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painkillers for toothache
I have ET and am on Pegasys Interferon. Hello My question is, I have very bad toothache and can’t see a dentist for a couple of weeks ! I want to take a painkiller stronger than paracetamol? Has anyone been in a similar situation and was able to take something stronger ? Thank you for reading this
I have ET and am on Pegasys Interferon. Hello My question is, I have very bad toothache and can’t see a dentist for a couple of weeks ! I want to take a painkiller stronger than paracetamol? Has anyone been in a similar situation and was able to take something stronger ? Thank you for reading this
Abrams
in
MPN Voice
10 months ago
No endo found in Lap, feel deflated :(
I felt so gutted no endometriosis was found- sounds ridiculous that I WANTED them to find it, but I wanted a reason for my
chronic
pain
. She has referred me to a bowel specialist- possible endometriosis on the bowel, but surely this would have been found in the lap?
I felt so gutted no endometriosis was found- sounds ridiculous that I WANTED them to find it, but I wanted a reason for my
chronic
pain
. She has referred me to a bowel specialist- possible endometriosis on the bowel, but surely this would have been found in the lap?
BlackcurrentSquash
in
Endometriosis UK
10 months ago
Treatment for life?
Hello. First time posting here. Diagnosed with CLL in July by flow test and Fish test. Although still technically in lymphocytosis. My chart says diagnosis: CLL. During the discussion in July my Dr told me of things they will be keeping an eye on. Then he said he won't discuss particular treatment plans
Hello. First time posting here. Diagnosed with CLL in July by flow test and Fish test. Although still technically in lymphocytosis. My chart says diagnosis: CLL. During the discussion in July my Dr told me of things they will be keeping an eye on. Then he said he won't discuss particular treatment plans
Quiltingone
in
CLL Support
11 months ago
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Headaches with GCA
Do you get headaches anywhere in your head or just in a certain place? And painkillers don't work.
Do you get headaches anywhere in your head or just in a certain place? And painkillers don't work.
Caulkhead63
in
PMRGCAuk
10 months ago
Rectal fissure - healed!
I'm not sure if this is the correct group to post in as I do not have IBS, however for 10+ years, I had a rectal fissure that just wouldn’t go away. I live in the Caribbean, have a healthy lifestyle and diet. Years ago, when first diagnosed with the fissure, I was prescribed Lidoprocto suppositories
I'm not sure if this is the correct group to post in as I do not have IBS, however for 10+ years, I had a rectal fissure that just wouldn’t go away. I live in the Caribbean, have a healthy lifestyle and diet. Years ago, when first diagnosed with the fissure, I was prescribed Lidoprocto suppositories
StogStog
in
IBS Network
10 months ago
knee replacement
hi had a meniscus op repair for torn cartlidge 2007 and have all sorts of problems since, with by right knee, swelling so much with walking and can’t stand in one position for long, and have a bakers cyst swelling pouch on the back crease of knee which is painful. my left leg has carried the right
hi had a meniscus op repair for torn cartlidge 2007 and have all sorts of problems since, with by right knee, swelling so much with walking and can’t stand in one position for long, and have a bakers cyst swelling pouch on the back crease of knee which is painful. my left leg has carried the right
Nat107
in
Arthritis Action
10 months ago
Endometriosis Symptoms?
I’ve not really been told much about the other symptoms of endo apart from
chronic
pelvis
pain
(which I am getting) My other symptoms are, awful acne, legit NO sex drive, I’ve dried up… if you know what I mean, excessive facial hair growth, my moods can be so low and dark and I am so tearful Bloods
I’ve not really been told much about the other symptoms of endo apart from
chronic
pelvis
pain
(which I am getting) My other symptoms are, awful acne, legit NO sex drive, I’ve dried up… if you know what I mean, excessive facial hair growth, my moods can be so low and dark and I am so tearful Bloods
EmilyKindon
in
Endometriosis UK
9 months ago
High neutrophil count😱
My wife's last blood test showed her platelets were up at @800 And her neutrophil count at over 70, her Hgb was 116, hematocrit was 0.38 which is high for her, but as it was only three weeks since she had three units of packed red cells and a bag of iron, that was expected. I read in the guardian of
My wife's last blood test showed her platelets were up at @800 And her neutrophil count at over 70, her Hgb was 116, hematocrit was 0.38 which is high for her, but as it was only three weeks since she had three units of packed red cells and a bag of iron, that was expected. I read in the guardian of
jointpain
in
MPN Voice
10 months ago
‘They thought I had cancer’: painkiller banned in UK linked to Britons’ deaths in Spain
Just want to make sure anyone with access to metamizole is aware of these possible issues. It is NOT available in the UK. [i]
‘They thought I had cancer’: painkiller banned in UK linked to Britons’ deaths in Spain
[/i] [i]Patients’ group says reactions to metamizole can cause sepsis and organ
Just want to make sure anyone with access to metamizole is aware of these possible issues. It is NOT available in the UK. [i]
‘They thought I had cancer’: painkiller banned in UK linked to Britons’ deaths in Spain
[/i] [i]Patients’ group says reactions to metamizole can cause sepsis and organ
helvella
Thyroid UK
in
Thyroid UK
10 months ago
7 weeks on and a million questions sorry
hi and good morning all, well I’m 7 weeks after icu ventilation and I have a million questions I’m hoping people could shed some light on so I don’t dr google everything and think I have every illness known to man!! I was on ventilation for 9 days in icu and I still have health issues popping up here
hi and good morning all, well I’m 7 weeks after icu ventilation and I have a million questions I’m hoping people could shed some light on so I don’t dr google everything and think I have every illness known to man!! I was on ventilation for 9 days in icu and I still have health issues popping up here
Alfiedude99
in
ICUsteps
10 months ago
Sacral Insufficiency Fractures
Hi, I've just joined this online community, which feels like a good start! I was diagnosed with sacral insufficiency fractures following a scan in February of this year. My symptoms - excruciating pain and limited mobility - started in September 2022 only 3 months after the finish of my pelvic radiotherapy
Hi, I've just joined this online community, which feels like a good start! I was diagnosed with sacral insufficiency fractures following a scan in February of this year. My symptoms - excruciating pain and limited mobility - started in September 2022 only 3 months after the finish of my pelvic radiotherapy
Poir
in
Pelvic Radiation Disease Association
10 months ago
I didn’t know if I’d be able to come back…..
