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Link between Endo and CFS/ME
Hi lovelies, I wonder if there is a link between Endo and chronic fatigue syndrome or even ME? I know we all complain of brain fog and extreme tiredness but I the experiences I have had over the last few years have been incredible. Yesterday for example, I could barely do anything I was so tired and
Hi lovelies, I wonder if there is a link between Endo and chronic fatigue syndrome or even ME? I know we all complain of brain fog and extreme tiredness but I the experiences I have had over the last few years have been incredible. Yesterday for example, I could barely do anything I was so tired and
Kaiser_susie
in
Endometriosis UK
7 years ago
Is there any substitute for GP forte 2 tablets ?
My mother 65 yr old taking GP forte 2 tablete. I heard it has significant side effects on kidney functioning in future can anybody suggests alternative to these tablete. After several searches I found black seed oil is perfect which can work similar to diabetic tablets and naturally create insulin in
My mother 65 yr old taking GP forte 2 tablete. I heard it has significant side effects on kidney functioning in future can anybody suggests alternative to these tablete. After several searches I found black seed oil is perfect which can work similar to diabetic tablets and naturally create insulin in
howalsada
in
Diabetes India
7 years ago
Road to a BMT... oops just got there
Hello Health Unlocked community, Since this forum and community offered me a great amount of support and kindness during our last crisis I thought I would come back to it. Last time you heard from me/us was when my husband Mark began failing on Ibrutinib in Feb. 2017 and he was going to start Venetoclax
Hello Health Unlocked community, Since this forum and community offered me a great amount of support and kindness during our last crisis I thought I would come back to it. Last time you heard from me/us was when my husband Mark began failing on Ibrutinib in Feb. 2017 and he was going to start Venetoclax
NMMP
in
CLL Support
7 years ago
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Constant aching...
Hi everyone Well I’ve suffered from ibs for over 20 years and I know it’s linked to anxiety and stress. I usually suffer from ibs d but it’s more ibs c now. I took the York test for ibs and cut out yeast, milk, gluten and wheat and dried fruit as well as nuts. I can’t afford to lose weight and I have
Hi everyone Well I’ve suffered from ibs for over 20 years and I know it’s linked to anxiety and stress. I usually suffer from ibs d but it’s more ibs c now. I took the York test for ibs and cut out yeast, milk, gluten and wheat and dried fruit as well as nuts. I can’t afford to lose weight and I have
Lynikinz
in
IBS Network
7 years ago
Chemo Might Be Next
I had check up with oncologist this week. Last January she told me that chemo would be sooner than later. I was able to avoid it all year. I have had CLL for 10 years. My WBC reached 193k. Last January I was at 150. Seems to be accelerating over the past 2 years. I have some swollen nodes. No other
I had check up with oncologist this week. Last January she told me that chemo would be sooner than later. I was able to avoid it all year. I have had CLL for 10 years. My WBC reached 193k. Last January I was at 150. Seems to be accelerating over the past 2 years. I have some swollen nodes. No other
GMa27
in
CLL Support
7 years ago
Mantel Cell Lymphomia
My partner was diagnosed with MCL three years ago. He underwent chemo and then had stem cell transplant. Recently, a blood test has indicated that his white blood cells have risen and that his platelets are now getting low. My partner looks and feels great, without showing any of the symptoms he first
My partner was diagnosed with MCL three years ago. He underwent chemo and then had stem cell transplant. Recently, a blood test has indicated that his white blood cells have risen and that his platelets are now getting low. My partner looks and feels great, without showing any of the symptoms he first
pollyg2016
in
CLL Support
7 years ago
My name is Rob from Florida. I appreciate all of you.
I currently have a gfr of 18 which just 11 months ago was between 29 and 32. I have heart disease and diabetes as well. I am 56 years old and am currently taking many tests to get on the donor list for the University of Miami. I am scared I am going to die. I try to stay positive but it is difficult.
