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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 , š¤¬ 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 , š¤¬ 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
Iām confused š
Isnāt the serum C reactive protein meant to be raised when we have an autoimmune
disease
like
hashimotos
? mine isnāt š¤ Or is it just the TPO that is raised? Thanks in advance for any help with thisā¦
Isnāt the serum C reactive protein meant to be raised when we have an autoimmune
disease
like
hashimotos
? mine isnāt š¤ Or is it just the TPO that is raised? Thanks in advance for any help with thisā¦
ThyroidObsessed
in
Thyroid UK
2 months ago
Wonderingā¦
Rightā¦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?
Rightā¦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. Iām 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? š¦
I have recently been diagnosed with diabetes type 2. Iām 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? š¦
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
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 havenāt 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 havenāt 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
7 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
6 hours ago
some suggestions - PCa websites?
Hey all: As Iāve mentioned before, Iām doing a comic about this experience. I want to have a short section at the end with websites that are good for learning about prostate cancer. I have room for a few more, and am looking for suggestions. Not an exhaustive list, but hoping for a useful list: Thanks
Hey all: As Iāve mentioned before, Iām doing a comic about this experience. I want to have a short section at the end with websites that are good for learning about prostate cancer. I have room for a few more, and am looking for suggestions. Not an exhaustive list, but hoping for a useful list: Thanks
Jpburns
in
Advanced Prostate Cancer
8 hours ago
nose bleed
was rushed to hospital 2weeks ago for pneumonia. Was discharged after a week. Wasnāt home 24 hrs. And out of the blue my nose started bleeding. It hasnāt stopped. Has this happened to anyone else and what did the doctors do to stop it?
was rushed to hospital 2weeks ago for pneumonia. Was discharged after a week. Wasnāt home 24 hrs. And out of the blue my nose started bleeding. It hasnāt stopped. Has this happened to anyone else and what did the doctors do to stop it?
Daytym
in
British Liver Trust
21 hours ago
1st transplant done in trial of Parkinsonās cell therapy ANPD001
This experimental therapy for Parkinsonās uses a type of stem cell called an induced pluripotent stem cell, or iPSC, which is able to generate nearly any type of cell in the body ā including dopamine-producing neurons. Its manufacturing is a three-step process. https://parkinsonsnewstoday.com/news
This experimental therapy for Parkinsonās uses a type of stem cell called an induced pluripotent stem cell, or iPSC, which is able to generate nearly any type of cell in the body ā including dopamine-producing neurons. Its manufacturing is a three-step process. https://parkinsonsnewstoday.com/news
Farooqji
in
Cure Parkinson's
24 hours ago
When were you going to mention I had early CKD? Oh I see, stage II isnāt anything to worry my little head about š
As my profile name implies, I have spent 20+ years in the healthcare industry. It took longer than Iād like to admit to awakening to how broken, corrupted and frankly dangerous this āHealthcare Industrial Complexā is. I recently had my annual exam with a PCP that I have always had great respect for
As my profile name implies, I have spent 20+ years in the healthcare industry. It took longer than Iād like to admit to awakening to how broken, corrupted and frankly dangerous this āHealthcare Industrial Complexā is. I recently had my annual exam with a PCP that I have always had great respect for
DisillusionedRN
in
Early CKD Support
1 day ago
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