Search
Search
About
Log in
Join
Experiences with
Potassium iodide
Posts
Communities
3,587 public posts
Filter results
Feel like my old self has died
Hi Feeling like I don’t really know which way to turn and would welcome any advice please. I don’t really post but read the posts daily. It’s the only way I’ve learnt anything about this god awful illness. After the RAI the Dr said i had Graves but the Dr who did my biopsies said Hashimotos. The first
Hi Feeling like I don’t really know which way to turn and would welcome any advice please. I don’t really post but read the posts daily. It’s the only way I’ve learnt anything about this god awful illness. After the RAI the Dr said i had Graves but the Dr who did my biopsies said Hashimotos. The first
kazb1966
in
Thyroid UK
6 years ago
Different brands of Levothyroxine.
I have been on Thyroxine since 1994 after receiving RAI but the whole experience has made me worse. Endo now has me on 75mcg but brain fatigue is a lot worse and my legs lack power. No matter what dosage I take , there is no improvement. I have now increased dosage to 100mcg- stopped taking all supplements
I have been on Thyroxine since 1994 after receiving RAI but the whole experience has made me worse. Endo now has me on 75mcg but brain fatigue is a lot worse and my legs lack power. No matter what dosage I take , there is no improvement. I have now increased dosage to 100mcg- stopped taking all supplements
delboy25
in
Thyroid UK
6 years ago
Restless leg syndrome Chanel 5 10pm tonight
Hi all, Tonight in Chanel 5 there is a documentary on restless leg syndrome. If you have it or even if you don’t it’s so well worth watching it or grab it on catch up. I have Graves and had RAI. I was left with secondary restless leg. When I took thyroxine it was so severe it moved to my hand. The sensation
Hi all, Tonight in Chanel 5 there is a documentary on restless leg syndrome. If you have it or even if you don’t it’s so well worth watching it or grab it on catch up. I have Graves and had RAI. I was left with secondary restless leg. When I took thyroxine it was so severe it moved to my hand. The sensation
rubyred
in
Thyroid UK
6 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
My take on stress free painless injections
Like many of us I have had a number of different injectors and I always wonder who I am going to get. Some have been more adept than others, though the aftermath has been more or less the same, except after my 3rd injection when every bone in my face became hot and extremely painful. For the 4th injection
Like many of us I have had a number of different injectors and I always wonder who I am going to get. Some have been more adept than others, though the aftermath has been more or less the same, except after my 3rd injection when every bone in my face became hot and extremely painful. For the 4th injection
Hidden
in
Macular Society
6 years ago
NHS V Private appointment
Attending NHS app tomorrow with endocrinologist sadly I do not hold much hope for outcome see previous entry . If I do not have any joy could anyone recommend specials in south west Wales and Bristol . My QOL has not been good since Diagnosis Graves Diaease followed by RAI
Attending NHS app tomorrow with endocrinologist sadly I do not hold much hope for outcome see previous entry . If I do not have any joy could anyone recommend specials in south west Wales and Bristol . My QOL has not been good since Diagnosis Graves Diaease followed by RAI
annie123
in
Thyroid UK
6 years ago
So many horrible symptoms
Hi everyone sine having RAI for Graves‘ disease five years ago I feel my get up and go has gone everything is an effort overwhelming fatigue on wakening ,hot flushes, strange intermittent fluttering around thyroid area that can last hours . Constipation, muscles ache all over . Shortness of breath oxygen
Hi everyone sine having RAI for Graves‘ disease five years ago I feel my get up and go has gone everything is an effort overwhelming fatigue on wakening ,hot flushes, strange intermittent fluttering around thyroid area that can last hours . Constipation, muscles ache all over . Shortness of breath oxygen
annie123
in
Thyroid UK
6 years ago
My cure for persistent Balanitis and/or Thrush. Stubborn penis rash that won't go away.
I found a cure for myself. Afetr suffering with this for 2 months and trying suggestions here, which failed for me, I went to a private doctor, this is the 2 things I did: 1) Applied Iodine by Betadine 60ml but any Iodine solution will do. It's a brown liquid and you mix it with around 50ml or so cold
I found a cure for myself. Afetr suffering with this for 2 months and trying suggestions here, which failed for me, I went to a private doctor, this is the 2 things I did: 1) Applied Iodine by Betadine 60ml but any Iodine solution will do. It's a brown liquid and you mix it with around 50ml or so cold
Pete55
in
Men's Health Forum
6 years ago
Hi all. My hypo thyroid symptoms seem worse to me despite medication and my endo saying I'm in range. By 12pm I feel totally unmedicated?
