Search
Search
About
Log in
Join
Experiences with
Colonic polyps
Posts
Communities
2,351 public posts
Filter results
adenomyosis sufferer
suffering today feeling like i'm going threw labour all over again adenomyosis is awful, i have a 3 procedure operation on 30th may, laparoscopy, histeroscopy polypectomy, has anybody els had this? x #adenomyosis
suffering today feeling like i'm going threw labour all over again adenomyosis is awful, i have a 3 procedure operation on 30th may, laparoscopy, histeroscopy polypectomy, has anybody els had this? x #adenomyosis
kellymiddleton130811
in
Adenomyosis Advice Association
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
What is Chronic Kidney Disease
Chronic Kidney Disease, which is always shorted as CKD, is a medical term used to describe the progressive loss of kidney function over several months or years. CKD in early stage is not deadly and also it causes no obvious discomforts. However, without effective and timely control, it progresses over
Chronic Kidney Disease, which is always shorted as CKD, is a medical term used to describe the progressive loss of kidney function over several months or years. CKD in early stage is not deadly and also it causes no obvious discomforts. However, without effective and timely control, it progresses over
Bangjun
in
Early CKD Support
6 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
Getting better
I have been too slow in sharing good news. Last week I learned that my bone marrow biopsy done 28 days after getting my CAR-T cells showed no copies of the DNA signature of my CLL- this is at least one log lower than the usual MRD testing by flow cytometry finding one cell in 100,000. More details on
I have been too slow in sharing good news. Last week I learned that my bone marrow biopsy done 28 days after getting my CAR-T cells showed no copies of the DNA signature of my CLL- this is at least one log lower than the usual MRD testing by flow cytometry finding one cell in 100,000. More details on
bkoffman
CLL CURE Hero
in
CLL Support
6 years ago
My cancer is in remission – what does this mean?
[i]"In the 1970s, only one cancer patient in three made it through the first five years after diagnosis. Today, this figure is around 70%, and exceeds 85% for some cancers that were previously fatal. So, remission might mean cure but we only know that over time." [/i] So concludes Ian Olver, Director
[i]"In the 1970s, only one cancer patient in three made it through the first five years after diagnosis. Today, this figure is around 70%, and exceeds 85% for some cancers that were previously fatal. So, remission might mean cure but we only know that over time." [/i] So concludes Ian Olver, Director
AussieNeil
Partner
in
CLL Support
6 years ago
Worried
Legs and feet are very swollen. left leg worse. esrd. not on dialysis yet. worried about CHF, Do i go to ER for this matter.
Legs and feet are very swollen. left leg worse. esrd. not on dialysis yet. worried about CHF, Do i go to ER for this matter.
rascal01
in
Kidney Dialysis
6 years ago
Letter to my MP regarding funding of Ibrutinib
Dear Mrs Hobhouse, I am a cancer patient and under treatment from the RUH since 2006 when I was first diagnosed with CLL. The disease is a slowly progressing one, and in 2010 after four years of ‘watch and wait’ I had six months of chemotherapy, and then another six months of chemotherapy in 2015. Last
Dear Mrs Hobhouse, I am a cancer patient and under treatment from the RUH since 2006 when I was first diagnosed with CLL. The disease is a slowly progressing one, and in 2010 after four years of ‘watch and wait’ I had six months of chemotherapy, and then another six months of chemotherapy in 2015. Last
Ruhi9
in
CLL 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
A year and four months out...
Was your transplant from a living donor or a cadaver? I remember getting a call from the Emory Transplant Center at about one o'clock in the morning telling me they had a matching kidney and to get there within four hours. This is my second kidney transplant, the first was from my mother.
Was your transplant from a living donor or a cadaver? I remember getting a call from the Emory Transplant Center at about one o'clock in the morning telling me they had a matching kidney and to get there within four hours. This is my second kidney transplant, the first was from my mother.
Hidden
in
Kidney Transplant Patient Support
6 years ago
Concerning blood results
Hi was wanting some support and advice from everyone on here. My blood platelets are elevated, my mean cell volume is down. After looking at blood under the microscope it’s been said that I have lymphocytosis with occasional abnormal lymphocytes and hypochromic microcytosis. These levels have been slowly
Hi was wanting some support and advice from everyone on here. My blood platelets are elevated, my mean cell volume is down. After looking at blood under the microscope it’s been said that I have lymphocytosis with occasional abnormal lymphocytes and hypochromic microcytosis. These levels have been slowly
Hanneesweedie
in
CLL Support
6 years ago
Copd and depression
Rgc1 I have copd and now I am quitting cigarettes,it has been a week and I can’t leave my apartment I fell totally depressed,The anxiety is off the charts when will the nicotine leave me be I need help any help
Rgc1 I have copd and now I am quitting cigarettes,it has been a week and I can’t leave my apartment I fell totally depressed,The anxiety is off the charts when will the nicotine leave me be I need help any help
Glenver
in
Lung Conditions Community Forum
6 years ago
Can I donate?
Hi everyone. My father started dialysis 2 weeks ago. He is on the waiting list for a kidney transplant. I still would like to ask whether I am able to donate my kidney to him. He says it wouldn't work because we share the same DNA.
Hi everyone. My father started dialysis 2 weeks ago. He is on the waiting list for a kidney transplant. I still would like to ask whether I am able to donate my kidney to him. He says it wouldn't work because we share the same DNA.
