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declining psa #6
Gm ladies n gentlemen, I’m here to give my results as I stated after stopping adt, post Rp, radiation n solely using ivermectin, cbd, turmeric n fish oil. My latest reading came in 1.34 down from 1.47 and continues to spiral down from starting this regiment at 1.92. Furthermore, prior to starting ivermectin
Gm ladies n gentlemen, I’m here to give my results as I stated after stopping adt, post Rp, radiation n solely using ivermectin, cbd, turmeric n fish oil. My latest reading came in 1.34 down from 1.47 and continues to spiral down from starting this regiment at 1.92. Furthermore, prior to starting ivermectin
Nfler
in
Advanced Prostate Cancer
8 months ago
Help with results please
Hi I wonder if anyone can help? I have just received these Blood Test results from my GP. My rheumatologist asked my doctor to do the Coeliac panel tests. The doctor's receptionist states that the nurse has checked and it is negative. I have continued to have multiple symptoms over the years, which
Hi I wonder if anyone can help? I have just received these Blood Test results from my GP. My rheumatologist asked my doctor to do the Coeliac panel tests. The doctor's receptionist states that the nurse has checked and it is negative. I have continued to have multiple symptoms over the years, which
lownook
in
Gluten Free Guerrillas
8 months ago
Question on Varicies
As most here know Margaret is no longer with us. And I am still digging more and more to understand what happened. Reading through her reports back in Oct of 2020, she had a fatty mass compressing the IVC and Portal. Which led to development of Varices. By December 2020 the fatty masses had vanished
As most here know Margaret is no longer with us. And I am still digging more and more to understand what happened. Reading through her reports back in Oct of 2020, she had a fatty mass compressing the IVC and Portal. Which led to development of Varices. By December 2020 the fatty masses had vanished
Wolivere
in
British Liver Trust
8 months ago
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Acute on Chronic Steroids
brother has had cirrhosis for last 3 years. Still drinking. Admitted to hospital Friday jaundice. Confusion HE I believe! Now on steroids. Has anyone any experience of this. Know that they are only given to certain people! Do you think this is now certain decline? Consultant said too early to tell
brother has had cirrhosis for last 3 years. Still drinking. Admitted to hospital Friday jaundice. Confusion HE I believe! Now on steroids. Has anyone any experience of this. Know that they are only given to certain people! Do you think this is now certain decline? Consultant said too early to tell
DQ33
in
British Liver Trust
8 months ago
Next Oxfordshire Lupus Group meeting - 6th December 2pm!
Following a successful first meeting for the Oxfordshire Lupus Group, we are thrilled to announced our next virtual meeting, which will be the 6th December at 2pm. This is a fantastic opportunity to meet others with lupus and associated conditions, friends and family also welcome to join! If you would
Following a successful first meeting for the Oxfordshire Lupus Group, we are thrilled to announced our next virtual meeting, which will be the 6th December at 2pm. This is a fantastic opportunity to meet others with lupus and associated conditions, friends and family also welcome to join! If you would
michaellasmith
Administrator
in
LUPUS UK
5 months ago
Options when Docetaxel stops working
Hi everyone- My brother was diagnosed with stage 4 prostate cancer in April of 2021. His PSA was 52 at the time of his diagnosis. He went on Lupron and Abiraterone which took his PSA to .03 and kept it low until Oct 2022. It went to 8.9 and his doctor put him on Docetaxel chemo. His PSA has continued
Hi everyone- My brother was diagnosed with stage 4 prostate cancer in April of 2021. His PSA was 52 at the time of his diagnosis. He went on Lupron and Abiraterone which took his PSA to .03 and kept it low until Oct 2022. It went to 8.9 and his doctor put him on Docetaxel chemo. His PSA has continued
TerryR123
in
Advanced Prostate Cancer
8 months ago
longest bout of AF , am I doing the right thing?
