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Post by Blossom/Jackie W. on Oct 20, 2011 8:34:24 GMT -5
Welcome to the COPD in Canada Forum! It’s great to have you here! Although we fly a Canadian flag, be assured our members here are from a number of different countries. Let’s face it….. the disease isn’t any different in Canada than in the USA or in the UK or Spain. You will find the people here to be caring, supportive, informative and helpful. We share information and knowledge and we learn from each other. From your first post on you’ll be made to feel at home, treated like a family member (because you are); as if you’ve been here forever….. And; there’s a LOT of good information on this site; feel free to try out the Search Tool whenever you want and/or just ask away. There’s no such thing as a dumb question so don’t ever think that way. We hope at some point you’ll introduce yourself; we’d love to get to know you! Also; because we do have members here from many different countries, it would be nice if you could add (if you haven’t already) where you’re from in your profile. It helps when we’re talking meds (different countries, different names; plus what might be approved in one country may not yet be in another. ) You can do this by looking to the top bar, click on the tab that says “Profile”, then click “Modify Profile”, put the info in and save the changes. Anyway…. Sometimes people simply come here to read and learn, some check in daily and others post or share something only occasionally. It doesn’t matter. What DOES matter is that you ARE here. You’re NOT ALONE out there. You have a larger group of friends and extended family than you think. We support each other because living with this disease can drag a person down. If you let us we’ll help “shore you up” when you need it, and in turn you can do the same for us when we need it. Although "joining" isn't a prerequsite to participate and post, there are some sections that are closed to guests or even members who are not "logged on." Not sure how to get started? Just jump right in anywhere, anytime any subject. Have a question? Don't worry about posting it in the "wrong place," we'll move it.... that's what the Admins are for. Perhaps you’re reading a thread (a message with different people contributing to) and you want to add something. Just look at the top right; in the red bar you’ll see “Reply” click on it and you’re off and running OR go to the bottom where it says “Quick Rely” and start typing. When you’re finished just hit “Post” There’s a whole lot of other things you can do as well but you’ll learn as you go along. Don’t ever be afraid to do a test post..... We've all been there.... My name is Jackie Whitaker, aka Blossom. and on behalf of my fellow members, Admins and Moderators .....WELCOME! (Note to Everyone: ALL previous Intros and Welcomes, going back to 2007, has been moved to the Archive Section.
philns.proboards.com/index.cgi?board=intros )
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Post by Deleted on Nov 3, 2011 22:53:08 GMT -5
helo Blossom my name is Roamingladytryinto (Pat) I am 62 years old am retired I have been told I have COPD and sleep apena. I use three inhalers just to breath and talk. I can not walk very far without having to sit down and rest and try to get my breath back. I have severe cronic back pain, bad eyes and a doctor that refuses to help me get tax disability credit. If it hadn't been for the previous doctor I would not be on CPP disability right now. The inhalers I use are Spiriva 18mcg (1xday)ventolin 100mcg 4xday flovent 250mcg 4xday and I still have breathing problems I am constantly clearing/coughing my throat just to breath as I can't seem to get any air in my lungs. I was a trucker for many years. I need to have the tax disability credit but this new doctor states I am not eligible for it. Yet Revenue Canada says I am eligible. Where I live in Ontario is a very remote area and we rely on locom doctors when the regular doctor can't handle the volume of patients.Question can a Locom Doctor fill out the form for Tax Disability Credit or not? And Am I eligible for the Tax Disability Credit. P.S. it takes me 1-2 hrs to dress and I sit down during that period just to get my breath and for the pain I am on oxycocet 325mg I have numerous other pills I am on too.
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Post by John on Nov 4, 2011 4:03:26 GMT -5
Welcome Pat . Good to see you . There are a number of our Canadian members that may be able to answer your questions or send you in the right direction . In the mean time  |
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Post by barbara41 on Nov 4, 2011 8:07:01 GMT -5
Pat
I've just looked at my husband's tax disability credit application - he applied in 2009 - and I can't see why a Locum doctor could not fill out the form. It just specifies ' medical doctor '. Maybe he/she is just not familiar with the form. Between your breathing and daily activity limitations I would think you would be eligible. An Occupational Therapist could also sign the form re your daily activity limitations but I don't know if you have access to one where you are. I don't know the link between CPP disability and tax credit disability but I would think that the CPP status would confirm your eligibility. The tax credit application requires the impairment to have lasted for a year and requires confirmation that your condition won't improve.
I hope I haven't confused the issue. Good luck with this ..
