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Post RP/SRT Pelvic Mass?
RRP 2/02, SRT 7/16, BCR 9/23 Latest PSA .17 I recently retired and have been spending more time sitting on my ass in front of the computer [like right now] than I should. Over the last couple of months I have begun to feel/sense that I am sitting on something, very similar to what I felt pre-RP. At
RRP 2/02, SRT 7/16, BCR 9/23 Latest PSA .17 I recently retired and have been spending more time sitting on my ass in front of the computer [like right now] than I should. Over the last couple of months I have begun to feel/sense that I am sitting on something, very similar to what I felt pre-RP. At
bldn10
in
Advanced Prostate Cancer
8 months ago
T3 trying to find someone to give me a T3 trial.
have a underactive thyroid low T3 symptoms Free T3 is very low at last blood test end of November trying to find a Dr in the Nottingham area who would prescribe T3 on a trial basis. So far no luck. Can you please private message me due to site guidelines. Willing to go private. Thanks
have a underactive thyroid low T3 symptoms Free T3 is very low at last blood test end of November trying to find a Dr in the Nottingham area who would prescribe T3 on a trial basis. So far no luck. Can you please private message me due to site guidelines. Willing to go private. Thanks
elwins
in
Thyroid UK
6 months ago
Nuelasta shot after Jevtana and Carboplatin treatment
I get a nuelasta shot 24 hours after receiving my Jevtana and Carboplatin iinfusion. I'm having major body aches for 2 to 3 days after receiving the shot to boost my white blood counts. None of my various pain medications works. Anyone have this problem or have an answer to help with the pain? Believe
I get a nuelasta shot 24 hours after receiving my Jevtana and Carboplatin iinfusion. I'm having major body aches for 2 to 3 days after receiving the shot to boost my white blood counts. None of my various pain medications works. Anyone have this problem or have an answer to help with the pain? Believe
robert570
in
Advanced Prostate Cancer
8 months ago
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Persistent AF
Hi everyone, I have been to see my cardiologist today. Had all the usual tests done he asked me how I was feeling I said I felt really well. He then told me I was no longer in Paroxysmal AF and I was in Persistent AF. How can they tell? I have got to have an echocardiogram done and a machine fitted
Hi everyone, I have been to see my cardiologist today. Had all the usual tests done he asked me how I was feeling I said I felt really well. He then told me I was no longer in Paroxysmal AF and I was in Persistent AF. How can they tell? I have got to have an echocardiogram done and a machine fitted
Gillybean123
in
AF Association
5 months ago
Have you visited the Arrhythmia Alliance website?
If you are new to the Forum, or would like updated information relating to a new medication, a scheduled procedure? an information booklet? Make a donation? Register for our monthly patient e-newsletter or simply just find out more about the charity and how we can help you. Our website contains a
If you are new to the Forum, or would like updated information relating to a new medication, a scheduled procedure? an information booklet? Make a donation? Register for our monthly patient e-newsletter or simply just find out more about the charity and how we can help you. Our website contains a
TracyAdmin
Partner
in
Sudden Cardiac Arrest & Heart Attack
5 months ago
Abalation Fears
Hi All Today I went and seen my Electrophysiology specialist and have booked in for an ablation in 2 weeks time. I am quite anxious about this whole procedure. He advised me it would be a 70% success rate and mentioned he does not like quoting over this rate. 70% is based on having no more AF episodes
Hi All Today I went and seen my Electrophysiology specialist and have booked in for an ablation in 2 weeks time. I am quite anxious about this whole procedure. He advised me it would be a 70% success rate and mentioned he does not like quoting over this rate. 70% is based on having no more AF episodes
Murphy10
in
Atrial Fibrillation Support
5 months ago
Discoid Lupus
Hello Everyone, I have been suffering with discoid lupus for 5 years now. i have had some pretty nasty flare ups since being diagnosed. One flare up resulted in having to spend 2 weeks in hospital. I recently had another flare up… After nearly 12 months in remission… And I started to get bald patches
Hello Everyone, I have been suffering with discoid lupus for 5 years now. i have had some pretty nasty flare ups since being diagnosed. One flare up resulted in having to spend 2 weeks in hospital. I recently had another flare up… After nearly 12 months in remission… And I started to get bald patches
