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Non-small-cell lung carcinoma
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Who the Hell is Ali ibn Isa?
He may be the guy who documented the very first written account of a TAB (Temporal Artery Biopsy) procedure; sometime between 940 to 1010 A.D!!! Go Ali! Another very technical (and to me, the layperson) mind boggling editorial about recent advances in giant cell arteritis and impacts to how the disease
He may be the guy who documented the very first written account of a TAB (Temporal Artery Biopsy) procedure; sometime between 940 to 1010 A.D!!! Go Ali! Another very technical (and to me, the layperson) mind boggling editorial about recent advances in giant cell arteritis and impacts to how the disease
Hidden
in
PMRGCAuk
6 years ago
Managing the Complications of Chronic Lymphocytic Leukemia (CLL) Online Program by The CancerCare Education Department (USA)
We appreciate your participation in Managing the Complications of Chronic Lymphocytic Leukemia (CLL), which took place on May 17. We hope you found this workshop informative and look forward to your feedback. If you were not able to attend this workshop, it is available on telephone replay 24 hours a
We appreciate your participation in Managing the Complications of Chronic Lymphocytic Leukemia (CLL), which took place on May 17. We hope you found this workshop informative and look forward to your feedback. If you were not able to attend this workshop, it is available on telephone replay 24 hours a
lankisterguy
Volunteer
in
CLL Support
6 years ago
Male hypo's support and advice
Hello everyone. I'm 41 male in the United States. I had aplastic anemia and a follow-up bone marrow transplant in 1998. The complications are GVH of the gut, low thyroid, and skin vitiligo. 200 mcg levo. Blood tests in April are the following Vit D 25, D3 19mg/dl Vit D D2 6mg D 25mg Folate 7.8 ng/ml
Hello everyone. I'm 41 male in the United States. I had aplastic anemia and a follow-up bone marrow transplant in 1998. The complications are GVH of the gut, low thyroid, and skin vitiligo. 200 mcg levo. Blood tests in April are the following Vit D 25, D3 19mg/dl Vit D D2 6mg D 25mg Folate 7.8 ng/ml
Jeffreyt
in
Thyroid UK
6 years ago
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Immunotherapy after 4 months hasn’t worked any suggestions other than more Chemotherapy?
Please see my previous post. Thank you
Please see my previous post. Thank you
ParchWoody
in
The Roy Castle Lung Cancer Foundation
6 years ago
Am I in crisis?
I have been suffering from occasional foot swelling and severe pain, for about 4-5yrs. It has recently become more frequent and more painful. Body is sore and always tired. However... I was told by doctor as a teen I have the sickle trait. My mother says I have sickle cell. Can trait become actual sickle
I have been suffering from occasional foot swelling and severe pain, for about 4-5yrs. It has recently become more frequent and more painful. Body is sore and always tired. However... I was told by doctor as a teen I have the sickle trait. My mother says I have sickle cell. Can trait become actual sickle
SarahXo
in
Sickle Cell Society
6 years ago
Stage 4 lung cancer
Hi Everyone! I'm on here on behalf of my partner, Jim, age 71. He was diagnosed with stage 4 lung cancer in January of this year and has been referred for chemotherapy but has heard a lot of bad things about it. He has stopped smoking and subtituted cigarettes with 10% CBD Vape which he uses frequently
Hi Everyone! I'm on here on behalf of my partner, Jim, age 71. He was diagnosed with stage 4 lung cancer in January of this year and has been referred for chemotherapy but has heard a lot of bad things about it. He has stopped smoking and subtituted cigarettes with 10% CBD Vape which he uses frequently
Wolfette1956
in
Lung Cancer Support
6 years ago
Thoughts on CLL treatment and watch and wait
I’d be really interested in other people’s thought processes about this. I’m not a haematologist, and this is all in the realm of theory and so may not stand up to clinical trials or the real world. I guess in a way I’m trying to synthesize a philosophy of treatment. 1. Why do we watch and wait? As
I’d be really interested in other people’s thought processes about this. I’m not a haematologist, and this is all in the realm of theory and so may not stand up to clinical trials or the real world. I guess in a way I’m trying to synthesize a philosophy of treatment. 1. Why do we watch and wait? As
AdrianUK
in
CLL Support
6 years ago
Lung Cancer Registry - Have You Participated?
