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B12 Folate and Ferritin
I have got a Vitamin D supplement. Can anybody recommend a brand of B12, Folate and Ferritin?
I have got a Vitamin D supplement. Can anybody recommend a brand of B12, Folate and Ferritin?
foamfollower
in
Thyroid UK
7 months ago
Small panic attacks
So yesterday I was walking the dog like I do everyday, I got so far from my house and started thinking what if I have a heart attack while I'm walking the dog, so I turned back and stayed about 5-7 mins from my house and made me feel better ,, but that's the worse thing someone can do, you need to face
So yesterday I was walking the dog like I do everyday, I got so far from my house and started thinking what if I have a heart attack while I'm walking the dog, so I turned back and stayed about 5-7 mins from my house and made me feel better ,, but that's the worse thing someone can do, you need to face
detour13
in
Anxiety and Depression Support
5 months ago
PSA Risen in Last 6 months
Have been on here a week ago, explaining that my husband (who was diagnosed 10years ago) has now been diagnosed with Gastroporesis, so not eating much due to constant nausea and vomiting. We are due to see his Urologist in 2 weeks time, so had the dreaded PSA blood test. It had been almost undetectable
Have been on here a week ago, explaining that my husband (who was diagnosed 10years ago) has now been diagnosed with Gastroporesis, so not eating much due to constant nausea and vomiting. We are due to see his Urologist in 2 weeks time, so had the dreaded PSA blood test. It had been almost undetectable
Hidden
in
Advanced Prostate Cancer
9 months ago
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ET: Changing from HU to Jakafi or an Interferon treatment
Hello everyone, I'd be really grateful for any guidance / advice on the following: ET / JAK2 were diagnosed 10 years ago following a stroke (fortunately without serious consequences) and I was put on HU plus Aspirin. Amazingly I had no side-effects (apart from a 'rash' on my lower legs after about
Hello everyone, I'd be really grateful for any guidance / advice on the following: ET / JAK2 were diagnosed 10 years ago following a stroke (fortunately without serious consequences) and I was put on HU plus Aspirin. Amazingly I had no side-effects (apart from a 'rash' on my lower legs after about
Bodensee
in
MPN Voice
9 months ago
Urso and gallstones
A recent ultrasound revealed possible gallstone blocking a bile duct. An MRCP was recommended and carried out a couple of weeks ago although more like an MRI as no contrast was administered. I now have an appointment in June but I'm not sure what for. My concern is from reading the Urso leaflet it
A recent ultrasound revealed possible gallstone blocking a bile duct. An MRCP was recommended and carried out a couple of weeks ago although more like an MRI as no contrast was administered. I now have an appointment in June but I'm not sure what for. My concern is from reading the Urso leaflet it
Cressy
in
PBC Foundation
5 months ago
confused whether to go ahead with laparoscopy
31 year old female Hi everyone I am due to have a diagnostic laparoscopy in 2.5 weeks. I am so nervous about the procedure and unsure whether to go ahead. My pain over the last few months has been manageable and my periods are ok. I don’t know whether I’m getting used to the pain. I have changed my
31 year old female Hi everyone I am due to have a diagnostic laparoscopy in 2.5 weeks. I am so nervous about the procedure and unsure whether to go ahead. My pain over the last few months has been manageable and my periods are ok. I don’t know whether I’m getting used to the pain. I have changed my
Penguinpal
in
Endometriosis UK
7 months ago
does having endo mean I am at high risk for ovarian cancer?
