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Petrified !!!!
Hello , I am 52 yrs old and this will be my first colonoscopy . For about a year I have has haemorrhoids on and off very itchy and sore bottom that goes with it. Felt the lump/s when I have had the attacks. No lumps present now. Have had some constipation lately and have seen a little blood when
Hello , I am 52 yrs old and this will be my first colonoscopy . For about a year I have has haemorrhoids on and off very itchy and sore bottom that goes with it. Felt the lump/s when I have had the attacks. No lumps present now. Have had some constipation lately and have seen a little blood when
Hidden
in
IBS Network
1 year ago
Second opinion required
Had a lot of dental work done last year and kind of still going through recovery. I had two extracts, three temp bridges one perm bridge that was fitted in July, four composite fillings, cap then ended up with a root filling through the cap. My bridge is so uncomfortable still unable to eat properly
Had a lot of dental work done last year and kind of still going through recovery. I had two extracts, three temp bridges one perm bridge that was fitted in July, four composite fillings, cap then ended up with a root filling through the cap. My bridge is so uncomfortable still unable to eat properly
janetmtt
in
Dentistry Health Support
5 months ago
trying to get a diagnoses
Hello, I was wondering if anyone can offer any advice or support. For years now Iv been having body pains being exhausted to the point I would fall asleep sat up. Not being able to do normal day to day things some days. . I got diagnosed with vit d deficiency I’m on tablets everyday for this for
Hello, I was wondering if anyone can offer any advice or support. For years now Iv been having body pains being exhausted to the point I would fall asleep sat up. Not being able to do normal day to day things some days. . I got diagnosed with vit d deficiency I’m on tablets everyday for this for
Rubydax
in
LUPUS UK
4 days ago
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Potential Lupus diagnosis
Hello, I have just joined this site and would be very grateful for any advice given. Sorry this might be a bit long winded🤪 So… my ethnicity is of Asian origin and ever since I can remember I don’t think a day has gone by where I don’t suffer from joint aches , muscle pain body stiffness and chronic
Hello, I have just joined this site and would be very grateful for any advice given. Sorry this might be a bit long winded🤪 So… my ethnicity is of Asian origin and ever since I can remember I don’t think a day has gone by where I don’t suffer from joint aches , muscle pain body stiffness and chronic
Perfumeflower57
in
LUPUS UK
7 days ago
just diagnosed with lupus
hi I’ve just been diagnosed with lupus via positive ANA test ! Only symptoms are the sun burning my neck and chest and my glands swell !! No medication given at the moment as I don’t have any other symptoms? Is there medication for this sun allergy ??? Thank you for any help !!!
hi I’ve just been diagnosed with lupus via positive ANA test ! Only symptoms are the sun burning my neck and chest and my glands swell !! No medication given at the moment as I don’t have any other symptoms? Is there medication for this sun allergy ??? Thank you for any help !!!
Edm174
in
LUPUS UK
10 days ago
I am lost, should I seek a second opinion?
