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Hashimoto's disease
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Hashimoto's and pain in muscles and joints
Hi I am new to the group.I am reaching out as I have a couple of questions.I have
Hashimotos
disease
and on an alternating dose of 125mg to 150mg each other day of levothyroxin.
Hi I am new to the group.I am reaching out as I have a couple of questions.I have
Hashimotos
disease
and on an alternating dose of 125mg to 150mg each other day of levothyroxin.
Hashiskip18
in
Thyroid UK
3 months ago
Hashimotos
Hi, My wife has been diagnosed with
Hashimotos
disease
by her doctors in Egypt. Thyroid disease runs in her family, her mother has it, but she regulates it with medicine and has never been diagnosed with Hashimotos.
Hi, My wife has been diagnosed with
Hashimotos
disease
by her doctors in Egypt. Thyroid disease runs in her family, her mother has it, but she regulates it with medicine and has never been diagnosed with Hashimotos.
Moonwai1986
in
Thyroid UK
1 month ago
Hashimoto diagnosis
I have just found out the I have
Hashimotos
Disease
and am going down the rabbit warren of Google trying to research what it is. How to live with it? What I can do to help myself? And generally get my head around the fact I have it.
I have just found out the I have
Hashimotos
Disease
and am going down the rabbit warren of Google trying to research what it is. How to live with it? What I can do to help myself? And generally get my head around the fact I have it.
Crazylegs16
in
Thyroid UK
7 months ago
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autoimmune and Hashimotos
I feel like I am on a one woman crusade in Scotland to get
Hashimotos
recognised for what it is an autoimmune
disease
, I now have four autoimmune diseases
Hashimotos
, Pernicious Anaemia, Coeliac
disease
, Hyperparathyroidism, and am being referred for testing for rheumatoid arthritis.
I feel like I am on a one woman crusade in Scotland to get
Hashimotos
recognised for what it is an autoimmune
disease
, I now have four autoimmune diseases
Hashimotos
, Pernicious Anaemia, Coeliac
disease
, Hyperparathyroidism, and am being referred for testing for rheumatoid arthritis.
Filicatlasy
in
Thyroid UK
2 months ago
Liothyronine
I explained I no longer needed to as the endo and previous surgery were happy to prescribe it , they now want me to have a telephone review with the gp to see if they can increase my T4 instead of giving me T3 , 🤬 I explained I don't convert and have barely any thyroid left due to
hashimotos
disease
I explained I no longer needed to as the endo and previous surgery were happy to prescribe it , they now want me to have a telephone review with the gp to see if they can increase my T4 instead of giving me T3 , 🤬 I explained I don't convert and have barely any thyroid left due to
hashimotos
disease
Jodiedebs
in
Thyroid UK
5 months ago
Difficulty in obtaining Morningside Liothyronine
I have been taking 5mcg of Liothyronine twice daily alongside 75mg of Levothyroxine prescribed by my consultant around 4 years ago. ( I have had
Hashimotos
'
disease
for almost 40 years)My problem is that I cannot obtain Morningside brand of Liothyronine from my usual pharmacies.
I have been taking 5mcg of Liothyronine twice daily alongside 75mg of Levothyroxine prescribed by my consultant around 4 years ago. ( I have had
Hashimotos
'
disease
for almost 40 years)My problem is that I cannot obtain Morningside brand of Liothyronine from my usual pharmacies.
Loubea53
in
Thyroid UK
10 months ago
I’m confused 😕
Isn’t the serum C reactive protein meant to be raised when we have an autoimmune
disease
like
hashimotos
? mine isn’t 🤔 Or is it just the TPO that is raised? Thanks in advance for any help with this…
Isn’t the serum C reactive protein meant to be raised when we have an autoimmune
disease
like
hashimotos
? mine isn’t 🤔 Or is it just the TPO that is raised? Thanks in advance for any help with this…
ThyroidObsessed
in
Thyroid UK
4 months ago
Wondering…
Right…another daft question, still trying to get my head around stuff: if you have hashis and hypothyroidism too, can an increase in symptoms at times sometimes be due to the
hashimotos
auto immune
disease
being more active rather than a problem with the hypo or levo dose?
