is a damn sight smarter than I am pointed out to me that I very likely upset some people in this community.
Although I have COPD I am in quite good health. I also realise that there are people on here who are probably in a bad way and I would not like to think that I contribute to them feeling down because of the provocative things I sometimes write.
In view of this I will not be sending any more posts.
This is a excellent site for people with breathing problems and I wish you all good health and happiness.
So long it was good to know you.
gus
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gustavski
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Sometimes what I need most on an off day is a smile at some smart a--ed comment someone, maybe even you might make. If any of us is going to make progress we must first learn to smile at ourselves. Perhaps we all need to take ourselves a little less seriously; even you when your wife maybe hurts your feelings a bit with some of her wisdom.
I enjoy your posts gus....they give me something else to think of apart from my breathing.
I used to book speakers for a women's group and even dreamt about the job last night as I used to get adverse comments from some members about my choice of subject.
One thing I learnt is that you can't please all the people all the time....that's life.
Don't be like that Gus. I have a habit of unintentionally saying things that might upset people too. The fact that you joined here is testament to your obvious interest in the subject. I too have COPD with heaps of other maladies but at my age you would expect that . I also get the shits with myself and tend to give them to other people so you're not alone old sausage.
Please stay and say hello to your I'm sure, loving wife.
Well Gus, you surprise me to say you are leaving, we are all different and express ourselves differently. Its your choice of course but you will be missed and don't feel you have to leave because of the way you express yourself. But what ever good luck for the future if you do leave.Nice to have met you.
I don't think I would have stayed with this forum, if all it was about was illness. Just as in life, we choose our friends, and perhaps respond to some more than others. But we have a good choice on here, thank goodness we are not all the same, that would be boring. Iris x
stay gus it doesn't matter what stage copd you have . we all have one thing in common the lung disease , your opinions might not be the same as others but it don't mean yours are wrong ,
Gus there are many people on here at different stages...think we can all gain from and appreciate someone not necessarily at a worse stage. Me. .I am at stage 4 and enjoy your posts 😊
See no reason for you to go?! If I am feeling low I can always avoid your post.... but on the whole I enjoy them. We have many different characters on here and you are just one of them. It is a choice which posts to read.
Hope you stay but all the best to you if we don't convince you to.
At least you have had the 'guts' so say sorry, not many people ever say that. I have coped pretty well up to now with COPD and other problems, but some days I get down so you have to think of people that are on an 'off day'. I can't see a reason for you to leave, you now know what you did wrong and hopefully it wont happen again, if it did I would be one of the first to object. Have a good day, Tatters.
The people on here who are " really ill " are some of the strongest, bravest , funniest people l have every had the privilege to know, and it would take more than your posts to upset them.
Please don't go Gus you ole salt !😀 I thnk you are good fun and just what we need, the severity of your copd is irrelevant, we're all in the same boat!😁 xxx
No no no, Gus, I love your posts, provocative, why not ? Gives us something to think about. I'm sure most on here will feel the same . Wait for the reaction and you will see. Take care. Christine. X
I have had it over 4 years mild with no change its not all doom and gloom theirs lots things you can do to beat it you tube lots great ideas on it breathing exercises etc
Look gus can l be honest with you? You're crazy and make us laugh sometimes and think too so what's wrong with that.
I have an odd sense of humour sometimes and your posts often fit with that so why not keep posting!
I am a carer so need cheering up at times. Just stay. Xx👍🏻😉😀
have I missed something. .your posts are welcome. ..and as far as am concerned look forward to them...
someone has already said that we need a difference in posts that gets people talking. ..and i think your posts do that....you can't get them all to please all....
if you stay then be prepared for a bit of stick every now and then....😆
how good your condition is...is fine with me also...
