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Autoimmune disease?
hello, Looking for advice/reassurance just need somewhere to unload really. It all started off with upper right sided abdominal pain which took me to the doctors back in February. Dull ache burning sensation not unbearable but I’m aware of the pain. Ultrasound scan on upper abdo normal. Bloods showed
hello, Looking for advice/reassurance just need somewhere to unload really. It all started off with upper right sided abdominal pain which took me to the doctors back in February. Dull ache burning sensation not unbearable but I’m aware of the pain. Ultrasound scan on upper abdo normal. Bloods showed
Farfield
in
British Liver Trust
1 month ago
Anyone know about Dr's or consultants prescribing metformin for endometriosis?
I recently got access to ALL my medical records from the consultants I had been referred to over the years and saw that in the past I had been prescribed metformin, altavita and amitryptaline at the same time by an endocrinologist. I presumed at the time it was for my underactive Thyroid and wasn't on
I recently got access to ALL my medical records from the consultants I had been referred to over the years and saw that in the past I had been prescribed metformin, altavita and amitryptaline at the same time by an endocrinologist. I presumed at the time it was for my underactive Thyroid and wasn't on
Escapologygirl
in
Endometriosis UK
1 month ago
Declining psa #9
Gm folks, hope all are having a wonderful New Year. I’m following up n giving results on using ivermectin, cbd oil, turmeric Vit b3,6,12 Vit c And zinc solely after eliminating ADT after 7 months, post Rp n rad… Psa dropped another .29 points to .66 down from .95 n psa was hovering 7 when I first got
Gm folks, hope all are having a wonderful New Year. I’m following up n giving results on using ivermectin, cbd oil, turmeric Vit b3,6,12 Vit c And zinc solely after eliminating ADT after 7 months, post Rp n rad… Psa dropped another .29 points to .66 down from .95 n psa was hovering 7 when I first got
Nfler
in
Advanced Prostate Cancer
6 months ago
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HiI found out I had APS during my 8th pregnancy in 2006. I had PEs. Fast forward to 2024. One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I
HiI found out I had APS during my 8th pregnancy in 2006. I had PEs. Fast forward to 2024. One of my adult daughters had PEs in pregnancy, horrific treatment from hospital, which was minutes from losing both my daughter and her baby (at 39 weeks) I'm now waiting to have a genetic test for APs as I
Dawnm10
in
Hughes Syndrome APS Forum
1 month ago
Shingles Jab
I noted that Lupus sufferers over 50 were supposed to be eligible for the Shingrix jab. However, after requesting one from the Surgery the receptionist said no. I did recently get the over 75s Covid booster without asking, courtesy of my immune system, , which I thought over the top. However, as rashes
I noted that Lupus sufferers over 50 were supposed to be eligible for the Shingrix jab. However, after requesting one from the Surgery the receptionist said no. I did recently get the over 75s Covid booster without asking, courtesy of my immune system, , which I thought over the top. However, as rashes
Stewart64
in
LUPUS UK
1 month ago
Join "Your Morning Wake-Up Call," a FREE virtual communication and cognition exercise series designed for individuals with Parkinson's
"Your Morning Wake-Up Call" features a comprehensive approach to enhancing communication and cognition, including: • Breath Exercises to strengthen breath support to help you communicate more effectively. • Voice and Speech Drills to improve your voice and enhance speech clarity. • Stimulating Cognitive
