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Experiences with
Livedo reticularis
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Covid vaccination brand
My concern is the Pfizer Covid vaccination because it gives me a leg rash -
Livedo
reticularis
, which worsens each time and never goes away it is not itchy but results in a very dry skin. Does anyone know if there is a different brand available? I had no problems with AZ?
My concern is the Pfizer Covid vaccination because it gives me a leg rash -
Livedo
reticularis
, which worsens each time and never goes away it is not itchy but results in a very dry skin. Does anyone know if there is a different brand available? I had no problems with AZ?
Rosie7may
in
Vasculitis UK
6 months ago
I’m scared
Weirdly I also developed onset
livedo
reticularis
. Anyway, my GP has mentioned if this continues I need to be referred to a specialist. But im just looking for some reassurance haha
Weirdly I also developed onset
livedo
reticularis
. Anyway, my GP has mentioned if this continues I need to be referred to a specialist. But im just looking for some reassurance haha
beetamer
in
MPN Voice
4 months ago
kali9
Symptoms I experience daily:
livedo
reticularis
, pain in my shoulders, ribcage, back muscles, breast bone, hands, knees, feet. I get swelling in the ball of the foot; my whole right foot is painful while on the left foot I get pain and sweeling on the ball of the foot and heel pain.
Symptoms I experience daily:
livedo
reticularis
, pain in my shoulders, ribcage, back muscles, breast bone, hands, knees, feet. I get swelling in the ball of the foot; my whole right foot is painful while on the left foot I get pain and sweeling on the ball of the foot and heel pain.
kali9
in
LUPUS UK
4 months ago
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Set of symptoms - who can relate?
I had mild occasional
livedo
reticularis
on the upper body, legs and arms, and petechiae on the arms and upper body, headache attacks, increased thirst over months that did not react to drinking, extreme brain fog after eating (especially breakfast), and malaise after cognitive and physical efforts.
I had mild occasional
livedo
reticularis
on the upper body, legs and arms, and petechiae on the arms and upper body, headache attacks, increased thirst over months that did not react to drinking, extreme brain fog after eating (especially breakfast), and malaise after cognitive and physical efforts.
rik_
in
Hughes Syndrome APS Forum
2 months ago
I'm not going nuts!
I also have a
livedo
reticularis
rash on my thighs, which I've had since childhood. I was put on aspirin for my last pregnancy. I get a butterfly facial rash every now and then and awful headaches, for which I take herbal remedies.
I also have a
livedo
reticularis
rash on my thighs, which I've had since childhood. I was put on aspirin for my last pregnancy. I get a butterfly facial rash every now and then and awful headaches, for which I take herbal remedies.
RabbitMum_1965
in
LUPUS UK
11 months ago
Stopping Injections After 3 Loading Doses
Hi! I’m new here and learning so much from reading all of the posts here. I was diagnosed with low B12 levels earlier on this year, although my PA antibodies came back negative. I was put on injections, and was meant to have 6 over 2 weeks followed by 1 every 3 months, however my GP had to stop them
Hi! I’m new here and learning so much from reading all of the posts here. I was diagnosed with low B12 levels earlier on this year, although my PA antibodies came back negative. I was put on injections, and was meant to have 6 over 2 weeks followed by 1 every 3 months, however my GP had to stop them
Hidden
in
Pernicious Anaemia Society
1 hour ago
Progress?
