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Non-small-cell lung carcinoma
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Tocilizumab
Hi. Has anyone had Tocilizumab injections for pmr? I've been looking at recent research which seems to suggest favourable outcomes for pmr sufferers who have problems tapering prednisolone.
Hi. Has anyone had Tocilizumab injections for pmr? I've been looking at recent research which seems to suggest favourable outcomes for pmr sufferers who have problems tapering prednisolone.
BlueMozart
in
PMRGCAuk
1 year ago
Join Us! Tuesday, February 14th, Gathering HOPE, a Social
Hello! For those of you who know me and to those of you I may not have spoken with or met yet, I am Michele Zeh, Manager of the Lung Cancer Living Room Series and I am excited to invite you to our monthly Gathering HOPE Social hosted now on our ZOOM link this coming Tuesday, February 14th, at 5pm PT
Hello! For those of you who know me and to those of you I may not have spoken with or met yet, I am Michele Zeh, Manager of the Lung Cancer Living Room Series and I am excited to invite you to our monthly Gathering HOPE Social hosted now on our ZOOM link this coming Tuesday, February 14th, at 5pm PT
Michelezeh
Partner
in
Lung Cancer Support
2 years ago
Red face / flushing. Possible rosacea
Hi I am 200 plus days post stem cell transplant. Since then I get flushed very easily. I have suffered with this in the past and still have it now but maybe worse I take a few medications still which may or may not help and wondered on any good way of controlling it my consultant has recommended me
Hi I am 200 plus days post stem cell transplant. Since then I get flushed very easily. I have suffered with this in the past and still have it now but maybe worse I take a few medications still which may or may not help and wondered on any good way of controlling it my consultant has recommended me
Kraskie1915
in
CLL Support
1 year ago
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Immunotherapy
Having had a lobectomy a few years ago on right lung, I now have 2 opacities on lower left lung. As there had only been one lesion seen on lower left lung I was offered radiotherapy. After last scan which showed another lesion adjacent to the first, I am told that 'radiotherapy is off the table'. At
Having had a lobectomy a few years ago on right lung, I now have 2 opacities on lower left lung. As there had only been one lesion seen on lower left lung I was offered radiotherapy. After last scan which showed another lesion adjacent to the first, I am told that 'radiotherapy is off the table'. At
ferntreegully
in
The Roy Castle Lung Cancer Foundation
2 years ago
Life beyond Myelofibrosis
I progressed from ET to Myelofibrosis a couple of years ago. I had an enlarged spleen and ruxolitinib lowered the platelets too much so I was switched to fedratinib. Depending on what predictive tool was used, I had a median predicted life span of between 2 and 14 years - not terribly helpful! I was
I progressed from ET to Myelofibrosis a couple of years ago. I had an enlarged spleen and ruxolitinib lowered the platelets too much so I was switched to fedratinib. Depending on what predictive tool was used, I had a median predicted life span of between 2 and 14 years - not terribly helpful! I was
Scaredy_cat
in
MPN Voice
1 year ago
introducing myself...
hello all, i'm new to this community and happy to be a part. i was diagnosed with AML in late august of last year and just underwent a Stem Cell Transplant at sloan kettering hospital in new york city in late march. i'm wondering if anyone out there has experienced the same? looking forward to hearing
hello all, i'm new to this community and happy to be a part. i was diagnosed with AML in late august of last year and just underwent a Stem Cell Transplant at sloan kettering hospital in new york city in late march. i'm wondering if anyone out there has experienced the same? looking forward to hearing
jmcasbar
in
Leukaemia Support
1 year ago
An update on my father’s immunotherapy for his lung cancer.
