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Adrenal cortex extract (ACE)
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forteo terrosa pen
there are few if any videos on administrating a dose of forteo. what's the volume of a single dose? are all the doses stored within the pen? it's it similar to insulin injecting?, because Mum will need to be shown m surely the nurses at the GP's will be able to do demonstrate and do the first shot
there are few if any videos on administrating a dose of forteo. what's the volume of a single dose? are all the doses stored within the pen? it's it similar to insulin injecting?, because Mum will need to be shown m surely the nurses at the GP's will be able to do demonstrate and do the first shot
MayGodBlessYou
in
Bone Health and Osteoporosis UK
1 year ago
forteo compared with terrosa
i'm still looking it up,but has anyone had experience using terrosa?, i think it's the australia-distributed version of forteo. thanks
i'm still looking it up,but has anyone had experience using terrosa?, i think it's the australia-distributed version of forteo. thanks
MayGodBlessYou
in
Bone Health and Osteoporosis UK
1 year ago
Throat tightness
Hello has anyone had tightness in throat like pressure feeling? I can breathe and swallow ok but it's so annoying. I've been suffering severe fatigue and feeling like my body is full of led my GP continues to take blood and did mention I have hyperthyroidism before Christmas but didn't give me any
Hello has anyone had tightness in throat like pressure feeling? I can breathe and swallow ok but it's so annoying. I've been suffering severe fatigue and feeling like my body is full of led my GP continues to take blood and did mention I have hyperthyroidism before Christmas but didn't give me any
Joylene123
in
Thyroid UK
5 months ago
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ACR (Microalbumin/Creatinine Ratio)
My Urine’s ACR result is 8.4 mg/mmol. HbA1C is 8.5. I am very worried. Kindly advise or provide insights.
My Urine’s ACR result is 8.4 mg/mmol. HbA1C is 8.5. I am very worried. Kindly advise or provide insights.
Limeandlemon
in
Diabetes India
5 months ago
Sugar Alcohols Ruined My Health: Learn from My Mistakes
Given the number of members who are intolerant to Teva levothyroxine, this video might be of some interest. Many suspect it is the mannitol content of Teva levothyroxine that lies behind the intolerance. After all, there were also many complaints around the world as Merck have slowly move from lactose
Given the number of members who are intolerant to Teva levothyroxine, this video might be of some interest. Many suspect it is the mannitol content of Teva levothyroxine that lies behind the intolerance. After all, there were also many complaints around the world as Merck have slowly move from lactose
helvella
Thyroid UK
in
Thyroid UK
5 months ago
High-Dose Vitamin B1 / Thiamine and Fat Soluble Benfotiamine Form
I am reposting a reply to the Vitamin B1 thread as I noticed a search on HealthUnlocked for Benfotiamine doesn't list the thread for Vitamin B1 and the information I posted doesn't fit in one reply. I'm not giving medical advice but I know a lot of people here are open to trying things and watch if
I am reposting a reply to the Vitamin B1 thread as I noticed a search on HealthUnlocked for Benfotiamine doesn't list the thread for Vitamin B1 and the information I posted doesn't fit in one reply. I'm not giving medical advice but I know a lot of people here are open to trying things and watch if
jazj
in
Advanced Prostate Cancer
6 months ago
prolia and forteo at the same time
well last week Mum's endo suggested forteo for 6-18mth, after 6 years prolia, then back to prolia. this was motivated due to possible vertebra fracture, he didn't push it, said to look it up, so i did, i was sort of keen for change, though thinking to stick to what you know, Mum also not keen on
well last week Mum's endo suggested forteo for 6-18mth, after 6 years prolia, then back to prolia. this was motivated due to possible vertebra fracture, he didn't push it, said to look it up, so i did, i was sort of keen for change, though thinking to stick to what you know, Mum also not keen on