Barbara41 - former caregiver to husband John
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Post by Blossom/Jackie W. on Nov 4, 2011 8:31:05 GMT -5
Hi Pat; Welcome to the group...... Barb's been around the block as have a few others here when it comes to the tax credit. There's a pretty decent (informative) 2 page thread that was started by Hugahusky as well back the first part of the year. You may find it helpful. (If you have further Q's, just ask..... Here's the link... philns.proboards.com/index.cgi?board=questions&action=display&thread=6916 |
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Post by Blossom/Jackie W. on Nov 25, 2011 7:32:08 GMT -5
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Post by John on Dec 26, 2011 7:39:32 GMT -5
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Post by sock on Jan 7, 2012 16:53:44 GMT -5
Hi there, im sock a 56 year old male with bad COPD.
Im on Advair 500
Spiriva once a day.
Ventolin x4 day.
I have my federal MMAR licence that i do not smoke anymore.
Im taking my life one step and one day at a time.
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Post by annabob on Jan 7, 2012 18:03:23 GMT -5
Welcome to the COPD forum. There a number of great people here, feel free to post at any time. Sock?? That is an unusual nickname. I am also on the same medication as you are. How long have you been living with COPD?  Comments - Graphics[/img][/url] |
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Post by sock on Jan 7, 2012 18:19:07 GMT -5
Thank you so much. Sock is my last cat...
I have had COPD for many years now, but its really starting up bad now.
Many panic episodes.
Right now i know i need to be here. As much as i would like to change.
I know it wont really get better. Life is good though.
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Post by Blossom/Jackie W. on Jan 7, 2012 19:19:38 GMT -5
Hi Sock.. and Welcome!
There's so many different folks who come here from e'where and with so many different situations.... I KNOW you'll find "your" spot ...
Somthing you said in your post.....
"Right now i know i need to be here. As much as i would like to change"
Is there somthing you feel you want or need to change? Or is it this danmned disease that we really can't change... only make life better along the road?
I can relate to the panic... sometmes it'll actually wake me up at night. Fortunately I recognize what it is and for the most part have learned to control it. Still tough though....
You know what though? What really strikes me as GREAT, was when you said....
"Life is good though. " That.... impressed me.
So; I hope you'll stick around, learn, contribute, share and help.... AND I look forward to getting to know you better!
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Post by aero63 on Jan 7, 2012 21:18:00 GMT -5
Hi Sock
Welcome aboard and I am glad you were able to find us and join.
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Post by sock on Jan 8, 2012 6:19:54 GMT -5
Well im on a couple of meds that are not related to COPD like Reminyl 8mg ER. for early dementia. I have been diagnosed with early dementia over two years ago. I have been taking Reminyl now for 26 months. Life is good indeed! And after all of this, Its not about me at all.  |
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Post by John on Jan 8, 2012 6:44:09 GMT -5
Welcome sock; I too take each day one step & one day @ a time . It;s much easier to live that way . There is a great group of people here . You are not alone and welcome aboard  |
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Post by susanny on Jan 8, 2012 22:08:12 GMT -5
Hey there Sock, pleased to meet you. You are welcome to stop over at the "Fence" and join us for a brief check in chat each day to keep up on each other. That way we kinda get an idea of how everyone's 'each day at a time' is going for that day, ya know?
What country are you from, btw? You mentioned that you had a federal MMAR license and I've never heard of that in the US. Could you explain what that is? Thanks.
I also live one day at a time, guess we pretty much all do. If a plan that was made doesn't look like it's going to work out, well, there's always tomorrow or the next day to get it done.
See ya around! Sue
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Post by sock on Jan 9, 2012 9:37:22 GMT -5
Thank you so much Sue.
Your in the U.S, I see.
Well the MMAR ( medical marihuana access regulations ) in Canada is Gov. approved marihuana for medical purposes.
This program started in 2001.
I was using said medication for Pegatron to clear the Hep-c virus and i did after six brutal months of treatment.
Im hep-c free now, but my plate is quite full.
I in no way endorse the smoking of anything in anyway...ever!
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Post by susanny on Jan 9, 2012 13:10:24 GMT -5
Thanks for explaining, Sock. My opinion is that marijuana is ok to use for medical purposes, preferably not smoking it of course. I am so glad you have recovered from the Hep C virus. Enough is enough for one person.
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Post by Deleted on Jan 22, 2012 16:20:57 GMT -5
Thanks Blossom
Just had my first copd flare up after being diagnosed in 2009 during cancer surgery which was removed successfully. 2 years have past and the Big C has not returned. Retired and living with my two ladies (one is a yorkie poo) who has decided she is my personal nurse. Thought I was lucky now I worry about the toll on my two ladies. All I can say is what a wake up.
To all you my deepest sympathy and empathy.
