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thyroid results
Could someone please help me understand my blood results which I had done by Medichecks (home testing kit) I have had underactive thyroid for the past 25years The doctors are always changing the brands I take I hadn’t had my thyroid levels tested for nearly 5 years with my GP, it’s as if they’d
Could someone please help me understand my blood results which I had done by Medichecks (home testing kit) I have had underactive thyroid for the past 25years The doctors are always changing the brands I take I hadn’t had my thyroid levels tested for nearly 5 years with my GP, it’s as if they’d
Horsemadlindy21
in
Thyroid UK
2 months ago
Blood test results
Hi all, can i have some help with blood test results? went to GP with symptoms of Hypothyroid, family history as both parents are diagnosed hypo. I was sent for full bloods incluing thyroid function 1/5/24 (bloods taken about 11am) HbA1c 31 mmol n/a Haemantinic serum vit b12 322ng/l 189-883
Hi all, can i have some help with blood test results? went to GP with symptoms of Hypothyroid, family history as both parents are diagnosed hypo. I was sent for full bloods incluing thyroid function 1/5/24 (bloods taken about 11am) HbA1c 31 mmol n/a Haemantinic serum vit b12 322ng/l 189-883
cheekysaph
in
Thyroid UK
10 days ago
Thybon Henning 20mcg T3 from Roseway
just posting this for comparison. I just had a private phone appointment with Roseway labs (£35) cheaper appointment as it’s a repeat, first appointment is £55. I will be trialling 10mcg T3 split 5/5 she suggested Thybon Henning (lactose free). 100 tablets for £60 via private prescription to cut into
just posting this for comparison. I just had a private phone appointment with Roseway labs (£35) cheaper appointment as it’s a repeat, first appointment is £55. I will be trialling 10mcg T3 split 5/5 she suggested Thybon Henning (lactose free). 100 tablets for £60 via private prescription to cut into
Regenallotment
in
Thyroid UK
5 months ago
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Endo finally tested FT3! Thoughts?
At my last endo appt early Dec, the consultant kept his same stance that my blood tests were all in range and my symptoms were all due to perimenopause. He said there was slight room for a small increase in levothyroxine so ive gone from 125x5/100x2 to 125x6 /100x1 and told me to speak to my gp and
At my last endo appt early Dec, the consultant kept his same stance that my blood tests were all in range and my symptoms were all due to perimenopause. He said there was slight room for a small increase in levothyroxine so ive gone from 125x5/100x2 to 125x6 /100x1 and told me to speak to my gp and
JUUJOO
in
Thyroid UK
3 months ago
Holding very low stable usPSA - 0.03X range for six years; no ADT, no chemo.
Eight years ago this month had RP after considerable investigation - nadir 0.050. Eleven months later had salvage RT; done at 0.10. Then after a year of pondering ADT and chemo, when my usPSA was back up to 0.10, I went to Europe for Ferrotran nano-MRI combined with Ga68 PSMA. The nanoMRI lite up
Eight years ago this month had RP after considerable investigation - nadir 0.050. Eleven months later had salvage RT; done at 0.10. Then after a year of pondering ADT and chemo, when my usPSA was back up to 0.10, I went to Europe for Ferrotran nano-MRI combined with Ga68 PSMA. The nanoMRI lite up
NanoMRI
in
Advanced Prostate Cancer
5 months ago
Blood test
Gp refuses to prescribe T3 as previously prescribe my old gp and refuses to increase T4 as apparently my thyroid result is normal ( I don't have one ) no mention of the T3 10 mcg plus T4 75mcg what's the point of this ? Apparently this abundant in detail result shows I don't need an increase in T4
