Search
Search
About
Log in
Join
Experiences with
Kidney diseases in childhood
Posts
Communities
61,067 public posts
Filter results
Addison's disease
Spoke with my GP yesterday regarding the extreme fatigue & rollercoaster of crashing following activity. He is now going to test & look at the possibility of Addison's. How does this mesh with PMR and Pred? I'd welcome any advice or better knowledge. Thanks.
Spoke with my GP yesterday regarding the extreme fatigue & rollercoaster of crashing following activity. He is now going to test & look at the possibility of Addison's. How does this mesh with PMR and Pred? I'd welcome any advice or better knowledge. Thanks.
Naim1
in
PMRGCAuk
28 days ago
Excess Folic Acid and Vitamin B12 Deficiency: Clinical Implications?
This is a very recent paper. Some of the areas covered are well-known. Such as not treating B12 deficiency with folic acid. But, in the more speculative parts, I think it does raise questions over the prescribing of high dose (e.g. 5 milligrams a day) of folic acid in those who are currently low in
This is a very recent paper. Some of the areas covered are well-known. Such as not treating B12 deficiency with folic acid. But, in the more speculative parts, I think it does raise questions over the prescribing of high dose (e.g. 5 milligrams a day) of folic acid in those who are currently low in
helvella
in
Pernicious Anaemia Society
28 days ago
Protein in my urine
Hi there! I am 6 months post kidney transplant. First I'd like to say that I was very blessed, I was approved and put on the list May 3, 2023 and I received my new kidney from a perfect match deceased donor June 13, 2023. My transplant team said that is very rare and very lucky. I have had some challenges
Hi there! I am 6 months post kidney transplant. First I'd like to say that I was very blessed, I was approved and put on the list May 3, 2023 and I received my new kidney from a perfect match deceased donor June 13, 2023. My transplant team said that is very rare and very lucky. I have had some challenges
SweetTexas75
in
Kidney Transplant
9 months ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
New diagnosis - what to expect/demand from GP
I had my second child in August 2022 and to be honest I've not felt right since. Since going back to work in June last year I've been permanently exhausted but it's just got worse and worse. Totally mental fog, can't focus, constantly yawning my head off. My body aches constantly but all the while I
I had my second child in August 2022 and to be honest I've not felt right since. Since going back to work in June last year I've been permanently exhausted but it's just got worse and worse. Totally mental fog, can't focus, constantly yawning my head off. My body aches constantly but all the while I
Whatdidyousay
in
Thyroid UK
1 month ago
Thyroid disease link with lupus and fibromyalgia
Hello I need to try to understand about my current situation I have underactive thyroid for which I’m prescribed levothyroxine But I have told my drs about feeling so wiped out so tired it hurts falling asleep during the day but not sleeping through the night I have been diagnosed with atrial
Hello I need to try to understand about my current situation I have underactive thyroid for which I’m prescribed levothyroxine But I have told my drs about feeling so wiped out so tired it hurts falling asleep during the day but not sleeping through the night I have been diagnosed with atrial
Dogsareangels
in
Thyroid UK
1 month ago
PMR/GCA and Sjogrens disease
Does anyone have Sjogren’s disease along with PMR/CGA? For months I’ve been struggling with worsening vision in my left eye, and trying to figure out if I was having a flare. The left eye vision is like it was before cataract surgery, worse some times than others, especially after reading. Opthomologist
Does anyone have Sjogren’s disease along with PMR/CGA? For months I’ve been struggling with worsening vision in my left eye, and trying to figure out if I was having a flare. The left eye vision is like it was before cataract surgery, worse some times than others, especially after reading. Opthomologist
Mstiles
in
PMRGCAuk
1 month ago
Gluten and B12 deficiency
Is there a link between B12 deficiency and gluten sensitivity? My neuropathy has massively improved since I started self injecting regularly but I’ve noticed it returns slightly after eating bread, pasta or other foods containing gluten. Alcohol has an effect too I think. Trying to put the pieces of
Is there a link between B12 deficiency and gluten sensitivity? My neuropathy has massively improved since I started self injecting regularly but I’ve noticed it returns slightly after eating bread, pasta or other foods containing gluten. Alcohol has an effect too I think. Trying to put the pieces of
Alilev
in
Pernicious Anaemia Society
1 month ago
Hello, any help welcome
Hi all,I've been told I have an underactive thyroid recently after feeling very tired and achy for a few months, and having a blood test. No treatment as yet, seems more tests are to follow. I've become much more tired, a bit weepy ( not like me at all😔). And, horror of horrors, I'm gaining weight
Hi all,I've been told I have an underactive thyroid recently after feeling very tired and achy for a few months, and having a blood test. No treatment as yet, seems more tests are to follow. I've become much more tired, a bit weepy ( not like me at all😔). And, horror of horrors, I'm gaining weight
cheeseandonioncrisps
in
Thyroid UK
1 month ago
Sarcoidosis
Hi I have Lupus and a few other auto diseases , just a quick question is Sarcoidosis any relation and do any of you have it , 💕
Hi I have Lupus and a few other auto diseases , just a quick question is Sarcoidosis any relation and do any of you have it , 💕
whatsit
in
LUPUS UK
1 month ago
who also has fibromyalgia and then lupus?
I was diagnosed with fibromyalgia in 2009 and then lupus last year. I think it was harder to get the diagnosis because a lot of syptoms overlap.
I was diagnosed with fibromyalgia in 2009 and then lupus last year. I think it was harder to get the diagnosis because a lot of syptoms overlap.
