Cold Weather And Copd
Feb 24, 2013
I was diagnosed with copd two years ago and use a serovent inhaler twice a day and have a ventolin for back up. This is my second winter since being diagnosed and the cold weather seems to be affecting me more this year. My spiro test in January showed a slight improvement but generally l feel more breathless and l wondered if maybe l should ask for a change of inhaler. Does anyone know of an alternative to serovent or is it just the weather making me feel worse.
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I know a lot of people that have cold extremities and they don't have COPD. My adoptive Mom was one of those people. Her hands and feet were always freezing cold and she did not have COPD. I've had cold feet and hands all of my life long before the diagnosis of COPD.
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I'm new to this diabetes thing. I was diagnosed a little over six months ago. There are so many things you have to remember. Summer is here and it is really getting warm outside and I know I have to carry my insulin with me. So, what do I need to do about my insulin & hot weather? I know I have to keep my insulin in the fridge at home and room temp is okay for the day but it is really get hot outside. How do I keep my meter, insulin and insulin strips protected?
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Just wondering if anyone has had this? If you live in an state that has high humidity (like the tropics) this sometimes 'tricks' your body into having a hot flash.....
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I'm now about 4 1/2 - 5 months post op. Walking again, doing great. We've had a lot of storms lately. Today I was doing great, then all of a sudden my foot started hurting, having pangs of pain/zingers, I was grocery shopping and noticed a turn in the weather. By the time it started pouring rain I was in uncomfortable pain. I just wanted to finish, get home and put ice on my foot, and I haven't done that in quite a while now.
It was like I felt the break in my heel, just an all over pain in my foot.
If I said that I 'knew' where the screws where, I think this crew are the only ones who would understand that...
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I have been experiencing clogged nose without colds, Pain around the eyes, forehead, the temple, migraine headaches, dizziness and imbalance when walking. A visit to the ENT showed normal hearing, no ear blockage or infections, no sinusitis or nasal polyps. His diagnosis is Vasomotor rhinitis. He said the weather, temperature, wind blowing triggers my blood vessels to swell and thus cause those symptoms. Anyone experiencing these weird feelings? Its so debilitating and affects my daily activities.
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I have COPD along with CHF. My blood pressure is normal. Have only 20% use of mitral valve. ( Cardiomyopathy). I was put on 60 mg of Furosemide (Diuretic) then 2.5 mg. Then after 2 months I am now at 7.5 mg.
My question is I have a constant cough, pulling up mucus. It starts with a real itchy throat and then the coughing. There is no relief. It goes on for anytime 7 to 15 minutes stop and then starts again. At night it is worse.
I am afraid that my COPD will get worse. Please let me hear from you if you have the same problems.
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I am a carer for my Hubby, who has Pleurisy at the moment. I am his carer & I am meant to be going into Hospital for a hip operation. I am full of acute Anxiety myself as I need to get my Husband better. He is on antibiotics and strong painkillers as well. He also suffers from arthritis and also is deaf & severely sighted.. I am giving him hot fluids as much as possible.
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i was lying down on my back last night and suddenly felt my whole chest (lungs maybe)inflate. Does anybody know why this happened as its happened quite a few times recently? This left me really gasping for breath.
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i was diagnosed with Emphysema in February and am having further tests. This has all come at me so quickly and caught me off guard. Is anybody else suffering with these headaches?
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i am 25 years old, i have been suffering from breathing difficulty or not able to take deep breath problem.. all day i feel like taking deep breath. but when i try for it.. am not able to take deep breath. during night time i sleep normal.
what could be the reason. anybody pls help.. my Xray CT scan all normal.
could this be psychological problem. doctors trying to say that also. if so. how to recover from this.. it feels like i don't have any life without solving this problem.
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Anyone get sore throat? I have a bad one. I read that it could turn into strep? Or just common? Remedies at all?
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I foolishly went back to smoking a while back because I feel BETTER when I smoke. I stopped, but get tempted because my breathing is much better when I do! I know it is insane, but has anyone experienced this? When I quit My breathing was much worse. I think it has to do with waking up your lungs, clearing them out, so you become sob. But I swear when I did smoke, I felt fine! So crazy.
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I gave up smoking at new year, just over two years ago. My dad died from emphysema when he has 60, and i always said that if i ever got a cough that reminded me of my dad i would quit. It got to the point where i was coughing myself to sleep each night, and i realised this wasn't just a cold that was going away, so i set myself a smoking deadline of new year (this was in the autumn) and did just that. Well 90% of my cough went away virtually overnight, but i was left with a niggly throat clearing thing, which wasn't too much hassle. Felt pretty good, and pleased with myself. So anyway, a couple of weeks ago i was doing a meditation app, and the instruction was to take a deep breath and hold it. It kind of took me by surprise, and the next day my back was hurting. So i made an appointment for the docs and she booked me in for a chest x ray and prescribed me a peak flow meter and some ventolin. 3 times a day i have to do a best of 3 reading, take two puffs of ventolin, then twenty mins later do another best of 3 reading. After three days of doing so i'm feeling constantly breathless, worse than i ever did, i still have that pain in the left side of my back, and i am sure now that indeed i have emphysema like my dad. I feel like crying all the time yet i'm putting a brave face on for everyone. I don't have any kids, and my boyfriend still smokes in the house. I try not to be around it, bit it's only a small house and difficult to avoid. He didn't see the long horrible death my dad had, both his parents are still fit and healthy. My morning peak flow reading is 350 and the other two (noon and night) are roughly 370 with hardly any difference from the ventolin except i think its giving me a dry throat. I guess my question is, has anyone else had COPD from age 40 and still lived a long time? How bearable is it? Because my dad carried on smoking quite far into his (he gave up when he went on oxygen) i'm finding it hard to expect anything different than he got. Also is it possible for the peak flow tests to be making me breathless?
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Had chest xray done .I have no cough slight out of breath has I have asthma. doctor's have now told me I have mild change if my lung copd.when I asked does this mean I have the decease she said it might just be from the damage from smoking all those years ago.am so worried and stressed. does this mean this is the beginning of a death sentence? not sleeping or eating.
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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 have recently been told that my diaphragm is not working properly and this could be the cause of my constant chest infections. Does anyone else have this problem?
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I have been recommended to use NAC as a COPD therapy so I guess I would like to hear something about this medication. Will it works, what are the possible side effects. I have also heard that if you are using it for a long time, combining it with copper supplements would be a smart thing to do. Why is that?
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I finally received Atrovent and a nebulizer yesterday and I may be crazy or just overly excited but I think I can tell a big difference already. Pharmacist said it was fast acting. Anyways, was going to clean house and light candles like normal and didn't know if there are certain smells I should avoid. Other than the obvious, smoke, fumes, etc. More like fragrances.
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I have just been diagnosed with stage 2 copd (emphysema). I have smoked for 48 years. I am 65 and told I have lungs of a 95 year old. I am struggling to stop smoking. If I cannot how fast will my progression be.
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I was just wondering if anyone in USA or Canada has heard of this and what they thought? I have talk to a Dr. and a Nurse from the States and they say it does work, but cost a few thousand . No one has called me back in Canada yet. Before I spend the money, just want to make sure it's safe and will help.
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