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SBRT #4
Update on yesterday's SBRT #4. The machine that is treating me (Varian Edge) takes two revolutions to administer the fraction. They line you up with lasers and images before, track the fiducials during the rotation (and the machine automatically holds the beam if you and/or your prostate move out of
Update on yesterday's SBRT #4. The machine that is treating me (Varian Edge) takes two revolutions to administer the fraction. They line you up with lasers and images before, track the fiducials during the rotation (and the machine automatically holds the beam if you and/or your prostate move out of
ToolBeltZia
in
Prostate Cancer Network
9 months ago
Post ablation tubal sterilisation syndrome (PATTS)
Has anyone else had both of these surgeries and gone on to have excruciating pain? During my surgery they found endometriosis and I've since had an MRI and CT scan (as well as lots of useless ultrasounds that find nothing). I've been diagnosed with deep infiltrating endo on ovaries, peritoneum and bowel
Has anyone else had both of these surgeries and gone on to have excruciating pain? During my surgery they found endometriosis and I've since had an MRI and CT scan (as well as lots of useless ultrasounds that find nothing). I've been diagnosed with deep infiltrating endo on ovaries, peritoneum and bowel
Malachitegoose
in
Endometriosis UK
7 months ago
NAC with ferritin deficiency or PA
Hi all. Just thought I’d pop in and ask my new friends if they know of any reason NAC shouldn’t be taken with iron tablets or B12, or whether NAC could actually have a negative effect on ferritin/B12 levels. Can’t find any info on this, so here I am 😊 I am awaiting latest blood results, so don’t
Hi all. Just thought I’d pop in and ask my new friends if they know of any reason NAC shouldn’t be taken with iron tablets or B12, or whether NAC could actually have a negative effect on ferritin/B12 levels. Can’t find any info on this, so here I am 😊 I am awaiting latest blood results, so don’t
MLJ2024
in
Pernicious Anaemia Society
7 months ago
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After 25 days back on prednisone...
Thank you to all who advised on my previous post. I have almost completed the first month back on 20mg day of prednisone. The effect was immediate, pain gone, stiffness gone, fatigue better, am motivated and catching up with chores I had neglected for months. I feel more positive now, even started
Thank you to all who advised on my previous post. I have almost completed the first month back on 20mg day of prednisone. The effect was immediate, pain gone, stiffness gone, fatigue better, am motivated and catching up with chores I had neglected for months. I feel more positive now, even started
Biba5
in
PMRGCAuk
7 months ago
Suspected IBS
I've had IBS symptoms for about 15 years. At first I thought it was intolerance to a few foods, and cutting those out seemed to help. But the symptoms seem to get worse and more frequent as I age. I am now 42 and get scared to go out to eat or be in the office all day (thankfully I WFH 4 days a week)
I've had IBS symptoms for about 15 years. At first I thought it was intolerance to a few foods, and cutting those out seemed to help. But the symptoms seem to get worse and more frequent as I age. I am now 42 and get scared to go out to eat or be in the office all day (thankfully I WFH 4 days a week)
Gaia_1
in
IBS Network
7 months ago
A plea from your brother
Click here to securely donate in any currency: https://malecare.org/donate Click here to securely donate in any currency:A Plea from Your Brother My prostate cancer diagnosis introduced me to Malecare - with the commanding encouragement of my urologist. My experiences validated the organization's remarkable
Click here to securely donate in any currency: https://malecare.org/donate Click here to securely donate in any currency:A Plea from Your Brother My prostate cancer diagnosis introduced me to Malecare - with the commanding encouragement of my urologist. My experiences validated the organization's remarkable
Darryl
Partner
in
Prostate Cancer Network
9 months ago
A plea from your brother
Click here to securely donate in any currency: https://malecare.org/donate A Plea from Your Brother My prostate cancer diagnosis introduced me to Malecare - with the commanding encouragement of my urologist. My experiences validated the organization's remarkable efforts in supporting men like me. I'm
Click here to securely donate in any currency: https://malecare.org/donate A Plea from Your Brother My prostate cancer diagnosis introduced me to Malecare - with the commanding encouragement of my urologist. My experiences validated the organization's remarkable efforts in supporting men like me. I'm
Darryl
Partner
in
Advanced Prostate Cancer
9 months ago
Generic B12-symptoms news article
Occasionally I see what I call a generic news article on issues pertaining to B12 deficiency. Typically the articles are not very good, misrepresenting some things, wrong about other things, and so forth. So I was surprised today when I saw one that is not so bad. Sure, it could be better, could be more
Occasionally I see what I call a generic news article on issues pertaining to B12 deficiency. Typically the articles are not very good, misrepresenting some things, wrong about other things, and so forth. So I was surprised today when I saw one that is not so bad. Sure, it could be better, could be more
WiscGuy
in
Pernicious Anaemia Society
7 months ago
constipation!!!