Good morning, not really after any advice just some thoughts from you lovely people. Basically in Oct ‘23 I had a massive variceal bleed, 6l blood transfusion and a 9% survival rate, very jaundice, lost over 3 stone bringing me to just under 6 stone, progonsees liver failure, put on a transplant list
Good morning, not really after any advice just some thoughts from you lovely people. Basically in Oct ‘23 I had a massive variceal bleed, 6l blood transfusion and a 9% survival rate, very jaundice, lost over 3 stone bringing me to just under 6 stone, progonsees liver failure, put on a transplant list
Starlight79
in
British Liver Trust
10 hours ago
Wednesday Word
[u][i]
ALT - Alanine Transaminase
[/i][/u] This is a blood test performed as part of your routine liver panel test. It is released more so by the [u][i]
hepatocytes -(liver cells)
[/i][/u] so it's associated more with hepatitis rather than PBC. ALT can be elevated in both non responders
[u][i]
ALT - Alanine Transaminase
[/i][/u] This is a blood test performed as part of your routine liver panel test. It is released more so by the [u][i]
hepatocytes -(liver cells)
[/i][/u] so it's associated more with hepatitis rather than PBC. ALT can be elevated in both non responders
DonnaBoll
Administrator
in
PBC Foundation
1 day ago
F3 Fibrosis Regression
hi all First post and have to say, read a lot of posts and can only thank everyone who contributes and helps educate others about their own personal way forward. So here is my question. How long does it realistically take ( with doing everything possible ) to regress from F3 severe fibrosis to F2?
hi all First post and have to say, read a lot of posts and can only thank everyone who contributes and helps educate others about their own personal way forward. So here is my question. How long does it realistically take ( with doing everything possible ) to regress from F3 severe fibrosis to F2?
Smif56
in
British Liver Trust
1 day ago
Post Op
Done my liver resection on 14 March 2024 coz found tumour in it since 2023. Went through Y90 treatment to shrink the tumour. Doc removed the tumour via keyhole with a drainage wound. After the op, stayed in hospital for 7 days till I’m stable and independent enough to walk on my own so wouldn’t be
Done my liver resection on 14 March 2024 coz found tumour in it since 2023. Went through Y90 treatment to shrink the tumour. Doc removed the tumour via keyhole with a drainage wound. After the op, stayed in hospital for 7 days till I’m stable and independent enough to walk on my own so wouldn’t be
SunnyShoe
in
British Liver Trust
2 days ago
always question
Just this morning there was a post about questioning the legitimacy of a survey about itching - and receiving payment for completing it. Some of you reached out to The PBC Foundation (as did I) to just make sure it was 'for real'. I am just as hopeful that when any of you don't feel the care you receive
Just this morning there was a post about questioning the legitimacy of a survey about itching - and receiving payment for completing it. Some of you reached out to The PBC Foundation (as did I) to just make sure it was 'for real'. I am just as hopeful that when any of you don't feel the care you receive
DonnaBoll
Administrator
in
PBC Foundation
2 days ago
Nicotine patches vs gum.
if you’re not aware, I’ve been experimenting with the nicotine patch. I found that it’s too much. I wonder if that why the trial failed. I found a couple pieces of gum, 3-4 a day as needed better. I will soon be off meds. They never really worked that good anyway. Nicotine works just as good if not
if you’re not aware, I’ve been experimenting with the nicotine patch. I found that it’s too much. I wonder if that why the trial failed. I found a couple pieces of gum, 3-4 a day as needed better. I will soon be off meds. They never really worked that good anyway. Nicotine works just as good if not
38yroldmale
in
Cure Parkinson's
3 days ago
Is it just me?