Gp refuses to prescribe T3 as previously prescribe my old gp and refuses to increase T4 as apparently my thyroid result is normal ( I don't have one ) no mention of the T3 10 mcg plus T4 75mcg what's the point of this ? Apparently this abundant in detail result shows I don't need an increase in T4
Jodiedebs
in
Thyroid UK
3 months ago
T3 and NDT help/advice
I have an Endo appt, 6 February, after a very long delay. I am struggling to function, despite an increase Levo to 125mg. The normal pattern; feel slightly better for a short few weeks then the awful symptoms come crashing back. I cannot function properly. I am trying to find out how to self
I have an Endo appt, 6 February, after a very long delay. I am struggling to function, despite an increase Levo to 125mg. The normal pattern; feel slightly better for a short few weeks then the awful symptoms come crashing back. I cannot function properly. I am trying to find out how to self
sunbee
in
Thyroid UK
5 months ago
Interpret test results - advice please
I've been on 75 mcg levothyroxine since 23 August 2023. I've taken levothyroxine since January 2023. Is this the correct dosage now? I've never had any of the conventional hypothyroid symptoms, except for extreme anxiety and disregulated nervous system, gut issues and tinnitus. On the 75mcg I feel
I've been on 75 mcg levothyroxine since 23 August 2023. I've taken levothyroxine since January 2023. Is this the correct dosage now? I've never had any of the conventional hypothyroid symptoms, except for extreme anxiety and disregulated nervous system, gut issues and tinnitus. On the 75mcg I feel
Green1957
in
Thyroid UK
5 months ago
puzzled by result of ft3
can anyone explain why my ft3 result would be lower although I had increased the dose ?
can anyone explain why my ft3 result would be lower although I had increased the dose ?
130396
in
Thyroid UK
5 months ago
??????? seriously ?
So my new Gp decided I was draining the NHS by taking T3 so as you may remember they refused to prescribe it even though endo first prescribe it 4 years ago and previous GP had no issues prescribing it, long story short they asked for a blood test as I argued if your refusing to prescribe me T3 ( I
So my new Gp decided I was draining the NHS by taking T3 so as you may remember they refused to prescribe it even though endo first prescribe it 4 years ago and previous GP had no issues prescribing it, long story short they asked for a blood test as I argued if your refusing to prescribe me T3 ( I
Jodiedebs
in
Thyroid UK
3 months ago
Genetic test positive
In November 2023 my iron labs were increased. Ferritin 117 TSAT 58 my doctor said we would retest in six month and do genetic testing but wasn’t concerned. My results just came in and it showed homogenous for H63D. I haven’t been able to speak with him yet. I am extremely scared.
In November 2023 my iron labs were increased. Ferritin 117 TSAT 58 my doctor said we would retest in six month and do genetic testing but wasn’t concerned. My results just came in and it showed homogenous for H63D. I haven’t been able to speak with him yet. I am extremely scared.
rupertj
in
Haemochromatosis Society UK
5 months ago
Gazdad,questions to ask gp ,please..
Hullo A-Team I beamed in recently re. My Mum's up coming blood test at her g.p, this has been allocated for 1 pm 21,march, could you please give me any info to ask for please, re . T4 , t3 etc? should, she take her daily potion (am.6ish,) 75-levo that day or fast somewhat? Nurse on phone said Not
Hullo A-Team I beamed in recently re. My Mum's up coming blood test at her g.p, this has been allocated for 1 pm 21,march, could you please give me any info to ask for please, re . T4 , t3 etc? should, she take her daily potion (am.6ish,) 75-levo that day or fast somewhat? Nurse on phone said Not
Gazdad
in
Thyroid UK
3 months ago
too much aldosterone and afib?