It really isn't about who is the sickest ! On here ,it's more about connecting with people who have the same condition in various stages ,who can offer advise ,share their experiences or just make a comment or share a story or photograph that will brighten up someone's day ,so ,,,,,please stay
Gus..., as you can see from the other posts..., all 29 of them at last count, your "wifey" couldn't be more wrong..., as "wifeys" often are...; stay/go do whatever suits you but know that in this group, you'll be missed and that there is no general "call" for your departure.
Hi gus, u dont have to leave, everybody is entitled to an opinion urs included, sense of humours will differ, , but that's what makes u all different. Initially it's only the lung condition itself that brings us to forums like this, that is the one thing we have in common, once we've joined personalities will come out in regards to posts. If u have offended someone then so be it, there will be 101 that u haven't, aslong as its not personal or aimed at an individual then it is always open to debate, u can't please everyone. People can either skip ur posts, read and not reply, comment their opinion in agreement or not, each to their own. Just accept and move on, but plz don't feel the need to leave 😜😋🙄😳😊 xx Sonia xx
Hi gustavski . Joining and fitting in with an established forum is not always easy but it is always sad when a member chooses to leave, unless they were here just to 'flame' and cause trouble (which happens occasionally but thankfully not often) and I am sure you do not fit into this category.
Members have their opinions on various subjects and will often share them. We will never have a situation where every member agrees so sometimes a different and opposing opinion will be presented. If you do not agree with it you are perfectly entitled to say so. The tricky bit is in how it is said. So, here is some advice for all members.
The Guidelines remind us that "the aim of this community is to provide a supportive, informative and friendly" place and that "participation in the site should be with respect, honesty and in the spirit of supporting and learning from your fellow users." We are also reminded "that the site is not a forum to 'name and shame' or to create negative feedback on individuals. There will be a “zero tolerance” approach to posts containing negative references to individuals." To maintain the community atmosphere this means we ignore what we don't like or we explain our different view without attacking the person holding the opposing view and if we think we are the one under attack we use the report button rather than retaliating.
Oh don't be a silly billy I don't come on here very often but when I do I see people with all sorts of illnesses that I have never heard of and hopefully will never get .... I have 1 lung, copd, collitis osteo-arthritis, tinitus ... erm I think that is all ...oh and heart failure.... Well up until Feb I was working with my sister in her cleaning company so even with this my tolerance to everything was probably higher than some others but I am just a 'carry on person' Only being told about the heart failure scupppering my chances of a new hip has made me give up working ....oh and the oxygen lead that I have to have 15/20 hours a day. But if I can come on now and again and have a laugh with somebody then that is great for me and them so don't go you contribute a lot and some of us need that xxxxxxx
Hi Gus, I'm not very well at the moment and it is taking a lot for me to come on here and answer your post.
From the number of replies you have received I am assuming that plenty of people will be asking you to stay on the forum but I haven't read any of their replies as I don't want to be influenced by anything they say.
I am sure that the variety of posts that you write have been enjoyed by most of the people who read them. As you say yourself, some of the things you write about are a bit provocative but from reading your posts I also know that no offence is meant. Possibly the way it is worded can make it come across in a different way than you mean it to. One of your posts that I answered last week was taken off but I know that nothing offensive was meant by it. I am sure it was explained to you why it was removed. I have had one of my posts edited which I found upsetting at the time but it is done to keep harmony on the forum and I have learned from it.
You say that your wife is smarter than yourself so why don't you let her read your posts before actually posting them to see what she thinks. She may see things in a different light and suggest a slight change so that what you write comes across as you mean it to.
There is no reason for you to leave the forum if you give a little extra thought not to what you write but how you write it. Guidance from your wife may make that difference.
I have enjoyed reading your posts. They generate a lot of interest and if you left I for one would miss reading them.
If you feel the need to talk then you have my permission to PM me.
Have a good think before deciding what to do.