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Post by Blossom/Jackie W. on Jan 22, 2012 18:54:34 GMT -5
Well Mart.... a big heart, lungful WELCOME! A few of us have been there with the Big C.... and; LC. Probably more than even we know here. Don't know where you're from, what stage of COPD or anything ... and.... the "other lady" but.... we'd love to get to know you if you want to share! |
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Post by susanny on Jan 22, 2012 23:30:33 GMT -5
Welcome and congratulations on your freedom from the Big C. Do you mind my asking what kind of cancer you beat? We have a full history of it throughout my family but fortunately I've been lucky so far. My mom fought 3 different kinds through her life, pancreatic being the last one. I'd love to hear more about your support system as it sounds like a terrific and strong one. Your Yorkie Poo sounds very loyal and adorable, what is her name? They are adorable little gems, aren't they?
I was diagnosed in 2006 and am severe COPD living on O2 24/7, retired since 2008. I have a wonderful husband of 39 yrs *just celebrated our anniversary Friday!. We have 2 great kids, a daughter and a son, who are very supportive as well. We've had several loving 4 legged friends, the last one just passing away a few months ago of a stroke. I miss him as he was my 'nursemaid' like your little one.
Well, now you know a little bit about one of us. I'd like to welcome you to join us at the 'FENCE' where we meet as often as we like, some of us daily and some less often, and tell about our experiences and such. It'll be nice to get to know you and for you to learn how we all are living with COPD.
Sue
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Post by John on Jan 23, 2012 12:32:13 GMT -5
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Post by merryfl on Feb 1, 2012 19:06:10 GMT -5
Hi to everyone. I see a lot of familiar names here - I'm a regular on Day-to-Day and used to be quite active on CI. I stop in here occasionally and decided I should just join up For those of you who don't know me - I'm a 59 year old female, and I live on a small farm in northern Florida (U.S.A.). I was diagnosed with COPD more than 20 years ago. It rapidly became severe and I went on disability in 2000. On March 30, 2009 I had a single lung transplant. What a joy not to need O2 any more!! I have had no problems with my transplant (knock wood), but am still learning to live within the limits inflicted on me by my super doctor. Sometimes it's a challenge, but always worth it. |
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Post by Suzanne (Suz) on Feb 1, 2012 19:15:58 GMT -5
Nice to meet you Merryfl..... I am 50 yrs old and was diagnosed with COPD Dec. 2008 just before Christmas, it was a shock. I have changed many things in my life since then and hopefully it will work. I keep in touch here for some great hints, cause who knows where I'll be in 10 yrs and maybe I will need help with O2 or something in the like. My hat's off to all of you battling this desease head on and still be standing..... you all amaze me and I hope I am that strong..... Today is easy for me, but I don't know about tomorrow...... in the meantime, welcome and make yourself at home!!! Suzanne
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Post by Blossom/Jackie W. on Feb 1, 2012 20:31:07 GMT -5
Well Merryfl.... it's lovely to see you and meet you! And.....Welcome! And Suz..... good to see you posting as well. I can see I've a few things to catch up on, and I will first thing in the morning, but for now if you don't mind it's my Jammie time (actually past  ) So ladies.... till the a.m., rest well... |
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Post by susanny on Feb 1, 2012 23:40:37 GMT -5
Welcome, Merry! It is always nice to see a new 'face' here and get to know her/him. Join us at the 'fence' and let us know about your transplant and the restrictions put on you. I'm interested, of course, as you never know whether I'll be in the same situation as you some day. I was diagnosed in '06 and retired in '08. Now that you don't need O2 any longer, do you think you'd be able to return to work at least part time? I miss that part of my life so much. Just being around people all the time.........right now I feel trapped.
So, let's get to know each other! I'm Sue, btw
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Post by John on Feb 2, 2012 16:38:21 GMT -5
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Post by Blossom/Jackie W. on Feb 3, 2012 15:09:34 GMT -5
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Post by Blossom/Jackie W. on Feb 5, 2012 7:25:44 GMT -5
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Post by Blossom/Jackie W. on Feb 10, 2012 8:46:15 GMT -5
Mumsie; I'm moving your post into it's own thread here so that folks can better see....
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Post by Blossom/Jackie W. on Feb 13, 2012 18:41:26 GMT -5
Hi Sue..... I see you found your way! Good for you! I've taken the liberty of temprarily copying your note over to Introductions & Welcomes. Just click on the link below. philns.proboards.com/index.cgi?action=display&board=introduce&thread=8949You're also now known as :Sue in Ontario" rather than a number. We look forward to getting to know you a lot better! Hey........ you found your way in! Way to go! |
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We have a number of new members . I want to wish you all a warm welcome . feel free to post or just watch . . Again 
)