Hello , an update on my father’s immunotherapy for lung cancer. Would really appreciate any thoughts , insight or experiences. Especially, but no only, those which can give my father some further hope. My father was disagnosed with Stage 4 lung cancer around 10 months ago. He started on chemo but
Hello , an update on my father’s immunotherapy for lung cancer. Would really appreciate any thoughts , insight or experiences. Especially, but no only, those which can give my father some further hope. My father was disagnosed with Stage 4 lung cancer around 10 months ago. He started on chemo but
Vip1
in
The Roy Castle Lung Cancer Foundation
2 years ago
cryoablation
Back again with an old problem. Had my cryoablation 15 months ago and went through the usual recovery with the help of all you nice folks. So I need some more help. The past 3 weeks my flutters have been returning. I've been stressed lately and I'm sure that helped to start them. So I went on Klor-con
Back again with an old problem. Had my cryoablation 15 months ago and went through the usual recovery with the help of all you nice folks. So I need some more help. The past 3 weeks my flutters have been returning. I've been stressed lately and I'm sure that helped to start them. So I went on Klor-con
mlp3434
in
AF Association
2 years ago
Lung Surgery Cancelled Twice
After an incidental find of a 19mm lung nodule and a clear PET scan in late October my respiratory consultant was sure it was a slow growing cancer caught early and recommended, which was agreed by me, that rather than a biopsy I go straight to surgery for a lung wedge resection to remove the nodule
After an incidental find of a 19mm lung nodule and a clear PET scan in late October my respiratory consultant was sure it was a slow growing cancer caught early and recommended, which was agreed by me, that rather than a biopsy I go straight to surgery for a lung wedge resection to remove the nodule
Domino13
in
The Roy Castle Lung Cancer Foundation
2 years ago
Would you be interested in new support if you have a mutation driven lung cancer, or have surgery as a treatment?
Hello all, On 16th February we will be starting an eight week programme of hour long on line support sessions for people with genetic mutation driven lung cancer. The sessions will be run by our facilitator and share coping ideas, practical tips and experience of treatment. If you would like to participate
Hello all, On 16th February we will be starting an eight week programme of hour long on line support sessions for people with genetic mutation driven lung cancer. The sessions will be run by our facilitator and share coping ideas, practical tips and experience of treatment. If you would like to participate
LorraineD
Roy Castle
in
The Roy Castle Lung Cancer Foundation
2 years ago
Pregnancy
Hi all I am 6.5 years post single lung transplant and recently found out I am 7 weeks pregnant . I'm super shocked as I was told I would never have another child ( I also have a 13 year old daughter) And im super worried about how my body is going to cope with this pregnancy. My transplant unit have
Hi all I am 6.5 years post single lung transplant and recently found out I am 7 weeks pregnant . I'm super shocked as I was told I would never have another child ( I also have a 13 year old daughter) And im super worried about how my body is going to cope with this pregnancy. My transplant unit have
Hidden
in
Lung Conditions Community Forum
2 years ago
Exhausted but happy.
I spent seven hours at the lung transplant clinic at Harefield yesterday. I was weighed and measured many times, sometimes with boots (dockers!) on sometimes off, ECG, echocardiogram, chest xray, blood tests, blood pressure test, lung function test, urine test, and finally mrsa test! Everone
I spent seven hours at the lung transplant clinic at Harefield yesterday. I was weighed and measured many times, sometimes with boots (dockers!) on sometimes off, ECG, echocardiogram, chest xray, blood tests, blood pressure test, lung function test, urine test, and finally mrsa test! Everone
Karenanne61
in
Lung Conditions Community Forum
2 years ago
Update on my previous post trapped nerve and PMR.
After an MRI on my spine I do not have a trapped nerve in my back and my pain is two vertebrae bones crumbling. I have come to the conclusion that the pain in my back and bottom area is mainly my PMR flare, it is so bad I can't move without pain while in bed. Tried increasing my pred dosage from 6mg
After an MRI on my spine I do not have a trapped nerve in my back and my pain is two vertebrae bones crumbling. I have come to the conclusion that the pain in my back and bottom area is mainly my PMR flare, it is so bad I can't move without pain while in bed. Tried increasing my pred dosage from 6mg
Washingup
in
PMRGCAuk
1 year ago
Hello there - any advice about Chemo (Carboplatin and Pemetrexed) and Immunotherapy (Pembrolizomab)?