Right…another daft question, still trying to get my head around stuff: if you have hashis and hypothyroidism too, can an increase in symptoms at times sometimes be due to the
hashimotos
auto immune
disease
being more active rather than a problem with the hypo or levo dose?
JoJoloveschocolate
in
Thyroid UK
3 months ago
hashimotos and b12
I have
hashimotos
disease
, I take 100mcg levo and previously to that, I also took liothyronine at 12.5 mcg daily which I self sourced ( due to issues I had with consultants regarding my tsh going down to 0.05 and the fact I dare take lio without their say so, I stopped taking it even though i told
I have
hashimotos
disease
, I take 100mcg levo and previously to that, I also took liothyronine at 12.5 mcg daily which I self sourced ( due to issues I had with consultants regarding my tsh going down to 0.05 and the fact I dare take lio without their say so, I stopped taking it even though i told
Rowing2
in
Pernicious Anaemia Society
2 months ago
The Wren Project Volunteers Outreach
The Wren Project is taking on volunteers to offer emotional listening support to individuals in distress with an autoimmune
disease
, including thyroid conditions such as Graves,
Hashimotos
and Autoimmune Thyroiditis.
The Wren Project is taking on volunteers to offer emotional listening support to individuals in distress with an autoimmune
disease
, including thyroid conditions such as Graves,
Hashimotos
and Autoimmune Thyroiditis.
TUKOffice
Thyroid UK
in
Thyroid UK
16 days ago
Hashimotos Disease and Diabetes type 2
I have recently been diagnosed with diabetes type 2. I’m active, not overweight and eat a very healthy diet. I understand that a side effect of Levothyroxine could possibly be responsible for glucose resistance. Does anyone have any further information? 🦋
I have recently been diagnosed with diabetes type 2. I’m active, not overweight and eat a very healthy diet. I understand that a side effect of Levothyroxine could possibly be responsible for glucose resistance. Does anyone have any further information? 🦋
MachuPichu33
in
Thyroid UK
1 year ago
Very sore and swollen hands. Is it possible I now have rheumatoid arthritis?
I have autoimmune thyroid
disease
(
hashimotos
) and coeliac
disease
. Is it possible to now have rheumatoid arthritis? I use voltarol max strength 12hr gel. Is there anything else I can buy over the counter or ask my GP for?
I have autoimmune thyroid
disease
(
hashimotos
) and coeliac
disease
. Is it possible to now have rheumatoid arthritis? I use voltarol max strength 12hr gel. Is there anything else I can buy over the counter or ask my GP for?
W3ndy2159
in
NRAS
1 year ago
Does PSA drop after starting ADT tell us anything?
My husband started Firmagon shots a month ago. Before starting his PSA was 5.9. It was tested a few days ago and it’s 1.4 now. Does this tell us anything of any significance? Thanks!
My husband started Firmagon shots a month ago. Before starting his PSA was 5.9. It was tested a few days ago and it’s 1.4 now. Does this tell us anything of any significance? Thanks!
EvFC
in
Advanced Prostate Cancer
2 hours ago
decompensated to compensated
hi as you know I have had decompensated cirrhosis diagnosed march 23, in January 24 I had a bleed from varices and have had 7 bands, next camera august, my next scan on liver is 18th June so next week, has anyone had this and after there liver went to compensated ? Thanks Leanne (King Billy is my
hi as you know I have had decompensated cirrhosis diagnosed march 23, in January 24 I had a bleed from varices and have had 7 bands, next camera august, my next scan on liver is 18th June so next week, has anyone had this and after there liver went to compensated ? Thanks Leanne (King Billy is my
Kingbilly3
in
British Liver Trust
3 hours ago
Does anyone take this supplement?