"Your Morning Wake-Up Call" features a comprehensive approach to enhancing communication and cognition, including: • Breath Exercises to strengthen breath support to help you communicate more effectively. • Voice and Speech Drills to improve your voice and enhance speech clarity. • Stimulating Cognitive
JMDean
in
Cure Parkinson's
6 months ago
Mr Alan M
I have been missed diagnosed with liver disease for years I believe that I am still around because I do not drink and I am quite strict with my diet etc. I have also taken a lot of over the counter medication for liver disease. I believe that the disease has been caused by DILI / prescribed medication
I have been missed diagnosed with liver disease for years I believe that I am still around because I do not drink and I am quite strict with my diet etc. I have also taken a lot of over the counter medication for liver disease. I believe that the disease has been caused by DILI / prescribed medication
TillySyd
in
British Liver Trust
6 months ago
Anyone used Dr Dani Gordon @The London Resilience Clinic
hi I have a diagnosis of Fibromyalgia, along with underactive thyroid, arthritis, chronic fatigue (long covid) and diverticula desiease (from pain relief meds). Although I have managed to cope and work full time for a number of years, I was hit with COVID and flu together at Christmas and it has
hi I have a diagnosis of Fibromyalgia, along with underactive thyroid, arthritis, chronic fatigue (long covid) and diverticula desiease (from pain relief meds). Although I have managed to cope and work full time for a number of years, I was hit with COVID and flu together at Christmas and it has
Field007
in
Fibromyalgia Action UK
1 month ago
C-Reactive Protein Test
Good day everyone. Has anyone has their levels checked? Does high levels correlate with PA and Autoimmune Gastritis? Thank you
Good day everyone. Has anyone has their levels checked? Does high levels correlate with PA and Autoimmune Gastritis? Thank you
Canadian77
in
Pernicious Anaemia Society
1 month ago
Been on Firmagon with Zytiga and Prednisone PSA rising, what can I do next?
Information in Bio Hoping to try a PARP inhibitor or Provenge perhaps, I don’t know much about this, but my medical oncologist keeps mentioning pluvicto, I’m not interested in doing that yet. Information from Bio below: Diagnosed 07/01/2022 Diagnosed By PSA Score 942.40 06/24-2022-07/06/2022
Information in Bio Hoping to try a PARP inhibitor or Provenge perhaps, I don’t know much about this, but my medical oncologist keeps mentioning pluvicto, I’m not interested in doing that yet. Information from Bio below: Diagnosed 07/01/2022 Diagnosed By PSA Score 942.40 06/24-2022-07/06/2022
Shorehousejam
in
Advanced Prostate Cancer
6 months ago
High-Dose Vitamin B1 / Thiamine and Fat Soluble Benfotiamine Form
I am reposting a reply to the Vitamin B1 thread as I noticed a search on HealthUnlocked for Benfotiamine doesn't list the thread for Vitamin B1 and the information I posted doesn't fit in one reply. I'm not giving medical advice but I know a lot of people here are open to trying things and watch if
I am reposting a reply to the Vitamin B1 thread as I noticed a search on HealthUnlocked for Benfotiamine doesn't list the thread for Vitamin B1 and the information I posted doesn't fit in one reply. I'm not giving medical advice but I know a lot of people here are open to trying things and watch if
jazj
in
Advanced Prostate Cancer
6 months ago
Understanding TSH Levels
HAD MY BLOOD TESTED IN JANUARY AND TSH Was .06 Gp said normal but no adjustment in meds as he said it was too high. Currently on 100mcg Thyroxine but feeling tired and usual symptoms of Underactive thyroid. Any advice appreciated. Thank you.
HAD MY BLOOD TESTED IN JANUARY AND TSH Was .06 Gp said normal but no adjustment in meds as he said it was too high. Currently on 100mcg Thyroxine but feeling tired and usual symptoms of Underactive thyroid. Any advice appreciated. Thank you.
JMF1
in
Thyroid UK
1 month ago
Does this look like lupus rash?