Hi I'm really struggling with my hypothyroidism since radio iodine treatment nearly two years ago. I started on Levo but found it difficult to tolerate finally giving up on it at 150mcg with itching, unbearable insomnia and huge weight gain. I went onto Naturethroid which was tolerated better and then
Hi I'm really struggling with my hypothyroidism since radio iodine treatment nearly two years ago. I started on Levo but found it difficult to tolerate finally giving up on it at 150mcg with itching, unbearable insomnia and huge weight gain. I went onto Naturethroid which was tolerated better and then
Shredder
in
Thyroid UK
6 years ago
Dr decreased my T3 & 4mo later 22 lbs of what I know is not fat as I consume less than 1200 calories daily, freezing cold/hairless/myxedema
Had RAI JUST OVER A YEAR ... went hypo quickly and symptomatic of hypo still. All the drs care about is a Tsh not that I put in 22 lbs of what feels like cold wet edema everywhere now even my stomach ( I can do 100 crunches ) and not break a sweat . I want to get off this crazy train !! Sick and tired
Had RAI JUST OVER A YEAR ... went hypo quickly and symptomatic of hypo still. All the drs care about is a Tsh not that I put in 22 lbs of what feels like cold wet edema everywhere now even my stomach ( I can do 100 crunches ) and not break a sweat . I want to get off this crazy train !! Sick and tired
MaryRAI
in
Thyroid UK
6 years ago
Euthyrox vs.Tirosint, my first question here!
Hello, it's my first post, I'm hipo (after RAI in 2012 due to Graves) on 125mcg Euthyrox+some T3 but I not doing well on it. I would like to know if 125 levothyroxine has the same potency as 125mcg Tirosint? I would like to buy some Tirosint but I'm afraid that 125mcg of Tirosint is more potent than
Hello, it's my first post, I'm hipo (after RAI in 2012 due to Graves) on 125mcg Euthyrox+some T3 but I not doing well on it. I would like to know if 125 levothyroxine has the same potency as 125mcg Tirosint? I would like to buy some Tirosint but I'm afraid that 125mcg of Tirosint is more potent than
hipolion
in
Thyroid UK
6 years ago
I have Graves Disease and I am being pressured in to making a definitive decision: RAI or surgery...
Hello, I have been diagnosed with Graves Disease since August 2015, aged 31. I have tried Block & Replace but unfortunately I relapsed last July after 6 months of no treatment. I am currently on 5mg of Carbimazole daily but my Endo is pushing me to make a definitive decision regarding the future of my
Hello, I have been diagnosed with Graves Disease since August 2015, aged 31. I have tried Block & Replace but unfortunately I relapsed last July after 6 months of no treatment. I am currently on 5mg of Carbimazole daily but my Endo is pushing me to make a definitive decision regarding the future of my
RhubarbAndCustard
in
Graves Disease Support
6 years ago
Thyroid Eye Disease & Prednisone | light at the end of the tunnel? :(
I have been diagnosed with TED by my endo and she has put me on a short course of 20mg of prednisone and referred me to a ted eye specialist. (i am also taking selenium, cut out gluten and have eye drops). This came 2 weeks after an RAI scan (where they use a tiny bit of iodine) and this apparently
I have been diagnosed with TED by my endo and she has put me on a short course of 20mg of prednisone and referred me to a ted eye specialist. (i am also taking selenium, cut out gluten and have eye drops). This came 2 weeks after an RAI scan (where they use a tiny bit of iodine) and this apparently
GraceLucy
in
Thyroid UK
6 years ago
Feeling confused...
Hi I am new to the forum and my brain is spinning at 100 miles an hour... I just wondered if people could give me some experience or suggestions of places to look for information - it is a mine field out there and struggling with where to start. Sorry for the long post, but here is the background...
Hi I am new to the forum and my brain is spinning at 100 miles an hour... I just wondered if people could give me some experience or suggestions of places to look for information - it is a mine field out there and struggling with where to start. Sorry for the long post, but here is the background...
