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Country 65
I have a cough all the time , doctor has given me Montelukast anyone tried this I have asthma so they say don't get out of breath only short of breath after coughing fit had this problem long time
I have a cough all the time , doctor has given me Montelukast anyone tried this I have asthma so they say don't get out of breath only short of breath after coughing fit had this problem long time
Country65
in
Lung Conditions Community Forum
7 years ago
Passive smoking
There has been a lot of discussion on here regarding nicotine etc. I just wanted to say that I am a big believer of 'each to their own'. However, people who smoke cigarettes, and e-cigarettes, rarely keep their smoke to themselves. As a life long NON-smoker with COPD, it does annoy me when people
There has been a lot of discussion on here regarding nicotine etc. I just wanted to say that I am a big believer of 'each to their own'. However, people who smoke cigarettes, and e-cigarettes, rarely keep their smoke to themselves. As a life long NON-smoker with COPD, it does annoy me when people
Hetty11
in
Lung Conditions Community Forum
7 years ago
First heamo dislysis
Hello all, went into hospital for a fistulagram this morning, all went ok, just about to have a cup of tea and told I did not have time as I was wanted in renal to start my dialysis- this was such a surprise as I was expecting 2nd week in September, best way to happen as no time to think about it. Everything
Hello all, went into hospital for a fistulagram this morning, all went ok, just about to have a cup of tea and told I did not have time as I was wanted in renal to start my dialysis- this was such a surprise as I was expecting 2nd week in September, best way to happen as no time to think about it. Everything
Philipjm
in
Dialysis Support
7 years ago
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Simply sleep
Hi all hope everyone is breathing well. I am having serious problems with sleeping my dr won't give me anything to help because of my breathing I was just wondering if anyone has any tips to help. I don't drink anything with caffeine after 4pm. Thank you for any suggestions
Hi all hope everyone is breathing well. I am having serious problems with sleeping my dr won't give me anything to help because of my breathing I was just wondering if anyone has any tips to help. I don't drink anything with caffeine after 4pm. Thank you for any suggestions
kazz01
in
Lung Conditions Community Forum
7 years ago
Update - in case anyone else is in a similar position!
I posted recently that the derm thought I had lichen aureus - well the biopsy results came back and it's granuloma annulare apparently. I've been put on tacrolimus. Wondering if anyone else with hypo has had or tried this? I'll update in a month or so even if no one has, just in case it helps anyone
I posted recently that the derm thought I had lichen aureus - well the biopsy results came back and it's granuloma annulare apparently. I've been put on tacrolimus. Wondering if anyone else with hypo has had or tried this? I'll update in a month or so even if no one has, just in case it helps anyone
brilliantbobbie
in
Thyroid UK
7 years ago
Are you kidding me??
Hi, I'm from the USA. I was reading the other day about a proposal that would cut the amount of nicotine in tobacco. I smoked all my adult life and it has really cost me....big time. I quit smoking after my diagnosis of Lung cancer in 2011. When I read that they were trying to get the FDA to cut the
Hi, I'm from the USA. I was reading the other day about a proposal that would cut the amount of nicotine in tobacco. I smoked all my adult life and it has really cost me....big time. I quit smoking after my diagnosis of Lung cancer in 2011. When I read that they were trying to get the FDA to cut the
girliegirl2012
in
Lung Conditions Community Forum
7 years ago
introducing my self suffering from GI and thyroid tips welcome
hello I am new to the group. I have been having problems with my tummy since i was a child but over the past years i have had all sorts of other issues such as under active thyroid, eczema, fatigue hair loss etc. Having tried NHS they did not recognise my under active thyroid and then I went privately
hello I am new to the group. I have been having problems with my tummy since i was a child but over the past years i have had all sorts of other issues such as under active thyroid, eczema, fatigue hair loss etc. Having tried NHS they did not recognise my under active thyroid and then I went privately
mitty1
in
IBS Network
7 years ago
Calcichew 500mg tablets are different sizes in container...
