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Adcal-D3 Caplets
Hi all,been on Adcal-D3 for 6years,2 in afternoon and 2 at bed time, just wondering how long you have to take them, 🤔 was worrying about kidney stones don't want them,seems it's the vit d that can cause them,but if they helping the bones . Xx
Hi all,been on Adcal-D3 for 6years,2 in afternoon and 2 at bed time, just wondering how long you have to take them, 🤔 was worrying about kidney stones don't want them,seems it's the vit d that can cause them,but if they helping the bones . Xx
Harrywogan
in
PMRGCAuk
1 year ago
Help with results and supplements please
I hope you can help me as I'm struggling. I haven't been feeling good for a long time - brainfog, poor memory, aches, fatigue, bloating, broken sleep, ringing in ears, pins n needles in fingers and toes, eyesight not so good.. currently on 125 eutirox and 10 liquid t3 liotir (im in Italy) I'm confused
I hope you can help me as I'm struggling. I haven't been feeling good for a long time - brainfog, poor memory, aches, fatigue, bloating, broken sleep, ringing in ears, pins n needles in fingers and toes, eyesight not so good.. currently on 125 eutirox and 10 liquid t3 liotir (im in Italy) I'm confused
Sandytango
in
Thyroid UK
1 year ago
1st BLOOD RESULT ON NDT
hi, thank you for looking and reading. I had a full thyroidectomy on 20 December 2022. I tried levothyroxine and was struggling to convert. I went on to NDT 7 weeks ago. I did my blood test this morning fasting and drinking only water at 7.30am, and I withheld the NDT for 24 hours. I appreciate my t3
hi, thank you for looking and reading. I had a full thyroidectomy on 20 December 2022. I tried levothyroxine and was struggling to convert. I went on to NDT 7 weeks ago. I did my blood test this morning fasting and drinking only water at 7.30am, and I withheld the NDT for 24 hours. I appreciate my t3
NIKEGIRL
in
Thyroid UK
1 year ago
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Rux Experience at 5 weeks
Started Rux at 10mg twice daily 5 weeks ago after MPN specialist suggested it might help with my non-specific symptoms she thinks may be related to my Type 2 CALR ET that came on when I stopped Peg 2 years ago. Bumped up to 15mg x2 - two weeks ago because platelets were going up every two weeks. I have
Started Rux at 10mg twice daily 5 weeks ago after MPN specialist suggested it might help with my non-specific symptoms she thinks may be related to my Type 2 CALR ET that came on when I stopped Peg 2 years ago. Bumped up to 15mg x2 - two weeks ago because platelets were going up every two weeks. I have
George1976
in
MPN Voice
1 year ago
anyone had prostap without Tibolone?
Hi I’m nearly 5 months in on the 3monthly prostap ( for fibroid shrinkage and pre hysterectomy) .. I didn’t take the Tibolone due to my fears for the first 3 months , but tried it on a half dose for about a month when I started the second 3month injection . Then I hated the side effects and they made
Hi I’m nearly 5 months in on the 3monthly prostap ( for fibroid shrinkage and pre hysterectomy) .. I didn’t take the Tibolone due to my fears for the first 3 months , but tried it on a half dose for about a month when I started the second 3month injection . Then I hated the side effects and they made
Batwoman3
in
Endometriosis UK
1 year ago
Help with latest blood test results and NDT dose please
Hello, long story short... I've had hypothyroidism for around 14 years now, I've had a mixture during those years of either levothyroxine - GP never prescribed the right dose and I had reactions to it, so started buying NDT and did well, until covid hit and I found it difficult to get it. My latest
Hello, long story short... I've had hypothyroidism for around 14 years now, I've had a mixture during those years of either levothyroxine - GP never prescribed the right dose and I had reactions to it, so started buying NDT and did well, until covid hit and I found it difficult to get it. My latest
pixieforest
in
Thyroid UK
1 year ago
Psoriasis of the Scalp eradicated
Hello I am new to this site but have had psoriasis of the scalp for over 20 years and probably like most others have tried various creams, lotions and potions which would give temporary relief but didn't cure it. I also have a thyroid condition and upon reading up found that patients with psoriasis
Hello I am new to this site but have had psoriasis of the scalp for over 20 years and probably like most others have tried various creams, lotions and potions which would give temporary relief but didn't cure it. I also have a thyroid condition and upon reading up found that patients with psoriasis
Delgor
in
Beyond Psoriasis
1 year ago
ME/CFS advice amongst other things...