Hello anyone I have got this constant gnawing ,scratching ,pinching ETC going on in my bum and for 3/4 months really bad constipation frightened to poop in case I "UNBLOCK" myself to the nasty stuff I just can't control I looked it up on DR GOOGLE and it came up with Proctalgia Fugax/ Levator Syndromeas
Hello anyone I have got this constant gnawing ,scratching ,pinching ETC going on in my bum and for 3/4 months really bad constipation frightened to poop in case I "UNBLOCK" myself to the nasty stuff I just can't control I looked it up on DR GOOGLE and it came up with Proctalgia Fugax/ Levator Syndromeas
bungi1961
in
Bowel Disease Support
8 months ago
Blood in Urine
Hi fellow fighters Had blood in my urine the last 10 days. Hoped it was a UTI but a course of antibiotics has failed. I had a bladder neck incision last June to help urinary flow. The urologist saw a suspicious patch and a biopsy confirmed it my prostate cancer has spread to my bladder. I’m hoping
Hi fellow fighters Had blood in my urine the last 10 days. Hoped it was a UTI but a course of antibiotics has failed. I had a bladder neck incision last June to help urinary flow. The urologist saw a suspicious patch and a biopsy confirmed it my prostate cancer has spread to my bladder. I’m hoping
Tonyliv
in
Advanced Prostate Cancer
9 months ago
Ibs sufferer any advice for nausea
hi 44 yr old in last 8 mths diagnosed with ibs m had a colonoscopy , bloods , stools samples taken and also had upper gi and ct scan with contrast all normal except calprocetin levels where high hence referral to gastologist My symptoms vary on flare up sometimes I be sat then all sudden I get funny
hi 44 yr old in last 8 mths diagnosed with ibs m had a colonoscopy , bloods , stools samples taken and also had upper gi and ct scan with contrast all normal except calprocetin levels where high hence referral to gastologist My symptoms vary on flare up sometimes I be sat then all sudden I get funny
Foody79
in
IBS Network
7 months ago
New Challenge!
Hi, I haven’t been on here for a while as was diagnosed with stage 2 breast cancer following a mammogram in late September. I underwent surgery for a mastectomy with a reconstruction on 15 th December and now starting my recovery! So going to be tricky managing my PMR symptoms as well as deal with this
Hi, I haven’t been on here for a while as was diagnosed with stage 2 breast cancer following a mammogram in late September. I underwent surgery for a mastectomy with a reconstruction on 15 th December and now starting my recovery! So going to be tricky managing my PMR symptoms as well as deal with this
GwenTheHen16
in
PMRGCAuk
9 months ago
I have my GP appt to discuss getting a diagnosis..... But do I ask for ANA tedt or referral to specialist???
Hi all, you were all so helpful when i first posted at the beginning of Feb! Finally the day is so close to discuss my possible lupus diagnosis (weds). I have took advice from your chats ,and written my symptoms down since start of Feb,and I'm ready to hopefully try to find a way forwards! But I guess
Hi all, you were all so helpful when i first posted at the beginning of Feb! Finally the day is so close to discuss my possible lupus diagnosis (weds). I have took advice from your chats ,and written my symptoms down since start of Feb,and I'm ready to hopefully try to find a way forwards! But I guess
Gingernat20
in
LUPUS UK
7 months ago
Metaxalone.