Hi everybody, Before I begin , I wish everybody a merry Xmas and a happy healthy new year!! My Xmas present has come early this year with my longest bout of AF ever! 40 hours and still going . I have an ablation booked for 18th January at St Bart’s , it will be my 3rd. A brief outline is I have had
Hi everybody, Before I begin , I wish everybody a merry Xmas and a happy healthy new year!! My Xmas present has come early this year with my longest bout of AF ever! 40 hours and still going . I have an ablation booked for 18th January at St Bart’s , it will be my 3rd. A brief outline is I have had
Kjsp
in
Atrial Fibrillation Support
4 months ago
Arginine and Taurine
Has anyone here had success with Arginine/Taurine/Magnesium? My Naturopath is willing to have me try but I am wondering if anyone has any firsthand knowledge out there of how long it takes to see results or not? Thanks!
Has anyone here had success with Arginine/Taurine/Magnesium? My Naturopath is willing to have me try but I am wondering if anyone has any firsthand knowledge out there of how long it takes to see results or not? Thanks!
MeganMN
in
AF Association
8 months ago
FENCHOL (in basil spice)
Has anyone here experimented with Fenchol and had good results? The easiest way to experiment with Fenchol would probably be to cover your food in basil spice for many days and wait to see if you notice any improvements. FENCHOL was recently proven to show improvements in Alzheimer's, but I noticed a
Has anyone here experimented with Fenchol and had good results? The easiest way to experiment with Fenchol would probably be to cover your food in basil spice for many days and wait to see if you notice any improvements. FENCHOL was recently proven to show improvements in Alzheimer's, but I noticed a
Discogs_discogs
in
Cure Parkinson's
8 months ago
Updates to the EULAR guidelines on managing lupus
The European Alliance of Associations for Rheumatology (EULAR) have updated their guidelines on how doctors should manage lupus. You can find out about how these guidelines are used in the UK, and how they've been updated, on our website here: https://lupusuk.org.uk/updates-to-the-eular-guidelines-on-managing-lupus
The European Alliance of Associations for Rheumatology (EULAR) have updated their guidelines on how doctors should manage lupus. You can find out about how these guidelines are used in the UK, and how they've been updated, on our website here: https://lupusuk.org.uk/updates-to-the-eular-guidelines-on-managing-lupus
Debbie_kinsey
Administrator
in
LUPUS UK
5 months ago
Low heart rate while resting
Hey guys. I'm kinda worried about my resting heart rate. If I'm sitting or laying it can go as low as 48bpm, even in sitting. My range is mostly between 48 and 56/57. As soon as I get up my heart rate also jumps quickly and sometimes I get a bit dizzy for few seconds like you would normally get when
Hey guys. I'm kinda worried about my resting heart rate. If I'm sitting or laying it can go as low as 48bpm, even in sitting. My range is mostly between 48 and 56/57. As soon as I get up my heart rate also jumps quickly and sometimes I get a bit dizzy for few seconds like you would normally get when
NewOne2023
in
Atrial Fibrillation Support
4 months ago
In a sexual relstionship with someone who has Lupus type SLE.
How do i maintain a healthy sexual relationship with someone who has Lupus. At times frustrated how do i treat person. Feel like have to be careful delicate with him. I cannot be in control and neither can he. Treating him very delicately intimacy problems sometimes communication barrier. Anyone advice
How do i maintain a healthy sexual relationship with someone who has Lupus. At times frustrated how do i treat person. Feel like have to be careful delicate with him. I cannot be in control and neither can he. Treating him very delicately intimacy problems sometimes communication barrier. Anyone advice
Tameeka723
in
LUPUS UK
5 months ago
Zanubrutinib and ACE inhibitors
I am approaching the start of treatment for the first time. I have for many years been taking an ACE inhibitor (perindropril) for high blood pressure, which is now well controlled. I have CLL, my lymphocyte count is doubling quickly (~2 months) and my haematologist is considering options for treatment
I am approaching the start of treatment for the first time. I have for many years been taking an ACE inhibitor (perindropril) for high blood pressure, which is now well controlled. I have CLL, my lymphocyte count is doubling quickly (~2 months) and my haematologist is considering options for treatment
Fogey
in
CLL Support
6 months ago
Scientists PREVENT DEATH of NEURONS in Alzheimer's research!