MayGodBlessYou
in
Osteoporosis Support
1 year ago
Turmeric
I have been amazed at the effect taking turmeric has had on the amount of pain I experience in my hands and how quickly this has happened. (Yes, I know about the placebo effect!) I would recommend anyone to try it (providing they check with their haems/doctors first). I take 2 capsules of turmeric extract
I have been amazed at the effect taking turmeric has had on the amount of pain I experience in my hands and how quickly this has happened. (Yes, I know about the placebo effect!) I would recommend anyone to try it (providing they check with their haems/doctors first). I take 2 capsules of turmeric extract
Mwalimu
in
MPN Voice
9 months ago
Magic Magnesium Malate
Has anyone else tried this New Nordic magic magnesium Malate. I'm taking one tablet a day instead of recommended two. Each tablet has 120mg of magnesium, some b vitamins, which I'm used to but 2 extracts new to me. One has maritime pine bark extract 150mg per 2 tabs and some long pepper extract. I
Has anyone else tried this New Nordic magic magnesium Malate. I'm taking one tablet a day instead of recommended two. Each tablet has 120mg of magnesium, some b vitamins, which I'm used to but 2 extracts new to me. One has maritime pine bark extract 150mg per 2 tabs and some long pepper extract. I
Camelia23
in
AF Association
6 months ago
Supplements for adrenal support
I’ve been researching supplements for low cortisol / adrenal support and find the whole subject very confusing. Some information suggests that high cortisol is the reason for adrenal fatigue and recommends supplements which are ‘calming’ and lower cortisol. Other sources claim, quite rightly, that
I’ve been researching supplements for low cortisol / adrenal support and find the whole subject very confusing. Some information suggests that high cortisol is the reason for adrenal fatigue and recommends supplements which are ‘calming’ and lower cortisol. Other sources claim, quite rightly, that
Hidden
in
Thyroid UK
1 year ago
Hi everyone and Happy New Year
my name is Jill and it’s been along while since I’ve posted anything. I was diagnosed in 1999. Aged 39. Despite being very unwell for months and being ‘fobbed ’ off by my Gp. By the time I was diagnosed I had Saddle Nose deformity. Like alot of you even as a nurse I was very scared and felt alone
my name is Jill and it’s been along while since I’ve posted anything. I was diagnosed in 1999. Aged 39. Despite being very unwell for months and being ‘fobbed ’ off by my Gp. By the time I was diagnosed I had Saddle Nose deformity. Like alot of you even as a nurse I was very scared and felt alone
Essex-jill
in
Vasculitis UK
6 months ago
DX 5 years on Dec 26th. What I’ve learned about my PD. Please Read! It might be helpful.
PD is very common in my family. My dad and his dad had it. I have almost no hope they will ever cure it because it’s so complex. Here is what caused my Parkinson’s. (IMO) 1.Genetics. This is something you cannot change. I know my genes have issues with clearing out toxins? PD is a man made disease
PD is very common in my family. My dad and his dad had it. I have almost no hope they will ever cure it because it’s so complex. Here is what caused my Parkinson’s. (IMO) 1.Genetics. This is something you cannot change. I know my genes have issues with clearing out toxins? PD is a man made disease
38yroldmale
in
Cure Parkinson's
6 months ago
thoughts, suggestions, experiences - prolia followed by forteo, endo said
he is a good endo, very bookish and conservative, clever specialist, ordered (another) scan - m.r.i - as possible fracture higher up than first x-ray taken. he reckons
after 6 years prolia
, do
forteo
no longer than eighteen months, can
review
at (did he say 6 months?) /a year
he is a good endo, very bookish and conservative, clever specialist, ordered (another) scan - m.r.i - as possible fracture higher up than first x-ray taken. he reckons
after 6 years prolia
, do
forteo
no longer than eighteen months, can
review
at (did he say 6 months?) /a year
MayGodBlessYou
in
Osteoporosis Support
1 year ago
First six-month blood test, and my lymphocytes have gone down!
