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Scientists say they have identified a root cause of lupus — one that could pave the way for new treatments
Scientists say they have identified a root cause of lupus — one that could pave the way for new treatments An imbalance of T cells, which play a key role in the body’s immune response, could explain most cases of the disease, according to new research. By Aria Bendix A key mystery behind one of the
Scientists say they have identified a root cause of lupus — one that could pave the way for new treatments An imbalance of T cells, which play a key role in the body’s immune response, could explain most cases of the disease, according to new research. By Aria Bendix A key mystery behind one of the
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 month ago
Scientists say they have identified a root cause of lupus — one that could pave the way for new treatments
Scientists say they have identified a root cause of lupus — one that could pave the way for new treatments An imbalance of T cells, which play a key role in the body’s immune response, could explain most cases of the disease, according to new research. By Aria Bendix A key mystery behind one of the
Scientists say they have identified a root cause of lupus — one that could pave the way for new treatments An imbalance of T cells, which play a key role in the body’s immune response, could explain most cases of the disease, according to new research. By Aria Bendix A key mystery behind one of the
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
1 month ago
Selegiline - Noticeably improved symptoms
My new neurologist started me on Selegiline 10 mg/day. In two weeks I reduced my Sinemet from two pills per day to one. My tremor is much calmer and I feel more clear. So far no negative side effects and I take the first 5 mg on an empty stomach.
My new neurologist started me on Selegiline 10 mg/day. In two weeks I reduced my Sinemet from two pills per day to one. My tremor is much calmer and I feel more clear. So far no negative side effects and I take the first 5 mg on an empty stomach.
Armyman
in
Cure Parkinson's
6 months ago
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Fibroscan Result - False?
Good Morning Everyone, I have been diagnosed with early cirrhosis last summer (July 2023) and have a Child Pugh A and a meld of 9. I have done two Elastology ultrasounds - first in July was 11.8 kpa and the second Nov 1st was 9.0 kpa. My liver enzymes are all in line and came back in line within
Good Morning Everyone, I have been diagnosed with early cirrhosis last summer (July 2023) and have a Child Pugh A and a meld of 9. I have done two Elastology ultrasounds - first in July was 11.8 kpa and the second Nov 1st was 9.0 kpa. My liver enzymes are all in line and came back in line within
Confused2024
in
British Liver Trust
6 months ago
Arthritis
does any one have Giant Cell arthritis. I am very poorly at the moment. I’m having test for it. I’ve been to my local hospital a few days now I’ve got to have a brain scan and maxillofacial appointment. Thanks
does any one have Giant Cell arthritis. I am very poorly at the moment. I’m having test for it. I’ve been to my local hospital a few days now I’ve got to have a brain scan and maxillofacial appointment. Thanks
Breavheart
in
LUPUS UK
1 month ago
Autoimmune neurological B12 deficiency
I came across this fascinating study on an autoimmune condition that results in B12 deficiency selectively in the central nervous system. Cerebrospinal fluid B12 is essentially non-existent but serum levels are normal, making this very hard to detect! https://www.medrxiv.org/content/10.1101/2023.08.21.23294253v1
I came across this fascinating study on an autoimmune condition that results in B12 deficiency selectively in the central nervous system. Cerebrospinal fluid B12 is essentially non-existent but serum levels are normal, making this very hard to detect! https://www.medrxiv.org/content/10.1101/2023.08.21.23294253v1
etreas
in
Pernicious Anaemia Society
1 month ago
help with new test results
hi, could someone please help with these results.iv been on levothyroxine 75mg for about 4 years . Diagnosed in 2019 as underactive thyroid. Thyroid function test Serum TSH level 2.15 mu/L [0.35 - 4.94] Serum free T4 level 13.2 pmol/L [9.0 - 19.0] Thyroid Therapy Levothyroxine (T4) It has come
hi, could someone please help with these results.iv been on levothyroxine 75mg for about 4 years . Diagnosed in 2019 as underactive thyroid. Thyroid function test Serum TSH level 2.15 mu/L [0.35 - 4.94] Serum free T4 level 13.2 pmol/L [9.0 - 19.0] Thyroid Therapy Levothyroxine (T4) It has come
Norrahsjake
in
Thyroid UK
1 month ago
neuropathy source
hi all, Does anyone else on here have Sjögren’s as well as PA? I am experiencing constant tingling and occasional burning/numbness in my fingers and toes. (specific fingers and toes, not all)….It got worse when I did a reloading series of dosages of B12. I’m curious - does neuropathy usually flow from
hi all, Does anyone else on here have Sjögren’s as well as PA? I am experiencing constant tingling and occasional burning/numbness in my fingers and toes. (specific fingers and toes, not all)….It got worse when I did a reloading series of dosages of B12. I’m curious - does neuropathy usually flow from
Lhood08
in
Pernicious Anaemia Society
1 month ago
Teesside Lupus Support group meetings
We are a group in the North East of England. We had a very welcoming and successful Event on Lupus and other associated chronic illnesses awareness on the 20th of July 2024. We are inviting any Lupies within our area who are looking for a place to go and meet and chat and do activities as well as share
We are a group in the North East of England. We had a very welcoming and successful Event on Lupus and other associated chronic illnesses awareness on the 20th of July 2024. We are inviting any Lupies within our area who are looking for a place to go and meet and chat and do activities as well as share
Pipido36
in
LUPUS UK
1 month ago
pernicious anemia diet
is there a certain diet that is recommended for pernicious anemia? I have been advised that even oats can be harmful? thanks
is there a certain diet that is recommended for pernicious anemia? I have been advised that even oats can be harmful? thanks
Damacian
in
Pernicious Anaemia Society
1 month ago
Do you stop Methotrexate whilst you have Covid?