Cazpurple
in
LUPUS UK
1 month ago
New to the scene
Hello, I’ve just signed up after probably a year of avoiding doing so, really hoping to connect with some people who understand rheumatoid arthritis and how to navigate it alongside the health system 🦓🐘🦒
Hello, I’ve just signed up after probably a year of avoiding doing so, really hoping to connect with some people who understand rheumatoid arthritis and how to navigate it alongside the health system 🦓🐘🦒
LoveIslandFan
in
NRAS
1 month ago
Another amazing research 💪🏼
🧐Scientists discover a cause of lupus and a possible way to reverse it😯❗ I recommend listening to the podcast that appears in the article, which sums it up very well: https://news.northwestern.edu/stories/2024/july/lupus-immune-response-reversal/ Mxx 💜💚
🧐Scientists discover a cause of lupus and a possible way to reverse it😯❗ I recommend listening to the podcast that appears in the article, which sums it up very well: https://news.northwestern.edu/stories/2024/july/lupus-immune-response-reversal/ Mxx 💜💚
Naladog
in
LUPUS UK
1 month ago
Creating a Framework for Treating Autoimmune Gastritis—The Case for Replacing Lost Acid
A paper from Bruce Wolffenbuttel and colleagues, released last February https://www.mdpi.com/2072-6643/16/5/662 Conclusion: [i]"Autoimmune gastritis is not a gastritis that needs acid suppression; rather, it may benefit from acid supplementation. The loss of stomach acid in AIG precedes nutrient deficiencies
A paper from Bruce Wolffenbuttel and colleagues, released last February https://www.mdpi.com/2072-6643/16/5/662 Conclusion: [i]"Autoimmune gastritis is not a gastritis that needs acid suppression; rather, it may benefit from acid supplementation. The loss of stomach acid in AIG precedes nutrient deficiencies
Technoid
in
Pernicious Anaemia Society
1 month ago
🐺New Lupus Research: Mechanism of lupus pathogenesis unveiled🦋
📚👩🏼🔬Professor Yoontae Lee’s team identifies target protein regulating autoimmune disease lupus: https://www.postech.ac.kr/eng/mechanism-of-lupus-pathogenesis-unveiled/ Happy reading 🧐 Xxx
📚👩🏼🔬Professor Yoontae Lee’s team identifies target protein regulating autoimmune disease lupus: https://www.postech.ac.kr/eng/mechanism-of-lupus-pathogenesis-unveiled/ Happy reading 🧐 Xxx
Naladog
in
LUPUS UK
1 month ago
Transplant Question
I’ve been wondering for awhile if kidney transplants are given once a person is past a certain age? I’m in the U.S. and I have a cousin who had severe liver disease. She was 75 & the state she lived in didn’t perform liver transplants on anyone over 68. I checked with my state, & liver transplants
I’ve been wondering for awhile if kidney transplants are given once a person is past a certain age? I’m in the U.S. and I have a cousin who had severe liver disease. She was 75 & the state she lived in didn’t perform liver transplants on anyone over 68. I checked with my state, & liver transplants
Halebopp
in
Kidney Disease
9 months ago
What to expect, medication etc - First appointment since Systemic Sclerosis diagnosis
Hi, I hope you can advise. Since November 2023 I have had Raynaud's, then December Severe Dry Eyes and mouth, In May 2023 landed up with medication for Sicca Sjogren's (Cyclosporine & Pilocarpine). Blood test done at the appointment showed Systemic Sclerosis (anti TH/TO) as well. I was advised of this
Hi, I hope you can advise. Since November 2023 I have had Raynaud's, then December Severe Dry Eyes and mouth, In May 2023 landed up with medication for Sicca Sjogren's (Cyclosporine & Pilocarpine). Blood test done at the appointment showed Systemic Sclerosis (anti TH/TO) as well. I was advised of this
Jules1821
in
Scleroderma & Raynaud's UK (SRUK)
1 month 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
1 month ago
Cutaneous scleroderma ?with Lupus overlap?
Recently saw Rheumatologist for 1st time confident that I’d get Sjogren’s diagnosis but came away with more than I’d bargained for with Cutaneous scleroderma possibly with Lupus overlap to add to my ever growing list of autoimmune conditions.
Recently saw Rheumatologist for 1st time confident that I’d get Sjogren’s diagnosis but came away with more than I’d bargained for with Cutaneous scleroderma possibly with Lupus overlap to add to my ever growing list of autoimmune conditions.
DebatDG9
in
PBC Foundation
1 month ago
Covid
just tested positive for the first time .. do I need any extra medication these days via nhs due to lupus ?
just tested positive for the first time .. do I need any extra medication these days via nhs due to lupus ?
Dressgirl52
in
LUPUS UK
1 month ago
Underactive thyroid
Hi, I’ve had underactive thyroid for a few years now but have never really done much research into the condition, I just take my meds and crack on. I have noticed more recently struggling more with tiredness, feeling groggy and just not feeling great. I’ve had blood tests etc and all is good so I am
Hi, I’ve had underactive thyroid for a few years now but have never really done much research into the condition, I just take my meds and crack on. I have noticed more recently struggling more with tiredness, feeling groggy and just not feeling great. I’ve had blood tests etc and all is good so I am
Jeo05
in
Thyroid UK
1 month ago
1
...
19
20
21
...
100
Next page
10
20
30
40
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Fertility Network UK
13273 results
Thyroid UK
6027 results
British Liver Trust
4556 results
View top 10 communities
Sort by
Most Relevant
Newest