I’m soon to be 55. I was diagnosed in the UK with MBL this summer. My lymphocytes were at six with over 50% of them monoclonal cells. I’ve just had my six-month check. I’ve come down to 4.8. I know that these numbers can move around quite a lot, but for now I’m really happy with the trend. I did change
I’m soon to be 55. I was diagnosed in the UK with MBL this summer. My lymphocytes were at six with over 50% of them monoclonal cells. I’ve just had my six-month check. I’ve come down to 4.8. I know that these numbers can move around quite a lot, but for now I’m really happy with the trend. I did change
Jazzandblues
in
CLL Support
6 months ago
Symptoms suddenly taking a turn for the worse
Hello everyone. I am new to the forum, and have some questions to ask, but also want to share my RLS story, as well as some things that I have found helpful in living with RLS. I have had RLS for over 40 years. At first it was fairly easily controlled with a good run or long walk, and later with magnesium
Hello everyone. I am new to the forum, and have some questions to ask, but also want to share my RLS story, as well as some things that I have found helpful in living with RLS. I have had RLS for over 40 years. At first it was fairly easily controlled with a good run or long walk, and later with magnesium
restlegs1
in
Restless Legs Syndrome
9 months ago
Too many vitamins ?
i was diagnosed 8 years ago with prostate cancer. I chose not to do anything until 4 months ago , when i felt in pain everywhere and went for treatment . I am now on Erleada and degarelix feeling much better and with the regular side effect of hot flashes and tireness. I took for 8 years and still
i was diagnosed 8 years ago with prostate cancer. I chose not to do anything until 4 months ago , when i felt in pain everywhere and went for treatment . I am now on Erleada and degarelix feeling much better and with the regular side effect of hot flashes and tireness. I took for 8 years and still
Raminagrobis
in
Advanced Prostate Cancer
9 months ago
No longer in NED.
I am freaking out right now. Right before I decide to celebrate with friends for my 5 year milestone, the cancer is active again and I feel defeated. I want to cancel the party next week. It’s all very overwhelming. I am ER/PR pos, HER2 neg. I’m in a lot of pain and although I am awaiting a chest
I am freaking out right now. Right before I decide to celebrate with friends for my 5 year milestone, the cancer is active again and I feel defeated. I want to cancel the party next week. It’s all very overwhelming. I am ER/PR pos, HER2 neg. I’m in a lot of pain and although I am awaiting a chest
Casual
in
SHARE Metastatic Breast Cancer
9 months ago
Prolia
I have just received an email from my GP who has arranged for a F2F appointment to see me beginning January to discuss me starting to take Prolia. My last Dexascan in 2021 did show that I have osteoporosis, and I did take Alendronic Acid for the first two years of having Polymyalgia. Since then I have
I have just received an email from my GP who has arranged for a F2F appointment to see me beginning January to discuss me starting to take Prolia. My last Dexascan in 2021 did show that I have osteoporosis, and I did take Alendronic Acid for the first two years of having Polymyalgia. Since then I have
Purplegloss
in
PMRGCAuk
6 months ago
Suppliments that help with chemo?
A friend on their own chemo journey recommended the following - wondering if anyone agrees, or is this the equivalent of snake oil? Thanks for any help you can give. Pao V “FM”® is a dietary supplement composed of Pao pereira extract (Geissospermum vellosii) and "Quassia amara" powder. Ginkgo V® is
A friend on their own chemo journey recommended the following - wondering if anyone agrees, or is this the equivalent of snake oil? Thanks for any help you can give. Pao V “FM”® is a dietary supplement composed of Pao pereira extract (Geissospermum vellosii) and "Quassia amara" powder. Ginkgo V® is
Tinuriel
in
Advanced Prostate Cancer
9 months ago
What does having a NEW KIDNEY feel like?
Hi All, I have been in the transplant list for a year now and still waiting to get called. I can’t just help to wonder what having a kidney transplant will feel like. Apart from the fact that it will be a gift of life and freedom from being tied down to dialysis. What does it feel like? Will you
Hi All, I have been in the transplant list for a year now and still waiting to get called. I can’t just help to wonder what having a kidney transplant will feel like. Apart from the fact that it will be a gift of life and freedom from being tied down to dialysis. What does it feel like? Will you
Imaanforever
in
Kidney Dialysis
7 months ago
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