Nora3le
in
Dialysis Support
6 years ago
Any help for insomnia
I was just started on daliresp for severe C.O.P.D. I am having terrible insomnia. Anyone else having same problem? Does any medicine help with insomnia? Thanks , Sam
I was just started on daliresp for severe C.O.P.D. I am having terrible insomnia. Anyone else having same problem? Does any medicine help with insomnia? Thanks , Sam
samferro
in
Lung Conditions Community Forum
6 years ago
More treatment confusion?!
Hi CLL'ers, I am very grateful for this forum. I'm on line a lot but this is the only place I go for CLL info. I saw my Dr. about a week ago and we have the same friendly debate-he wants to begin treatment and I don't. My white count is at 30 thousand, no doubling of the Absolute count, lots of fatigue
Hi CLL'ers, I am very grateful for this forum. I'm on line a lot but this is the only place I go for CLL info. I saw my Dr. about a week ago and we have the same friendly debate-he wants to begin treatment and I don't. My white count is at 30 thousand, no doubling of the Absolute count, lots of fatigue
lorna222
in
CLL Support
6 years ago
NEVER GIVE UP!
I’m a 71 year old female of Irish decent. I was diagnosed with CLL in 1991. It remained in remission until January 2017. My oncologist started me on IMBRUVICA (3 capsules, 140mg each) in March 2017. The only “side effect” was bone pain in the beginning. Dr. H assured me that it was temporary & was
I’m a 71 year old female of Irish decent. I was diagnosed with CLL in 1991. It remained in remission until January 2017. My oncologist started me on IMBRUVICA (3 capsules, 140mg each) in March 2017. The only “side effect” was bone pain in the beginning. Dr. H assured me that it was temporary & was
maowen46
in
CLL Support
6 years ago
Questions for consultant?
49 Years old, in UK (Yorkshire) Diagnosed 2 years ago, blood counts steadily rising. I am no longer working (As a p/t Teacher) due to fatigue. Started FCR Chemo due to fatigue (On Cycle 1) . No swollen lymph nodes etc but CT scan showed Spleen enlarged and lesions on Liver. Biopsy revealed CLL progression
49 Years old, in UK (Yorkshire) Diagnosed 2 years ago, blood counts steadily rising. I am no longer working (As a p/t Teacher) due to fatigue. Started FCR Chemo due to fatigue (On Cycle 1) . No swollen lymph nodes etc but CT scan showed Spleen enlarged and lesions on Liver. Biopsy revealed CLL progression
AntonMB
in
CLL Support
6 years ago
Transplant in sight
It's been a while since I last posted but I finally feel that the transplant is in reach. Ibruitinib and Venetoclax combination is having an amazing impact with WBC now in the normal range at 8.90. Lymphocytes down to 5.90 and once they reach 4.50 or below, my bone marrow will be checked for % of CLL
It's been a while since I last posted but I finally feel that the transplant is in reach. Ibruitinib and Venetoclax combination is having an amazing impact with WBC now in the normal range at 8.90. Lymphocytes down to 5.90 and once they reach 4.50 or below, my bone marrow will be checked for % of CLL
KAS8
in
CLL Support
6 years ago
Petition: Provide funding for biomedical research into Myalgic Encephalomyelitis (ME & CFS)
Myalgic Encephalomyelitis (ME) often referred to as Chronic Fatigue Syndrome (CFS) a debilitating chronic neuroimmune disease worsen after even minimal physical, emotional or mental activity causing many symptoms of which the main two are chronic pain and severe fatigue.It is estimated that 7 million
Myalgic Encephalomyelitis (ME) often referred to as Chronic Fatigue Syndrome (CFS) a debilitating chronic neuroimmune disease worsen after even minimal physical, emotional or mental activity causing many symptoms of which the main two are chronic pain and severe fatigue.It is estimated that 7 million
Admin_AFMCG
Administrator
in
Andover Fibromyalgia & ME Community Group
6 years ago
Anyone have bizarre auto-immune issue connected to CLL?
Looking to see if anyone else out there has dx of CLL yet not the typical cll picture. I’m inquiring for my dearest friend whom was dx 3 years ago. Was w/w for 1.5 years, had to start treatment. Did ibrutinib, now started rutuxin.... multiple blood/platlets transfusions, nuelasta shots for extreme neutropenia
Looking to see if anyone else out there has dx of CLL yet not the typical cll picture. I’m inquiring for my dearest friend whom was dx 3 years ago. Was w/w for 1.5 years, had to start treatment. Did ibrutinib, now started rutuxin.... multiple blood/platlets transfusions, nuelasta shots for extreme neutropenia
Lauriesue4
in
CLL Support
6 years ago
Komshaz
Hello every1...please i want to know if anyone experienced a GFR of 32 has gone up by eating rite and doing exercise...doing a low protien diet.. no meat ,no salt,or sugar..
Hello every1...please i want to know if anyone experienced a GFR of 32 has gone up by eating rite and doing exercise...doing a low protien diet.. no meat ,no salt,or sugar..
Komalshahz
in
Early CKD Support
6 years ago
1
...
59
60
61
...
100
Next page
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
CLL Support
1441 results
Lung Conditions Community Forum
217 results
Diabetes India
81 results
View top 10 communities
Sort by
Most Relevant
Newest