me or does anyone else experience an intermittent clunky sensation from their new hip one walking? I'm 5 weeks in with a ceramic on ceramic. No other problems and if this how it's going to be I can live with it. I have read that some people with ceramic hips experience clicking. . Just wondered if I describe clicking as clunking!
View 27 RepliesI'm going to start off by saying my condition/illness or whatever it may be is a medical mystery to six doctors (physicians, neurologists, psychiatrists) and that I am unemployed and rejecting job offers because my condition limits my abilities and brain function. It is a roadblock in my life and I can't seem to drive around it. I am a healthy and fit 24 y/o male who has been suffering from transient, hard to describe disorientating episodes/spells that I first had the pleasure of experiencing at 18. Since then, the episodes have occurred almost daily but do not last all day long - they are TRIGGERED by certain situations and environments. I can feel the spells gradually, but pretty quickly coming on (they don't occur at the drop of a hat) and I actually have the ability to stop them by laying down in a dark room and literally putting a pillow over my face and just "shutting down" for a couple minutes. Weird, I know. The "spells" last anywhere from 10 minutes to multiple hours, depending on if I get to a dark room with a pillow. I've tried multiple migraine medications and none have even remotely helped.
Triggers:
-Focusing on something for more than a few minutes - even talking to a person! I can't even talk to a freaking family member face-to-face without falling into one of these spells. One minute I'm fine and then there's a total disconnect between what I'm seeing and my cognitive function. Depth perception also throws me off here.
-Similar to focusing...when I'm talking for an extended period of time. It feels like my brain is totally deprived of oxygen and I then fall into one of these disorienting episodes
-Light contrast situations, especially when I'm in a well-lit room when it's dark outside. It's like my brain doesn't "agree" with what i'm seeing and the light situation
Symptoms:
In addition to feeling extremely disoriented, the other symptoms include a general feeling of disconnectedness, brain fog, a headache of pinpoint pain in the back right of my head that occurs during most of the episodes, a massive drop in mood and overall emotion (apathy I guess you could say), a minor lack of memory of anything that occurred during one of these episodes (for example if I read 5-10 pages during one of the spells I wouldn't remember specific details of the read but would remember the general theme and whatnot), and extreme cognition trouble (speaking, writing and even focusing on a person and their eyes). One minute I'm thinking and speaking clearly and the next minute one of these episodes can surface and I start to totally jumble my thoughts, words and sentences and I sound like a complete idiot. At this point in the dizzy spell, I want to just lay in bed and cover a pillow over my face in the dark. When I do that, it's literally like hitting the reset button and the symptoms decrease significantly.
I have had an EEG and and a brain MRI - both normal.
These episodes or spells or whatever they are are affecting my quality of life. I used to be a very happy, energetic and social person and now this issue is somewhat holding me back, though I do go up against it daily in hopes that I can increase my tolerance of the spells, which I can't.
Since I posted a thread about self-catheterization -- more formally called Clean Intermittent Catheterization (CIC) -- there have been a few different discussions on the topic in various threads. I thought it might make sense to bring those discussions over to a dedicated thread. With that in mind, I will summarize and/or copy and paste some of what was said before into this thread for better continuity.
My story in a nutshell. 68 years old with BPH probably since my late 20’s. Watch and Wait strategy with on-and-off trials of Tamsulosin (Flomax) with poor results. Symptoms were the normal retention issues resulting in frequent urination with incomplete emptying, urgency, and having to go to the bathroom at night in increasing frequencies. Near the end, two or three uti’s per year often accompanied by gross hematuria (bleeding).
Two years ago things got significantly worse and I couldn’t urinate on my own without physically pushing against my bladder (Crede Maneuver). That led to another trip to the urologist where ultrasound showed significant retention and hydronephrosis (water in the kidneys). I was told I needed an operation (this facility primarily did Turps) but first I had to rehabilitate my bladder because at the time it was too flaccid (stretched) for a good surgical outcome. I was given the choice of wearing a Foley Catheter for six weeks, or a program of self-catheterization (CIC) in order to decompress the bladder. I chose CIC so I didn’t have to wear a Foley 24/7, and also because I felt it put me more in control.
Six weeks later my bladder was rehabilitated to the extent they could do a Turp, and the hydronephrosis was gone. After doing some research and a lot of thinking I decided to put off the Turp due to the potential of irreversible side effects, primarily retrograde ejaculation. Two years later, I am still doing CIC while waiting for newer procedures with better outcomes and fewer side effects.
