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Suspected ulcerative colitis and nausea
Hi all hope all is wellI have been suffering with suspected ulcerative colitis for a while now and have lately started to feel nauseous and not wanting to eat much especially in the morning. I go dizzy alot too and have daily urgency to pass BM every morning most times quite soft with blood. I eat only
Hi all hope all is wellI have been suffering with suspected ulcerative colitis for a while now and have lately started to feel nauseous and not wanting to eat much especially in the morning. I go dizzy alot too and have daily urgency to pass BM every morning most times quite soft with blood. I eat only
Sooty712
in
Crohn's and Colitis Support
3 months ago
How much loading to do in resistance training if one has osteoporosis?
So dad has bone mets and dexa showed osteoporosis in some places like femur and osteopenia in some places. Hips are OK. Attaching the report. How does one decide how much resistance training is OK ? Can the resistance training be risky in contributing to fractures ? I know resistance training
So dad has bone mets and dexa showed osteoporosis in some places like femur and osteopenia in some places. Hips are OK. Attaching the report. How does one decide how much resistance training is OK ? Can the resistance training be risky in contributing to fractures ? I know resistance training
Tinkudi
in
Advanced Prostate Cancer
3 months ago
PV and AMD?
I've had PV since 2015 and have been on Jakafi for 18 months. I've recently been diagnosed with age-related macular degeneration and have been treated with intravitreous avastin. I've seen some papers suggesting that AMD is more common for people with MPNs. Has anyone else had this experience? Steve
I've had PV since 2015 and have been on Jakafi for 18 months. I've recently been diagnosed with age-related macular degeneration and have been treated with intravitreous avastin. I've seen some papers suggesting that AMD is more common for people with MPNs. Has anyone else had this experience? Steve
sbs_patient
in
MPN Voice
9 months ago
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angular cheilitis
I’ve suffer a lot from this I get it around 3/4 times a year but usually lasts about a week. I’m on my third week struggling with this and can’t find a lip balm or treatment. I heard Daktarin oral gel but it’s sold out everywhere and the pharmacy said they even finding it hard to get it in for people
I’ve suffer a lot from this I get it around 3/4 times a year but usually lasts about a week. I’m on my third week struggling with this and can’t find a lip balm or treatment. I heard Daktarin oral gel but it’s sold out everywhere and the pharmacy said they even finding it hard to get it in for people
Ladybitsandbobs
in
NRAS
9 months ago
Diagnosed today with an acoustic Neuroma.
Hi Everyone. I have just been told this morning that my MRI confirmed an acoustic neuroma. The ENT Doctor said he is now referring me to a specialist in Manchester. Can anyone tell me what to expect now ? Did anyone have any treatment for it ? Thank you.
Hi Everyone. I have just been told this morning that my MRI confirmed an acoustic neuroma. The ENT Doctor said he is now referring me to a specialist in Manchester. Can anyone tell me what to expect now ? Did anyone have any treatment for it ? Thank you.
Reddington__
in
Acoustic Neuroma Support
9 months ago
PIC - Punctate Inner Choroidopathy
Hi. I have just received a diagnosis for the above condition. I understand it’s extremely rare and would like to hear about other people’s experiences. I’m literally just on the journey and have had the first of 3 ‘rescue’ injections to prevent further sight loss. Would be good to connect with others
Hi. I have just received a diagnosis for the above condition. I understand it’s extremely rare and would like to hear about other people’s experiences. I’m literally just on the journey and have had the first of 3 ‘rescue’ injections to prevent further sight loss. Would be good to connect with others
Rome2023
in
Macular Society
9 months ago
small eyey
I don’t look like my eyes are normal size but the consultant says they are small, not deep and short ??? Says cataract op would be difficult when the time comes . Says further laser surgery not possible. has anyone else been told this ? I worries me for the future
I don’t look like my eyes are normal size but the consultant says they are small, not deep and short ??? Says cataract op would be difficult when the time comes . Says further laser surgery not possible. has anyone else been told this ? I worries me for the future
Sufitzy
in
Glaucoma UK
9 months ago
left atrial appendage occlusion interesting paper
there a differences of views on left atrial appendage closure primarily due to the purpose of the left appendage not being known. This is an interesting research paper bringing together all the studies - study looks at LAA closure alone and not with a mini maze or catheter ablation specifically
there a differences of views on left atrial appendage closure primarily due to the purpose of the left appendage not being known. This is an interesting research paper bringing together all the studies - study looks at LAA closure alone and not with a mini maze or catheter ablation specifically
MummyLuv
in
AF Association
1 year ago
Angular Cheilitis?