Hello It’s been months since I posted to all the lovely supportive people here. I’m very sorry but I couldn’t face it as I had an injury, which a physio said meant that I might not be able to run again. I was devastated. But the amazing news is after nearly 4 months of not running I started very slowly
Hello It’s been months since I posted to all the lovely supportive people here. I’m very sorry but I couldn’t face it as I had an injury, which a physio said meant that I might not be able to run again. I was devastated. But the amazing news is after nearly 4 months of not running I started very slowly
LindySearle
Graduate10
in
Bridge to 10K
10 months ago
Tylenol
i seem to be suffering from
chronic
lower back/hip
pain
(four months now) . My question is…..is it okay to take Tyelenol as long as you follow the recommended dosage?
i seem to be suffering from
chronic
lower back/hip
pain
(four months now) . My question is…..is it okay to take Tyelenol as long as you follow the recommended dosage?
Gaspereaux
in
PBC Foundation
10 months ago
Back and hips - is this a Flare??
Hi wonderful people, When I first had PMR and at each previous flare, the pain has been across my shoulders and down the backs of my legs. I am currently feeling it badly in my lower back and pelvic girdle and am not sure if it is a flare or summat else. I am somewhat stressed and know that this
Hi wonderful people, When I first had PMR and at each previous flare, the pain has been across my shoulders and down the backs of my legs. I am currently feeling it badly in my lower back and pelvic girdle and am not sure if it is a flare or summat else. I am somewhat stressed and know that this
MDT1
in
PMRGCAuk
10 months ago
Edinburgh Endo Clinic
Hello! Just wondering if anyone has been on a loooong waiting list to be seen by an Endo specialist for the first time since diagnosis? Currently, it's an 80-week waiting time in Edinburgh. I know there is an option to go privately but I am just totally shocked that someone has to suffer from pain etc
Hello! Just wondering if anyone has been on a loooong waiting list to be seen by an Endo specialist for the first time since diagnosis? Currently, it's an 80-week waiting time in Edinburgh. I know there is an option to go privately but I am just totally shocked that someone has to suffer from pain etc
Axolotl23
in
Endometriosis UK
10 months ago
Migrane World Summit
I watched: Why sleep problems plague kids and adults Brain retraining for
Chronic
Pain
After a big heated debate my son eventually watched the first video, wish me luck for the others. I am not sure if re-watching them counts until you tick "watched" we will see.
I watched: Why sleep problems plague kids and adults Brain retraining for
Chronic
Pain
After a big heated debate my son eventually watched the first video, wish me luck for the others. I am not sure if re-watching them counts until you tick "watched" we will see.
Lady4
in
Functional Neurological Disorder - FND Hope
1 year ago
What does having a NEW KIDNEY feel like?
Hi All, I have been in the transplant list for a year now and still waiting to get called. I can’t just help to wonder what having a kidney transplant will feel like. Apart from the fact that it will be a gift of life and freedom from being tied down to dialysis. What does it feel like? Will you
Hi All, I have been in the transplant list for a year now and still waiting to get called. I can’t just help to wonder what having a kidney transplant will feel like. Apart from the fact that it will be a gift of life and freedom from being tied down to dialysis. What does it feel like? Will you
Imaanforever
in
Kidney Dialysis
10 months ago
Pain in the spleen/splenomegaly
Hello, maybe someone has an idea. After 5 years w&w my spleen has now enlarged (splenomegaly). I've also been having pain on my left side for a few days now. Are there any natural or herbal ways I can support my spleen? Because I don't want to have a spleen removed. I don't take any other medicine,
Hello, maybe someone has an idea. After 5 years w&w my spleen has now enlarged (splenomegaly). I've also been having pain on my left side for a few days now. Are there any natural or herbal ways I can support my spleen? Because I don't want to have a spleen removed. I don't take any other medicine,
Omaschnabel
in
CLL Support
1 year ago
I make trying to suppress EBV a leg of my supplement strategy.
I replied to a comment with this comment, then decided to share it as a post also:
As somebody who has been exposed to EBV (mono), I make trying to suppress EBV a leg of my supplement strategy. I need to write up everything I think helps with EBV, but here is a short list: -
Lactobacillus
I replied to a comment with this comment, then decided to share it as a post also:
As somebody who has been exposed to EBV (mono), I make trying to suppress EBV a leg of my supplement strategy. I need to write up everything I think helps with EBV, but here is a short list: -
Lactobacillus
Bolt_Upright
in
Cure Parkinson's
8 months ago
Mutation Levels
I have seen other discussions re bad mutations , on my regular letter to my doctor from my haematologist it states : Chronic Lymphocytic Leukemia associated with high risk variants including loss of the LEU and ATM genes. As per my normal blood results, do these have a high and low level and if so
I have seen other discussions re bad mutations , on my regular letter to my doctor from my haematologist it states : Chronic Lymphocytic Leukemia associated with high risk variants including loss of the LEU and ATM genes. As per my normal blood results, do these have a high and low level and if so
uide3095
in
CLL Support
1 year ago
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