I will detail my experiences with CIC in following posts -- but to summarize, once mastered, it’s a painless five minute procedure that allows you to empty your bladder completely any time you want. With CIC, I therefore have no retention issues, no urgency, and in most cases sleep 6-8 hours through the night without having to get up and go to the bathroom. No UTI’s in over 18 months. And because my bladder has been partially rehabilitated, I can urinate normally about 50% of the time without using the Crede maneuver. My IPSS Score (International Prostate Symptom Score) would be Zero (the best), albeit with a little mechanical assist.
As of now, nothing that I have read about the various current procedures has tempted me to have an operation. That could, or could not change, in the future, but the nice thing about CIC is that you can stop it any time you want with no repercussions. The caveat is that CIC should be done under the supervision of a doctor who will monitor your BPH as required. Similar to seeing a doctor on a regular basis during a Watch n’ Wait BPH strategy.
I know many of you here have already had operations like Turp, and in most cases people seem pleased with the outcomes. CIC certainly isn’t’ for everyone, and I can understand why someone does not want to carry around a urinary “tool box” with them. On the other hand, with practice, it’s not the traumatic and scary procedure some think. I can honestly say right now that for me it’s about as traumatic as brushing my teeth.
I’m offering my experiences and thoughts on CIC for any of those who haven’t yet made up their mind on an operation. It even can make sense for those of you who don’t need an operation yet, but want to increase their IPSS quality of life score. In fact, wish I had done CIC earlier while on Watchful Waiting. Didn’t realize how much BPH had been affecting me for most of my adult life until I was able to empty my bladder completely.
CIC doesn’t have to be a permanent solution, it could just part of a waiting strategy like I’m on, until better surgical operations are developed with better outcomes and fewer permanent side effects.
For any number of reasons, the majority of urologists don’t seem to offer CIC as an alternative to surgery. My current urologist doesn’t as far as I know, but he’s OK with what I’m doing because it works for me. So, either you have to find a urologist you can convince to go along, or go to some of the major teaching hospitals where CIC is probably more in use and better understood. That is where I was taught, albeit not very well, but that is another story.
I've been avoiding going to the Dr's for a while now, as I'm very scared.
Every few months, I have a day or so where I urinate blood. Also some blood clots. No real pain.
Then it will seemingly disappears for a few months, and will then return for a day or so.
I'm assuming it's something terrible.
Other symptoms seem to be frequent/weak urination.
Sometimes a mild/dull pain in one of my testicles.
Has anyone experienced this? WHy would it be every few months like this?
I plan to call my GP tomorrow as it happened again a minute ago for the first time in a few months and i'm plucking up the courage.
I'm petrified of the cystoscopy. (pain and embarrassment)
I had my urine tested for an unrelated issue a while ago, and it was apparently 'clean' (even though this was only a day after i'd been urinating what looked like almost pure blood)
How can this be?
I was hoping for some advice on a problem that I've had for 3 years. My main problem has been on and off vertigo and imbalance, however I don't think I have rotational vertigo because most of the time I just feel like inside my head is spinning? It also feels as if the ground is sinking beneath me.
Dizziness started 3 years ago, about 2 months after a serious bout of the flu which took months to recover from. At the time my ears were extremely blocked and I would do the Valsalva maneuver to help unclog my ears. It wasn't until now that I discovered you aren't supposed to do that? Anyway my dizziness was consistent 24/7 for nearly 1 year, at which time my symptoms seemed to disappear. As of April this year my symptoms returned.
Over the years I have been to numerous GP's, ENT's, neurologist, and all of which were unsure of what was going on. Most of them have said they don't believe it's Meniere's disease. My main GP said I DIDN'T have fluid in my middle ears, however since then 2 GP's have both confirmed that I DO.
Current symptoms:
Brain fog
Dizziness/vertigo
My ears feel wet in the morning. Not enough to wet pillow
Tinnitus in both ears, slightly more prominent on the left side
Fatigue
Difficulty concentrating/problems with memory
Tingling/electric shock feeling on left side of scalp behind left ear
Anxiety
GERD and gastritis
A couple of things seem to exacerbate these symptoms, such as anxiety, hot and humid weather, having a hot shower (I now have to have cold showers, before I would have to sit down), menstrual cycle.
So I am pretty convinced that I either have a perilymph fistula or middle ear fluid. I have been using Nasonex for a couple of months which seemed to improve symptoms but now I am starting to feel worse again. My now current GP has suggested Ventilation tubes/grommets, however if I actually have a perilymph fistula will this improve symptoms or not have any benefit at all? I also have been prescribed SERC but I do not think it will help, as 2 years ago I took it and it made my symptoms WORSE.