I have hypoparathyroidism. I've been taking Calcichew 500mg tablets for years. Recently, I discovered my new (latest) container of Calcichew tablets were different sizes. Larger ones (those I'm used to) mixed with smaller tablets. Should I be worried? Family members (on my behalf) went to talk to
I have hypoparathyroidism. I've been taking Calcichew 500mg tablets for years. Recently, I discovered my new (latest) container of Calcichew tablets were different sizes. Larger ones (those I'm used to) mixed with smaller tablets. Should I be worried? Family members (on my behalf) went to talk to
zolo
in
Thyroid UK
7 years ago
Long Term Treatment
Believe it, or not, and it does amaze me.....It's been Twenty Years, since I Collapsed with Vasculitis. I was given or, more correctly, my Mother was told that I had 'Less Than An Hour' to live. I AM aware that it is only due to the skills/care of Surgeons/Doctors, along with my Mother's ceaseless love
Believe it, or not, and it does amaze me.....It's been Twenty Years, since I Collapsed with Vasculitis. I was given or, more correctly, my Mother was told that I had 'Less Than An Hour' to live. I AM aware that it is only due to the skills/care of Surgeons/Doctors, along with my Mother's ceaseless love
AndrewT
in
Vasculitis UK
7 years ago
Is exercise always beneficial??
Hello there. After a lazy holiday away and a few housebound rainy days lately, I have come to the startling conclusion that my brisk daily dog walks (2 x 1 hours) are actually making my chest very much worse. My diagnosis is Lupus/UCTD with resp muscle weakness & small Airways Disease. I'm 50, slim
Hello there. After a lazy holiday away and a few housebound rainy days lately, I have come to the startling conclusion that my brisk daily dog walks (2 x 1 hours) are actually making my chest very much worse. My diagnosis is Lupus/UCTD with resp muscle weakness & small Airways Disease. I'm 50, slim
Fennella02
in
Lung Conditions Community Forum
7 years ago
COPD advice please...
Hello everyone, I was diagnosed with COPD when I was 58 and gave up smoking 3 years ago I am 66 now and in Stage 4. Although I am still fairly active, walking, shopping etc., I have slowed down dramatically, can no longer hurry or run and normal household chores are a real chore now, frequently getting
Hello everyone, I was diagnosed with COPD when I was 58 and gave up smoking 3 years ago I am 66 now and in Stage 4. Although I am still fairly active, walking, shopping etc., I have slowed down dramatically, can no longer hurry or run and normal household chores are a real chore now, frequently getting
SteveHill
in
Lung Conditions Community Forum
7 years ago
Question on Complete Stem Cell Transplant
Has anyone out there ever had a complete stem cell transplant? I will be going with my sister in law this coming week to Emory Hospital in Atlanta to find out the details. Would like to hear the good and the bad if you or if you know anyone who has had this done. She has CLL but has the P17 deletion
Has anyone out there ever had a complete stem cell transplant? I will be going with my sister in law this coming week to Emory Hospital in Atlanta to find out the details. Would like to hear the good and the bad if you or if you know anyone who has had this done. She has CLL but has the P17 deletion
evetom
in
CLL Support
7 years ago
What meds. are okay to take with Copd?
I know I have posted about the bad affects of antidepressants. However, I also know that I need something to help me have a better outlook these days. I have heard Celexa is bad, and that is what I currently take. :o It helps me some, but I heard/read it's bad with all of our breathing issues, and
I know I have posted about the bad affects of antidepressants. However, I also know that I need something to help me have a better outlook these days. I have heard Celexa is bad, and that is what I currently take. :o It helps me some, but I heard/read it's bad with all of our breathing issues, and
phyllis_liberty
in
COPD Friends
7 years ago
CLL and Low estrogen treatments
Does anyone have any information about CLL and taking either Black Cohosh or Estrovera for low estrogen? Or any other insights into managing low estrogen and CLL? Thanks.