Just wondering if anyone suffers from Angular Cheilitis with their RA keep getting it and mentioning to the GP but he just ignored it. I've had my B12 checked and it was ok. I've read sulfasalazine can cause it. I'm also on Benepali jab once a week. Ive also read it could be folate levels but I think
Just wondering if anyone suffers from Angular Cheilitis with their RA keep getting it and mentioning to the GP but he just ignored it. I've had my B12 checked and it was ok. I've read sulfasalazine can cause it. I'm also on Benepali jab once a week. Ive also read it could be folate levels but I think
Haz58
in
NRAS
7 months ago
2.5 year old, suddenly bedwetting
Hi all, my 2.5 year old has been night potty trained for 5 months with max 2 or 3 wee accidents in that time, but suddenly started bedwetting practically every night for a Week.She has always struggled with infrequent poos, likely caused by withholding. My gp agrees the bedwetting is likely due to impacted
Hi all, my 2.5 year old has been night potty trained for 5 months with max 2 or 3 wee accidents in that time, but suddenly started bedwetting practically every night for a Week.She has always struggled with infrequent poos, likely caused by withholding. My gp agrees the bedwetting is likely due to impacted
Blando
in
ERIC
9 months ago
Further update Gallbladder removal
So I am home after a long day. Had to get up at 5am to be at hospital by 7am. All the usual preps and questions then operation took place at 10am. Because I have an LBBB (No underlying heart issues) They were extra careful with monitoring so had an extra canula thingy in my inner wrist to monitor heart
So I am home after a long day. Had to get up at 5am to be at hospital by 7am. All the usual preps and questions then operation took place at 10am. Because I have an LBBB (No underlying heart issues) They were extra careful with monitoring so had an extra canula thingy in my inner wrist to monitor heart
Manderson27
in
British Liver Trust
9 months ago
Neutrophils
Hi everyone new here. I've just got my bloods back from gp and I have low white cell count (neutrophils) this leaves me open to infection as I'm sure your all aware that is a side effect of Roactemra. The consultant has now stopped my injection for 1 week and then repeat bloods in 4 weeks. My question
Hi everyone new here. I've just got my bloods back from gp and I have low white cell count (neutrophils) this leaves me open to infection as I'm sure your all aware that is a side effect of Roactemra. The consultant has now stopped my injection for 1 week and then repeat bloods in 4 weeks. My question
Headpain24
in
PMRGCAuk
3 months ago
IBS or something more?
Hi, this is my first post on here, and I'm just wondering if anyone can calm my anxiety and mind...For the past 4 years, I've had what I can only call unusual symptoms...bloating, passing a lot of blood from my back passage (clots included and the amount I'd pass during a heavy period), a lot of mucus
Hi, this is my first post on here, and I'm just wondering if anyone can calm my anxiety and mind...For the past 4 years, I've had what I can only call unusual symptoms...bloating, passing a lot of blood from my back passage (clots included and the amount I'd pass during a heavy period), a lot of mucus
SES05
in
IBS Network
3 months ago
Fostair - lactose-free?
I just had a telephone consult with my respiratory consultant. As the steroid in my Seretide inhaler is thought likely to be the cause of my recently diagnosed adrenal insufficiency, he proposes to switch me from Seretide to Fostair as the steroid in that is less potent. I am seeing conflicting information
I just had a telephone consult with my respiratory consultant. As the steroid in my Seretide inhaler is thought likely to be the cause of my recently diagnosed adrenal insufficiency, he proposes to switch me from Seretide to Fostair as the steroid in that is less potent. I am seeing conflicting information
JumpJiving
in
Asthma Community Forum
9 months ago
radiation treatments led to perforated colon?