I am wondering if I may have damaged my ears years ago when I had the flu by constantly trying to pop my ears. I have been allergy tested for Molds, grass, pet dander and dust mites, all negative. I have also been tested for MS which was negative, and all the routine blood tests etc. MRI showed I have a mid-septal deviation (my nose isn't straight) and previously enlarged adenoids, but apparently was of no clinical significance.
I don't have any problem falling asleep, the longest it takes if 20 minutes sometimes. But I ONLY sleep for 5 hours, maybe 6 if I'm lucky. So I try to make myself stay up until 11pm so I can get up at my normal time of 5am. This is very hard because I will usually fall asleep in front of the tv around 9/930.I get up from the couch around 1030/11 and go to my bed, but then wake up at 3 am like clockwork. Last night I fell asleep in front of the tv at 930, got into my bed at 1030, but then woke up at 230! I usually can't fall back asleep either, or maybe dose in and out if I'm lucky. My mind is already awake then.I tried Melatonin years ago, and it worked for the first couple of days to a week. But then I built up a resistance to it and I had to keep increasing the dosage until it didn't help at all anymore.I have gone through different prescribed meds that didn't really work. The one that worked the best(Trazodone) had a side effect that I didn't like(woke up with an extremely dry mouth), and I built up a resistance to that too. I just wanted to see if there were any other meds out there, OTC or prescription, that may work?
View 1 RepliesI have been taking this drug for over 6 months now. 40mg twice a day The cluster headaches that have plagued my life are now down to a bare minimum.....(not totally gone away) and manageable.
HOWEVER! I have gained about 1.5 stone in weight, particularly around my middle. This is highly unusual for me.
My GP states this is NOT a recognised side effect and I simply must be eating more due to feeling better! As my eating habits have not changed at all, I find this very hard to accept. If I am to take this drug for the rest of my days, At this rate I will be enormous! this is only a temporary side effect?
I recently had blood tests done Which show high cholesterol. However I have been experiencing intermittent chest pains and aching in arms and legs. I also feel like I have to take a big breath every now and then as my breathing has been quite short recently. I get extremely exhausted after minor exercise or simply walking to the shop. I have also felt my body heating up very rapidly like I was sitting next to a fire then return to normal after a few minutes.
View 1 RepliesI am a female that is 23 and I am quite overweight (BMI around 47). I would like to know if I am experiencing angina or if it could be something else. My stomach doctor has ruled out a hiatal hernia. I've also had EKGs and two heart ultrasounds and they were all fine.
So the symptom I'm having is just sharp pain in the middle of my chest. It comes and goes, but is frequent. I've been having this since I woke up about 11am and it is 4:30p now. I've not felt right all day. I've been to sleep twice since I woke up and still it is happening. I've been having a little trouble breathing as well. My forehead felt weird this morning too. I couldn't describe how it felt to my mother.
There is a clinic nearby and I don't know whether I should go to it. Every time they do a test on me for anything, it is always negative. I just don't want to make them waste their time or make myself look like a fool/hypochondriac.
I've tried about 3 other boards and seems like 100's of site but I cannot find anyone with similar symptoms to what I have. On feb 14, I got a huge euphoric feeling in my head, followed by rapid heart rate, tingling in my fingers and toes, and a feeling that I was going to have a mental breakdown. I went to the ER and got blood pressure/blood sugar/EKG test and a physical test and they determined I was fine and gave me Ativan to take. The next day I started feeling pains in my head that would last for 2-5 seconds and then go away, come back in a different spot later. They hit me anywhere from in my brain, in my sinus (although no sinus pain since Monday), different parts of my skull and on the sides of my head. Most of the pains are on the skull (bone). I mentioned to my doc and he switched me to clonazepam and told me to come back in two weeks to see if I need an MRI.
That appt is next Wednesday and as it has been 3 weeks of the pain not getting better or worse I'm almost positive I'll still have it by then. On a side note, in the past my headaches were in my brain and would be a constant pain for a few hours, and would only come ones a month or so. These pains are not nearly as painful and do not last for more than 20 seconds, but they happen at all times of the day (although in he morning I can lay in bed for a half hour and have no pain, then they come shortly after i get up. I've looked at brain tumour symptoms and I don't really have any of them, the pain is light, my cognitive skills are the same, no nausea, dizziness, etc. The only thing I have is chronic anxiety because of the pains and the fact that they could be something serious. So basically, should I try to get an MRI before meeting my family doc next week? I live in Canada so everything is covered.
Had this condition for about 1 year blood tests do not show any problem so why is this happening?