I currently have a gfr of 18 which just 11 months ago was between 29 and 32. I have heart disease and diabetes as well. I am 56 years old and am currently taking many tests to get on the donor list for the University of Miami. I am scared I am going to die. I try to stay positive but it is difficult.
rcoffino
in
Early CKD Support
7 years ago
Any post-polyp success stories?
My illusive polyp is finally gone and I'm very pleased! It was spotted 8 months ago just as we were about to start our first cycle. 2 months later I had a hysteroscopy with local anasthetic but they couldn't find it so assumed it had gone by itself. And then just before our first FET it was seen on
My illusive polyp is finally gone and I'm very pleased! It was spotted 8 months ago just as we were about to start our first cycle. 2 months later I had a hysteroscopy with local anasthetic but they couldn't find it so assumed it had gone by itself. And then just before our first FET it was seen on
Llama1
in
Fertility Network UK
7 years ago
Am I taking too much tumeric root?
I have been taking tumeric root for two years and wondering if there could be adverse issues. I take about a 2 inch root blended with ginger root, cayenne pepper, ceylon cinnamon, cucumber, lemon with rind, almond butter, kale or other leafy greens and coconut water. It makes about 12 ounces of smoothie
I have been taking tumeric root for two years and wondering if there could be adverse issues. I take about a 2 inch root blended with ginger root, cayenne pepper, ceylon cinnamon, cucumber, lemon with rind, almond butter, kale or other leafy greens and coconut water. It makes about 12 ounces of smoothie
hazy0
in
Lung Conditions Community Forum
7 years ago
NICE publish guidance to enable NHS England commissioning of Venetoclax for treating CLL; within CDF managed access agreement.
Today The National Institute for Health and Care Excellence (NICE) have published technology appraisal guidance [TA487] https://www.nice.org.uk/guidance/ta487 No surprises this is in line with the final Appraisal Determination (FAD) last Month and outline article here ( NICE use the Cancer Drugs Fund
Today The National Institute for Health and Care Excellence (NICE) have published technology appraisal guidance [TA487] https://www.nice.org.uk/guidance/ta487 No surprises this is in line with the final Appraisal Determination (FAD) last Month and outline article here ( NICE use the Cancer Drugs Fund
HAIRBEAR_UK
Administrator
in
CLL Support
7 years ago
Vitamin D deficiency linked to increased risk for renal disease in patients with SLE
Vitamin D deficiency linked to increased risk for renal disease in patients with SLE November 9, 2017
Michelle A. Petri
SAN DIEGO — Low levels of vitamin D were associated with elevated rates of end-stage renal disease among patients with systemic lupus erythematosus, according to findings
Vitamin D deficiency linked to increased risk for renal disease in patients with SLE November 9, 2017
Michelle A. Petri
SAN DIEGO — Low levels of vitamin D were associated with elevated rates of end-stage renal disease among patients with systemic lupus erythematosus, according to findings
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
7 years ago
Overdosing?
