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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
2 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
6 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
14 days ago
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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
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
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 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
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
1 month 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
11 months ago
The role of PSMA PET/CT in predicting downgrading in patients with Gleason score 4+4 prostate cancer in prostate biopsy - W Jour Uro 5/21/24
[i]An interesting investigation aimed at validating the use of PSMA PET/CT in patients to adjust the Gleason score (downward) of their cancer based on conventional pre-surgery biopsy, scans (ultrasound & MRI). In this instance the focus was on downgrading from a high-risk of 8 to an intermediate-risk
[i]An interesting investigation aimed at validating the use of PSMA PET/CT in patients to adjust the Gleason score (downward) of their cancer based on conventional pre-surgery biopsy, scans (ultrasound & MRI). In this instance the focus was on downgrading from a high-risk of 8 to an intermediate-risk
cujoe
in
Fight Prostate Cancer
2 hours ago
Any Carnivore dieters who are taking Parkinson’s medication?
Hello, I am a 42 year old woman, diagnosed with Parkinson’s, 17 years ago, at the age of 40. started Kinson Parkinson’s medication 4 years ago but I’m experiencing increased meds off times. I heard about the Carnivore diet and I am very interested in trying it, but I am not sure joe I can do it successfully
Hello, I am a 42 year old woman, diagnosed with Parkinson’s, 17 years ago, at the age of 40. started Kinson Parkinson’s medication 4 years ago but I’m experiencing increased meds off times. I heard about the Carnivore diet and I am very interested in trying it, but I am not sure joe I can do it successfully
Seekerofhealth
in
Cure Parkinson's
8 hours ago
Protein supplements
I've been reading a lot about needing proteins to help with thyroid issues. Has anyone embarked on this route ?
I've been reading a lot about needing proteins to help with thyroid issues. Has anyone embarked on this route ?
HHHJC
in
Thyroid UK
11 hours ago
PCA Prognosis?
Hi All! I am due for my 4rd Lupron treatment and follow-up next week. My bloodwork is done and my PSA is still <.01 for 9 months now. I have BRCA 1 and 2. When my Urologist gave me my initial diagnosis after my biopsies (Gleason 4+3=7 and 11 of 12 biopsies positive). nHe gave me a full report
Hi All! I am due for my 4rd Lupron treatment and follow-up next week. My bloodwork is done and my PSA is still <.01 for 9 months now. I have BRCA 1 and 2. When my Urologist gave me my initial diagnosis after my biopsies (Gleason 4+3=7 and 11 of 12 biopsies positive). nHe gave me a full report
Sagewiz
in
Advanced Prostate Cancer
18 hours ago
Two updates in the Guidelines for PBC
PRACTICE GUIDANCE Primary biliary cholangitis: 2021 practice guidance update from the American Association for the Study of Liver Diseases Lindor, Keith D.*,1; Bowlus, Christopher L.2; Boyer, James3; Levy, Cynthia4; Mayo, Marlyn5 Author Information Hepatology 75(4):p 1012-1013, April 2022. | DOI
PRACTICE GUIDANCE Primary biliary cholangitis: 2021 practice guidance update from the American Association for the Study of Liver Diseases Lindor, Keith D.*,1; Bowlus, Christopher L.2; Boyer, James3; Levy, Cynthia4; Mayo, Marlyn5 Author Information Hepatology 75(4):p 1012-1013, April 2022. | DOI
DonnaBoll
Administrator
in
PBC Foundation
1 day ago
hepatic Encephalopathy
morning, can anyone advice me about hepatic Encephalopathy ? I have stage 4 liver desease and was feeling so confused last night with things like time and thinking lights were off but were on is this the start of it? Last time I was like this was last march when I had my diagnoses, I take lactose which
morning, can anyone advice me about hepatic Encephalopathy ? I have stage 4 liver desease and was feeling so confused last night with things like time and thinking lights were off but were on is this the start of it? Last time I was like this was last march when I had my diagnoses, I take lactose which
Kingbilly3
in
British Liver Trust
1 day ago
Some good news to start the day: Complete Response in First Patient Ever Treated with 2 Doses of Cu-67 SAR-bisPSMA at 8GBq...6 months
I have already written about this, but then he approached the 6 months mark, so... "The patient remains with undetectable levels of Prostate Specific Antigen (PSA) for almost 6 months, following the administration of the second dose of 67Cu-SAR-bisPSMA. PSA is a marker used to assess clinical response
I have already written about this, but then he approached the 6 months mark, so... "The patient remains with undetectable levels of Prostate Specific Antigen (PSA) for almost 6 months, following the administration of the second dose of 67Cu-SAR-bisPSMA. PSA is a marker used to assess clinical response
Maxone73
in
Advanced Prostate Cancer
1 day ago
Lixisenatide as a treatment for early Parkinson’s disease progression
In this randomized controlled trial, lixisenatide reduced motor disability progression in Parkinson’s patients. 2. Individuals in the lixisenatide group experienced greater gastrointestinal side effects rates than individuals in the placebo group. Evidence Rating Level: 1 (Excellent) https:/
In this randomized controlled trial, lixisenatide reduced motor disability progression in Parkinson’s patients. 2. Individuals in the lixisenatide group experienced greater gastrointestinal side effects rates than individuals in the placebo group. Evidence Rating Level: 1 (Excellent) https:/
Farooqji
in
Cure Parkinson's
2 days ago
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