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Help!! Am I losing my mind?
Hi all, I've been a lurked for some time and have found a lot of posts helpful. For over 3 years now I've been having lots of random symptoms, aches, pains, minor small joint swelling, chronic fatigue, b12 deficiency, hair loss, fluctuating weight, chillblains, ? Reynauds...the list is endless. Bloods
Hi all, I've been a lurked for some time and have found a lot of posts helpful. For over 3 years now I've been having lots of random symptoms, aches, pains, minor small joint swelling, chronic fatigue, b12 deficiency, hair loss, fluctuating weight, chillblains, ? Reynauds...the list is endless. Bloods
Hayleybabes1982
in
LUPUS UK
8 years ago
Osteoporosis - My Experience.
After a dexascan in 2008 because of family with osteoporosis, I was diagnosed with osteopenia, given a supply of Calcium with vitamin D3 and told to come back in three years. Turned up at the doctors three yars later (2011) and was told that NICE had upped the time between scans to 5 years. I actually
After a dexascan in 2008 because of family with osteoporosis, I was diagnosed with osteopenia, given a supply of Calcium with vitamin D3 and told to come back in three years. Turned up at the doctors three yars later (2011) and was told that NICE had upped the time between scans to 5 years. I actually
Aristotle13
in
Bone Health and Osteoporosis UK
8 years ago
Constant thrush
Me and my boyfriend keep getting thrush infections, we've had it at least 4/5 times this year already. I know that I'm the main factor for it as I've always suffered from thrush and have to be on high steroid cream to treat it and I follow the full instructions given by the doctor each time which clears
Me and my boyfriend keep getting thrush infections, we've had it at least 4/5 times this year already. I know that I'm the main factor for it as I've always suffered from thrush and have to be on high steroid cream to treat it and I follow the full instructions given by the doctor each time which clears
Vickeeet
in
BASHH
8 years ago
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Help needed please!
Hi everybody. My first post here. A dear friend of mine introduced me to this forum and I've spent weeks reading posts and learning lots from all you knowledgeable people out there. In May this year I went to my GP after feeling rotten for at least a year, just getting worse. Symptoms like incredible
Hi everybody. My first post here. A dear friend of mine introduced me to this forum and I've spent weeks reading posts and learning lots from all you knowledgeable people out there. In May this year I went to my GP after feeling rotten for at least a year, just getting worse. Symptoms like incredible
EMTaylor
in
Thyroid UK
8 years ago
Vitamins and supplements advice
I would be very grateful for advice on which brand of and what dose to buy in the following please? Selenium Magnesium (to help with sleep, I'm haven't been sleeping well at all) Vitamin B1 Vitamin B12 I am currently taking:- Vitamin D3 (1000 iu) with K2-MK7 Vitamin C & Rose Hips 1000 mg Gentle Iron
I would be very grateful for advice on which brand of and what dose to buy in the following please? Selenium Magnesium (to help with sleep, I'm haven't been sleeping well at all) Vitamin B1 Vitamin B12 I am currently taking:- Vitamin D3 (1000 iu) with K2-MK7 Vitamin C & Rose Hips 1000 mg Gentle Iron
cc251254
in
Thyroid UK
8 years ago
TSH 3.83 - Dr says normal, is that right?
T4 = 13.2pmol/L TSH = 3.83 mU/L Vitamin D3 = 34 nmol/L Folate = 10.6 ug/L Ferritin = 4 ug/L (noted as low and prescribed supplements) Red blood cell count = 4.95 10*12/L
T4 = 13.2pmol/L TSH = 3.83 mU/L Vitamin D3 = 34 nmol/L Folate = 10.6 ug/L Ferritin = 4 ug/L (noted as low and prescribed supplements) Red blood cell count = 4.95 10*12/L
Grifter
in
Thyroid UK
8 years ago
Still shattered
Hello everyone happy Friday! Well I started taking NDT beginning of July as I was perpetually tired and suffering from 6 migraines a week been on T3/T4 combo since Dec 2015 but endo. wouldn't increase the dose. I had my six monthly/in reality 8 monthly check in with the endo the beginning of August.
