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Switching to Lupron?
I've been on Firmagon for two years. PSA undetectable (<.064), all scans negative. Will switching to a six month Lupron shot cause testosterone flare?
I've been on Firmagon for two years. PSA undetectable (<.064), all scans negative. Will switching to a six month Lupron shot cause testosterone flare?
epfj3333
in
Advanced Prostate Cancer
9 months ago
Shall I raise my Levo
I’ve been on 115mcg of T4 now for around 3 months. For one month I did the carnivore/keto diet with a little T3 but it was so hard to stick to. I’ve been eating normally again with no T3 now for about 2-3 weeks. My levels are still quite low so I’m thinking of going up to 125mcg per day does this sound
I’ve been on 115mcg of T4 now for around 3 months. For one month I did the carnivore/keto diet with a little T3 but it was so hard to stick to. I’ve been eating normally again with no T3 now for about 2-3 weeks. My levels are still quite low so I’m thinking of going up to 125mcg per day does this sound
ockerdoc
in
Thyroid UK
1 month ago
Liver Results and Spleen Pain
Hi, so take a immune Upadacitinib for my skin and have took for 2 years now, I am M 41 and do like the occasional drink, I was diagnosed with NAFLD around 6 months ago and have cut down drinking, my levels have always been fine other than GGT which was around 200. I have recently had further bloods
Hi, so take a immune Upadacitinib for my skin and have took for 2 years now, I am M 41 and do like the occasional drink, I was diagnosed with NAFLD around 6 months ago and have cut down drinking, my levels have always been fine other than GGT which was around 200. I have recently had further bloods
kevsmt5111
in
British Liver Trust
1 month ago
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1 year post diagnosis
I am a 54 yo male living in Vegas, I found out I was Jak2 positive last year, looked at labs before doctor and freaked. I have been having slightly higher RBC and Platelets for around 6-7 years. I used to donate blood pretty regularly and took testosterone, so the doctors kinda ignored it. I was a paramedic
I am a 54 yo male living in Vegas, I found out I was Jak2 positive last year, looked at labs before doctor and freaked. I have been having slightly higher RBC and Platelets for around 6-7 years. I used to donate blood pretty regularly and took testosterone, so the doctors kinda ignored it. I was a paramedic
FINFAN1970
in
MPN Voice
1 month ago
T3 battles
I’m on T3 only, taking 30mcg in one dose daily. Spoke to the endocrinologist this morning and after explaining to her that the reason I don’t take levothyroxine is because it made me far worse she said she’s never heard anyone that’s happened to. I told her I currently have symptoms of being under medicated
I’m on T3 only, taking 30mcg in one dose daily. Spoke to the endocrinologist this morning and after explaining to her that the reason I don’t take levothyroxine is because it made me far worse she said she’s never heard anyone that’s happened to. I told her I currently have symptoms of being under medicated
ScriptMaz
in
Thyroid UK
1 month ago
Can anyone Assist?
A couple of weeks ago, I partially read a lengthy and extremely interesting post explaining many aspects of PCa..., also the link between PSA and PCa and many other facts. I flagged the post to read later but for some reason the post has been deleted. Can anyone point me to this post as from what
A couple of weeks ago, I partially read a lengthy and extremely interesting post explaining many aspects of PCa..., also the link between PSA and PCa and many other facts. I flagged the post to read later but for some reason the post has been deleted. Can anyone point me to this post as from what
StuartS
in
Advanced Prostate Cancer
9 months ago
Best way to take NDT
Hello, today is my first day taking NDT. I was on a T4/T3 combo for the last two years. I usually chewed my meds (T4, T3) and tried to grind them as much as possible with my teeth before drinking a glass of water. What is the best way to take NDT? Can I take it in the same way to ensure good absorption
Hello, today is my first day taking NDT. I was on a T4/T3 combo for the last two years. I usually chewed my meds (T4, T3) and tried to grind them as much as possible with my teeth before drinking a glass of water. What is the best way to take NDT? Can I take it in the same way to ensure good absorption
helloworl
in
Thyroid UK
1 month ago
T3 NHS Prescription in SW London
Hi all,
Has anyone found a NHS endocrinologist who will prescribe Liothyronine in SW London?!