Does anyone have any information about CLL and taking either Black Cohosh or Estrovera for low estrogen? Or any other insights into managing low estrogen and CLL? Thanks.
cjspolyar
in
CLL Support
7 years ago
A great success by approaching things from the other direction!
I will keep this short, so if any one wants to ask me more about this they can do so. I posted some time ago about approaching RLS from the viewpoint of fixing my sleep problems first, not the RLS. And that is what I have been doing. After more than 6 years of having great difficulty sleeping, with
I will keep this short, so if any one wants to ask me more about this they can do so. I posted some time ago about approaching RLS from the viewpoint of fixing my sleep problems first, not the RLS. And that is what I have been doing. After more than 6 years of having great difficulty sleeping, with
lauraflora
in
Restless Legs Syndrome
7 years ago
CLL in stage zero.
Hello, I am new to this group and wanted to introduce myself. I was diagnosed with CLL two years ago and remain in stage zero. I am 57 years old and they found it by chance when I was having stomach problems. My could go up and down a little but not enough for treatment. The only thing that concerns
Hello, I am new to this group and wanted to introduce myself. I was diagnosed with CLL two years ago and remain in stage zero. I am 57 years old and they found it by chance when I was having stomach problems. My could go up and down a little but not enough for treatment. The only thing that concerns
noeagaman
in
CLL Support
7 years ago
Unmutated Newbie
Hello, all ~ First off, thanks to everyone for sharing information and personal experiences with CLL! I was diagnosed in March of this year, am stage 0, normal karyotype, just barely over the cutoff between mutated/unmutated. My CLL doc considers me intermediate risk due to being unmutated (and positive
Hello, all ~ First off, thanks to everyone for sharing information and personal experiences with CLL! I was diagnosed in March of this year, am stage 0, normal karyotype, just barely over the cutoff between mutated/unmutated. My CLL doc considers me intermediate risk due to being unmutated (and positive
yazbe
in
CLL Support
7 years ago
what is the time period for take insulin in same place in the body ?
Hi, what is the time period for take insulin in same place in body. can we continue same place everyday? my doc. suggested to take insulin 4 times a day rapid 3 time and lantuas at before bed? present i am taking rapid insulin to stomach and lantus on legs. But i found it's not affecting. can you please
Hi, what is the time period for take insulin in same place in body. can we continue same place everyday? my doc. suggested to take insulin 4 times a day rapid 3 time and lantuas at before bed? present i am taking rapid insulin to stomach and lantus on legs. But i found it's not affecting. can you please
RajpsChai
in
Diabetes India
7 years ago
Over nine years of blogging since transplant for CLL (chronic lymphocytic leukemia) on July 1, 2008
Hi, What a long strange trip it’s been. I just posted one of my old school blog post about my CLL journey: http://bkoffman.blogspot.com Some of you have been along for most of my almost 12 year CLL/ITP/ HSCT/ clinical trial journey and the last 9+ years of blogging about it, and the last 2 + years of
Hi, What a long strange trip it’s been. I just posted one of my old school blog post about my CLL journey: http://bkoffman.blogspot.com Some of you have been along for most of my almost 12 year CLL/ITP/ HSCT/ clinical trial journey and the last 9+ years of blogging about it, and the last 2 + years of
bkoffman
CLL CURE Hero
in
CLL Support
7 years ago
The CLL Tribune is full of articles written by CLL experts and fellow patients.
Hi, Last week we proudly published the latest issue of The CLL Tribune (http://www.cllsociety.org/newsletter/). We're so grateful to the patients and physicians who share their experiences and expertise to enrich our CLL Society community. If you would like to share your story, or have ideas for future
Hi, Last week we proudly published the latest issue of The CLL Tribune (http://www.cllsociety.org/newsletter/). We're so grateful to the patients and physicians who share their experiences and expertise to enrich our CLL Society community. If you would like to share your story, or have ideas for future
bkoffman
CLL CURE Hero
in
CLL Support
7 years ago
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