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Copd asthma edema in feet

Recently my feet are puffier then usual ,I'm not but seems like I get more out of breath when my feet are puffy I was recently prescribed predestone and my feet became puffier then usual for a few days,they seem to have gone down to more normal also I seem to be getting varicose veins and little dark coloured veins in feet my feet are usually a bit numb,everything seems worse since having covid back in March.im really sick of seeing drs who dont really know much about long covid ,I'm 72 feel like I'm just wasting what time I have left going for more X-rays seeing specialists ect copd does not seem to improve .I'm on trimbow atm I can't tell if making things easier can't sleep due to having to spit every couple hrs climate here in Australia isn't good bush fires floods heatwave, thanks iv decided to not watch tv news any more I'm afraid state of politics is way too depressing thanks all.

  1. Hi . It used to be that we had to make a real effort to absorb the news -- buy a newspaper and read it, select a TV newscast to watch and then be available to commit to the newscast at the time that it airs. That's not the case anymore. It can be really difficult to avoid. So, I hope you are able to make a conscious effort to tune it out. As a former journalist, I have always encouraged people to be informed, but your health comes first.
    Have you ever seen a cardiologist about the swelling in your legs. So often, swelling in the feet and legs is caused by circulation issues. It might be helpful to get a cardiologist's perspective. Warmly, Lori (Team Member)

    1. Thanks Lori for reply ,I was feeling bit down that day ,it just seems every time I go to drs or waiting for a result since covid I expect to hear negative info ,so hard to even get an appointment some days .thanks

      1. Long Covid is still such a mystery, unfortunately. And there are so many people out there who are suffering without answers. Davoe, have you ever checked out some of the groups online for people with long covid? At the very least, you'll be able to talk with people that understand your experience and help you to feel a little less alone. I just did a quick Google search and there were quite a few websites that came up for Australia, so maybe that would be a good place to start. Facebook is another good option for connection, and perhaps our colleagues at the Social Health Network can point you toward others in that situation. I'm thinking about you. -Melissa, team member

    2. After my my stemi last year with 4 stents. I was advised to pay close attention to any swelling in the legs or ankle areas. Stage 3 doesn't help either. Just last week had the PAD procedure test done. Found mild to moderate restrictions. AND on to the next adventure. Just like it never ends. I wish you the best in health. Yes i am staying positive. Never a dull moment.

      1. I am glad you are remaining postive and hopeful. Though the test results must have been hard to hear, it was discovered early. Hopefully, with treatment, you can slow any progression. Sending lots of gentle hugs your way. - Lori (Team Member)

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