St. Patrick’s Day I collapsed in pain and was rushed to ER. A CT ABD PE revealed a perforated colon near my rectum, broad internal infection (sepsis) with kidneys and liver shutting down. A life flight, three surgeries later, 3 weeks sedated and immobile in an ICU, and seven weeks in hospital rehabs
St. Patrick’s Day I collapsed in pain and was rushed to ER. A CT ABD PE revealed a perforated colon near my rectum, broad internal infection (sepsis) with kidneys and liver shutting down. A life flight, three surgeries later, 3 weeks sedated and immobile in an ICU, and seven weeks in hospital rehabs
kreg001
in
Advanced Prostate Cancer
3 months ago
Hashi symptoms still or tired/dry eyes?
Hey everyone, Still on my journey to "optimal" health and lab's whilst having Hashimoto's. Diagnosed 18 month ago. I have a strange one for you, or, not so strange, right now I'm not sure. So, currently on 162.5mcg of Levo and 10 mcg of Lio. I would say symptom wise I am feeling the best I have in
Hey everyone, Still on my journey to "optimal" health and lab's whilst having Hashimoto's. Diagnosed 18 month ago. I have a strange one for you, or, not so strange, right now I'm not sure. So, currently on 162.5mcg of Levo and 10 mcg of Lio. I would say symptom wise I am feeling the best I have in
dexterholland91
in
Thyroid UK
9 months ago
Bowel changes and pain. Positive faecal calprotectin, negative CT
Hello! I've had longstanding pelvic and back pain for some years now (gynaecology have been no help at all unfortunately) but since last October, my bowels have been affected (pain before and after going to the toilet, and alternating loose stools and constipation. I'm thinking there must be swelling
Hello! I've had longstanding pelvic and back pain for some years now (gynaecology have been no help at all unfortunately) but since last October, my bowels have been affected (pain before and after going to the toilet, and alternating loose stools and constipation. I'm thinking there must be swelling
Jennyjenjen01
in
Crohn's and Colitis Support
3 months ago
Mebeverine
Has anyone else found that their symptoms of IBS increase after taking mebervive. I was prescribed it, and when I have taken it my stomach flares up, I get major bloating and really sharp stomach pains? Has anyone else had this or is it just me?
Has anyone else found that their symptoms of IBS increase after taking mebervive. I was prescribed it, and when I have taken it my stomach flares up, I get major bloating and really sharp stomach pains? Has anyone else had this or is it just me?
Loveheartsx
in
IBS Network
3 months ago
IBS struggle
Hi. I've been struggling with IBS for a few years now. I am also allergic to dairy products. I try and have a healthy diet but it is very difficult. I eat low FODMAP dinners most days and have low FODMAP lunches when I'm at work. I take biomel powder in my banana and peanut butter smoothie twice a day
Hi. I've been struggling with IBS for a few years now. I am also allergic to dairy products. I try and have a healthy diet but it is very difficult. I eat low FODMAP dinners most days and have low FODMAP lunches when I'm at work. I take biomel powder in my banana and peanut butter smoothie twice a day
JadeDrane
in
IBS Network
3 months ago
The difference between ET and JAK2 ET…?
I’m a little confused about these two. My SIL doesn’t have the JAK2 tho I do have it. I don’t understand the differences between the two diagnoses 😊 I am 60 and my SIL is 42. She is on drugs as well for Ulcerative Colitis. They are anti rejection drugs. She was diagnosed with ET a year or 2 ago
I’m a little confused about these two. My SIL doesn’t have the JAK2 tho I do have it. I don’t understand the differences between the two diagnoses 😊 I am 60 and my SIL is 42. She is on drugs as well for Ulcerative Colitis. They are anti rejection drugs. She was diagnosed with ET a year or 2 ago
Pachena
in
MPN Voice
1 year ago
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