Beryl2485
in
LUPUS UK
6 months ago
Liver Ultrasound Question
Hello! I had an abdominal ultrasound today including my liver due to a recent blood test showing very high on all the liver tests… my GP is suspecting Non-alcoholic fatty liver… I know I have to wait for the ultrasound report to come back, but the radiologist who did the scan said that my liver was
Hello! I had an abdominal ultrasound today including my liver due to a recent blood test showing very high on all the liver tests… my GP is suspecting Non-alcoholic fatty liver… I know I have to wait for the ultrasound report to come back, but the radiologist who did the scan said that my liver was
Hidden
in
British Liver Trust
6 months ago
Marshmallow
hi 3 weeks ago I was admitted to A&E in ambulance with severe central chest pain I was informed I was having a heart attack and admitted to CCU 3 days later transferred to Coventry UHT hospital underwent angioplasty procedure as one coronary artery was 99% blocked Cardiologist explained 2 others
hi 3 weeks ago I was admitted to A&E in ambulance with severe central chest pain I was informed I was having a heart attack and admitted to CCU 3 days later transferred to Coventry UHT hospital underwent angioplasty procedure as one coronary artery was 99% blocked Cardiologist explained 2 others
Marshmallow888
in
British Heart Foundation
10 months ago
GP appointment and blood tests - will recent steroid injection skew results?
Afternoon everyone, I had a GP appointment yesterday to discuss my symptoms. Went through everything that has happened since the summer. She sent me for blood tests today which included CRP, ESR, Rheumatoid factor and various other tests relating to autoimmune conditions. She insisted I call back for
Afternoon everyone, I had a GP appointment yesterday to discuss my symptoms. Went through everything that has happened since the summer. She sent me for blood tests today which included CRP, ESR, Rheumatoid factor and various other tests relating to autoimmune conditions. She insisted I call back for
MsWhistledown
in
PMRGCAuk
6 months ago
rheumatoid arthritis
Hi I’m Lynne. I’ve had Rheumatoid Arthritis for around 5 years. I’m on (tocilizumab) and Methotrexate injections once a week plus 10 mg steroids . I’ve had lots of falls because of my knee giving way. I’m trying to build up my muscles but finding this difficult because I’ve got a tear in shoulder from
Hi I’m Lynne. I’ve had Rheumatoid Arthritis for around 5 years. I’m on (tocilizumab) and Methotrexate injections once a week plus 10 mg steroids . I’ve had lots of falls because of my knee giving way. I’m trying to build up my muscles but finding this difficult because I’ve got a tear in shoulder from
linnypin1
in
NRAS
6 months ago
Hemorrhoids from higher cholesterol
I thought I'd ask if this is common for other people. I suspect my Hemorrhoids have got quite bad as a result of slightly underactive thyroid. My cholesterol is mildly high - 5.7 when it should be below 5. Also I have gilberts syndrome which is high bilirubin. When I fasted or went more than 6 hrs without
I thought I'd ask if this is common for other people. I suspect my Hemorrhoids have got quite bad as a result of slightly underactive thyroid. My cholesterol is mildly high - 5.7 when it should be below 5. Also I have gilberts syndrome which is high bilirubin. When I fasted or went more than 6 hrs without
SteveT3
in
Thyroid UK
6 months ago
GCA diagnostic dilemma
Thank you everyone who has helped so far. Last night I had a message from Rheumy saying I should go to the hospital for an emergency biopsy, with the headache and unusual severe temporal pain being the driver. He said that U/S was so ‘operator sensitive’ as to be unreliable in this ‘locality’. The
Thank you everyone who has helped so far. Last night I had a message from Rheumy saying I should go to the hospital for an emergency biopsy, with the headache and unusual severe temporal pain being the driver. He said that U/S was so ‘operator sensitive’ as to be unreliable in this ‘locality’. The
Predderman2020
in
PMRGCAuk
8 months ago
Weight problems and insensitive people
I've been so self conscious since gaining so much weight from my underactive thyroid that I'm basically a hermit in my own home, I barely go outdoors, for fear of being called up on my weight gain, or "looking well". Today I decided to go outdoors only to bump into an old acquaintance who couldn't resist
I've been so self conscious since gaining so much weight from my underactive thyroid that I'm basically a hermit in my own home, I barely go outdoors, for fear of being called up on my weight gain, or "looking well". Today I decided to go outdoors only to bump into an old acquaintance who couldn't resist
Foxxyyh
in
Thyroid UK
6 months ago
any tests for Familial hypocholesterolemia?
