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Hypomyelination and congenital cataract
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Atelectasis?
I have seen several people refer to this here, but didn't know what it was. My PET/CT scan on Friday showed some mildly alarming things -- bone met in spine is shrinking, but a bunch of subcentimeter but metabolically active lymph nodes around the lungs (hila, paratrachea, mediastinal-pleural). Not
I have seen several people refer to this here, but didn't know what it was. My PET/CT scan on Friday showed some mildly alarming things -- bone met in spine is shrinking, but a bunch of subcentimeter but metabolically active lymph nodes around the lungs (hila, paratrachea, mediastinal-pleural). Not
TammyCross
in
SHARE Metastatic Breast Cancer
6 months ago
Recurrence?im scared
I don't know where to start because I'm scared to death. I already made a post about my situation but I need to talk more about it with people who understand my situation. My mother, my beloved mother... my reason for living. In 2020 she underwent surgery for stage one seromucinous adenocarcinoma
I don't know where to start because I'm scared to death. I already made a post about my situation but I need to talk more about it with people who understand my situation. My mother, my beloved mother... my reason for living. In 2020 she underwent surgery for stage one seromucinous adenocarcinoma
Belindajames
in
My Ovacome
4 months ago
Reaction to Taxol (Paclitaxel) and alternatives?
Hi- I was diagnosed with primary peritoneal cancer in Jan 2024. I had my first chemo last week and reacted to the taxol (paclitaxel) so could only receive bev and carboplatin. I will be switched to taxotere for my next treatment. Wondering if anyone else has had a reaction to taxol and then received
Hi- I was diagnosed with primary peritoneal cancer in Jan 2024. I had my first chemo last week and reacted to the taxol (paclitaxel) so could only receive bev and carboplatin. I will be switched to taxotere for my next treatment. Wondering if anyone else has had a reaction to taxol and then received
ajtbq
in
SHARE Ovarian Cancer Support
6 months ago
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Ranolazine (used for angina) could potentially be repurposed for PCa. Only mouse studies so far.
“Treatment of cancer patients with lipid metabolic inhibitors like ranolazine could potentially re-activate the immune cells to restore and enhance cellular-mediated antitumor immunity and tumor regression.” Targeting Fat Oxidation in Mouse Prostate Cancer Decreases Tumor Growth and Stimulates Anti-Cancer
“Treatment of cancer patients with lipid metabolic inhibitors like ranolazine could potentially re-activate the immune cells to restore and enhance cellular-mediated antitumor immunity and tumor regression.” Targeting Fat Oxidation in Mouse Prostate Cancer Decreases Tumor Growth and Stimulates Anti-Cancer
Graham49
in
Advanced Prostate Cancer
6 months ago
Result of Liver Biopsy - Any Insights?
This is the result of my liver biposy. Any insights on the comment? ----- CLINICAL HISTORY>>:: Prostate Ca with hepatic mets ?Small cell transformation versus other. FINAL DIAGNOSIS>>:: LIVER NODULE, CORE BIOPSY: - POORLY DIFFERENTIATED PROSTATIC ADENOCARCINOMA WITH SMALL CELL TRANSFORMATION
This is the result of my liver biposy. Any insights on the comment? ----- CLINICAL HISTORY>>:: Prostate Ca with hepatic mets ?Small cell transformation versus other. FINAL DIAGNOSIS>>:: LIVER NODULE, CORE BIOPSY: - POORLY DIFFERENTIATED PROSTATIC ADENOCARCINOMA WITH SMALL CELL TRANSFORMATION
skiingfiend
in
Advanced Prostate Cancer
6 months ago
High risk vs. aggressive cancer
I understand the definition of high-risk prostate cancer (Gleason, PSA and/or spread), but that doesn't necessarily seem to be the same thing as aggressive cancer. How can aggressiveness be determined for high risk, localized cancer? Thanks for any insight and information.
I understand the definition of high-risk prostate cancer (Gleason, PSA and/or spread), but that doesn't necessarily seem to be the same thing as aggressive cancer. How can aggressiveness be determined for high risk, localized cancer? Thanks for any insight and information.