I wonder if any of you have heard of the Lung Cancer Registry? https://www.lungcancerregistry.org/ The Registry is a joint effort of the Bonnie J Addario Lung Cancer Foundation (ALCF), the American Lung Association (ALA), and the International Association for the Study of Lung Cancer (IASLC). Its purpose
I wonder if any of you have heard of the Lung Cancer Registry? https://www.lungcancerregistry.org/ The Registry is a joint effort of the Bonnie J Addario Lung Cancer Foundation (ALCF), the American Lung Association (ALA), and the International Association for the Study of Lung Cancer (IASLC). Its purpose
Surviventhrive
in
Lung Cancer Support
6 years ago
Husband with Stage 4 lung cancer
My husband feels very weak. Does anyone have any suggestions to help him feel stronger or is this how it is going to be? He was diagnosed a little over a year ago. Has had Chemo and is now on Opdivo.
My husband feels very weak. Does anyone have any suggestions to help him feel stronger or is this how it is going to be? He was diagnosed a little over a year ago. Has had Chemo and is now on Opdivo.
Horselover13
in
Lung Cancer Support
6 years ago
Here it is. Times piece today on CLL and access to drugs. Skip dumb comments....
The Times chief reporter, Sean O’Neill, is writing about his leukaemia for the first time to highlight the unfair NHS policy on who can be offered life-saving drugs We had spent a glorious August day high in the Picos mountains in northern Spain, whizzing by cable car to the 1,800m peak of Fuenta De
The Times chief reporter, Sean O’Neill, is writing about his leukaemia for the first time to highlight the unfair NHS policy on who can be offered life-saving drugs We had spent a glorious August day high in the Picos mountains in northern Spain, whizzing by cable car to the 1,800m peak of Fuenta De
romarin
in
CLL Support
6 years ago
Stage 4 adenocarcinom
My husband was diagnosed with adenocarcinoma stage 4 nsc lung cancer poorly differentiated. He had a liquid biopsy and dna sequencing done and was started on 2 chemo drugs and immunotherapy (kaytruda). He also has a plural effusion and the lung is collapsed. We were told that the tumors were massive
My husband was diagnosed with adenocarcinoma stage 4 nsc lung cancer poorly differentiated. He had a liquid biopsy and dna sequencing done and was started on 2 chemo drugs and immunotherapy (kaytruda). He also has a plural effusion and the lung is collapsed. We were told that the tumors were massive
Marian54
in
Lung Cancer Support
6 years ago
Stem cell transplant outcomes
Hi Y'All, I have post-PV Myelofibrosis and am getting to the stage where I can see transfusions looming and therefore my best chance for stem cell transplant (SCT) will soon be gone. I have so far resisted SCT because the outcomes are so unpredictable (especially if u don't have a related donor, which
Hi Y'All, I have post-PV Myelofibrosis and am getting to the stage where I can see transfusions looming and therefore my best chance for stem cell transplant (SCT) will soon be gone. I have so far resisted SCT because the outcomes are so unpredictable (especially if u don't have a related donor, which
jane13
in
MPN Voice
6 years ago
High GGT post treatment for Acute Myeloid Leukaemia
Hi I have a GGT reading of 900. It has been rising steadily since a successful stem cell transplant in August. I drink very little and am only a bit overweight. My disease is in remission but am still not feeling well. Many of my symptoms - nausea, fatigue and loss of appetite could be caused by liver
Hi I have a GGT reading of 900. It has been rising steadily since a successful stem cell transplant in August. I drink very little and am only a bit overweight. My disease is in remission but am still not feeling well. Many of my symptoms - nausea, fatigue and loss of appetite could be caused by liver
Hidden
in
British Liver Trust
6 years ago
Any bowel problems with GPA?