hi, this will be a bit of a long one sorry. I am really confused and don’t know whether to accept my gps answer or go private for a second opinion. My issues started more noticeably in October last year when I started heavily bleeding and having long periods and very short periods of time of not bleeding
hi, this will be a bit of a long one sorry. I am really confused and don’t know whether to accept my gps answer or go private for a second opinion. My issues started more noticeably in October last year when I started heavily bleeding and having long periods and very short periods of time of not bleeding
Han99m
in
Thyroid UK
16 days ago
Don't know where to start
After 4 years I still don't really know what I have.Initially diagnosed with Undifferentiated Inflammatory Arthritis, then discovered by accident that it had changed to Connective Tissue Disease and Lupus. I also discovered only yesterday that at some point I tested positive for ANA which I've never
After 4 years I still don't really know what I have.Initially diagnosed with Undifferentiated Inflammatory Arthritis, then discovered by accident that it had changed to Connective Tissue Disease and Lupus. I also discovered only yesterday that at some point I tested positive for ANA which I've never
Brychni
in
LUPUS UK
19 days ago
I’ll health retirement
Hi All I posted on here a couple of months back about I’ll health retirement with the NHS pension I got a letter back today saying I don’t qualify for tier one or two reason being there is still ongoing issues not resolved I was diagnosed with Fibro in 2022 and mainly bedbound most days I was
Hi All I posted on here a couple of months back about I’ll health retirement with the NHS pension I got a letter back today saying I don’t qualify for tier one or two reason being there is still ongoing issues not resolved I was diagnosed with Fibro in 2022 and mainly bedbound most days I was
10x10
in
Fibromyalgia Action UK
20 days ago
Intrinsic factor
I seem to be at a sticking point with the findings of the intrinsic factor test. This is due to the way they now interpret the test results. My test result was Au/ml 1.63 ... Which I jumped with joy over as I thought "at last, this proves I have been telling the truth". How wrong I was. It is no longer
I seem to be at a sticking point with the findings of the intrinsic factor test. This is due to the way they now interpret the test results. My test result was Au/ml 1.63 ... Which I jumped with joy over as I thought "at last, this proves I have been telling the truth". How wrong I was. It is no longer
Allywales8663
in
Pernicious Anaemia Society
1 month ago
ANA test results
Hi, I’m reaching out in the hope someone is able to help me translate my ANA blood tests. I’ve had symptoms for over a year, predominantly fatigue/exhaustion, painful joints, mouth sores, feet that turn purple when cold (I also have a coeliac disease diagnosis from 2015). My results are back on
Hi, I’m reaching out in the hope someone is able to help me translate my ANA blood tests. I’ve had symptoms for over a year, predominantly fatigue/exhaustion, painful joints, mouth sores, feet that turn purple when cold (I also have a coeliac disease diagnosis from 2015). My results are back on
PurpleKoala24
in
LUPUS UK
1 month ago
unknown rash
hi everyone! Last week I posted pictures of my son’s face rash asking if it looked like cutaneous lupus. For those who are just reading now, he had this rash for about two months now— started on his ear which was raw red then went away. A few weeks later the rash developed bright red spots on his face
hi everyone! Last week I posted pictures of my son’s face rash asking if it looked like cutaneous lupus. For those who are just reading now, he had this rash for about two months now— started on his ear which was raw red then went away. A few weeks later the rash developed bright red spots on his face
Demaso33
in
LUPUS UK
2 months ago
Horrible food and mouth taste
I am trying to find out which tablet can spoil taste a food. Dose anyone have this problem on Prednisonal ?
I am trying to find out which tablet can spoil taste a food. Dose anyone have this problem on Prednisonal ?
Doublef
in
PMRGCAuk
6 months ago
unknown face rash
hi— My five-year-old son has had a rash on his face for over a month now. The rash initially started on his ear but resolved,, however the face stayed the same. We’ve taken him to his pediatrician emergency room and dermatologist and nobody knows what it is. Right after the spots started to appear he
hi— My five-year-old son has had a rash on his face for over a month now. The rash initially started on his ear but resolved,, however the face stayed the same. We’ve taken him to his pediatrician emergency room and dermatologist and nobody knows what it is. Right after the spots started to appear he
Demaso33
in
LUPUS UK
2 months ago
Oral Thrush
Hi Apert from intense oral hygiene, keto diet, no alcohol, using doctor prescribed oral mouth rinse for at least 10 days can anyone suggest anything that will work and get rid of this awful feeling in my mouth. . Was pre diabetic before steroids now awaiting next bloods so suspecting steroid induced
Hi Apert from intense oral hygiene, keto diet, no alcohol, using doctor prescribed oral mouth rinse for at least 10 days can anyone suggest anything that will work and get rid of this awful feeling in my mouth. . Was pre diabetic before steroids now awaiting next bloods so suspecting steroid induced
merle1010
in
PMRGCAuk
6 months ago
Help I don’t understand
So for the last 4 months I’ve been having pain in my muscles and head as well as tingling and a burning sensation. Also extreme fatigue and a red rash on my cheeks and trouble swallowing.My doctor gave me prednisone to treat because crp and esr were high. She also started me on plaquenil. Now before
So for the last 4 months I’ve been having pain in my muscles and head as well as tingling and a burning sensation. Also extreme fatigue and a red rash on my cheeks and trouble swallowing.My doctor gave me prednisone to treat because crp and esr were high. She also started me on plaquenil. Now before
Jadaboo4
in
LUPUS UK
3 months ago
Does anyone with LUPUS get reoccurring Shingles/ Herpes Zoster infections?
