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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
5 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
5 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
5 months ago
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Cortisol saliva test results
I’ve just had my third cortisol saliva test done and am interested to get advice from the experts on here eg the very knowledgeable humanbean! It basically tells the story of how I feel. Unable to get out of bed without a cup of tea. Able to do some light jobs/activities in the morning. Tired after
I’ve just had my third cortisol saliva test done and am interested to get advice from the experts on here eg the very knowledgeable humanbean! It basically tells the story of how I feel. Unable to get out of bed without a cup of tea. Able to do some light jobs/activities in the morning. Tired after
CornishChick
in
Thyroid UK
4 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
5 months ago
Researchers from WEHI and Trento University (Italy) have answered an age-old question: which function helps mutant p53 fuel tumour growth?
The study revealed that the
loss of function
in the mutated p53 protein is the critical factor in cancer growth, disproving the previously suggested gain-of-function role. Using CRISPR gene editing, the researchers removed various mutated forms of p53 and found no change in cancer cell behavior
The study revealed that the
loss of function
in the mutated p53 protein is the critical factor in cancer growth, disproving the previously suggested gain-of-function role. Using CRISPR gene editing, the researchers removed various mutated forms of p53 and found no change in cancer cell behavior
Maxone73
in
Advanced Prostate Cancer
7 months ago
Progressing nanotechnology to improve targeted cancer treatment: not related to prostate cancer only
The article emphasizes the challenges in transitioning from lab findings to clinical applications, stressing the need for further research to optimize nanocarriers for cancer therapy. It explores the potential of nanocarriers and compounds for selective tumor targeting, including liposomes, nanoparticles
The article emphasizes the challenges in transitioning from lab findings to clinical applications, stressing the need for further research to optimize nanocarriers for cancer therapy. It explores the potential of nanocarriers and compounds for selective tumor targeting, including liposomes, nanoparticles
Maxone73
in
Advanced Prostate Cancer
7 months ago
update: Zanabrutinib vs Obenven (O&V)
We are praying for Gods wisdom (James1:5), and we’re leaning toward the Zanabrutinib. The infusions and time and distance will be impactful to my husbands work and he’s prefer to go the simpler route. We learned he’s still 13Q and TP53 negative and his lymph nodes are reduced (we have used ALT for
We are praying for Gods wisdom (James1:5), and we’re leaning toward the Zanabrutinib. The infusions and time and distance will be impactful to my husbands work and he’s prefer to go the simpler route. We learned he’s still 13Q and TP53 negative and his lymph nodes are reduced (we have used ALT for
Cb1391
in
CLL Support
7 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
5 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
5 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
5 months ago
continuing back pain
I was diagnose with 2b Ovarian Cancer in April 22. I had surgery and 6 rounds of Chemo. I have a very supportive team . I have had an MRI , CT and spinal x-ray all have shown degenerative changes to my spine. There is no evidence of recurrence. My CA125 is 13. The problem is I’m consumed with anxiety
I was diagnose with 2b Ovarian Cancer in April 22. I had surgery and 6 rounds of Chemo. I have a very supportive team . I have had an MRI , CT and spinal x-ray all have shown degenerative changes to my spine. There is no evidence of recurrence. My CA125 is 13. The problem is I’m consumed with anxiety
Hota
in
My Ovacome
7 months ago
CRS4PC and Zytiga side effects ?
My hubby is 69 and recently started Zytiga three weeks ago and it seems that he has developed moderate fatigue and low appetite since one week ago. I’m wondering if this could be a side effect of the Zytiga or if anyone thinks it’s an immunity infection attack.
My hubby is 69 and recently started Zytiga three weeks ago and it seems that he has developed moderate fatigue and low appetite since one week ago. I’m wondering if this could be a side effect of the Zytiga or if anyone thinks it’s an immunity infection attack.