Gem_gems
in
Thyroid UK
6 years ago
Testing for iodine deficiency
I've been using the search box to find out which is the best method to test iodine levels,but some posts are quite old & I am still confused.Please would people post or PM the latest thinking on the most accurate private test
I've been using the search box to find out which is the best method to test iodine levels,but some posts are quite old & I am still confused.Please would people post or PM the latest thinking on the most accurate private test
Naomi8
in
Thyroid UK
6 years ago
Pro BNP
I had a heart attack 4 years ago - from my very stressful job- and it was not properly diagnosed so when I eventually got help there was serious permanent damage. I understood the blood test called ProBNP showed results that indicated heart muscle damage (5500 was the score). In subsequent years the
I had a heart attack 4 years ago - from my very stressful job- and it was not properly diagnosed so when I eventually got help there was serious permanent damage. I understood the blood test called ProBNP showed results that indicated heart muscle damage (5500 was the score). In subsequent years the
annemk
in
AF Association
6 years ago
Iodine testing options
Id like to test my iodine level but have found the various, past HU responses a bit confusing. Some may also be out of date eg Blue Horizon dont seem to do it now (they did last December for £49 incl a 20% discount). Any views on the best method? Note: I had it done by blood test with BH 15 months ago
Id like to test my iodine level but have found the various, past HU responses a bit confusing. Some may also be out of date eg Blue Horizon dont seem to do it now (they did last December for £49 incl a 20% discount). Any views on the best method? Note: I had it done by blood test with BH 15 months ago
userotc
in
Thyroid UK
6 years ago
Is there any response to graves besides burn it with RAI?
Is there any response to Graves besides burn it with RAI? Ive been struggling with my thyroid for almost two years now, graves specifically before that I was hypo but never diagnosed. I got a new Endo this is the third suppose to be best in the state, and i tel lhim that I am looking for another option
Is there any response to Graves besides burn it with RAI? Ive been struggling with my thyroid for almost two years now, graves specifically before that I was hypo but never diagnosed. I got a new Endo this is the third suppose to be best in the state, and i tel lhim that I am looking for another option
bd8510
in
Graves Disease Support
6 years ago
The Thyroid Hormone Inactivating Type 3 Deiodinase Is Essential for Optimal Neutrophil Function: Observations From Three Species
OK, OK - so Deiodinase Type 3 is essential for the functioning of neutrophils. But
WHY
? [Many years ago, I remember reading the idea that in certain circumstances thyroid hormone(s) would be deiodinated in order to release iodine atoms - with the iodine then being available to kill bacteria (or
OK, OK - so Deiodinase Type 3 is essential for the functioning of neutrophils. But
WHY
? [Many years ago, I remember reading the idea that in certain circumstances thyroid hormone(s) would be deiodinated in order to release iodine atoms - with the iodine then being available to kill bacteria (or
helvella
Thyroid UK
in
Thyroid UK
6 years ago
Sore Feet and Aching Body
Hi, had Graves disease, got nuclear iodine, now thyroid under active. Using the medication and my levels have stabilized. Want to know if anybody else suffers from sore feet and aching body? And what could be the cause. Thank you.
Hi, had Graves disease, got nuclear iodine, now thyroid under active. Using the medication and my levels have stabilized. Want to know if anybody else suffers from sore feet and aching body? And what could be the cause. Thank you.
AMCB
in
Thyroid UK
6 years ago
Nausea and underactive thyroid.
Hello! I am just wondering if it is normal to get nausea after starting Levothyroxine? 9th Feb my GP tested TSH only and Vit D levels. TSH 7.6 (range 0.27-4.2) Vit D 118 (range >51) I was started on 50mg Levothyroxine end of Feb but had a few adverse reactions (which my specialist nurse says is nothing
Hello! I am just wondering if it is normal to get nausea after starting Levothyroxine? 9th Feb my GP tested TSH only and Vit D levels. TSH 7.6 (range 0.27-4.2) Vit D 118 (range >51) I was started on 50mg Levothyroxine end of Feb but had a few adverse reactions (which my specialist nurse says is nothing
melon_one
in
Thyroid UK
6 years ago
1
...
89
90
91
...
100
Next page
50
60
70
80
90
100
Filter results
Clear filters
Posted in
All communities
Thyroid UK
2973 results
NRAS
59 results
Macular Society
56 results
View top 10 communities
Sort by
Most Relevant
Newest