Regards. John
PS: If they can put up with me on here they can put up with anyone. 😳😂😂😂
Do you really have to leave , I have seen you around on here , but it's always seemed OK to me . If you feel you may have hurt / offended anyone then you can adjust the way you write . I don't think you have to go , stay and work through it , I know you will feel better in the end and you need this site as much. as anyone . 😇
Hi gus I see nothing wrong with your posts. If some one dosnt agree with what you say they don't need to answer it. There is no reason why you should leave. Please don't go.
Gus if we were all the same the world would be a boring place.As you can see that you are wanted on this sight and you have made some people laugh and by the looks off things you have made some friends.
Please think about staying,what ever your health conditions are.
I am new here and live your post. Please stay. My doc say I am mild for emphazema but I feel moderate. Lung capacity at 75%. . We are all different and at different stages. We are all needed to help on another. Please reconsider Gus.
Have I missed something Gus? I haven't been upset by your posts. I have enjoyed many of them.
We all have or care for someone who has lung problems. Apart from that similarity we are all different. Someone said, you are you & I am me & that is ok. I hope you will reconsider & stay please. Love Margaret x
Hi Gus, I appreciate your wife's thoughtfulness for our feelings. 😊 I am one of those with severe emphysema and I can honestly say that I have never been offended by any of your posts. You have a knack for getting people talking and that's what forums are for. Obviously you can see that you're a valued member here, hopefully you'll stay on.
Sometimes I think that all mails should be prefaced with some sort of warning. Just because we are on this forum it does not mean that we are all the same we are not. Some of us like cricket some do not, (I don't understand them and feel a little sorry for them but that leaves more room for me so it's ok) some have emphysema some do not. We are all different and that is ok.
Not all of the people on this forum actually send/write posts, but that does not mean that they do not learn something from them or enjoy them. If you really want to leave then sorry to see you go, but don't leave just because some people are different and may not be as open minded as others.
Why should you go Gus? This site is for you and me and everyone else who is suffering from lung disease. The camaraderie is great, so please stay with us.
Well all has been said Gus. Shame if you decide to go. You remind me a lot of my husband who also is mild at the moment, hopefully will stay that way please God. But he also is a dab hand of casting the line and see what he can reel in. I love that kind of banter others may not. We are all different, thank the Lord. Keep letting rip with your comments, especially now that the darker nights are drawing in . By the way are you dressing for Halloween or going as yourself!
So long? Where are you going - why are you going? 55 replies to your post caught my eye - haven't read all of them yet but so far, they all seem to be asking the same question. Yes you're somewhat provocative at times but you're entitled to your opinions, and (I think) we're entitled to challenge them - or better still (tongue in cheek here) to try and change them😁😁 You shouldn't go, it makes a change to be challenged by non health or family related matters and it exercises the grey matter! Think again young man!
Dear gus, I n health and in sickness, you are here to stay. You encourage us. Moreover you might tell us wht you do to keep so healthy. There's no shame in feeling good.
Gus as I'm typing this reply I see you've had 59 replies(and loads and loads of people "liking" these replies), so don't leave. Read what people have written before you call it a day,please.
Gus, I'm relatively new to this forum and I'm in a similar situation to yours. I have COPD but I'm still relatively healthy. I've been hesitant to post things for precisely the reason your wife pointed out--since I'm not nearly as ill as many of the folks on this forum I'm afraid that my comments and complaints will come off as offensive, or fall into the "what does he have to complain about" category. But as many other folks have pointed out, we're all in different places on the same spectrum. Therefore nobody's experiences or comments are more valid or invalid than anyone else's. There's a lot of my current life experience I'd like to share: my growing dependence on supplemental oxygen, coping with decreasing lung function, dealing with the emotional ramifications of an increasing inability to do things I used to do, how I deal with people at work, on the street, in my everyday encounters, strategies for coughing up phlegm every day without scaring young children and animals. There's a lot to having COPD and a lot we can offer each other in the way of perspective, encouragement, compassion, advice and good humor. So even though I'm not a regular reader of your posts, please give your exit a second thought. You can see you have a lot of followers here and a lot of people who will miss sharing your thoughts and comments if you go. If you step on someone's toes once in awhile--guess what? So do we all. We just apologize and move on. Hope you'll do the same and keep writing.
