COPD :: Stage 2 With 61 Percent Lung Function
Jul 12, 2014
I was told way back in August of 2013 I had copd. Smoked for 33 years. Started when I was 13. Did stop smoking in October. Now on 12 meds daily and get out of breath doing just about anything. I own a lawn mowing biz but getting harder and harder to do my job and getting ticked off clients because I cant keep up. Have been getting real depressed about everything. Someone told me to keep a daily blog about my life with copd. Started that about a month ago. Its somewhat therapeutic, it at least lets me get stuff off my chest so to speak. And maybe someone will read it and go hey i'm going through the same crap. In my case its hard to find folks going through it or those that do who even want to talk about it. So if your getting depressed i would recommend doing a blog. No one may ever read it, but you will be able to get out all the stuff you want to say. Thanks for listening and i hope you find what you're looking for.
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I went for a CAT scan for my heart and it was discovered that I have two nodules measuring 4mm in each lung. I haven't seen the doctor as yet. Has anyone experienced this and what was done for it? I am quite anxious.
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I 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!!
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My daughter recently had an encounter with unprotected sex with her boyfriend, he proceeded to tell her after sex that he had herpes and had only had it for 7 months with only 2 outbreaks, who knows if this is true or not. She broke up with him and I told her to go to the gynecologist and get screened for STDs. she has had no outbreaks and they have not had sex for 2 weeks. they said her pap smear was fine and they did blood work on her for hsv1 and hsv2. the MD called and said that her HSV1 was 67 percent and HSV 2 was 2.75. he said this was very low and that she has probably had it for a long time and did not contact it from this recent partner. I also read that combined testing of hsv1 and hsv2 can be false positives. she has had absolutely no symptoms at all. does this mean she has genital herpes or is there any other test that can be done to make sure she doesn't have it. she is 22 and having major panic and anxiety or this, it is breaking my heart.
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So ended up having to go to er last night and was told that I was half a cm and 50 percent effaced! Then doc said I was full cm today but was given a shot last night to stop contractions cause they were every 15 mins ! I'm almost 38 weeks and supposed to have c section the 22nd. Now on major bed rest why won't they just take her ?
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I was recently in a coma and was given a 15 percent chance to live just how serious is that.
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I have been diagnosed with Endometriosis in the lung. I was wondering if any one else out their had this condition? It's such a rare condition doctors don't know what to do...
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Is there a medication to remove the scar on my right lung?
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I had a Mri scan for back pain, result found 2 small nodules in lung. Seeing specialist in July, I get a little short of breath and a little wheezy at times nothing to alarm myself, but I have terrible fatigue also have red lumps on forehead chin and buttocks. Worried this could be sarcoidosis my father had this sadly died 26 years, I have read different views on this being hereditary, so worried seems ages till July I am female age 55 & a smoker, any thoughts ?
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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 have just been diagnosed with CKD stage 3 (GFR 48) and I can't understand why. I have low blood pressure and don't have diabetes. I am slim fit and healthy and age 52 so not that old. I also have a low white blood count. Can anyone shed some light? My GP does not seem worried, and so nor should I be, but I feel uncomfortable not knowing what has caused this.
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How can I improve my Stage 3 kidney disease, having a G.F.R. of 34?
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I'm 10 weeks pregnant with our first child and I think I've hit the emotional eat everything stage. I can't stop eating I'm like the hungry caterpillar or something, but my husband's in Arizona for work and I'm in Virginia and I just wanted to talk to him so I hop on FB and I see he shared a video about 40 minutes ago so I send him a simple hello message and no response. It just makes me feel like hey pregnant wife should be the first thing you talk to when you get off work considering I'm your wife and pregnant with our baby. I went from so mad that I wanted to punch something to crying am I wrong for feeling this way ?
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Hi! I'm going to preface this post with some background information: I'm 19 and I've been suffering with constipation for my entire life (my parents have videos of me straining to have a BM when I was still in pampers). It wasn't until last year that I was diagnosed with constipation by delayed colonic transit and put on Miralax to help move my BM's.