View 6 RepliesI am a 49 year old woman and I have a 8mm noncalcified nodule in the middle lobe of my right lung. For some reason, it does NOT show up on an X-ray but it was found on a CT. Shouldn't it show on an x-ray also?? The ER found it by accident...they thought I had a blood clot that had travelled to my lung...nope! It's a nodule. It was found 51 weeks ago and I did have another scan 2 months after it was found and there was no change in the size. But, since I don't have health insurance, I have been unable to have another CT scan as recommended (every 3 months). My husband makes too much money for us to qualify for any financial assistance but we can't afford a pulmonologist or scan. I have been a smoker for 30 years and I do get backaches and I can't do much without getting short of breath but that doesn't mean it's cancer. My main question is why is it not showing on an X-ray...I've had 2 since they found it on a CT scan so unless it mysteriously disappeared, I don't understand. I have been checked for histoplasmosis and other things like that and they were all negative. Can anyone tell me why it's not apparent on a chest x-ray???? Thanks!!
View 1 RepliesFor about 6 weeks I've had stomach irritation, intermittent pain in left and right side with tenderness under the ribs, headaches, lower and upper abdomen pain, bloating, belching, an intermittent sharp pain like an electric shock at the top and just to the right of my abdomen, and most recently floating stools.
To be honest the pain isn't unbearable, just irritating, very uncomfortable and persistent which is getting me down. I wake every day with the same series of pains and bothersome bloating and burning. I've been on omeprazole for about four weeks which doesn't seem to have sorted it.
one week ago injured my middle finger and recieved a cut on top of my knuckle. seemed to be healing ok then out of no where yesterday it sweeled up. very painfull if moved or if i reach in my pocket. no oosing any fluid please help!
View 1 RepliesAbout 6 weeks ago I began to experience some ear problems. It started with muffled hearing, tinnitus, and mild pain. I went to primary care provider and she prescribed amoxicillin three times a day for the middle ear infection. A couple of days later my symptoms got a lot worse. I lost most of the hearing in my right ear and I had severe jolting pain that radiated to my whole head and eyes. I went to the ER and was given a shot of penicillin and was also diagnosed with strep throat. I was referred to ENT because my eardrum had actually burst. The ENT doc prescribed ear drops and a higher dose of amoxicillin with clavu k. Another week passed and the symptoms continued to get worse. I followed up with ENT last week and he said my right ear looked really bad inside and I am probably going to need surgery to fix it. He also said to stop taking my antibiotics and ear drops.
Okay, this is why I think I may have Lyme. Throughout all of this I was experiencing flu and other symptoms that I didn't pay much attention to because I was focused on the ear infection. In the beginning I felt unusual muscle twitching in my limbs with achy pain. I just dismissed it as normal body functions. Fast forward to this week, the muscle twitching is now more severe and present all over my body (almost every voluntary muscle). There is some accompanying pain/soreness from the constant twitching. I am also having heart palpitations, anxiety, depression (a first for me), joint pain, dizziness, painful headache, and brain fog/"out of it" feeling. I am also unusually sensitive to cold and some of my muscles feel "electric." I went to the ER yesterday and they did some bloodwork, an EKG, and a chest x-ray but everything was normal. The EKG showed a left axis deviation in my heart but the doc said it was nothing because I am a little stocky.
I don't know what to do. I am getting worse everyday, especially after stopping the antibiotics. My doctors appear to think that my symptoms are psychosomatic even though my anxiety has been under control for weeks. The only thing they're sure I have is an ear infection, but even that isn't responding to antibiotics.
I have pets and they play in a backyard that is filled with squirrels, rats, opossums, and birds. I sleep with one of my dogs and I have found a few ticks in my bed before. I didn't think they bit humans but about 2 months ago I did develop a weird rash on my upper buttox that became a huge cyst (I sleep belly-down). It lasted a few weeks but it completely disappeared a couple of weeks ago. I just thought it was a big zit and didn't think much of it. Maybe this could have been a bite?
Sorry, about the long read. I am a recently discharged disabled veteran and I receive healthcare through the VA. Appointments are always weeks away due to huge backlogs, which makes it even more frustrating. The appointments are also always rushed and my doctors are quick to make the "anxiety" diagnosis if they don't find anything obvious.
I am not looking for a diagnosis. I am mainly seeking advice on what I should do and if my symptoms may sound like Lyme. I would also like to ask how I can approach my doctor with the possibility of Lyme Disease without being dismissed right away. I am really starting to get scared because I have been getting progressively worse over a period of almost 2 months.
I am possibly thinking of paying for a private home detox. They have suggested it will be using valium as opposed to Librium. I was just wondering if anyone else on here had been through one?
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