Corgi16
in
Advanced Prostate Cancer
5 months ago
Colonoscopy
Hello, I’ve been having various bowel issues for the past few months, ie. constipation, bloating, slight pain in lower back, bit of diarrhoea and my Dr would like me to go for a colonoscopy. As there’s no bleeding, I assumed it could be something else. Am I wrong to think this? Any advice welcome
Hello, I’ve been having various bowel issues for the past few months, ie. constipation, bloating, slight pain in lower back, bit of diarrhoea and my Dr would like me to go for a colonoscopy. As there’s no bleeding, I assumed it could be something else. Am I wrong to think this? Any advice welcome
CoffeeLover55
in
Bowel Disease Support
5 months ago
Figuring things out - first year since diagnosis
Hi, I'm posting here as I don't know anyone in real life with lupus and have been struggling to work out what my expectations should be in terms of symptoms. I was diagnosed just over a year ago following about a year of strange symptoms - GI issues, weight loss, Raynaud's, mouth ulcers, hand and wrist
Hi, I'm posting here as I don't know anyone in real life with lupus and have been struggling to work out what my expectations should be in terms of symptoms. I was diagnosed just over a year ago following about a year of strange symptoms - GI issues, weight loss, Raynaud's, mouth ulcers, hand and wrist
CGSLE
in
LUPUS UK
4 months ago
Oxynorm
I'm too .... shattered... to give a nicely put story even a short n sweet would be too much right now. So in the meantime I would love to hear your thoughts on Oxynorm as pain relief for brutal endometriosis. It's helping reasonably well for me (though not fully I may add) Many thanks in advance
I'm too .... shattered... to give a nicely put story even a short n sweet would be too much right now. So in the meantime I would love to hear your thoughts on Oxynorm as pain relief for brutal endometriosis. It's helping reasonably well for me (though not fully I may add) Many thanks in advance
Roellen
in
Endometriosis UK
5 months ago
Long time sufferer from gastric problems
I am female, 83 years old and have had stomach problems for most of my life, I have not been diagnosed with IBS but have all the symptoms. I keep trying probiotics, imodium , kaolin and morphine mixture but nothing helps for long.
I am female, 83 years old and have had stomach problems for most of my life, I have not been diagnosed with IBS but have all the symptoms. I keep trying probiotics, imodium , kaolin and morphine mixture but nothing helps for long.
cal428orie
in
IBS Network
5 months ago
Lupus or another Autoimmune Disease?
I’m 50 yr old female with issues, RLS, Hashimotos, Autoimmune Atrophic Chronic Gastritis, intestinal Metaplasia, Iron Deficiency Anemia w/transfusions, B12 deficiency, and now this horrible hip and joint pain. I know if you have one Autoimmune Disease you’re likely to have more. I’ve had a full work
I’m 50 yr old female with issues, RLS, Hashimotos, Autoimmune Atrophic Chronic Gastritis, intestinal Metaplasia, Iron Deficiency Anemia w/transfusions, B12 deficiency, and now this horrible hip and joint pain. I know if you have one Autoimmune Disease you’re likely to have more. I’ve had a full work
Milescircus
in
LUPUS UK
4 months ago
Final Path Report After RALP (Dad - 74, G7- 4+3) , what’s next ?
Hi All, I had posted about a month ago about my dad with G7 - 4+ 3. We originally thought there were bone Mets but it just turned out to be another bone anomaly identified in the PSMA PET scan. We went ahead with RALP and have shared the final path report here. While the MRI showed no signs of
Hi All, I had posted about a month ago about my dad with G7 - 4+ 3. We originally thought there were bone Mets but it just turned out to be another bone anomaly identified in the PSMA PET scan. We went ahead with RALP and have shared the final path report here. While the MRI showed no signs of
EzioAudi7
in
Advanced Prostate Cancer
7 months ago
blood tests
hi lovely people, I was wondering if you could give me any advice. I’m relatively new to all of this and I’ve had a very bad experience at my last hospital. I was misdiagnosed most of last year with Complex Regional Pain disease. My rheumatologist wouldn’t even consider an autoimmune disease. Anyway
hi lovely people, I was wondering if you could give me any advice. I’m relatively new to all of this and I’ve had a very bad experience at my last hospital. I was misdiagnosed most of last year with Complex Regional Pain disease. My rheumatologist wouldn’t even consider an autoimmune disease. Anyway
Tonkie
in
LUPUS UK
4 months ago
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