Ever Since My Spontaneous Pneumothorax, Difficulty Exercising
Apr 2, 2014
Ever since my spontaneous pneumothorax I have had a lot of trouble with exercising. All the doctors have given me a clean bill of health and yet I can't run a 1/4 mile without being completely out of breath. Has anyone else experienced this? I need help because I am trying to be a peace officer and it is what I have been working toward for years. I have to be able to run for this job and right now I can't.
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I am a woman of 42 very energetic but one morning I woke up with the most severe pain in my right shoulder and pain down my arm I started crying because I was scared my husband told me to get an ambulance but I said I would be ok, I got dressed for work I dropped the twins off at school then went to work, I walked down to the hospital that is where I work and my boss took one look at me and told me to get to a&e, I went for the x ray then was taken straight to HDU and they told me my lung had collapsed and they needed to put a tube in god I have never felt pain like it, I cried and screamed all the way through, after that I was put on the ward and 6 days later it had not healed up there was a hole in it so they had to transfer me to leeds where I could have the operation done, I had a tiny bit of my lung removed and it was stuck on to my chest wall with irritant powder it helps the lung stick better, when I came to after the operation I was in so much pain and the tablets were not helping they were trying all sorts to get it right, I have been home nearly two weeks and the pain is still there but not has bad its more my ribs and across my stomach and that is what is worrying me and the chance that I might have to have it done again and also there is a 40% chance it can happen to my left lung, I am so scared to do anything in case it happens again, but I am glad I had it done, but it goes to show it can happen to anyone.
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tuberculosis..? difficulty swallowing , difficulty breathing, cough out blood, dark-brown phlegm, cough doesn't go and mucus, weight loss,tired always......
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Spontaneous splenic rupture in infectious mononucleosis. How will his body fight the infection without his spleen.
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Back in April 2014 I had an operation on my lung to fix it to my chest wall. (Pleurodesis) (VATS).
I used to smoke about 6/7 a day for 3 years before that.
I'm 20 years old now and it's been 16 months since I had the operation.
Basically I miss being able to smoke with friends at the pub or when I'm out etc.
Would it hurt me or would there be bad results if I were to smoke 1 or 2 a MONTH. Literally only 1 or 2. (I barely go out)
I don't want to hear the "Smoking is never good." blah blah blah. I just need to know whether 1 or 2 a month would have catastrophic issues on my lung.
It will be tobacco also (Roll ups) not cigarettes.
Dan
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I was wondering if anyone else's calf muscle tends to get a bit painful and tight after exercising, also think i over did things yesterday as my knee feels really swollen today
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Has anyone else had a blackout or faintness when exercising whilst having atrial fibrillation?
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I had all my lung drama in the 1980s, two collapses on each side, then followed by each a major lung op, one side using a blebectomy (I think it was called) which was a partial lobectomy that was then stapled back together. The other was a filler where they used some seal to fill the space between the lung and the pleura. So many years later, I survived without needing other operations but heres what happened to my lungs...!
Not sure exactly, but my chest cage, lung cage, shrank relatively suddenly - the doctor noticed the xrays looked as if they belonged to different people. Then I experienced permanent shortness of breath, I have now lived with this for six years. It was accompanied by permanent elevated adrenaline and heart pounding, none of which has been diagnosed by the doctor who always say 'everything is within normal range'. I exercise as much as I can to keep my breathing in as good a shape as possible but I feel like if they opened me up they would find an awful mess in their. I cycle a lot and swim as much as possible - I was always super active - but my breathing capacity in exercise is so much less than it was. I am 50 now and know that damage is also due to binge smoking throughout my life but I haven't smoked for a long time. I'd love to know if other people have had this or varied reactions from their lung op history and what they did about it, especially what their solutions have been. MY SOLUTIONS HAVE BEEN variously holding my breath under water for as long as possible to try and expand my lung capacity - not for the pre-op pneumo people!, Yoga, Stretching, breathing in a spine stretching folded position, meditation, cycle till you are out of breath, Buteko methods of CP and green juicing for best method of getting positive amount of super nutrients to the brain and blood stream oxygene. This might have helped someone, it helped me but it took me years to discover all the different methods I now incorporate. My condition puts me in a state of constant panic that I need to daily manage.
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I recently started exercising, elliptical, treadmill and weights. I have a lump/knot, its soft yet harder underneath. It is halfway between my calf and heel, good in size. It isn't painful, unless you are pressing in on it. I am not sure if I have just overdone it or if I have pulled a muscle or tendon. It isn't bruised or red, maybe a slight warm to touch at most. Any suggestions?
My family physician wasn't sure if it was a pulled something or maybe even a vein. I have googled and not really came up with much, I have ruled out trigger as it isn't actually up in the calf muscle itself and it isn't hard?
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I am a 27 years old male and have been suffering from some left chest pain for the past two weeks. The pain worsens when taking a deep breath, exercising, lying down, and even talking. Along with the the chest pain I get a sharp stabbing pain in my back when doing all the same activities. The weirdest thing is I have a hard lump on my chest that is painful to touch. It doesn't get better with ice or heat and pain medications don't seem to help either.
