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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
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
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
8 months ago
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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
3 months ago
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
19 days 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
2 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
27 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
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
8 days 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
10 months ago
Hives and hypothyroid??
I have
hashimotos
disease
/ It looks like a heat rash/allergy rash but I have not been anywhere hot or had anything new to trigger an allergy. TIA
I have
hashimotos
disease
/ It looks like a heat rash/allergy rash but I have not been anywhere hot or had anything new to trigger an allergy. TIA
Tired2022
in
Thyroid UK
1 year ago
multiple autoimmune
This has been going on for 20 years first Sarcoidosis, then
Hashimotos
, then Hyperparathyroidism, then Coeliac
disease
, then Pernicious Anemeia and now testing for Rheumatoid Arthritis.
This has been going on for 20 years first Sarcoidosis, then
Hashimotos
, then Hyperparathyroidism, then Coeliac
disease
, then Pernicious Anemeia and now testing for Rheumatoid Arthritis.
Filicatlasy
in
LUPUS UK
9 months ago
Recent NHS bloods due to hypertension
Hello everyone I'm hoping some kind soul will help me understand my latest blood results I'll post them here.I have very high blood pressure thyroid
disease
hashimotos
and osteoarthritis the doctors have today started me on blood pressure medicine I've resisted as long as possible but with a bp of
Hello everyone I'm hoping some kind soul will help me understand my latest blood results I'll post them here.I have very high blood pressure thyroid
disease
hashimotos
and osteoarthritis the doctors have today started me on blood pressure medicine I've resisted as long as possible but with a bp of
pet-lamb
in
High Blood Pressure Support
4 months ago
Parkinson's Drugs Summary
Found this lecture helpful to know what my options are after the neurologist chose for me. Currently on madopar with entacapone newly added. Feel a little better. Time will tell. https://youtu.be/LJVcrvrFYJs?si=Km9qcU_fC71QRSbz
Found this lecture helpful to know what my options are after the neurologist chose for me. Currently on madopar with entacapone newly added. Feel a little better. Time will tell. https://youtu.be/LJVcrvrFYJs?si=Km9qcU_fC71QRSbz
Thal
in
Cure Parkinson's
2 hours ago
After Pluvicto #6 results
Finished my 6th and final Pluvicto and am now getting lab results. I see that somehow I neglected to put results after #5 -- may have been distracted by doctors freaking out that my kidney function was going down and my calcium shot up. My nuclear medicine doc made a judgement call to give me a full
Finished my 6th and final Pluvicto and am now getting lab results. I see that somehow I neglected to put results after #5 -- may have been distracted by doctors freaking out that my kidney function was going down and my calcium shot up. My nuclear medicine doc made a judgement call to give me a full
Miccoman
in
Advanced Prostate Cancer
7 hours ago
Cirosis
I have high liver enzymes. AST 91. Alt 134. Ggt 235. Fibroscan cap 366 and kpa 5.6. What does this mean .
I have high liver enzymes. AST 91. Alt 134. Ggt 235. Fibroscan cap 366 and kpa 5.6. What does this mean .
Curryblue
in
British Liver Trust
14 hours ago
Next NoSilverBullet Zoom Webinar on 13 May: Live interview of Dr M Okun on "Practical strategies for living a happier life with Parkinson's"
I am delighted to announce that our next NoSilverBullet Zoom webinar will be taking place at 7pm London time on Monday, the 13th of May. I will have the pleasure of interviewing Dr Michael Okun on the topic of "Practical strategies for living a happier life with Parkinson's". Dr Okun is a worldwide
I am delighted to announce that our next NoSilverBullet Zoom webinar will be taking place at 7pm London time on Monday, the 13th of May. I will have the pleasure of interviewing Dr Michael Okun on the topic of "Practical strategies for living a happier life with Parkinson's". Dr Okun is a worldwide
Michel0220
in
Cure Parkinson's
14 hours ago
How Long To Discontinue 5-ARIs and/or Select Supplements to "Unmask" PSA?
Disregarding the discussion as whether to temporarily discontinue or not discontinue in fht efirst place... Purportedly some substances may "mask" PSA. I believe the general rule of thumb is on 5-ARIs like Avodart (Dutasteride) you are supposed to double the PSA reading to get the "real" PSA? In addition
Disregarding the discussion as whether to temporarily discontinue or not discontinue in fht efirst place... Purportedly some substances may "mask" PSA. I believe the general rule of thumb is on 5-ARIs like Avodart (Dutasteride) you are supposed to double the PSA reading to get the "real" PSA? In addition
jazj
in
Advanced Prostate Cancer
1 day ago
Chronic Liver Disease Post Transplant
Hi, I had a liver transplant in October 2017 and apart from a little set back right at the beginning, meaning I was in Addenbrookes for 5 weeks, I have been really well. I haven’t even had Covid! However a couple of months ago, I had a CT scan which showed that I have chronic liver disease. To say
Hi, I had a liver transplant in October 2017 and apart from a little set back right at the beginning, meaning I was in Addenbrookes for 5 weeks, I have been really well. I haven’t even had Covid! However a couple of months ago, I had a CT scan which showed that I have chronic liver disease. To say
Dawnejoy
in
British Liver Trust
1 day ago
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