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I need help
Waiting on a laparoscopy but they can’t tell me how long the wait will be due to covid. I’m losing the will to live. The back ache, tummy ache, the burning sensation in my back, constipation, bloating and swelling. My lower abdomen is now hard to touch, I’m finding it hard to finish my meals. I take
Waiting on a laparoscopy but they can’t tell me how long the wait will be due to covid. I’m losing the will to live. The back ache, tummy ache, the burning sensation in my back, constipation, bloating and swelling. My lower abdomen is now hard to touch, I’m finding it hard to finish my meals. I take
saint_ellen
in
Endometriosis UK
3 years ago
IBS back pain and pain killers
When my. IBS has flares up it aggravates my back problems. I used to manage the back pain with pain killers and anti inflamatories. I think the latter are why IBS got bad. I am now in extreme pain and paracetamol is not doing mu h on its own. Codeine usually leads to constipation which also affects
When my. IBS has flares up it aggravates my back problems. I used to manage the back pain with pain killers and anti inflamatories. I think the latter are why IBS got bad. I am now in extreme pain and paracetamol is not doing mu h on its own. Codeine usually leads to constipation which also affects
Tomuch
in
IBS Network
3 years ago
Test results query.
Good morning all. So after trying Probiotics a while ago without any improvement, (thank you Nackapan!!) my partner ordered a hair sample test for me. It shows a Streptomyces and Thermophilus imbalance. Does this mean I should percivere with probiotics? Also. It shows low Vitamin A, low vitamin B1 and
Good morning all. So after trying Probiotics a while ago without any improvement, (thank you Nackapan!!) my partner ordered a hair sample test for me. It shows a Streptomyces and Thermophilus imbalance. Does this mean I should percivere with probiotics? Also. It shows low Vitamin A, low vitamin B1 and
Ritchie1268
in
Pernicious Anaemia Society
3 years ago
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What do you use to manage your pain?
Hello everyone, I come here looking for some help desperately. I had surgery booked to treat my endometriosis but after starting the surgery the surgeon ran into complications and couldn't actually treat me. I have been suffering for many years with pain on and off and it had always been put down to
Hello everyone, I come here looking for some help desperately. I had surgery booked to treat my endometriosis but after starting the surgery the surgeon ran into complications and couldn't actually treat me. I have been suffering for many years with pain on and off and it had always been put down to
Shels97
in
Endometriosis UK
3 years ago
I have had chest pain for 7 years..
Hi all It all started 7 years ago, I didn't do anything to cause it, atleast not from what I remember. I just had this chest at the centre of my chest going through to the tip of my left shoulder, like a spear going through my body. At 14 years of age I assumed the worse of course, but i went to the
Hi all It all started 7 years ago, I didn't do anything to cause it, atleast not from what I remember. I just had this chest at the centre of my chest going through to the tip of my left shoulder, like a spear going through my body. At 14 years of age I assumed the worse of course, but i went to the
David89898
in
Pain Concern
3 years ago
Prescribed medication Nd RLS
Does anyone know which sleeping tablets and pain killers make RLS worse? After fairly major surgery I was given sleeping tablets in the hospital and was up all night walking around with terrible RLS. I was prescribed amitriptyline to take home and it definitely aggravated the RLS.
Does anyone know which sleeping tablets and pain killers make RLS worse? After fairly major surgery I was given sleeping tablets in the hospital and was up all night walking around with terrible RLS. I was prescribed amitriptyline to take home and it definitely aggravated the RLS.
Stelladevico
in
Restless Legs Syndrome
3 years ago
Newbie - need some help!