Hello everyone happy Friday! Well I started taking NDT beginning of July as I was perpetually tired and suffering from 6 migraines a week been on T3/T4 combo since Dec 2015 but endo. wouldn't increase the dose. I had my six monthly/in reality 8 monthly check in with the endo the beginning of August.
tootired
in
Thyroid UK
8 years ago
Parkinsons detox
I just joined this forum after seeing my mom struggle so much with her PD. Over the years have introduced mucana , a few supplements , exercise etc , but a recent fall has really pushed her back where she is tired, sleepy and can barely walk (she was only walking with the helper before also) . Wish
I just joined this forum after seeing my mom struggle so much with her PD. Over the years have introduced mucana , a few supplements , exercise etc , but a recent fall has really pushed her back where she is tired, sleepy and can barely walk (she was only walking with the helper before also) . Wish
mymomhaspd
in
Cure Parkinson's
8 years ago
Vitamin regimen - looking to make changes!
Hi all, I made a long Vit D post here but am splitting this lot out. https://healthunlocked.com/thyroiduk/posts/134080785/vitamin-d-deficiency I am currently taking the following: - Levothyroxine 100mcg (increased 4/7/16 from 75mcg) - Vit D 1600iu colecalciferol - H&B Calcium 333.3mg , Magnesium
Hi all, I made a long Vit D post here but am splitting this lot out. https://healthunlocked.com/thyroiduk/posts/134080785/vitamin-d-deficiency I am currently taking the following: - Levothyroxine 100mcg (increased 4/7/16 from 75mcg) - Vit D 1600iu colecalciferol - H&B Calcium 333.3mg , Magnesium
queenmabroo
in
Thyroid UK
8 years ago
Vitamin D deficiency
Hi all! Full blood tests at end of post but starting with my questions! I am hypothyroid taking 100mcg of levothyroxine. As this thread has become really long I'm going to start a second about my other vitamins etc (will add link!) So I had a recent blood test which shows that my vitamin D is still deficient
Hi all! Full blood tests at end of post but starting with my questions! I am hypothyroid taking 100mcg of levothyroxine. As this thread has become really long I'm going to start a second about my other vitamins etc (will add link!) So I had a recent blood test which shows that my vitamin D is still deficient
queenmabroo
in
Thyroid UK
8 years ago
Possible secondary endo
Hi ladies I'm new here. Just wanting some advice please. I had an emergency c section in November 2013 my first child I was 29.since then iv been on the depo injection and femodette pill aswel as breast feeding till may this year. (My periods have always been bad since they started and iv always been
Hi ladies I'm new here. Just wanting some advice please. I had an emergency c section in November 2013 my first child I was 29.since then iv been on the depo injection and femodette pill aswel as breast feeding till may this year. (My periods have always been bad since they started and iv always been
Hidden
in
Endometriosis UK
8 years ago
Newcomer - B12 Deficiency Advice Please
Hi All, I'm new to here having ended up here through a worry more recently about a B12 deficiency. Just to give you a bit of info, I'm 26 average fit and healthy woman, eat a good balanced diet but do have IBS. I've suffered with chronic fatigue for a long while now which I'm really struggling with lately
Hi All, I'm new to here having ended up here through a worry more recently about a B12 deficiency. Just to give you a bit of info, I'm 26 average fit and healthy woman, eat a good balanced diet but do have IBS. I've suffered with chronic fatigue for a long while now which I'm really struggling with lately
2torts
in
Pernicious Anaemia Society
8 years ago
test results, advice on to how to get gp to increase dose.
Last Nov I was finally given levo (50mcg) by my gp after months of increasing TSH tests and feeling really bad and when retested was told I was in range although still feeling rough and in the higher part of the range (I think it was 3.7). I successfully used the nice guidelines to get an increase to
Last Nov I was finally given levo (50mcg) by my gp after months of increasing TSH tests and feeling really bad and when retested was told I was in range although still feeling rough and in the higher part of the range (I think it was 3.7). I successfully used the nice guidelines to get an increase to
bd79og
in
Thyroid UK
8 years ago
Is this Pityriasis Rosea?