I was diagnosed with PMR September 2023 but I'm unable to have steroids. Due to a heart condition I'm also unable to have Immuno suppresants. My Rheumy has now prescribed Metaxalone for pain relief. Reading the side effects I'm not sure I'm happy to take them as they can affect your kidneys and liver
I was diagnosed with PMR September 2023 but I'm unable to have steroids. Due to a heart condition I'm also unable to have Immuno suppresants. My Rheumy has now prescribed Metaxalone for pain relief. Reading the side effects I'm not sure I'm happy to take them as they can affect your kidneys and liver
Joann63
in
PMRGCAuk
7 months ago
Is it safe to take mesalazine/octasa long term?
Hi everyone, I'm Claire and was diagnosed with mild/moderative ulcerative colitis last year. Apart from an initial flare up (followed by diagnostic procedures leading to the diagnosis), my only symptoms have been an uncomfortable/slightly painful feeling in my stomach/upper intestine. My gastroenterologist
Hi everyone, I'm Claire and was diagnosed with mild/moderative ulcerative colitis last year. Apart from an initial flare up (followed by diagnostic procedures leading to the diagnosis), my only symptoms have been an uncomfortable/slightly painful feeling in my stomach/upper intestine. My gastroenterologist
Claire_lc
in
Crohn's and Colitis Support
7 months ago
Iron plus zinc better for iron deficiency anemia
reading about zinc I came across the following article. I mean it focuses on chronic kidney desease but I found this gem of info stating that zinc combined with iron is better than iron alone. Now I'm not iron deficient. But I thought this might be interesting for those who are. Beware too much zinc
reading about zinc I came across the following article. I mean it focuses on chronic kidney desease but I found this gem of info stating that zinc combined with iron is better than iron alone. Now I'm not iron deficient. But I thought this might be interesting for those who are. Beware too much zinc
B12life
in
Pernicious Anaemia Society
7 months ago
11 months Post SCT
I’ve been wanting to update my Stem Cell Transplant journey with good news and today I was going to post that, instead I’ve been told that a lot of my lymph nodes are enlarged again. It’s so disappointing to say the least, not what I was expecting as I feel quite well and most of the GVHD issues have
I’ve been wanting to update my Stem Cell Transplant journey with good news and today I was going to post that, instead I’ve been told that a lot of my lymph nodes are enlarged again. It’s so disappointing to say the least, not what I was expecting as I feel quite well and most of the GVHD issues have
Billarina
in
CLL Support
2 months ago
I have RLS and recently updated iron labs revealed the following: Ferritin=59.2ng/mL & Transferrin Saturation = 53%.
I have been taking oral iron supplements (Iron sulfate 325mg) and Vitamin C 200 mg daily on an empty stomach but the ferritin has been going up but slowly but the transferrin saturation has gone up much higher. Should I continue with my iron supplements?
I have been taking oral iron supplements (Iron sulfate 325mg) and Vitamin C 200 mg daily on an empty stomach but the ferritin has been going up but slowly but the transferrin saturation has gone up much higher. Should I continue with my iron supplements?
DTache
in
Restless Legs Syndrome
7 months ago
Is it safe to take mesalazine/octasa long term for ulcerative colitis?
Hi everyone, I'm Claire and was diagnosed with mild/moderative ulcerative colitis last year. Apart from an initial flare up (followed by diagnostic procedures leading to a diagnosis), my only symptoms have been an uncomfortable/slightly painful feeling in my stomach/upper intestine. My gastroenterologist
Hi everyone, I'm Claire and was diagnosed with mild/moderative ulcerative colitis last year. Apart from an initial flare up (followed by diagnostic procedures leading to a diagnosis), my only symptoms have been an uncomfortable/slightly painful feeling in my stomach/upper intestine. My gastroenterologist
Claire_lc
in
IBS Network
7 months ago
New to Forum, but not to IBS
Hi all, I was diagnosed with IBS some 30 years ago, but think I had it a long time before that. I used to have flare ups, but now I have symptoms most days and not having stomach discomfort takes me by surprise.Had lots of tests, blood and stools, nothing found. But GP thought upper right quadrant
Hi all, I was diagnosed with IBS some 30 years ago, but think I had it a long time before that. I used to have flare ups, but now I have symptoms most days and not having stomach discomfort takes me by surprise.Had lots of tests, blood and stools, nothing found. But GP thought upper right quadrant
Linpin63
in
IBS Network
7 months ago
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