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my mom age 57 is facing a difficulty in breath taking. we shown her so many doctors (nuemeralogist,cardiologist,physician etc) but no body can understand why it happens. she is having BP also.
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I am 4 months into my third depression in 30 years and this time along with all the usual symptoms there is a really debilitating problem with doing anything. This is not just demotivation but it feels physical. I will try and explain each activity is made up of individual movements so making a cup of tea involves standing up, walking to the kitchen, picking up the kettle, walking to the tap, turning the tap on, etc, etc. Well, each time one movement ends I have great difficulty moving onto the next one. There appears to be a block which takes huge amounts of willpower to overcome only to be back there again after the next movement. Often I will get so far and then give up. It has got to the point when I can spend all day unable to motivate myself to do anything because things just seem so pointless and hard work. Going to work at the moment is impossible and I am off sick but I now worry about how on earth I am going to go back. I have just been forcing myself until a couple of weeks back when I just gave up and rang in sick. After the initial relief that I could rest, the guilt kicked in and what I'd hoped would be rest is now anxiety riddled. Does anyone have any idea what on earth this troublesome symptom is? It feels like there is lubrication missing in my brain as if it's seized up. It's really horrible.
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After taking citalopram 10mg for 4 weeks started little bit difficult to breathe for 5 days already and everytime i feel pain in heart area. Can it be allergy? i never felt like this before, today i have to rise to 20 mg and im panicking.
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I have to force much effort to speak sometime because extra spit in my mouth like allergy and my word are out of order and missing.
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I am desperate and scared. I've always been a "slow swallower" but a couple of weeks ago things got much worse. I suddenly had extreme difficulty swallowing water. I was drinking a glass full and it made me feel like gagging, I had to stop and spit it out, I could not swallow. Ever since then it is extremely hard to swallow water. Oranje juice is a little easier and solids generally are okay. It is the initiation of a swallow that is hard. The water is in my mouth and I don't just automatically swallow, I have to think about i, it takes about 15 seconds to get a mouthful down. And I feel so much like gagging every time I have water in my mouth. It is worse if someone is in the room with me.
Everything I read points to something bad - ALS, brain tumors, etc. I am crying and crying I am so scared. The doctor doesn't know and won't' rule anything out until I have the swallowing evaluation (barium) and the ENT visit.
Also scaring me into thinking it is ALS is that I have had problems with my voice for several months, hoarseness, can't project, people can't hear me, I always have to repeat myself, I stumble and slur over words..
I'm scared of the swallow test, I read you have to drink 3 ounces of water as fast as you can. It makes me cry to think about that, it will take me 10 minutes.
I am so scared, can anyone give me any reassuring words? Has anyone ever had something like this happen and it wasn't serious?
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All my life I have struggled with waking up in the morning. I am female, aged 71, and can remember this problem going right back to my childhood. I think I may have something called Delayed Sleep Phase Syndrome. It doesn't matter what time I go to bed, I find it almost impossible to fall asleep before about 1 am, but the problem in the morning is even worse. I don't think I've ever woken naturally and feeling awake and alert. I am drowsy and dopey and half asleep and if I don't have to get to a job or a meeting I can easily fall back asleep for another 2 hours. It takes three different alarms to wake me up, and most mornings I just feel sick and awful. Do other people have this problem and how do they cope?
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Recently when I find it difficult to begin certain letters, such as 'a', 'v', 'r' and 'd', when I am writing. I am studying Physics, and so write a lot of maths. I have never previously had any trouble writing letters, and consider myself to have neat handwriting. I have tried different pens, pencils e.t.c, and worry this might have some link with Parkinson’s disease, which runs in my Dad's side of the family. I am a male aged 18.
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I've been taking ramipril now for 9 years with no significant side effects, but lately I've developed a dry mouth and difficulty in swallowing. I've had various blood tests which have all been ok. Could Ramipril cause this condition after so many years ?
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My wife was prescribed 10 milligrams/day dose of ramipril and nearly passed out in town, palpitations, difficulty breathing and pain in the chest. She was admitted to hospital with a view that she might have had a heart attack. They put a camera up her femoral artery but her heart was clear, no problems.
her blood pressure was 90 over 45. we stopped her taking the Ramipril and all her symptoms disappeared. It was as if the tablets were producing the palpitations and the chest pains which she was taking more and more tablets for.
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Im a student à 21 years old. In two weeks, I will be on exams. It's a very stressful period for me. Its a period during which Ive some sleep issues. Ive some difficulties in order to fall asleep. And when I finally fell asleep, I wake up between two and three times a night.
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i am having difficulty in sleeping for several days already. the doctor prescribed me with seroxat 25mg, had taken only one but causes me jerky movements and confusions. i am afraid to take another. had slept for only 6 hours the most. the drug that helped me sleep were hydroxyzine and benadryl but no pharmacy sell these products in Ar-Ar city, KSA. it cause me anxiety. i can still focused on my job but the thought of not able to sleep results in sleepless nights.
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