I don't know if you're going to have the same experience I'm having, but for me supplemental oxygen is a small portable O2 concentrator that the doc gave me to use while exercising. I've been exercising regularly for over ten years now (generally 30-40 min at the gym 3-4 times a week) but in the last year or so when I exercised my blood oxygen levels were dropping like my Giants in the National League West. (If you haven't noticed, I'm from the States, so for me there's nothing in life that can't be expressed with a baseball metaphor.) Anyway, it's like a 7-8 pound battery powered boombox in a handy little backpack and I dial it up to 3 liters a minute and that manages to keep my blood sats up around 90% more or less while I'm on the exercise bike. (It was dropping down into the low 80's, even the high 70's on a particularly good day.)
I also use the box at home when I'm particularly short of breath, like after I've had a good bout of coughing and airway clearance or when the air is particularly hot and smoky (I live in California). I've even started bringing it with me when I go out and about and expect to do a fair amount of walking, like I did today. It works pretty well. My biggest issue is the social aspect of getting used to having people see me with the cannula up my nose. It's OK with family and close friends, but it bugs the hell out of me to be wearing it when I run into people I don't know that well or haven't seen in awhile. Not that I'm ashamed of it. There's no shame in having to wear this. This is an accommodation that I need, through no fault of my own. It just is. But what I object to is having to share my private health information with everyone. I'm just not used to leading with "Hi, I'm Bob, I've got bronchiectasis. How are you?" I know, I know, if my lung function continues to slide like my damn Giants then I may well get to where I have to wear a cannula 24/7, and I'm not going to become a recluse when and if that happens. I recognize sometimes our health condition gets to the point where we have to wear it like a sign on our foreheads for all the world to see. But I'm just not there yet. I may have to be dragged to that point kicking and screaming. We'll see.
So that's a brief rundown of my experience with supplemental O2 to date. Almost but not quite as effective as two fingers of single malt at the end of the day. But I can't get the insurance to pay for the Scotch.
New York Giants?!? No my friend, the San Francisco Giants. My Giants left New York in 1958. You must be referring to that American football team that plays in New Jersey. I'm one of those uncommon Yanks who doesn't really care all that much for football. I'll watch a game now and then and I follow the season but I don't sacrifice my Sundays to watching six hours of pickup truck and light beer commercials--I mean football broadcasts. No, for me baseball is the true American pastime. Yes, it can be mystifying and frustratingly slow but it's the only professional sport to my knowledge to have inspired a literature, and there's nothing like having your favorite team slowly rip your heart out over an entire summer to make you forget your COPD. At least it works that way for me!
Well to be quite frank with you I know very little about what the Americans call football and we here in the land of the cucumber sandwiches call soccer. It seems to me to be a form of Rugby plus knee pads, shoulder pads, helmets and crotch protectors. I believe it is called the Grid Iron.
Baseball.. now there is a sport I think I could get fond of. It seems to me to be a glamorous version of rounders that I played as a child. That seems to have gone out of fashion. We all played in the street then. No chance of doing that now with Britain having the highest density of cars for the roads in Europe.
I think I started to like baseball when Joe DiMaggio married MM.
Gus we need things to think about other than our health - please don't go - When I read jokes on here I often share them with a friend. Just like we share humor, we also share bad news. We need both.
hi gus we all have diferant illnesses to cope with and we are here for each other tell you wife she is a lovely lady but you dont upset us we want you to stay take care ,
hey Gus can you please just go, all these friends begging asking you to stay is bringing tears to my eyes and I just can't take anymore you know what I mean ? but you can stay if you realy want too
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Who's eligible for covid anti-virals?
Lung nodule thanks every one who replied 
Who could you ask about if your entitled to any benifits. 
Concern with my upcoming procedures.
so who plays the Harmonica? 