Unfortunately, because this diagnosis came so late, I've been straining to have BM's for the past 19 years, changes in lifestyle (diet, exercise, fiber supplement, etc.) all for naught. This straining led to hemorrhoids, which brings me to this forum. I've been dealing with hemorrhoids since elementary school, and when I have a flare up, I'm practically debilitated from the pain– my last flare-up kept me awake for 3 days straight and gave me multiple migraines. The flare-ups happen once every few months, but can last up to a week.
I wanted to know if anyone on here has had a hemorrhoidectomy, and what their experience with the procedure was like. I'm figuring that my hemorrhoids are AT LEAST a stage 3, and the surgery looks like the most permanent option. Also, if anyone has constipation by delayed colonic transit and as a result have developed hemorrhoids: how have you dealt with it? What has worked for you?
I see a lot of the post-op for a hemorrhoidectomy has to do with the intake of fiber, but too much fiber can actually make me MORE constipated. :(
Any thoughts, opinions, or personal experiences would be a LIFESAVER. Thanks for listening to my rambles!
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I am a 34 year old male who was diagnosed with hemochromatosis only after a liver biopsy because i only have one of the genetic markers. When diagnosed my ferritin was over 5000. Shortly after i was diagnosed with stage 4 cirrhosis of the liver. Is anyone out there in the same boat as me.
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I have recently been diagnosed with Parkinson's disease and am worried and confused. Are there exercises I should do? I am not on medicine but I understand that there are some that should be considered. Which ones are best for the early stage of the disease.
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I recovered from stg 3 Sarc (in lungs, lymph, joints, sinus) 13yrs ago, after 5yrs of illness and 2yrs of steroids.
I now have Erythema Nodosum (sp?) - red painful bumps on lower legs.
Research suggests that 'EN' is associated with a specific version of Sarc, Lofgren syndrome, which is usually resolves quickly and without treatment.
I'm scared to go to the Dr, as I don't want to face the tension & round of tests to exclude a Sarc relapse. It's not something I want to go through again...
I wonder if it's very likely for a relapse to come with a whole new presentation of the Sarc? Or is it unlikely to be sarc, as I never had EN the last time?
Does anyone have any experience or advice which may help me decide what to do?
Best wishes to all who are currently battling with their Sarc, I truly understand your pain and your exhaustion. I was not expected to recover last time - but I did.
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Falling pregnant after having a transplant for 25 years and 20% kidney function. What r the risks?
I have recently got engaged and my fianc and I would love nothing more than to have a child, however my renal specialist has advised my against falling pregnant due to the risks and it may send me into renal failure.
Does anyone have any info on this or any similar experience with this?
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We'll I'm afraid iv had to go back up to 5mg again,I think I was trying to come of them to fast, after 22 years,I wish I'd never taken even one, I was told by my gp that cutting down 1 mg a month,I'd be fine,got down to 3 I've never experienced anything like this in my life,I was lying on the floor,not being able to function,I'm now being referred to a shrink,to see,what's wrong with me,when in fact there's nothing wrong with me,apart from,I can't seem to get of these tablets,as they do stuff to your brain,chemical imbalance or something,I'm, still going to try again,but,very slowly next time,
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I'm a 37 year old man who was diagnosed with HSP in 2007. My symptom was the rash which appeared all over my legs and buttocks. The rash went away but left me with stage 3/4 kidney disease. I feel very scared this will lead to total kidney failure. My recent results doesn't look good with my creatine being 216. This has ruled my life and I'm so upset this could happen to me. The doctors don't know anything. All they have done is put me on 10mg of Ramipril and basically hope for the best. I'm getting married in July to my beautiful fiancé who I love so much but I seem to focus more on this disease and what might happen to me in the near future than her. I'm going to try an alternative way to help my condition. Systematic ideology (excuse the spelling) This focuses on strict diet control, with taking 100 percentage herbal ingredients. The therapy focuses on targeting muscle groups and emotional part of the body. Has anyone else tried this? Would love to hear from anyone in the same boat as me and is there anyone out there that has been in the same situation and continued in stage 3 for a very long time.
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My son is 8 years old and has today been diagnosed with first stage Perthes.
His foot turns in when he walks and he has pain in his knee.
Please can someone tell me how to make life in the house easier!
He has been told not to put any weight on his leg at all and has been given a pair of crutches, but is a wheelchair better?
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