RugbyVLS
in
Advanced Prostate Cancer
6 months ago
brachytherapy
my hubbie has just had brachytherapy for stage 3 prostate and has been in great pain since Thursday. He’s been told it’s normal and to suck it up but he’s not sleeping and is struggling to wee without great pain (tears) . Any advice as to what has worked for you to manage post op brachytherapy please
my hubbie has just had brachytherapy for stage 3 prostate and has been in great pain since Thursday. He’s been told it’s normal and to suck it up but he’s not sleeping and is struggling to wee without great pain (tears) . Any advice as to what has worked for you to manage post op brachytherapy please
bikebabe
in
Prostate Cancer Network
6 months ago
Anyone? 😁
LOL I’m popping on here, again, for your honest opinion and advice. I have been OFF all forms of treatment since the beginning of January (when I was told there was evidence that Ibrance and Anastrazole were failing). A brief stint with Xeloda (for 6 days...6 days of pure torture)…and to tell you
LOL I’m popping on here, again, for your honest opinion and advice. I have been OFF all forms of treatment since the beginning of January (when I was told there was evidence that Ibrance and Anastrazole were failing). A brief stint with Xeloda (for 6 days...6 days of pure torture)…and to tell you
CTGirl1962
in
SHARE Metastatic Breast Cancer
6 months ago
Colonoscopy
hello everyone😊 I wrote on here about 2 weeks ago for some advice in regards to a colonoscopy, I wanted to update you on my progress so that anyone who may be feeling afraid or anxious about this process can hopefully take something from this Today I had my colonoscopy, terrified and lost count of
hello everyone😊 I wrote on here about 2 weeks ago for some advice in regards to a colonoscopy, I wanted to update you on my progress so that anyone who may be feeling afraid or anxious about this process can hopefully take something from this Today I had my colonoscopy, terrified and lost count of
Purplecake97
in
Colon Cancer Connected
8 hours ago
Article states b2 deficiency the cause of functional b12 deficiency
what do you all think about this article which states serum b12 can be falsely elevated if there is a b2 deficiency which causes inactive cobalomine to result in elevated serum b12 https://www.iomcworld.org/articles/paradoxical-vitamin-b12-deficiency-normal-to-elevated-serum-b12-with-metabolic-vitamin-b12
what do you all think about this article which states serum b12 can be falsely elevated if there is a b2 deficiency which causes inactive cobalomine to result in elevated serum b12 https://www.iomcworld.org/articles/paradoxical-vitamin-b12-deficiency-normal-to-elevated-serum-b12-with-metabolic-vitamin-b12
B12life
in
Pernicious Anaemia Society
22 hours ago
Famotidine as a substitute for Omeprazole?
Hello friends, Has anyone been prescribed Famotidine to replace Omeprazole? I’ve been experiencing gut issues for several months now and my gp has suggested a change in H2 antagonist to see if the frequency symptoms resolve. The list of potential side effects on the PIL don’t inspire me to make the
Hello friends, Has anyone been prescribed Famotidine to replace Omeprazole? I’ve been experiencing gut issues for several months now and my gp has suggested a change in H2 antagonist to see if the frequency symptoms resolve. The list of potential side effects on the PIL don’t inspire me to make the
Heron82
in
PMRGCAuk
2 days ago
After 25 years they have stopped my B12 - what can I do?
I'm in my early sixties. Generally very good health. On no medication. About twenty five years ago my then brilliant GP did a blood test for B12. A few days later rang me to come to the surgery immediately where he injected B12 himself. Apparently I had dangerously low levels of B12 that indicated I
I'm in my early sixties. Generally very good health. On no medication. About twenty five years ago my then brilliant GP did a blood test for B12. A few days later rang me to come to the surgery immediately where he injected B12 himself. Apparently I had dangerously low levels of B12 that indicated I
DIYenthusiast
in
Pernicious Anaemia Society
2 days ago
peptic ulcers?