hi! I an 26 and I have recently been diagnosed with moderate endometriosis. I am having a hard time coming to terms with it all and I consulted dr Google. I came across studies that show endo is a precursor to ovarian cancer and increases risk. I already have health anxiety however now I have gotten
hi! I an 26 and I have recently been diagnosed with moderate endometriosis. I am having a hard time coming to terms with it all and I consulted dr Google. I came across studies that show endo is a precursor to ovarian cancer and increases risk. I already have health anxiety however now I have gotten
JS1001
in
Endometriosis UK
9 months ago
shift work
Hi all, so glad I found this group.Diagnosed 10 years ago and have always worked night shifts, I’m now being told I must work 12 hour days (7-7.30)as well even though occupational health advise nights only, stiffness and pain in the mornings make it impossible to be anywhere for 7am in the morning, nevermind
Hi all, so glad I found this group.Diagnosed 10 years ago and have always worked night shifts, I’m now being told I must work 12 hour days (7-7.30)as well even though occupational health advise nights only, stiffness and pain in the mornings make it impossible to be anywhere for 7am in the morning, nevermind
Nitenurse63
in
NRAS
7 months ago
Endo in bowel tips
I was just wondering if anybody could help in regards to having endometriosis in their bowel, as I've found it quite hard to find out about it when researching. My surgeon found it on the outside of my bowel, and I am seeing a colon specialist to see if it has entered my bowel. I was just wondering if
I was just wondering if anybody could help in regards to having endometriosis in their bowel, as I've found it quite hard to find out about it when researching. My surgeon found it on the outside of my bowel, and I am seeing a colon specialist to see if it has entered my bowel. I was just wondering if
shaqshuka101
in
Endometriosis UK
7 months ago
Ablation No2 15th May
Hi all,I'm having my 2nd ablation in Nuffield St Barts in London with Professor Schilling Wed 15th May for breakthrough Afib. Will also be having EP study combined. I had a spate of VT picked up on my Wellue device and I only had it when I was on Propafenone, stopped that and straight back on the Amioderone
Hi all,I'm having my 2nd ablation in Nuffield St Barts in London with Professor Schilling Wed 15th May for breakthrough Afib. Will also be having EP study combined. I had a spate of VT picked up on my Wellue device and I only had it when I was on Propafenone, stopped that and straight back on the Amioderone
Quest4NSR
in
Atrial Fibrillation Support
5 months ago
constipation help
hope you knowledgeable people can help me. I was shouted at by my gp and bought to tears. She insisted I follow her Plan. 3 docusate and 1 fybogel sachet daily. To ignore what other drs have said. I began with this on 1st March, I’m now on day 6, have still not opened my bowels. I have terrible
hope you knowledgeable people can help me. I was shouted at by my gp and bought to tears. She insisted I follow her Plan. 3 docusate and 1 fybogel sachet daily. To ignore what other drs have said. I began with this on 1st March, I’m now on day 6, have still not opened my bowels. I have terrible
Laxido21
in
IBS Network
7 months ago
NICE guideline on B12 Deficiency diagnosis and monitoring in over 16s
The Vitamin B12 Deficiency Guideline in Over 16's has been published.
What does this mean for those with Pernicious Anaemia whether formally diagnosed or not?
What does it mean with those struggling to get sufficiently frequent treatment for their B12 deficiency?
What does
The Vitamin B12 Deficiency Guideline in Over 16's has been published.
What does this mean for those with Pernicious Anaemia whether formally diagnosed or not?
What does it mean with those struggling to get sufficiently frequent treatment for their B12 deficiency?
What does
PAScomms
in
Pernicious Anaemia Society
7 months ago
Steroid inhalers and oral thrush.
Have recently started Relvar Ellipta inhaler and would like to know how to treat oral thrush? With many thanks. 🤗
Have recently started Relvar Ellipta inhaler and would like to know how to treat oral thrush? With many thanks. 🤗
Lupino
in
Lung Conditions Community Forum
7 months ago
delayed reconstruction
I had a subdural haemorrhage in may 2023 removing most of the right side of my scull even encroached my forehead that’s some 10 months ago now. I was supposed to receive reconstructive surgery and have titanium implant to protect the sensitive area where my skin is my only protection to my brain. That
I had a subdural haemorrhage in may 2023 removing most of the right side of my scull even encroached my forehead that’s some 10 months ago now. I was supposed to receive reconstructive surgery and have titanium implant to protect the sensitive area where my skin is my only protection to my brain. That
Jodieb73
in
Headway
9 months ago
Had results but still confused 🤷🏻♀️
After having biopsy samples taken during an incomplete colonoscopy back on 20th Jan and then having the CT pneumocolon on 8th Feb I have finally had the results read out to me by the med sec….not sure if it’s left me with more questions rather than answers 🤷🏻♀️ The biopsy results show inflammation
After having biopsy samples taken during an incomplete colonoscopy back on 20th Jan and then having the CT pneumocolon on 8th Feb I have finally had the results read out to me by the med sec….not sure if it’s left me with more questions rather than answers 🤷🏻♀️ The biopsy results show inflammation
PinkBubblez1
in
Colon Cancer Connected
7 months ago
Genetic Testing?