Hi, I'm sure some of you will know me and my story from my posts on this forum. I have hashimoto's hypothyroidism and suffered for over 4 years now and the situation is getting worse. It's destroying my life and my beautiful family, the mental strain over the last 2 weeks has been unbearable and I feel
Hi, I'm sure some of you will know me and my story from my posts on this forum. I have hashimoto's hypothyroidism and suffered for over 4 years now and the situation is getting worse. It's destroying my life and my beautiful family, the mental strain over the last 2 weeks has been unbearable and I feel
joey82
in
Thyroid UK
1 year ago
At wits end
Hi, I feel very anxious and depressed. Getting really horrible feelings. I’m on duloxetiene, and have just increased it from 30mg to 60mg a few days ago. I have just had a blood test and they say my vitamin D is borderline so I am just starting 1000 IOU’s of vitamin D tablets. I haven’t worked for almost
Hi, I feel very anxious and depressed. Getting really horrible feelings. I’m on duloxetiene, and have just increased it from 30mg to 60mg a few days ago. I have just had a blood test and they say my vitamin D is borderline so I am just starting 1000 IOU’s of vitamin D tablets. I haven’t worked for almost
Emma143
in
Anxiety Support
1 year ago
Vitamin D
Vitamin D is often mentioned here, as is fibromyalgia. I thought some here might be interested in this article: https://www.hcplive.com/view/vitamin-d-may-improve-quality-of-life-in-fibromyalgia
Vitamin D is often mentioned here, as is fibromyalgia. I thought some here might be interested in this article: https://www.hcplive.com/view/vitamin-d-may-improve-quality-of-life-in-fibromyalgia
WiscGuy
in
Pernicious Anaemia Society
1 year ago
B12 only half the battle -- and an odd symptom
Back story: I was B12, Folate, Vit. D deficient with extremely low Ferritin (9). These deficiencies have been going on for years and docs were pretty clueless, made me feel like I was a drama queen about it all, and I had an allergy to B12 shots. Was finally sent to a hematologist who was ON this -
Back story: I was B12, Folate, Vit. D deficient with extremely low Ferritin (9). These deficiencies have been going on for years and docs were pretty clueless, made me feel like I was a drama queen about it all, and I had an allergy to B12 shots. Was finally sent to a hematologist who was ON this -
vagabondbeauty
in
Pernicious Anaemia Society
1 year ago
Back in the thyroid zone!
Been a while but I’ve been over on another site PMRGCAUK, jeez these autoimmune diseases , the gift that keeps on giving ! Long story but on Pred for that , tapering into my 10th month. Fabulous group, as is this, but taken my eye off the ball with the thyroid lately! Anyway availed of the Blue Horizon
Been a while but I’ve been over on another site PMRGCAUK, jeez these autoimmune diseases , the gift that keeps on giving ! Long story but on Pred for that , tapering into my 10th month. Fabulous group, as is this, but taken my eye off the ball with the thyroid lately! Anyway availed of the Blue Horizon
Romilly2
in
Thyroid UK
1 year ago
Bloods Back
Good evening, NHS Bloods are back: Ferritin 22ug/L (15-300ug/L) B12 317ng/L (180-900mg/L) Vit D 42 nmol/L Folate 4.9ug/L > 3ug/L I’ve really appreciated the support and guidance people have given. It’s a weekend of studying the best Vits for me. Thank you so much yet again ❤️
Good evening, NHS Bloods are back: Ferritin 22ug/L (15-300ug/L) B12 317ng/L (180-900mg/L) Vit D 42 nmol/L Folate 4.9ug/L > 3ug/L I’ve really appreciated the support and guidance people have given. It’s a weekend of studying the best Vits for me. Thank you so much yet again ❤️
Tinker72
in
Thyroid UK
1 year ago
D3 supplimenting
As I a Hashimoto's I often see that it's important to take optimal doses of D3 daily. I also have to wear 50 factor SPF on my face because of solar keratosis. I have been taking high doses especially through the winter, but my latest blood test shows I' m too high Serum total 25-hydroxy vitamin D level