Wondering if anyone else isn't sold on the concept of taking a sledgehammer to the immune system to treat RRMS. I am looking forward to these meds finishing clinical trials: * Vidofludimus calcium [It's both anti-EBV and neuroprotective effect] (Link: https://multiplesclerosisnewstoday.com
Wondering if anyone else isn't sold on the concept of taking a sledgehammer to the immune system to treat RRMS. I am looking forward to these meds finishing clinical trials: * Vidofludimus calcium [It's both anti-EBV and neuroprotective effect] (Link: https://multiplesclerosisnewstoday.com
By-Design-1000
in
My MSAA Community
3 days ago
b12 liver stores
Hi everyone, Just a quick question for those of us with PA. When we have b12 loading doses I have read this replenishes liver stores. Can anyone tell me does this b12 always successfully make it into the liver stores? I ask because my body does not reflect this. Loading doses did nothing to alleaviate
Hi everyone, Just a quick question for those of us with PA. When we have b12 loading doses I have read this replenishes liver stores. Can anyone tell me does this b12 always successfully make it into the liver stores? I ask because my body does not reflect this. Loading doses did nothing to alleaviate
brenanddave
in
Pernicious Anaemia Society
3 days ago
Ultrasound/Biopsy show cirrhosis, but fibroscan score is 7.4
I’m somewhat perplexed… since my diagnosis I’ve been told I have cirrhosis, because of my biopsy and ultrasound results. A recent fibroscan score was 7.4, which is fibrosis. Although some parts of the fibroscan were as high as 8. Can someone explain this? My dr. was very vague in his explanation. Thank
I’m somewhat perplexed… since my diagnosis I’ve been told I have cirrhosis, because of my biopsy and ultrasound results. A recent fibroscan score was 7.4, which is fibrosis. Although some parts of the fibroscan were as high as 8. Can someone explain this? My dr. was very vague in his explanation. Thank
Danteskid
in
PBC Foundation
4 days ago
Update
Just thought I would update my situation after being diagnosed with Nash in 2019. After changing my diet and losing 20 kilos I have been told by my surgeon who recently performed an operation to repair a large hiatus hernia that I do not have Nash. My liver has returned to its normal size and it's a
Just thought I would update my situation after being diagnosed with Nash in 2019. After changing my diet and losing 20 kilos I have been told by my surgeon who recently performed an operation to repair a large hiatus hernia that I do not have Nash. My liver has returned to its normal size and it's a
Mizcole
in
Living with Fatty Liver and NASH
4 days ago
1st year
Just a little post on good news . Im just about to go out and have lunch with all my family to celebrate my 1st year of Liver Transplant 🎉🎉🥳🥳💕💕. I hope everyone else has a great day 💕💕. Stay safe all Dogbot 🐶Dave
Just a little post on good news . Im just about to go out and have lunch with all my family to celebrate my 1st year of Liver Transplant 🎉🎉🥳🥳💕💕. I hope everyone else has a great day 💕💕. Stay safe all Dogbot 🐶Dave
Dogbot
in
British Liver Trust
5 days ago
AASLD organization
www.aasld.org This is the site for the [u][i]
American
[/i][/u] Association for the Study of Liver Diseases. They make the AASLD Guidelines for the Diagnosis and Treatment of PBC. Every one should take the time to read this. Take a copy of it to your doctor as well. They should be familiar
www.aasld.org This is the site for the [u][i]
American
[/i][/u] Association for the Study of Liver Diseases. They make the AASLD Guidelines for the Diagnosis and Treatment of PBC. Every one should take the time to read this. Take a copy of it to your doctor as well. They should be familiar
DonnaBoll
Administrator
in
PBC Foundation
6 days ago
Coping
My story starting in 2020,light headed,weight loss,in and out if the toilet.When i eventually went to the hospital was tokd Cirrhosis,been in and out since,they never explained diet so i have had a couple of burst blood vessels not nice. Now i am aware this us my 1st week of rabbit food!! No booze for
My story starting in 2020,light headed,weight loss,in and out if the toilet.When i eventually went to the hospital was tokd Cirrhosis,been in and out since,they never explained diet so i have had a couple of burst blood vessels not nice. Now i am aware this us my 1st week of rabbit food!! No booze for
Rawai
in
British Liver Trust
6 days ago
Has methotrexate caused liver damage
I had a blood test which showed raised levels of ALP 136, Aspartate Transaminase 68. My GP said that my RA meds have caused damage to my liver!!! I am having a liver fibroscan tommorrow to check for fatty liver. Very anxious but will need to take it one step at a time. Any guidance and advice welcome
I had a blood test which showed raised levels of ALP 136, Aspartate Transaminase 68. My GP said that my RA meds have caused damage to my liver!!! I am having a liver fibroscan tommorrow to check for fatty liver. Very anxious but will need to take it one step at a time. Any guidance and advice welcome
Beanyynwa
in
NRAS
7 days ago
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