Two antibiotics. Eight Prednisolone, Two Carbocisteine, One Tiotropium, Two Fostair....who needs breakfast ha ha
Two antibiotics. Eight Prednisolone, Two Carbocisteine, One Tiotropium, Two Fostair....who needs breakfast ha ha
caz1951
in
COPD Friends
7 years ago
Copd and cannabis
I am just curious as to weather cannabis oil can help with copd as i have been diegnosed with it about 5 years ago and untill now the inhailours have worked great but just getting over a cold ( i know a cold ) but my chest is hurting and i have a nasty cough,dr said i have just got over a chest infection
I am just curious as to weather cannabis oil can help with copd as i have been diegnosed with it about 5 years ago and untill now the inhailours have worked great but just getting over a cold ( i know a cold ) but my chest is hurting and i have a nasty cough,dr said i have just got over a chest infection
Tezstee
in
Lung Conditions Community Forum
7 years ago
A not-so-dumb question about IGHV clonal evolution
As part of a discussion a week ago titled "Warning this may be a dumb question" ( https://healthunlocked.com/cllsupport/posts/private/136589626/warning-this-may-be-a-dumb-question ) DMary wrote the following: "A helpful private message told me that IgVH mutation doesn't change and suggested I look at
As part of a discussion a week ago titled "Warning this may be a dumb question" ( https://healthunlocked.com/cllsupport/posts/private/136589626/warning-this-may-be-a-dumb-question ) DMary wrote the following: "A helpful private message told me that IgVH mutation doesn't change and suggested I look at
gardening-girl
in
CLL Support
7 years ago
Year after CLL diagnosis~
After a yr of this CLL diagnosis I am still frustrated with the "wait and see" approach. I understand for older patients waiting but I am 54 and have been an active horseback rider my whole life. Now I have fatigue, muscle and joint pain, which the drs say is not specifically related to CLL. My lumph
After a yr of this CLL diagnosis I am still frustrated with the "wait and see" approach. I understand for older patients waiting but I am 54 and have been an active horseback rider my whole life. Now I have fatigue, muscle and joint pain, which the drs say is not specifically related to CLL. My lumph
Nettiehudson
in
CLL Support
7 years ago
Research survey on CLL/SLL
Hi We are doing some research in follow up to our abstract from ASH 2016 and would appreciate your help. Participate in an important Survey for Patients with CLL/SLL • Have you been diagnosed with chronic lymphocytic leukemia or small lymphocytic lymphoma? • Do you reside in the United States? If the
Hi We are doing some research in follow up to our abstract from ASH 2016 and would appreciate your help. Participate in an important Survey for Patients with CLL/SLL • Have you been diagnosed with chronic lymphocytic leukemia or small lymphocytic lymphoma? • Do you reside in the United States? If the
bkoffman
CLL CURE Hero
in
CLL Support
7 years ago
Radiation as sll treatment
Hello! I saw my cll specialist for the first time today and since I have sll (p17 del) in the early stages he is referring me to a radiation oncologist for a consult. Has anyone done radiation on sll? The cancer is in my inguinal (groin) nodes on both sides and not detectable anywhere else including
Hello! I saw my cll specialist for the first time today and since I have sll (p17 del) in the early stages he is referring me to a radiation oncologist for a consult. Has anyone done radiation on sll? The cancer is in my inguinal (groin) nodes on both sides and not detectable anywhere else including
Lrd38
in
CLL Support
7 years ago
Cll I just got diagnosed with cll my white blood count is 20,000
I have been diagnosed with cll my white blood cell count is 20,000 no other symptoms I feel fine
I have been diagnosed with cll my white blood cell count is 20,000 no other symptoms I feel fine
Pinafi
in
CLL Support
7 years ago
Peritoneal Dialysis
I would just like to share my experience with peritoneal dialysis. If you haven't read my previous post introducing myself, here a shorter version. I started off with emergency hemodialysis due to high blood pressure. Once my blood pressure was stabilized I was able to get my surgery for my catheter
I would just like to share my experience with peritoneal dialysis. If you haven't read my previous post introducing myself, here a shorter version. I started off with emergency hemodialysis due to high blood pressure. Once my blood pressure was stabilized I was able to get my surgery for my catheter
PUREkatniss
in
Kidney Dialysis
7 years ago
Crying with frustration and pain
I am in the middle of a really bad bout of IBS, stomach cramps lasted 4 days, now day 3 of severe rectal pain. I know it will pass but the thought of the days until it does is literally making me sit and cry. I can't find any relief, have taken Colofac and pain killers to no avail. As for food, I
I am in the middle of a really bad bout of IBS, stomach cramps lasted 4 days, now day 3 of severe rectal pain. I know it will pass but the thought of the days until it does is literally making me sit and cry. I can't find any relief, have taken Colofac and pain killers to no avail. As for food, I
lizziep
in
IBS Network
7 years ago
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