I have been doing a lot of research on how to fix cramping. Let me first say, no pickle juice does not work. I also do not have fluid taken off during dialysis. I add 400ml of saline each treatment. I also have no fluid restrictions and so I do drink a lot of water. And none of my mineral labs indicate
I have been doing a lot of research on how to fix cramping. Let me first say, no pickle juice does not work. I also do not have fluid taken off during dialysis. I add 400ml of saline each treatment. I also have no fluid restrictions and so I do drink a lot of water. And none of my mineral labs indicate
Bassetmommer
in
Kidney Dialysis
6 hours ago
Elevated liver enzymes but no cause?
Hello, just wondering if anybody else has elevated liver enzymes but no cause found? ALT and AST have been raised for months but doctors can’t find a cause. I’ve had SO many tests, scans etc, and everything is normal? Yet they keep coming back raised. I take 1.25mg bisoprolol but doctors are certain
Hello, just wondering if anybody else has elevated liver enzymes but no cause found? ALT and AST have been raised for months but doctors can’t find a cause. I’ve had SO many tests, scans etc, and everything is normal? Yet they keep coming back raised. I take 1.25mg bisoprolol but doctors are certain
Gingernut64
in
British Liver Trust
8 hours ago
Docetaxal chemotherapy
I have had prostate cancer since 2017. First I had radiation and then Lupron for three years. When my PSA started to rise I took abiraterone and Lupron for 3 more years and was undetectable. It started to rise again to 1.78. Then I was put on Xtandi but after a week I developed a full body rash. When
I have had prostate cancer since 2017. First I had radiation and then Lupron for three years. When my PSA started to rise I took abiraterone and Lupron for 3 more years and was undetectable. It started to rise again to 1.78. Then I was put on Xtandi but after a week I developed a full body rash. When
Gern
in
Advanced Prostate Cancer
11 hours ago
Subarachnoid Hemorrhage & Tinnitus
Hi I had a Subarachnoid hemorrhage 4 weeks ago with no Aneurysms or other abnormalities found after an Angiogram. I feel very lucky & grateful to be one of the lucky ones. I've been taking 5mg of Amlodipine for 2 weeks to stop BP peaking & have since had mild tinnitus. I'm seeing GP next week for BP
Hi I had a Subarachnoid hemorrhage 4 weeks ago with no Aneurysms or other abnormalities found after an Angiogram. I feel very lucky & grateful to be one of the lucky ones. I've been taking 5mg of Amlodipine for 2 weeks to stop BP peaking & have since had mild tinnitus. I'm seeing GP next week for BP
Aquawhite
in
Headway
11 hours ago
Please could I ask what your thoughts are on Stem Cell Therapy?
My wife was diagnosed with PD in 2015. She was fine until summer 2021 when she had a fall in the garden and ended up in hospital for 3 weeks. She was then put on Sinemet Plus 25/100 mg. Since then her deterioration has been quite fast. Rigidity, stiffness, slow movement and exhaustion getting worse
My wife was diagnosed with PD in 2015. She was fine until summer 2021 when she had a fall in the garden and ended up in hospital for 3 weeks. She was then put on Sinemet Plus 25/100 mg. Since then her deterioration has been quite fast. Rigidity, stiffness, slow movement and exhaustion getting worse
Jade77
in
Cure Parkinson's
15 hours ago
The most informative web page I have seen about vision loss after stroke is from the RNIB.
Hi folks was searching for info on loss of vision after TIA and came across this page from the Royal National Institute for the Blind. It's really informative so I thought I'd share it. https://www.rnib.org.uk/your-eyes/eye-conditions-az/stroke-related-eye-conditions/#what-are-some-of-the-common-visual-symptoms-of-stroke
Hi folks was searching for info on loss of vision after TIA and came across this page from the Royal National Institute for the Blind. It's really informative so I thought I'd share it. https://www.rnib.org.uk/your-eyes/eye-conditions-az/stroke-related-eye-conditions/#what-are-some-of-the-common-visual-symptoms-of-stroke
pinkvision
in
Headway
18 hours ago
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