Ideally Charing Cross/Chelsea Westminster… Details: I have been taking 100mcg Levothyroxine daily and 10mcg (morning) and 5mcg (afternoon) Liothyronine for 3 years which has made a world of difference
Hi all,
Has anyone found a NHS endocrinologist who will prescribe Liothyronine in SW London?!
Ideally Charing Cross/Chelsea Westminster… Details: I have been taking 100mcg Levothyroxine daily and 10mcg (morning) and 5mcg (afternoon) Liothyronine for 3 years which has made a world of difference
Meebles
in
Thyroid UK
1 month ago
Reverse T3, stress and temperature
hello. I am one of a few outliers here, not hashi, but some classic low thyroid symptoms eg loss of eyebrows, leg hair, and in bloods, poor converter and not high t3, and for me most telling, low temperature and heart rate. (i am not posting results today) People have suggested it is central hypothyroidism
hello. I am one of a few outliers here, not hashi, but some classic low thyroid symptoms eg loss of eyebrows, leg hair, and in bloods, poor converter and not high t3, and for me most telling, low temperature and heart rate. (i am not posting results today) People have suggested it is central hypothyroidism
lauriegraham
in
Thyroid UK
1 month ago
PLMD medication
Hello I just joined because i was recently diagnosed with PLMD. The doctors don't really seem very informed about this condition. My ferritin level was fine around 200 so I decided to not supplement that even though the hospital advised me to. I then went onto take Pramipexole (didn't help) for
Hello I just joined because i was recently diagnosed with PLMD. The doctors don't really seem very informed about this condition. My ferritin level was fine around 200 so I decided to not supplement that even though the hospital advised me to. I then went onto take Pramipexole (didn't help) for
drover123
in
Restless Legs Syndrome
1 month ago
CDK12 gene mutation
My husband continues to be hormone sensitive but Sept. 4, 2023 he developed intense and unrelenting pain in his right mandible. The oncologist and palliative care nurse prescribed morphine and dilaudid to help reduce the pain. These pain meds are helping although he can still feel pain and gets breakthrough
My husband continues to be hormone sensitive but Sept. 4, 2023 he developed intense and unrelenting pain in his right mandible. The oncologist and palliative care nurse prescribed morphine and dilaudid to help reduce the pain. These pain meds are helping although he can still feel pain and gets breakthrough
Decktime
in
Advanced Prostate Cancer
7 months ago
GP Coming - what to ask
having my annual review tomorrow and GP is coming to see me. Looking at all my past results I wonder, with them being up and down constantly, whether I am one of those whereby Levo no longer works for me and might be keeping me ill. Diagnosed back in 2005 and it's too far back to remember how I was
having my annual review tomorrow and GP is coming to see me. Looking at all my past results I wonder, with them being up and down constantly, whether I am one of those whereby Levo no longer works for me and might be keeping me ill. Diagnosed back in 2005 and it's too far back to remember how I was
Jefner
in
Thyroid UK
1 month ago
T4 keeps dipping and Endo says levels are still “good” (but I feel exhausted)
Hi all, I used to be on: -150mg of Levo And - 1.5 grains of ERFA NDT which was very suitable for years. My T4 would usually come out in between 18 to 20 pmol/L (range is 9.0 to 23.0 pmol/L), and my T3 whilst on the upper end of acceptable, would come out in between 4.6 and 6.5 pmol/L (range is
Hi all, I used to be on: -150mg of Levo And - 1.5 grains of ERFA NDT which was very suitable for years. My T4 would usually come out in between 18 to 20 pmol/L (range is 9.0 to 23.0 pmol/L), and my T3 whilst on the upper end of acceptable, would come out in between 4.6 and 6.5 pmol/L (range is
hormonaljunkie
in
Thyroid UK
1 month ago
Is lactose intolerance and soya sensitivity affecting absorption of T4?