In Feb, I noticed that a mole my husband has on his side, had a rash like a haloaround it. The rash then developed mainly on his truck and back, but also on his legs and arms. The GP has diagnosed Pityriasis Rosea but it's non typical in that it's not itchy or sore. However, it does look like hives
In Feb, I noticed that a mole my husband has on his side, had a rash like a haloaround it. The rash then developed mainly on his truck and back, but also on his legs and arms. The GP has diagnosed Pityriasis Rosea but it's non typical in that it's not itchy or sore. However, it does look like hives
Juliegc
in
MY SKIN
8 years ago
Any suggestions welcomed
Ok here goes, not having a great time of it lately. Retired on ll health end of March and had a couple of months of feeling quite good. It was if the stress of work no longer being there just made me feel so much better. It was quite stressful getting to the retirement point! Anyway I was on 15mg of
Ok here goes, not having a great time of it lately. Retired on ll health end of March and had a couple of months of feeling quite good. It was if the stress of work no longer being there just made me feel so much better. It was quite stressful getting to the retirement point! Anyway I was on 15mg of
Griggser
in
PMRGCAuk
8 years ago
Recently diagnosed in the last few years?
I was diagnosed in July 2014 and have gained support, understanding and information from others who have been recently diagnosed. I had intense vertigo, facial twitching and fatigue like I've never experienced that brought me in for diagnosis. I thought I might have a brain tumor. Now two years later
I was diagnosed in July 2014 and have gained support, understanding and information from others who have been recently diagnosed. I had intense vertigo, facial twitching and fatigue like I've never experienced that brought me in for diagnosis. I thought I might have a brain tumor. Now two years later
Kokomo26
in
My MSAA Community
8 years ago
Seven essential vitamins as we age.
By the time we hit our forties, our body starts to change. Muscle mass starts to deteriorate, the likelihood of putting on weight increases, the onset of menopause is nigh, and the risk of chronic diseases like cancer, heart disease and diabetes begins to increase. And while it is always important to
By the time we hit our forties, our body starts to change. Muscle mass starts to deteriorate, the likelihood of putting on weight increases, the onset of menopause is nigh, and the risk of chronic diseases like cancer, heart disease and diabetes begins to increase. And while it is always important to
patliputra
in
Diabetes India
8 years ago
From 2000 people with Hashimoto's- the nine most helpful strategies.
This is an email I received from Isabella Wentz. 'After implementing carefully researched lifestyle changes, I was able to see a tremendous improvement in my health. I decided to summarize my research an improvements in my book, Hashimoto's the Root Cause in 2013. When I initially published the book
This is an email I received from Isabella Wentz. 'After implementing carefully researched lifestyle changes, I was able to see a tremendous improvement in my health. I decided to summarize my research an improvements in my book, Hashimoto's the Root Cause in 2013. When I initially published the book
Scazzoh
in
Thyroid UK
8 years ago
MS for at least 36 years
My MS was diagnosed in 1980 after several years of symptoms. I was on Avonex for 3 years (2001-2004) and then Copaxone (2006-2009) but currently am taking no MS drugs, though I do take 5,000 IU of vitamin D3 daily. I taught in the Chicago City College system for several years and have a Ph.D. I also
My MS was diagnosed in 1980 after several years of symptoms. I was on Avonex for 3 years (2001-2004) and then Copaxone (2006-2009) but currently am taking no MS drugs, though I do take 5,000 IU of vitamin D3 daily. I taught in the Chicago City College system for several years and have a Ph.D. I also
agate
in
My MSAA Community
8 years ago
Concerns about daughter
Hi folks, I have been diagnosed with SLE for 4 years now and have severe organ involvement, heart/lungs. Looking back I think I have had this all of my life. My daughter who has recently turned 4 has a sore and swollen vagina, she can be up 3/4 times a night crying in pain and this has been this case
Hi folks, I have been diagnosed with SLE for 4 years now and have severe organ involvement, heart/lungs. Looking back I think I have had this all of my life. My daughter who has recently turned 4 has a sore and swollen vagina, she can be up 3/4 times a night crying in pain and this has been this case
mcjm
in
LUPUS UK
8 years ago
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