hi there, Asking for hubby 54 who runs twice a week, plays table tennis, walks 40 mins a day, healthy diet (although we are looking at sugars, fats and the various debates), has done dry January due to a dodgy bilirubin result which corrected in 4 weeks not drinking. Cholesterol blood tests from
hi there, Asking for hubby 54 who runs twice a week, plays table tennis, walks 40 mins a day, healthy diet (although we are looking at sugars, fats and the various debates), has done dry January due to a dodgy bilirubin result which corrected in 4 weeks not drinking. Cholesterol blood tests from
Regenallotment
in
Cholesterol Support
5 months ago
shortness of breath subsequent to zoledronic acid infusion
Because of GI problems, bisphosphonate tablets are not an option for me, so I have gone down the infusion path. I had my first infusion on December 28th, and experienced about three days of bad muscle pain, which then resolved itself. It was a couple of weeks later that I noticed that my ankles were
Because of GI problems, bisphosphonate tablets are not an option for me, so I have gone down the infusion path. I had my first infusion on December 28th, and experienced about three days of bad muscle pain, which then resolved itself. It was a couple of weeks later that I noticed that my ankles were
Angel_doll
in
PMRGCAuk
5 months ago
Monitor for Afib
Hi all,Having gone into permanent Afib after a covid infection with no previous history I've had a cardioversion whist on amiodarone. As far as I'm aware I'm still in sinus rhythm and now off amiodarone (thank goodness). I'm on the waiting list for an ablation. My question is it worth getting some kind
Hi all,Having gone into permanent Afib after a covid infection with no previous history I've had a cardioversion whist on amiodarone. As far as I'm aware I'm still in sinus rhythm and now off amiodarone (thank goodness). I'm on the waiting list for an ablation. My question is it worth getting some kind
JoDogBlue
in
Atrial Fibrillation Support
5 months ago
Spontaneous Subdural Hematoma
I am 58 years old. A few months I started to develop headaches and neck pain that gradually increased in severity. I eventually went to the ER and was diagnosed with a minor subdural hematoma (SDH) based upon a CT Scan and was sent home for follow-up with a neurosurgeon. I have had no recent head
I am 58 years old. A few months I started to develop headaches and neck pain that gradually increased in severity. I eventually went to the ER and was diagnosed with a minor subdural hematoma (SDH) based upon a CT Scan and was sent home for follow-up with a neurosurgeon. I have had no recent head
TWF64
in
Headway
8 months ago
Discoid lupus
Hi. I have just got results of biopsy. I have discoid lupus, I have also had full blood checks and came back clear. Every where I read says discoid lupus only affects the skin. But I have been experiencing joint pain pretty much every part of my body where there's joints, stiffness, extreme fatigue.
Hi. I have just got results of biopsy. I have discoid lupus, I have also had full blood checks and came back clear. Every where I read says discoid lupus only affects the skin. But I have been experiencing joint pain pretty much every part of my body where there's joints, stiffness, extreme fatigue.
Kddp
in
LUPUS UK
6 months ago
afib and chest infection
hi. My afib has been steady for around 3 months (ie no episodes). My HR runs around 52-60. I’ve started with a chest infection yesterday (can remember feeling like this for a long time) I checked my afib via Apple Watch and although it says I’m in sinus rhythm my HR is low to mid 90’s. Could this
hi. My afib has been steady for around 3 months (ie no episodes). My HR runs around 52-60. I’ve started with a chest infection yesterday (can remember feeling like this for a long time) I checked my afib via Apple Watch and although it says I’m in sinus rhythm my HR is low to mid 90’s. Could this
macymoo007
in
AF Association
5 months ago
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