Summary:
"Researchers have unveiled the mystery behind neuron death in Alzheimer’s disease. A groundbreaking study reveals that neurons undergo a programmed cell death, necroptosis, when exposed to amyloid plaques and tau tangles, hallmark proteins linked to Alzheimer’s. The study pinpoints
Summary:
"Researchers have unveiled the mystery behind neuron death in Alzheimer’s disease. A groundbreaking study reveals that neurons undergo a programmed cell death, necroptosis, when exposed to amyloid plaques and tau tangles, hallmark proteins linked to Alzheimer’s. The study pinpoints
PDWarrior1900
in
Cure Parkinson's
8 months ago
FIB4 Test
Did a follow up visit today with my hepatologist and he did this FIB4 calc for me. He extracted my data and assessed. Liver disease is frequently asymptomatic, challenging early identification in the primary care setting. The fibrosis 4 (FIB4) index is a liver fibrosis biomarker that is a potential
Did a follow up visit today with my hepatologist and he did this FIB4 calc for me. He extracted my data and assessed. Liver disease is frequently asymptomatic, challenging early identification in the primary care setting. The fibrosis 4 (FIB4) index is a liver fibrosis biomarker that is a potential
ninjagirlwebb
in
PBC Foundation
8 months ago
Hope for the future
New research into autoimmune liver condition suggests unique cell movements may be driving disease A Birmingham study reveals a novel cellular phenomenon could be responsible for the onset of primary biliary cholangitis (PBC). Research suggests that a recent understanding of cell movements may
New research into autoimmune liver condition suggests unique cell movements may be driving disease A Birmingham study reveals a novel cellular phenomenon could be responsible for the onset of primary biliary cholangitis (PBC). Research suggests that a recent understanding of cell movements may
DonnaBoll
Administrator
in
PBC Foundation
2 months ago
Thoughts and Help
Hello all! I am new here. I know this is a lupus / autoimmune group, but before joining I noticed some helpful posts for other conditions, so I am hoping I can find some advice here. I have been dealing with declining health for a few years now, but have not received any diagnoses. I do have a positive
Hello all! I am new here. I know this is a lupus / autoimmune group, but before joining I noticed some helpful posts for other conditions, so I am hoping I can find some advice here. I have been dealing with declining health for a few years now, but have not received any diagnoses. I do have a positive
Hidden
in
LUPUS UK
5 months ago
AST 29/Alt 20
According to the ommi calculator my results are indicative of cirrhosis. it says 1.45 too high I have been getting liver pain and muscle cramps and esophogus problems for quite a while now any thoughts.
According to the ommi calculator my results are indicative of cirrhosis. it says 1.45 too high I have been getting liver pain and muscle cramps and esophogus problems for quite a while now any thoughts.
Oldbloke1
in
British Liver Trust
8 months ago
Post cardioversion
1 week post cardioversion and am in NSR, and no palpitations any more. However I am still feeling exhausted and steps and hills are a real problem ........anyone else had the same experience ?
1 week post cardioversion and am in NSR, and no palpitations any more. However I am still feeling exhausted and steps and hills are a real problem ........anyone else had the same experience ?
OldTown
in
AF Association
4 months ago
Newly Discovered Trigger of Parkinson’s Upends Common Beliefs
Degeneration of dopaminergic neurons is widely accepted as the first event that leads to Parkinson’s. But the new study suggests that a dysfunction in the neuron’s synapses — the tiny gap across which a neuron can send an impulse to another neuron — leads to deficits in dopamine and precedes the neurodegeneration
Degeneration of dopaminergic neurons is widely accepted as the first event that leads to Parkinson’s. But the new study suggests that a dysfunction in the neuron’s synapses — the tiny gap across which a neuron can send an impulse to another neuron — leads to deficits in dopamine and precedes the neurodegeneration
Farooqji
in
Cure Parkinson's
8 months ago
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