Hi, for several months now I've had a change in bowel habit. Colonoscopy clear thank goodness. But the problem continues and have had a couple of episodes of near incontince of faeces. And deep rectal pain. Just wondered if any one else has had similar symptoms.
Hi, for several months now I've had a change in bowel habit. Colonoscopy clear thank goodness. But the problem continues and have had a couple of episodes of near incontince of faeces. And deep rectal pain. Just wondered if any one else has had similar symptoms.
ludo
in
Vasculitis UK
6 years ago
Lobotomy right top lung lobe
I am 72 and had robot-assisted surgery on 3/20/18. While I was in the hospital 2 days I did not experience any problems during my stay, my only problem since has been a shortness of breath and feeling tired. Has anyone else had this problem and how long did it last?
I am 72 and had robot-assisted surgery on 3/20/18. While I was in the hospital 2 days I did not experience any problems during my stay, my only problem since has been a shortness of breath and feeling tired. Has anyone else had this problem and how long did it last?
WFM1
in
Lung Cancer Support
6 years ago
reducing
haven,t posted for long time, but been reading some of your reduction plans, i started at 40 mg, oct 2016, got down to 10 mg last spring, when i told my rheumy in august last yr about my 49 yr son diagnosed , with cancer, multiple myeloma, and that he would be having a stem cell transplant in januar
haven,t posted for long time, but been reading some of your reduction plans, i started at 40 mg, oct 2016, got down to 10 mg last spring, when i told my rheumy in august last yr about my 49 yr son diagnosed , with cancer, multiple myeloma, and that he would be having a stem cell transplant in januar
arvine
in
PMRGCAuk
6 years ago
CALR Type 1 & 2 Have Contrasting OS Outcomes
Hey everyone, As an update, since my last post (ASXL1 Mutation Detected), I recently came across some very useful articles concerning the CALR mutations & ASXL1 and their ability to be included as Prognostically significant, and naturally wanted to share those findings hopefully to the benefit of others
Hey everyone, As an update, since my last post (ASXL1 Mutation Detected), I recently came across some very useful articles concerning the CALR mutations & ASXL1 and their ability to be included as Prognostically significant, and naturally wanted to share those findings hopefully to the benefit of others
socrates_8
in
MPN Voice
6 years ago
Getting back up and running
Earlier this month I braved my first run since my pneumothorax back in January. Unsurprisingly it was considerably slower and more difficult than immediately prior to the collapse but it felt great to be back out there again. Psychologically it's a huge lift as it's a sign that I'm getting stronger
Earlier this month I braved my first run since my pneumothorax back in January. Unsurprisingly it was considerably slower and more difficult than immediately prior to the collapse but it felt great to be back out there again. Psychologically it's a huge lift as it's a sign that I'm getting stronger
dodgylungrunner
British Lung Foundation
in
Lung Conditions Community Forum
6 years ago
Just been to see my consultant.
Just been to see my respritory consultant, he asked me about having a lung transplant, this was a surprise as I didn't think I would ever be offered one. I will have to go to Newcastle for tests, I'm not worried. I know it's not gaurnteed be the offer is there. I'm also being assessed for home oxygen
Just been to see my respritory consultant, he asked me about having a lung transplant, this was a surprise as I didn't think I would ever be offered one. I will have to go to Newcastle for tests, I'm not worried. I know it's not gaurnteed be the offer is there. I'm also being assessed for home oxygen
Damon1864
Volunteer
in
Lung Conditions Community Forum
6 years ago
Report on the 2018 Lung Cancer Leadership Conference
“Lung Cancer Leadership Conference” - that is an intriguing title for a conference. Free to Breathe has held this conference for several years. The event was not offered in 2017, as Free to Breathe and the Lung Cancer Research Foundation (LCRF) merged, but it was back this year, and I was invited to
“Lung Cancer Leadership Conference” - that is an intriguing title for a conference. Free to Breathe has held this conference for several years. The event was not offered in 2017, as Free to Breathe and the Lung Cancer Research Foundation (LCRF) merged, but it was back this year, and I was invited to
scifiknitter
Blogger
in
Lung Cancer Support
6 years ago
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