Hi lovely people, I have Covid and am wondering if I should miss my Methotrexate out this week. I was given antivirals, but had to stop because of an allergic reaction after 24 hours. What have you done in the same position please? My Rheumatoid is well controlled at the moment.
Hi lovely people, I have Covid and am wondering if I should miss my Methotrexate out this week. I was given antivirals, but had to stop because of an allergic reaction after 24 hours. What have you done in the same position please? My Rheumatoid is well controlled at the moment.
Lotttie4
in
NRAS
1 month ago
Underactive thyroid
I Was diagnosed with under active thyroid 10 years ago age 50, I have struggled with tiredness my go will not change the 50mg dose of levothyroxine. I have just had it re tested and tsh level is 0.97 I am also anemic come back in the same blood tests so starting iron. Any thoughts please
I Was diagnosed with under active thyroid 10 years ago age 50, I have struggled with tiredness my go will not change the 50mg dose of levothyroxine. I have just had it re tested and tsh level is 0.97 I am also anemic come back in the same blood tests so starting iron. Any thoughts please
JUNEO
in
Thyroid UK
1 month ago
Taste alteration
Hi, Has anyone experienced loss of taste after transplant? My partner says everything tastes absolutely horrendous. Will this come back?!
Hi, Has anyone experienced loss of taste after transplant? My partner says everything tastes absolutely horrendous. Will this come back?!
Gemmax
in
British Liver Trust
6 months ago
Creatine and Whey protein
I was diagnosed with Parkinson's in July 2020. In the last year I have lost weight by around 3.5 kg I went to a nutritionist because of the weight loss and, in particular, the loss of muscle mass.In addition to a diet and the recommendation to continue going to the gym twice a week for bodybuilding,
I was diagnosed with Parkinson's in July 2020. In the last year I have lost weight by around 3.5 kg I went to a nutritionist because of the weight loss and, in particular, the loss of muscle mass.In addition to a diet and the recommendation to continue going to the gym twice a week for bodybuilding,
Crepe
in
Cure Parkinson's
6 months ago
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
1 month 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
1 month ago
delay..
I need to apologize to so many of our newer members. Beginning in this role February 1st, I am still learning. I just found out, being new as the facilitator of this amazing group, how to find the names of the 'new' members..... let me introduce myself to all of you. Hi - and welcome! My name is
I need to apologize to so many of our newer members. Beginning in this role February 1st, I am still learning. I just found out, being new as the facilitator of this amazing group, how to find the names of the 'new' members..... let me introduce myself to all of you. Hi - and welcome! My name is
DonnaBoll
Administrator
in
PBC Foundation
6 months ago
New Research: multisensory gamma stimulation promotes the influx of cerebrospinal fluid and the efflux of interstitial fluid in mice
New Research: multisensory gamma stimulation promotes the influx of cerebrospinal fluid and the efflux of interstitial fluid in mice:
• How 40Hz sensory gamma rhythm stimulation clears amyloid in Alzheimer's mice 2024 https://medicalxpress.com/news/2024-02-40hz-sensory-gamma-rhythm-amyloid.html
New Research: multisensory gamma stimulation promotes the influx of cerebrospinal fluid and the efflux of interstitial fluid in mice:
• How 40Hz sensory gamma rhythm stimulation clears amyloid in Alzheimer's mice 2024 https://medicalxpress.com/news/2024-02-40hz-sensory-gamma-rhythm-amyloid.html
Bolt_Upright
in
Cure Parkinson's
6 months ago
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
overdose
I was diagnosed Feb 1 2024. Is it possible to overdose on Co-Beneldopa 200 MG. I take three doses a day [3 x 200 mg]. I try to take them at 8-hour intervals but often screw up, as my memory is so bad. Any side effects of Co-Beneldopa?
I was diagnosed Feb 1 2024. Is it possible to overdose on Co-Beneldopa 200 MG. I take three doses a day [3 x 200 mg]. I try to take them at 8-hour intervals but often screw up, as my memory is so bad. Any side effects of Co-Beneldopa?
disilusioned
in
PSP Association
6 months ago
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