As I a Hashimoto's I often see that it's important to take optimal doses of D3 daily. I also have to wear 50 factor SPF on my face because of solar keratosis. I have been taking high doses especially through the winter, but my latest blood test shows I' m too high Serum total 25-hydroxy vitamin D level
Everdean
in
Thyroid UK
1 year ago
Titration of blood tests newly diagnosed
Hello... new diagnosis hashimotos in march , started on 50mcg thyroxine 18th march, repeat bloods in 3 months . Today I asked my GP for rationale for the three months having asked for a immediate review which she refused saying that the levels would not show up with a test now which I challenged the
Hello... new diagnosis hashimotos in march , started on 50mcg thyroxine 18th march, repeat bloods in 3 months . Today I asked my GP for rationale for the three months having asked for a immediate review which she refused saying that the levels would not show up with a test now which I challenged the
Hidden
in
Thyroid UK
1 year ago
questions before private endo
Recent blood tests have revealed the following. Blood test taken without medication and food at 9 am, followed protocol re avoiding biotin before etc. Medication 100 mg levothyroxine ( accord) CRP - 0.14 < 3 Ferritin 23 (30 - 150) B Active 73 (37.5 - 188) Folate Serum 31.9 (8.83 - 60.8) Vit D
Recent blood tests have revealed the following. Blood test taken without medication and food at 9 am, followed protocol re avoiding biotin before etc. Medication 100 mg levothyroxine ( accord) CRP - 0.14 < 3 Ferritin 23 (30 - 150) B Active 73 (37.5 - 188) Folate Serum 31.9 (8.83 - 60.8) Vit D
Hopeful129
in
Thyroid UK
1 year ago
NHS Attitudes on Worth of Life
My deep apologies to everyone for this post but I think it’s going to be a long one. Partly about PA and partly on NHS attitudes I am encountering about the worth of life. Warning for sensitive members, this post might be shocking. So you will know me through my posts regarding seizures and both neurological
My deep apologies to everyone for this post but I think it’s going to be a long one. Partly about PA and partly on NHS attitudes I am encountering about the worth of life. Warning for sensitive members, this post might be shocking. So you will know me through my posts regarding seizures and both neurological
RoseFlowerDew
in
Pernicious Anaemia Society
1 year ago
Depression and tsh?
Hey guys, I am back again! So recently tsh was 4.43 range 0.35 - 4.94, so doctor said your thyroid is back to normal, I argued that I was still at the upper end of the range and convinced this was causing my low mood and anxiety. I asked for more levothyroxine but he declined, I still argued with him
Hey guys, I am back again! So recently tsh was 4.43 range 0.35 - 4.94, so doctor said your thyroid is back to normal, I argued that I was still at the upper end of the range and convinced this was causing my low mood and anxiety. I asked for more levothyroxine but he declined, I still argued with him
Dollc86
in
Thyroid UK
1 year ago
Vitamin D supplementation.
I have finally got my nine weeks done on no change to thyroid meds after a period of changing meds too quickly for my body to cope properly. I will post the full results when I have had a proper chance to study them. Trying to understand them for myself. Since January (mental issues and big physicals
I have finally got my nine weeks done on no change to thyroid meds after a period of changing meds too quickly for my body to cope properly. I will post the full results when I have had a proper chance to study them. Trying to understand them for myself. Since January (mental issues and big physicals
arTistapple
in
Thyroid UK
1 year ago
Vitamin
Hi currently on 50mcg of levothyroxine just wondering what is the best vitamins to take currently take roughly about 3000iu of vitamin D and B complex and B12 spray and omega 3 daily any advice thanks.
Hi currently on 50mcg of levothyroxine just wondering what is the best vitamins to take currently take roughly about 3000iu of vitamin D and B complex and B12 spray and omega 3 daily any advice thanks.
Campy1967
in
Thyroid UK
1 year ago
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