So I am waiting to be diagnosed with Lupus/ Mix Connective Tissue Disease. I have a lot of the symptoms for lupus like the face rash, other rashes on my body. Severing from fatigue, mouth ulcers really bad migraines. My body gets swollen and holds a lot of fluid. Joint pain as well as stomach issues.
So I am waiting to be diagnosed with Lupus/ Mix Connective Tissue Disease. I have a lot of the symptoms for lupus like the face rash, other rashes on my body. Severing from fatigue, mouth ulcers really bad migraines. My body gets swollen and holds a lot of fluid. Joint pain as well as stomach issues.
Severancered9
in
LUPUS UK
3 months ago
German tara
Hi everyone I've being getting a tube off biogenesis gel for dry mouth last night was the first dry mouth since afore xmas it was great I woke up at 2 my mouth completely dry no moisture at all in mouth tongue could off used it for sanding that rough had some water but still abit dry but
Hi everyone I've being getting a tube off biogenesis gel for dry mouth last night was the first dry mouth since afore xmas it was great I woke up at 2 my mouth completely dry no moisture at all in mouth tongue could off used it for sanding that rough had some water but still abit dry but
Germantara
in
Lung Conditions Community Forum
6 months ago
Need Help With Results From Blood Test
Hello everyone, I recently started having burning sensations, tingling and pain in my head, leg, feet and arms, also brain fog, dry mouth, and muscle pain in chest with extreme fatigue. Also had a red rash under both of my eyes.My GP ordered blood work and my platelets were high, iron low, protein and
Hello everyone, I recently started having burning sensations, tingling and pain in my head, leg, feet and arms, also brain fog, dry mouth, and muscle pain in chest with extreme fatigue. Also had a red rash under both of my eyes.My GP ordered blood work and my platelets were high, iron low, protein and
Jadaboo4
in
LUPUS UK
3 months ago
Enterosgel
Hi I’ve been suffering from haemorrhoids for a few months. It’s been getting better very gradually by eating a very high fibre diet to keep my stool very soft. But this has had the side effect of causing urgency several times a day. It’s making it very difficult to leave the house. I’ve had ibs for
Hi I’ve been suffering from haemorrhoids for a few months. It’s been getting better very gradually by eating a very high fibre diet to keep my stool very soft. But this has had the side effect of causing urgency several times a day. It’s making it very difficult to leave the house. I’ve had ibs for
MurphysSoulMate
in
IBS Network
6 months ago
Adenomyosis, Endometriosis and Autoimmune diseases
Hi ladies, this question is just out of curiosity because I see several posts about a lot of us having a combination of Endometriosis/ Adenomyosis and autoimmune disease. Following all my symptoms (that got even worse since I have no therapy but only medication to ease the pain) now I got a possible
Hi ladies, this question is just out of curiosity because I see several posts about a lot of us having a combination of Endometriosis/ Adenomyosis and autoimmune disease. Following all my symptoms (that got even worse since I have no therapy but only medication to ease the pain) now I got a possible
Taikaei
in
Endometriosis UK
3 months ago
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