Hi everyone, I recently posted that I’m due a colonoscopy after having a qfit result of >200 with visible blood on my stool, this symptom comes and goes (months between each time) I have discovered today that Ulcers run in my family, on my mums side my great grandad had a duodenal ulcer, my nan had
Hi everyone, I recently posted that I’m due a colonoscopy after having a qfit result of >200 with visible blood on my stool, this symptom comes and goes (months between each time) I have discovered today that Ulcers run in my family, on my mums side my great grandad had a duodenal ulcer, my nan had
Purplecake97
in
Colon Cancer Connected
2 days ago
Update
Hi everyone, I’m on a steroid taper of 10/5 daily so will be on 5 mg when I start Mycophenolate on 20th of this month, I’m starting on a low dose gradually increasing. Hopefully this will take away the inflammation and remove bilateral pleural effusion’s and pericardial effusion caused by Serositis as
Hi everyone, I’m on a steroid taper of 10/5 daily so will be on 5 mg when I start Mycophenolate on 20th of this month, I’m starting on a low dose gradually increasing. Hopefully this will take away the inflammation and remove bilateral pleural effusion’s and pericardial effusion caused by Serositis as
Numptybrain
in
PMRGCAuk
2 days ago
ongoing chronic constipation.. ‘opioid bowel & interstitial cystitis… test results!
following months of waiting I eventually paid to see a private bowel surgeon. Worth every penny. She organised tests through NHS. Won’t bore with details- but I have a dysfunctional opioid bowel ( due to severe back problems). A large rectocele & possibly a cystocele I’m having a transit study…
following months of waiting I eventually paid to see a private bowel surgeon. Worth every penny. She organised tests through NHS. Won’t bore with details- but I have a dysfunctional opioid bowel ( due to severe back problems). A large rectocele & possibly a cystocele I’m having a transit study…
Beakybird58
in
IBS Network
2 days ago
Diverticular disease
hi all Been having abdominal pains since January. Had the fight of my life with gps to get any thing done first visit gp told me it was ibs and he had seen worse. Any way prescription for mebeverine and off I went. All was well for about 3 days then the pain was back but 1000 times worse couldn’t
hi all Been having abdominal pains since January. Had the fight of my life with gps to get any thing done first visit gp told me it was ibs and he had seen worse. Any way prescription for mebeverine and off I went. All was well for about 3 days then the pain was back but 1000 times worse couldn’t
Mrdd
in
Bowel Disease Support
3 days ago
Apixaban and iron
I am taking Apixaban 5mg bd and iron bisglycinate 60mg. Is the iron reducing the effectiveness of the Apixaban and vice versa? If so, what is the solution to raising the ferritin levels?
I am taking Apixaban 5mg bd and iron bisglycinate 60mg. Is the iron reducing the effectiveness of the Apixaban and vice versa? If so, what is the solution to raising the ferritin levels?
Dires
in
Restless Legs Syndrome
3 days ago
Was thinking of Dr. Chandy yesterday, God bless him for having such courage
Long story but I have had a couple of head MRIs due to lesions that are perpendicular in nature. To check if they have increased. I had access to my own scans so I knew that they were checking for MS. As I could read the medical terminology. But my GP (newish to me) never told me. I don't know why, it
Long story but I have had a couple of head MRIs due to lesions that are perpendicular in nature. To check if they have increased. I had access to my own scans so I knew that they were checking for MS. As I could read the medical terminology. But my GP (newish to me) never told me. I don't know why, it
Litatamon
in
Pernicious Anaemia Society
3 days ago
IBS D
having real problems at the minute bad flare up having to get up through the night multiple times loose just like water bad cramps thought i had appendicitis.Been to Gastro said ibs no weight loss and 3 normal FITS really got a grip this time so fed up taking Alverine 120mg any suggestions would be appreciated
having real problems at the minute bad flare up having to get up through the night multiple times loose just like water bad cramps thought i had appendicitis.Been to Gastro said ibs no weight loss and 3 normal FITS really got a grip this time so fed up taking Alverine 120mg any suggestions would be appreciated
Harold2
in
IBS Network
4 days ago
Ferrocalm
I started taking Ferrocalm about 18 weeks ago and suffered adjustment symptoms from day 1 which still persist. I have had severe intractable iBS-C for 10 years which has not responded to all allopathic treatments including Amitriptyline which didn’t work at 100mg at night! I was fully investigated
I started taking Ferrocalm about 18 weeks ago and suffered adjustment symptoms from day 1 which still persist. I have had severe intractable iBS-C for 10 years which has not responded to all allopathic treatments including Amitriptyline which didn’t work at 100mg at night! I was fully investigated
Pangea56
in
IBS Network
4 days ago
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