Hi all, I guess I'm just looking for someone to tell me I'm not going mad... I have booked a doctor's appointment, the first one to pursue a possible endo diagnosis, but I'm panicking that I'll just get told to get on with it or put on the pill etc. I have been struggling with increasingly worse periods
Hi all, I guess I'm just looking for someone to tell me I'm not going mad... I have booked a doctor's appointment, the first one to pursue a possible endo diagnosis, but I'm panicking that I'll just get told to get on with it or put on the pill etc. I have been struggling with increasingly worse periods
effie_97
in
Endometriosis UK
3 years ago
Pain & swelling control
Hi folks finally started methotraxte 26/07/21. There were times when I screamed and broke down crying with the pain, sure other people had a similar experience, not helped by the hospital losing my test results and having to undergo the X rays again, which took some time to organise. Still get pain
Hi folks finally started methotraxte 26/07/21. There were times when I screamed and broke down crying with the pain, sure other people had a similar experience, not helped by the hospital losing my test results and having to undergo the X rays again, which took some time to organise. Still get pain
Ritaritis
in
NRAS
3 years ago
Help with pain
Hey .. I'm new on here.. I suffer with pain daily.. this really affects me & my mood.. it's tiring & debilitating.. I take pain killers but they don't really help alot.. So what I want to know is.. how do you cope with being constantly in pain? Does it hold you back like it does me? Even something
Hey .. I'm new on here.. I suffer with pain daily.. this really affects me & my mood.. it's tiring & debilitating.. I take pain killers but they don't really help alot.. So what I want to know is.. how do you cope with being constantly in pain? Does it hold you back like it does me? Even something
Mummabear123
in
Endometriosis UK
3 years ago
Lyrica for pain
I have taken Lyrica for pain for about 5 years. I take only 100mg 2x a day. While it's not perfect, it does take the edge off the pain. Especially sitting long periods, which now I don't have a choice really anymore. I'm progressive MS in a power wheelchair about 98% of the time. I do walk a bit each
I have taken Lyrica for pain for about 5 years. I take only 100mg 2x a day. While it's not perfect, it does take the edge off the pain. Especially sitting long periods, which now I don't have a choice really anymore. I'm progressive MS in a power wheelchair about 98% of the time. I do walk a bit each
palomino27
in
My MSAA Community
3 years ago
Update on oestrogen treatment for non absorption of liothyronine. A warning!
In November last year, I started seeing an endo privately for my hypo problems. He told me he was an expert. He was very definite that my hypo symptoms were due to me not absorbing liothyronine as I should. He was very definite that the cause of this was my having lost too much oestrogen when I went
In November last year, I started seeing an endo privately for my hypo problems. He told me he was an expert. He was very definite that my hypo symptoms were due to me not absorbing liothyronine as I should. He was very definite that the cause of this was my having lost too much oestrogen when I went
dizzy864
in
Thyroid UK
3 years ago
Should I have the laparoscopy?
I have had very irregular periods my whole life, a couple of occasions I’ve continued to bleed after my period should have finished or my period returned within a week. I get a lot of back pain and feels like I have a fork scratching away at my uterus especially in the weeks leading to my period. Sometimes
I have had very irregular periods my whole life, a couple of occasions I’ve continued to bleed after my period should have finished or my period returned within a week. I get a lot of back pain and feels like I have a fork scratching away at my uterus especially in the weeks leading to my period. Sometimes
Puddd
in
Endometriosis UK
3 years ago
Coping with dogs cancer diagnosis
Hi guys, I don't know if anyone out there can relate, give advice or just hear a girl out. My dog recently had biopsies of 2 lumps on his side and they were confirmed as mast cell tumors (the one lump i had checked over a year ago and was told it was a bite) He had them removed last Tuesday (5 lumps
Hi guys, I don't know if anyone out there can relate, give advice or just hear a girl out. My dog recently had biopsies of 2 lumps on his side and they were confirmed as mast cell tumors (the one lump i had checked over a year ago and was told it was a bite) He had them removed last Tuesday (5 lumps
Flossybubble
in
Anxiety and Depression Support
3 years ago
ET PAINS
does any body feel very pain in the body and severe headache squeeze pain vertigo? 6 months diagnosed still taking pain killers?
does any body feel very pain in the body and severe headache squeeze pain vertigo? 6 months diagnosed still taking pain killers?
shiela23
in
MPN Voice
3 years ago
Endo diet and sweet tooth what can you eat?
