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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
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
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
23 days 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
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
9 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
4 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
3 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
2 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
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
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
5 days 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
Aches and pains
Having thyroid
disease
or
hashimotos
which i have is obviously a autoimmune disorder. Unfortunatley for me i have 6 autoimmune conditions. Their symtoms all overlap which mainly consist and well documented that aching joints and muscle pain are part of the condition.
Having thyroid
disease
or
hashimotos
which i have is obviously a autoimmune disorder. Unfortunatley for me i have 6 autoimmune conditions. Their symtoms all overlap which mainly consist and well documented that aching joints and muscle pain are part of the condition.
Mellymoos
in
Thyroid UK
1 year ago
could be of interest for those on BAT
Extreme responses to immune checkpoint blockade following bipolar androgen therapy and enzalutamide in patients with metastatic castration resistant prostate cancer https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585736/
Extreme responses to immune checkpoint blockade following bipolar androgen therapy and enzalutamide in patients with metastatic castration resistant prostate cancer https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7585736/
Maxone73
in
Advanced Prostate Cancer
4 hours ago
Essential read & listen (watch) resources for ALL PCa patients - The 2023 Walsh Guide & Peter Attia's podcast with Dr. Ed. Schaeffer -10/23
Two recent resources that all PCa patients should take the time to get/use/access. The first is the 2023 updated edition of the patient guide, [i]
Dr. Patrick Walsh's Guide to Surviving Prostate Cancer.
[/i] And the second is a [i]
Dr. Peter Attia podcast interview with Ed Schaeffer, MD & PhD[
Two recent resources that all PCa patients should take the time to get/use/access. The first is the 2023 updated edition of the patient guide, [i]
Dr. Patrick Walsh's Guide to Surviving Prostate Cancer.
[/i] And the second is a [i]
Dr. Peter Attia podcast interview with Ed Schaeffer, MD & PhD[
cujoe
in
Fight Prostate Cancer
16 hours ago
Time to adjust my course, any suggestions?
Psa is on a steady increase again. I was taking extandi for a year up until 11 /23 over that yr my Psa had dropped from 29, 11/22 to 1.4 ,11/23. I was having significant SEs, brain fog mainly so I decided to switch to nubeqa (daralutimide) even tho there was a steady drop in PSA on extandi. Nubeqa
Psa is on a steady increase again. I was taking extandi for a year up until 11 /23 over that yr my Psa had dropped from 29, 11/22 to 1.4 ,11/23. I was having significant SEs, brain fog mainly so I decided to switch to nubeqa (daralutimide) even tho there was a steady drop in PSA on extandi. Nubeqa
rick8637
in
Advanced Prostate Cancer
2 days ago
Liver Cancer
I was diagnosed with liver cancer by my consultant yesterday (Friday 31st May 2024). They are going to take a liver biopsy in a couple of weeks as I am going on holiday next Monday. Then once this is done I will be having radiography. I am going to be positive and hopefully fight this all the way
I was diagnosed with liver cancer by my consultant yesterday (Friday 31st May 2024). They are going to take a liver biopsy in a couple of weeks as I am going on holiday next Monday. Then once this is done I will be having radiography. I am going to be positive and hopefully fight this all the way
Mick1414
in
British Liver Trust
2 days ago
New saliva test for PCa screening
It will be presented this weekend. They claim that it is more specific than PSA screening and also can be done at home using supplied by mailed kits.
It will be presented this weekend. They claim that it is more specific than PSA screening and also can be done at home using supplied by mailed kits.
Justfor_
in
Fight Prostate Cancer
2 days ago
discomfort under ribs
I feel fine, then I get pain around liver area and get stomach cramps which I end up having to poo the colour is quite yellowish (sorry for details!) once I have been feel much better this has been going on for some weeks now it is definitely worse if I were to eat food with fats in, any ideas please
I feel fine, then I get pain around liver area and get stomach cramps which I end up having to poo the colour is quite yellowish (sorry for details!) once I have been feel much better this has been going on for some weeks now it is definitely worse if I were to eat food with fats in, any ideas please
Suecong
in
British Liver Trust
2 days ago
Aside from easing motor symptoms of Parkinson’s disease, deep brain stimulation (DBS) may also slow disease progression
https://parkinsonsnewstoday.com/news/dbs-reduces-toxic-clumping-parkinsons-rat-brain-cells-study/
https://parkinsonsnewstoday.com/news/dbs-reduces-toxic-clumping-parkinsons-rat-brain-cells-study/
Farooqji
in
Cure Parkinson's
2 days ago
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