Hi everyone. I started with a flat purple rash last Tuesday. It’s spread across my stomach and down the front of my thighs. Then a more sporadic raised rash started on shoulders, back, and then my hands and arms on Friday evening. The first marks on upper body looked like I’d scratched the skin. Yesterday
Hi everyone. I started with a flat purple rash last Tuesday. It’s spread across my stomach and down the front of my thighs. Then a more sporadic raised rash started on shoulders, back, and then my hands and arms on Friday evening. The first marks on upper body looked like I’d scratched the skin. Yesterday
Hidden
in
LUPUS UK
1 month ago
Anti-Androgen Therapy and Bone Tumors in Prostate Cancer
Sorry guys, but I found this and all I can say is it scared the hell out of me. Now I don't know what to think. Maybe someone can sort it out. https://journals.lww.com/oncology-times/fulltext/2021/08050/anti_androgen_therapy_can_fuel_spread_of_bone.16.aspx Jeff Dunn AO, Professor and CEO of the Prostate
Sorry guys, but I found this and all I can say is it scared the hell out of me. Now I don't know what to think. Maybe someone can sort it out. https://journals.lww.com/oncology-times/fulltext/2021/08050/anti_androgen_therapy_can_fuel_spread_of_bone.16.aspx Jeff Dunn AO, Professor and CEO of the Prostate
85745
in
Advanced Prostate Cancer
6 months ago
1st consult questions to ask please
hi, please can someone guide me on which questions to ask? My brother has got his first appointment at Leeds liver Unit next week. He’s got Class C liver cirrhosis, was diagnosed in July as he was decompensated with ascites and hepatic encephalopathy and almost died. He’s seen gastro ONCE since being
hi, please can someone guide me on which questions to ask? My brother has got his first appointment at Leeds liver Unit next week. He’s got Class C liver cirrhosis, was diagnosed in July as he was decompensated with ascites and hepatic encephalopathy and almost died. He’s seen gastro ONCE since being
MrsAlien
in
British Liver Trust
6 months ago
Don't know what's real anymore...
Some know my story so far, but briefly, rheumatologist diagnosed sjogren's after several years of UCTD and has now referred but to a sjogren's specialist. I saw him about a month ago and he's not convinced it's sjogren's and is running more tests and told me to stop taking Amitryptiline as tris can
Some know my story so far, but briefly, rheumatologist diagnosed sjogren's after several years of UCTD and has now referred but to a sjogren's specialist. I saw him about a month ago and he's not convinced it's sjogren's and is running more tests and told me to stop taking Amitryptiline as tris can
Mctd
in
LUPUS UK
1 month ago
Biomarkers to Assess Multiple Sclerosis
Some review and maybe something new.
Recent research on fluid biomarkers in multiple sclerosis (MS) frames an emerging picture of two aspects of the disease: inflammatory activity measured with
neurofilament light chain
(NfL), and disease progression independent of relapses, with promising
Some review and maybe something new.
Recent research on fluid biomarkers in multiple sclerosis (MS) frames an emerging picture of two aspects of the disease: inflammatory activity measured with
neurofilament light chain
(NfL), and disease progression independent of relapses, with promising
BettysMom
in
My MSAA Community
1 month ago
Getting bombarded with ads for RA treatment Honey bee venom cream?.
Amazing too good to be true claims for this but there seems to be a few bits of research on it being anti inflammatory. Anyone tried it ? Still taking the meds....
Amazing too good to be true claims for this but there seems to be a few bits of research on it being anti inflammatory. Anyone tried it ? Still taking the meds....
welsh12
in
NRAS
6 months ago
Levothyroxine side effects
I have been on 150mcg levothyroxine constant since January 1st this year. Around the 20th February I started with shortness of breath and irregular heart beats which have continued daily and my t4 and tsh have gradually got better to where last weeks blood test show they are now within range. I am adamant
I have been on 150mcg levothyroxine constant since January 1st this year. Around the 20th February I started with shortness of breath and irregular heart beats which have continued daily and my t4 and tsh have gradually got better to where last weeks blood test show they are now within range. I am adamant
Andrew36
in
Thyroid UK
1 month ago
itchy skin
hi have any of you ladies out there had itchy skin with underactive thyroid. Mine is mainly on my back. I have used most creams to get rid of it but it comes and goes and it’s back again driving me mad at the moment. Could anyone recommend any remedies to help? Thanks
hi have any of you ladies out there had itchy skin with underactive thyroid. Mine is mainly on my back. I have used most creams to get rid of it but it comes and goes and it’s back again driving me mad at the moment. Could anyone recommend any remedies to help? Thanks
Purpleprincess1963
in
Thyroid UK
1 month ago
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