Does anyone have an experience to share about getting genetic testing done on your biopsy samples? I'm interested in three tests: (1) a DECIPHER test, (2) a full gene sequencing of tumor DNA and RNA (e.g., at Claris Labs), and (3) the Artera AI analysis of digitized pathology slides. Also, if anyone
Does anyone have an experience to share about getting genetic testing done on your biopsy samples? I'm interested in three tests: (1) a DECIPHER test, (2) a full gene sequencing of tumor DNA and RNA (e.g., at Claris Labs), and (3) the Artera AI analysis of digitized pathology slides. Also, if anyone
janebob99
in
Prostate Cancer Network
9 months ago
Burning tongue and metallic taste .
I was dx 10 years ago. Had FCR, Ibrutinib, and Venetoclax. I am on Venetoclax now for 18 months after 6 times of V+O. A year ago I lost my taste sense and everything tastes metallic,but the worse is a burning tongue sensation. Does it have any connetion to CLL or Venetoclax ?Gidi
I was dx 10 years ago. Had FCR, Ibrutinib, and Venetoclax. I am on Venetoclax now for 18 months after 6 times of V+O. A year ago I lost my taste sense and everything tastes metallic,but the worse is a burning tongue sensation. Does it have any connetion to CLL or Venetoclax ?Gidi
GIDI
in
CLL Support
5 months ago
lung nodule / proposed surgery / scared and confused
Hello, thank you for this site. My best to all on this site for health and happiness. I’m not even sure where I may be at on this journey but am certainly scared and confused . In March of 2022 I had a kidney stone and a lung nodule was detected on right lower lobe and suggested follow up in 3 -6 months
Hello, thank you for this site. My best to all on this site for health and happiness. I’m not even sure where I may be at on this journey but am certainly scared and confused . In March of 2022 I had a kidney stone and a lung nodule was detected on right lower lobe and suggested follow up in 3 -6 months
ghostyinmass
in
Lung Cancer Support
9 months ago
Update finally on treatment
Hello ladies and gentlemen, I am finally on treatment, it took nearly 4 months from dx to treatment (due to moving from South Carolina to Seattle area). I am on Ibrance (Dec. 13th) and letrozole (Nov. 16th). And I am on palliative care for pain management since I have neuropathy in my left arm and hand
Hello ladies and gentlemen, I am finally on treatment, it took nearly 4 months from dx to treatment (due to moving from South Carolina to Seattle area). I am on Ibrance (Dec. 13th) and letrozole (Nov. 16th). And I am on palliative care for pain management since I have neuropathy in my left arm and hand
monkeygirl62
in
SHARE Metastatic Breast Cancer
9 months ago
Update following meeting with MO
For those following my journey, I had a face-to-face meeting with my MO today and learnt a few things I didn't know. Firstly, the genetic test of the liver tumour the NHS do only tests for BRCA - no other genes. The reason appears to be that the only treatment they would offer is a Parp inhibitor so
For those following my journey, I had a face-to-face meeting with my MO today and learnt a few things I didn't know. Firstly, the genetic test of the liver tumour the NHS do only tests for BRCA - no other genes. The reason appears to be that the only treatment they would offer is a Parp inhibitor so
Benkaymel
in
Advanced Prostate Cancer
9 months ago
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