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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
5 months ago
Levothyroxine without prescription
I have been diagnosed with
Hashimotos
disease
which my GP tells me is nit treatable until my levels get so bad it present as hypothyroidism.
I have been diagnosed with
Hashimotos
disease
which my GP tells me is nit treatable until my levels get so bad it present as hypothyroidism.
Gillm84
in
Thyroid UK
28 days ago
Slippery elm and thyroid meds
Does anyone with
hashimotos
thyroid
disease
take slippery elm? I want to try this but Im trying to work out how to stop it affecting absorption of thyroid meds (thyroxine and Liithyronine which I take on waking and at 9 pm. I usually take peptac at 11 pm.
Does anyone with
hashimotos
thyroid
disease
take slippery elm? I want to try this but Im trying to work out how to stop it affecting absorption of thyroid meds (thyroxine and Liithyronine which I take on waking and at 9 pm. I usually take peptac at 11 pm.
Tessica
in
Acid Reflux Support
2 months ago
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Gastritis and Hashimotos
Does anyone with
hashimotos
thyroid
disease
take slippery elm? I want to try this for gastritis but Im trying to work out how to stop it affecting absorption of thyroid meds (thyroxine and Liithyronine which I take on waking and at 9 pm. I usually take peptac also at 11 pm.Thanks
Does anyone with
hashimotos
thyroid
disease
take slippery elm? I want to try this for gastritis but Im trying to work out how to stop it affecting absorption of thyroid meds (thyroxine and Liithyronine which I take on waking and at 9 pm. I usually take peptac also at 11 pm.Thanks
Tessica
in
Thyroid UK
2 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
3 months ago
Help getting a levothyroxine prescription
Has anyone had a diagnosis of
hashimotos
disease
and recieved any treatment or has anyone went private and been given levothyroxine or have any advice on how to get it? Thanks in advance
Has anyone had a diagnosis of
hashimotos
disease
and recieved any treatment or has anyone went private and been given levothyroxine or have any advice on how to get it? Thanks in advance
Gillm84
in
Thyroid UK
28 days 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
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
4 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
7 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
1 year ago
Megaloblastic anemia and very low b12
I only have one other health issue and that's
hashimotos
thyroid
disease
. Thank you
I only have one other health issue and that's
hashimotos
thyroid
disease
. Thank you
Plumpudding
in
Pernicious Anaemia Society
2 days ago
Liver nodules
I also have
hashimotos
, addisons
disease
and sjogrens syndrome I was wondering if these autoimmune conditions could be causing nodules and just pray it's not cancer! Thanks for reading
I also have
hashimotos
, addisons
disease
and sjogrens syndrome I was wondering if these autoimmune conditions could be causing nodules and just pray it's not cancer! Thanks for reading
Kjs1993
in
British Liver Trust
3 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
6 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
5 months ago
Thyroid autoantibodies/TPO test results
Is this high or very high, please, and has anyone with similar readings gone on to discover that they have hyperparathyroid
disease
plus
Hashimotos
?
Is this high or very high, please, and has anyone with similar readings gone on to discover that they have hyperparathyroid
disease
plus
Hashimotos
?
Hidden
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
4 months ago
Post Surgery Query
Hi there, I had a lap, hysteroscopy and curettage 3 days ago. Unattached ovary from back of uterus and removed the scar tissue from it, excision of 3 points of endo on other ovary, slight ablation of endo on bladder and removed a big piece of tissue from top to bottom of uterus. Reading everything
Hi there, I had a lap, hysteroscopy and curettage 3 days ago. Unattached ovary from back of uterus and removed the scar tissue from it, excision of 3 points of endo on other ovary, slight ablation of endo on bladder and removed a big piece of tissue from top to bottom of uterus. Reading everything
Oneday_
in
Endometriosis UK
36 minutes ago
Circulating Lipid Profiles Associated With Resistance to Androgen Deprivation Therapy in Localized Prostate Cancer
Circulating Lipid Profiles Associated With Resistance to Androgen Deprivation Therapy in Localized Prostate Cancer Authors: Hui-Ming Lin, PhD https://orcid.org/0000-0003-4892-6008, Xiaoyu Yang, MS https://orcid.org/0009-0001-0035-9289, Margaret M. Centenera, PhD https://orcid.org/0000-0002-2206-0632
Circulating Lipid Profiles Associated With Resistance to Androgen Deprivation Therapy in Localized Prostate Cancer Authors: Hui-Ming Lin, PhD https://orcid.org/0000-0003-4892-6008, Xiaoyu Yang, MS https://orcid.org/0009-0001-0035-9289, Margaret M. Centenera, PhD https://orcid.org/0000-0002-2206-0632
podsart
in
Advanced Prostate Cancer
4 hours ago
At what PSA will a PSMA PET scan be useful?
Hi everyone My father has been on Lupron for 3 years now. We stopped Abi last year due to rising blood sugar levels. His PSA used to hover between 0.6-0.8 (with an occasional spike to 1.2). PSA in May 24 was 0.6. Today, however, his PSA came back as 2.5. Plan is to restart Abi and monitor. But I wanted
Hi everyone My father has been on Lupron for 3 years now. We stopped Abi last year due to rising blood sugar levels. His PSA used to hover between 0.6-0.8 (with an occasional spike to 1.2). PSA in May 24 was 0.6. Today, however, his PSA came back as 2.5. Plan is to restart Abi and monitor. But I wanted
Rodeoz15
in
Advanced Prostate Cancer
5 hours ago
Recurrent prostate cancer at 5 months after radical prostatectomy, with psa up to 0.2. PSMA and MRI negative. Now on Leuprolide and Nubeqa.
My Gleason was 9. Incontinence has been an issue since the RP and even though it has improved still leaked around 30 ml a day. Delaying radiation that I was recommended by one institution but some Oncologists say to delay radiation for more recovery. Even though my PSA is 0.01 on the meds, i worry
My Gleason was 9. Incontinence has been an issue since the RP and even though it has improved still leaked around 30 ml a day. Delaying radiation that I was recommended by one institution but some Oncologists say to delay radiation for more recovery. Even though my PSA is 0.01 on the meds, i worry
Chipichape1
in
Advanced Prostate Cancer
23 hours ago
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