Hello I’ve posted about changing my diet to see if it helps obviously the last time I tried it I didn’t stick to it as I am trying again… Basically I had. Endo confirmed in 2015 via a lap The symptoms came back after my first child and then even worse symptoms after I had my second 2 years ago I went
Hello I’ve posted about changing my diet to see if it helps obviously the last time I tried it I didn’t stick to it as I am trying again… Basically I had. Endo confirmed in 2015 via a lap The symptoms came back after my first child and then even worse symptoms after I had my second 2 years ago I went
Prettythings1
in
Endometriosis UK
3 years ago
Let's talk about pain management
Chronic abdominal pain is a main symptom of chronic pancreatitis. While there is no cure, there are many different techniques that have helped patients deal with their pain. Here are five pain management strategies that have helped pancreatitis deal with their pain, based on expert recommendations:
Chronic abdominal pain is a main symptom of chronic pancreatitis. While there is no cure, there are many different techniques that have helped patients deal with their pain. Here are five pain management strategies that have helped pancreatitis deal with their pain, based on expert recommendations:
Sofia_MC
Partner
in
Chronic Pancreatitis Support
3 years ago
SLE & Covid
Swinging temp, tonsillitis, cough, plus lupus in overdrive: oral sores cover entire roof of mouth and palate, rash extra red and fiery, swelling /
facial
oedema on top form 😫 and I won’t mention the excruciating
pain
. Exhausted Love Green tomatoes
Swinging temp, tonsillitis, cough, plus lupus in overdrive: oral sores cover entire roof of mouth and palate, rash extra red and fiery, swelling /
facial
oedema on top form 😫 and I won’t mention the excruciating
pain
. Exhausted Love Green tomatoes
Greentomatoes
in
LUPUS UK
3 years ago
RLS COPING MECHANISMS
What I might do to calm my legs before bedtime: 1. Stretching 2. Messaging 3. Walking about 4. Drink a glass of water 5. Take a bath to relax 6. Make myself a cup of Pukka Nighttime Tea 7. DISTRACTION: Looking at old photo albums, play Bridge or Scrabble on phone, try on clothes, do my nails. 8.
What I might do to calm my legs before bedtime: 1. Stretching 2. Messaging 3. Walking about 4. Drink a glass of water 5. Take a bath to relax 6. Make myself a cup of Pukka Nighttime Tea 7. DISTRACTION: Looking at old photo albums, play Bridge or Scrabble on phone, try on clothes, do my nails. 8.
Felicity21
in
Restless Legs Syndrome
3 years ago
Sulfrazalazine and anti inflammatory tab mix?
Hi all, Does anyone know if you can take sulfrazalazine and ibuprofen or other anti inflammatory tabs celecoxib together or is it a no go? Partner has started sulfrazalazine a week ago and pain is getting to him a bit. He was able to take the anti inflammatories prior to starting Sulfra to help with
Hi all, Does anyone know if you can take sulfrazalazine and ibuprofen or other anti inflammatory tabs celecoxib together or is it a no go? Partner has started sulfrazalazine a week ago and pain is getting to him a bit. He was able to take the anti inflammatories prior to starting Sulfra to help with
Lgrattan03
in
NRAS
3 years ago
Priorities for achalasia research
One of the exercises we have been undertaking in Achalasia Action is trying to work out what research would gain most support from those with achalasia. After all, people with achalasia are the ones most affected! So this is a brief summary of our work so far, and we would value any comments, suggestions
One of the exercises we have been undertaking in Achalasia Action is trying to work out what research would gain most support from those with achalasia. After all, people with achalasia are the ones most affected! So this is a brief summary of our work so far, and we would value any comments, suggestions
Alan_M
Partner
in
Achalasia Action
3 years ago
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