Hi, so I was diagnosed just before Christmas (Is cancer the Christmas Grinch? 🤔 It was in my case....) Anyway, having been diagnosed with NSCL cancer I've now been put on a treatment plan, and start on Monday next week. Has anyone got any top tips for getting through the next few months? It all sounds
Hi, so I was diagnosed just before Christmas (Is cancer the Christmas Grinch? 🤔 It was in my case....) Anyway, having been diagnosed with NSCL cancer I've now been put on a treatment plan, and start on Monday next week. Has anyone got any top tips for getting through the next few months? It all sounds
Boo_Radley
in
The Roy Castle Lung Cancer Foundation
2 years ago
No offer of treatment.
My dear friend and colleague was diagnosed with stage 4 lung cancer in December. She has had a biopsy and been told there is no treatment available for her. She is just being given pain relief. She did not want to know how long she might have left. She sleeps most of the day and can't walk from the
My dear friend and colleague was diagnosed with stage 4 lung cancer in December. She has had a biopsy and been told there is no treatment available for her. She is just being given pain relief. She did not want to know how long she might have left. She sleeps most of the day and can't walk from the
Loppydune
in
The Roy Castle Lung Cancer Foundation
2 years ago
FDA Approves Cell Therapy for Patients with Blood Cancers to Reduce Risk of Infection Following Stem Cell Transplantation- Released 4/17/23
Today [4/17/23], the U.S. Food and Drug Administration approved Omisirge (omidubicel-onlv), a substantially modified allogeneic (donor) cord blood-based cell therapy to quicken the recovery of neutrophils (a subset of white blood cells) in the body and reduce the risk of infection. The product is intended
Today [4/17/23], the U.S. Food and Drug Administration approved Omisirge (omidubicel-onlv), a substantially modified allogeneic (donor) cord blood-based cell therapy to quicken the recovery of neutrophils (a subset of white blood cells) in the body and reduce the risk of infection. The product is intended
PhysAssist
in
MPN Voice
1 year ago
'Astonishing' Results: Skip Salvage Chemo, Go Straight to HSCT from ASH 2022 [For Refractory AML/Relapsed AML]
NEW ORLEANS — Investigators confessed to being "astonished" by results of a randomized trial showing that patients with acute myeloid leukemia who have a poor response following induction therapy do just as well going on to immediate allogeneic transplant as they would if they had received an intensive
NEW ORLEANS — Investigators confessed to being "astonished" by results of a randomized trial showing that patients with acute myeloid leukemia who have a poor response following induction therapy do just as well going on to immediate allogeneic transplant as they would if they had received an intensive
PhysAssist
in
MPN Voice
1 year ago
Hi, im new here
Hi, im really wondering if i have developed fibromyalgia. I have recently recovered from treatment for blood cancer by having a stem cell transplant (14 months ago) im struggling to return to work full time, im suffering everyday with pain ,fatigue, weakness, dizziness, brain fog, sometimes my skin
Hi, im really wondering if i have developed fibromyalgia. I have recently recovered from treatment for blood cancer by having a stem cell transplant (14 months ago) im struggling to return to work full time, im suffering everyday with pain ,fatigue, weakness, dizziness, brain fog, sometimes my skin
Marchhare7
in
Fibromyalgia Action UK
1 year ago
billionaires
i dot know how many of you heard the " Doc vs Parkinson's" story A doctor who paid almost 20 million dollars to get a stem cell transplant of brain about 3 years ago. He had PD for 15 years and now his symptoms are reversing. Are people with money, power and PD are getting efficient treatment and
i dot know how many of you heard the " Doc vs Parkinson's" story A doctor who paid almost 20 million dollars to get a stem cell transplant of brain about 3 years ago. He had PD for 15 years and now his symptoms are reversing. Are people with money, power and PD are getting efficient treatment and
Rupa88
in
Cure Parkinson's
1 year ago
Abnormal cells
hello! I’m just wanting some help on something we are quiet distressed with at the moment, My nan has been told she has lung cancer, She went for a PET Scan which showed 3 red areas (bowel, lung, spine) We were told these are abnormal cells. She’s now waiting on more tests which are weeks away
hello! I’m just wanting some help on something we are quiet distressed with at the moment, My nan has been told she has lung cancer, She went for a PET Scan which showed 3 red areas (bowel, lung, spine) We were told these are abnormal cells. She’s now waiting on more tests which are weeks away
Qwerty500
in
The Roy Castle Lung Cancer Foundation
2 years ago
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