SlowDragon If I have a lactose intolerance and sensitivity to soya, could this be affecting my T4 absorption or conversion to T3? If so, would liquid thyroxine help or do I need T3 added? I recall reading a post regarding this from you but I am unsure where it is now. I avoid lactose and soya but
SlowDragon If I have a lactose intolerance and sensitivity to soya, could this be affecting my T4 absorption or conversion to T3? If so, would liquid thyroxine help or do I need T3 added? I recall reading a post regarding this from you but I am unsure where it is now. I avoid lactose and soya but
Sailing14
in
Thyroid UK
1 month ago
Private GP visit
I saw I private GP today as I felt with more time to go through my symptoms and tests I might get somewhere. But she is of the opinion that my B12, ferritin and folate levels were all fine and nothing to worry about. They are within range. I asked about my symptoms, but she didn’t feel they warranted
I saw I private GP today as I felt with more time to go through my symptoms and tests I might get somewhere. But she is of the opinion that my B12, ferritin and folate levels were all fine and nothing to worry about. They are within range. I asked about my symptoms, but she didn’t feel they warranted
Chickens44
in
Pernicious Anaemia Society
1 month ago
St George’s NHS 1st Appointment Query
Is anyone treated under St George’s NHS? I had a question about the first appointment. The letter states to bring a urine sample. Was this necessary?
Is anyone treated under St George’s NHS? I had a question about the first appointment. The letter states to bring a urine sample. Was this necessary?
Curious123
in
Thyroid UK
1 month ago
Test Result Feedback
Any feedback on below bloods? On 600mcg levothyroxine total per week. Am working on the iron at the moment. Vit B12 and D are fine. Trying to de-stress where I can. TSH 0.52 mIU/L (0.4 - 4) 3.3% Free T4 (fT4) 15.6 pmol/L (9 - 25) 41.3% Free T3 (fT3) 5.7 pmol/L (3.5 - 6.5) 73.3% T4:T3 Ratio 2.737
Any feedback on below bloods? On 600mcg levothyroxine total per week. Am working on the iron at the moment. Vit B12 and D are fine. Trying to de-stress where I can. TSH 0.52 mIU/L (0.4 - 4) 3.3% Free T4 (fT4) 15.6 pmol/L (9 - 25) 41.3% Free T3 (fT3) 5.7 pmol/L (3.5 - 6.5) 73.3% T4:T3 Ratio 2.737
Curious123
in
Thyroid UK
1 month ago
Gabapentin and liver resection
The help I have been given from this forum has been invaluable, I don't know where I would be without it. I have weaned myself off of Pramipexole and am now using Gabapentin, I don't think I have suffered anything like some of the other members. My question is, I need to up the dose, I am taking 1 x
The help I have been given from this forum has been invaluable, I don't know where I would be without it. I have weaned myself off of Pramipexole and am now using Gabapentin, I don't think I have suffered anything like some of the other members. My question is, I need to up the dose, I am taking 1 x
Ozzey
in
Restless Legs Syndrome
1 month ago
Splitting NDT - SHBG and cortisol changes - help!
Hi all, I have started splitting my Armour dose, taking less in the morning and more in the afternoon. I had a test for ft3 ft4, but also checked cortisol and SHBG. I was so surprised. My ft4 is similar to where it was before splitting, my ft3 is a tad higher. SHBG went up from 62 to 79.9. Cortisol
Hi all, I have started splitting my Armour dose, taking less in the morning and more in the afternoon. I had a test for ft3 ft4, but also checked cortisol and SHBG. I was so surprised. My ft4 is similar to where it was before splitting, my ft3 is a tad higher. SHBG went up from 62 to 79.9. Cortisol
Incoguto
in
Thyroid UK
1 month ago
Genetic diagnosis
Hi all, sorry I haven't posted anything for ages but sometimes life is like that. I have finally got some sort of diagnosis. I had more genetic testing a couple of years ago and they have found that I have two anomalies on gene SPG7. This means that my disability is more spastic based than ataxia.
Hi all, sorry I haven't posted anything for ages but sometimes life is like that. I have finally got some sort of diagnosis. I had more genetic testing a couple of years ago and they have found that I have two anomalies on gene SPG7. This means that my disability is more spastic based than ataxia.
ww-wibblywobbly
in
Ataxia UK
1 month ago
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