I began my journey with Atrial fibrillation in 2010. Low potassium and high blood pressure was considered to be the instigator. I found out a year ago that I have a tumor on an adrenal gland that is producing too much aldosterone. Too much aldosterone causes low potassium and high blood pressure. I currently
I began my journey with Atrial fibrillation in 2010. Low potassium and high blood pressure was considered to be the instigator. I found out a year ago that I have a tumor on an adrenal gland that is producing too much aldosterone. Too much aldosterone causes low potassium and high blood pressure. I currently
Amcech
in
Atrial Fibrillation Support
5 months ago
Figuring things out - first year since diagnosis
Hi, I'm posting here as I don't know anyone in real life with lupus and have been struggling to work out what my expectations should be in terms of symptoms. I was diagnosed just over a year ago following about a year of strange symptoms - GI issues, weight loss, Raynaud's, mouth ulcers, hand and wrist
Hi, I'm posting here as I don't know anyone in real life with lupus and have been struggling to work out what my expectations should be in terms of symptoms. I was diagnosed just over a year ago following about a year of strange symptoms - GI issues, weight loss, Raynaud's, mouth ulcers, hand and wrist
CGSLE
in
LUPUS UK
2 months ago
OK just spoke to gp reception about my T3 being re installed because endo does not want to deal with me! 😠
Hi everyone ❤️ So I've just spoke to gp reception about me calling in to get my T3 prescription, but we're told it had been stopped, this was Friday last week, I explained I had around 4 /5days left. I also explained the endo did not want to deal with me and said she would only prescribe T4, which definitely
Hi everyone ❤️ So I've just spoke to gp reception about me calling in to get my T3 prescription, but we're told it had been stopped, this was Friday last week, I explained I had around 4 /5days left. I also explained the endo did not want to deal with me and said she would only prescribe T4, which definitely
birkie
in
Thyroid UK
5 months ago
Adding more T3? or keep as is?
Hello All, I am looking to see any suggestions regarding adding more T3 to my current regimen. I am on 175 Tirosint T4 and 10mcg T3; I have Hashimoto’s and have been working on my iron by adding iron bisglycinate, which has helped as I am not dizzy, lightheaded, and have more focus. I also noticed
Hello All, I am looking to see any suggestions regarding adding more T3 to my current regimen. I am on 175 Tirosint T4 and 10mcg T3; I have Hashimoto’s and have been working on my iron by adding iron bisglycinate, which has helped as I am not dizzy, lightheaded, and have more focus. I also noticed
Kava3
in
Thyroid UK
3 months ago
Lupus or another Autoimmune Disease?
I’m 50 yr old female with issues, RLS, Hashimotos, Autoimmune Atrophic Chronic Gastritis, intestinal Metaplasia, Iron Deficiency Anemia w/transfusions, B12 deficiency, and now this horrible hip and joint pain. I know if you have one Autoimmune Disease you’re likely to have more. I’ve had a full work
I’m 50 yr old female with issues, RLS, Hashimotos, Autoimmune Atrophic Chronic Gastritis, intestinal Metaplasia, Iron Deficiency Anemia w/transfusions, B12 deficiency, and now this horrible hip and joint pain. I know if you have one Autoimmune Disease you’re likely to have more. I’ve had a full work
Milescircus
in
LUPUS UK
3 months ago
Increasing Levo but not feeling great
hellooooo I've been having some trouble with increasing my levothyroxine lately and wondered if you could help please? I've been taking levothyroxine for about 4 years roughly and it's very slowly been increasing (as expected). I started on 25, then 50, then I was on 75 for about two and a half
hellooooo I've been having some trouble with increasing my levothyroxine lately and wondered if you could help please? I've been taking levothyroxine for about 4 years roughly and it's very slowly been increasing (as expected). I started on 25, then 50, then I was on 75 for about two and a half
Hidden
in
Thyroid UK
2 months ago
Where to find T3 in UK
Hello everyone, Happy New Healthy Year first. I am seeing a lot of people taking T3. Where do you get it please? Many thanks Fede
Hello everyone, Happy New Healthy Year first. I am seeing a lot of people taking T3. Where do you get it please? Many thanks Fede
Fedeg
in
Thyroid UK
5 months ago
Underactive
Hi,Hoping someone can help, been on different doses of thyroxine but my doctor has put me on 75mg. I fee worse just so tired, my joints are aching just feel like my body is shutting down have no energy and feeling low plus my memory is not so good, my weight has gone up any advice would be great?
Hi,Hoping someone can help, been on different doses of thyroxine but my doctor has put me on 75mg. I fee worse just so tired, my joints are aching just feel like my body is shutting down have no energy and feeling low plus my memory is not so good, my weight has gone up any advice would be great?
Frustrated44
in
Thyroid UK
5 months ago
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