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update on 3 questions i posted = numbness & tingling? vitamins? weight gain?
For those that may have read my questions that i posted in the week i would like to thank you for your replies,i thought you might like to know how i got on at the doctors today where i asked him the same questions plus a couple others. On the numbness and tingling i told him that my hands are getting
For those that may have read my questions that i posted in the week i would like to thank you for your replies,i thought you might like to know how i got on at the doctors today where i asked him the same questions plus a couple others. On the numbness and tingling i told him that my hands are getting
pinkblossom
in
Fibromyalgia Action UK
12 years ago
anglia
hi have been on methotrexate & various other tabs & steroid jabs, at present just injecting 25mg met about a year ago started with a spoty rash which is gradualy spreading & itching am using steroid cream but not working ra ok at moment but rash not good any ideas please
hi have been on methotrexate & various other tabs & steroid jabs, at present just injecting 25mg met about a year ago started with a spoty rash which is gradualy spreading & itching am using steroid cream but not working ra ok at moment but rash not good any ideas please
anglia
in
NRAS
12 years ago
Hair Thinning..
It's been 7 months since i was told i had cd. blood test showed low calcuim and d3 levels. i have been gf since then.i have a really good diet fresh meat/fish fruit veg..so why now am i getting hair loss? i'm feeling so much better in myself and most of the symptoms i had have gone. i'm off to see my
It's been 7 months since i was told i had cd. blood test showed low calcuim and d3 levels. i have been gf since then.i have a really good diet fresh meat/fish fruit veg..so why now am i getting hair loss? i'm feeling so much better in myself and most of the symptoms i had have gone. i'm off to see my
Hidden
in
Gluten Free Guerrillas
12 years ago
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Has anyone tried Vitamin D3
Since April last year I have been experimenting with Vitamin D3 I started taking 5000iu a day and from the first pill my RLS/Spasm's in my arms and legs stopped and my neuropathic pain decreased, however after 2 months my RLS/Spasm's and pain came back, I researched vitamin d and I found that for
Since April last year I have been experimenting with Vitamin D3 I started taking 5000iu a day and from the first pill my RLS/Spasm's in my arms and legs stopped and my neuropathic pain decreased, however after 2 months my RLS/Spasm's and pain came back, I researched vitamin d and I found that for
StevenSims
in
Restless Legs Syndrome
12 years ago
Vit D Toxicity.
Recently been transferred off Calcichew and given Colecalciferol 20,000 unit capsules instead. Dosage; 1 daily for 1 week then once weekly afterwards. Took them for 4 days, evening of 4th day, severe vomiting and diarrhoea started (Monday). yesterday (Thursday), called Doc to enquire. At first he
Recently been transferred off Calcichew and given Colecalciferol 20,000 unit capsules instead. Dosage; 1 daily for 1 week then once weekly afterwards. Took them for 4 days, evening of 4th day, severe vomiting and diarrhoea started (Monday). yesterday (Thursday), called Doc to enquire. At first he
Midori
in
Fibromyalgia Action UK
12 years ago
Vitamin D Dekristol recall - check your prescription!
Thanks to our fellow members Thyroid UK for this warning - well spotted! We have been alerted a few minutes ago to the recall of Dekristol 20,000 and 50,000 IU vitamin D capsules. Please be careful to check the exact product - this is only the specific capsules identified - not all Dekristol products
Thanks to our fellow members Thyroid UK for this warning - well spotted! We have been alerted a few minutes ago to the recall of Dekristol 20,000 and 50,000 IU vitamin D capsules. Please be careful to check the exact product - this is only the specific capsules identified - not all Dekristol products
FionaGFG
Administrator
in
Gluten Free Guerrillas
12 years ago
Neuropathic Pain
Hi, I have a rare disease Adrenomyeloneuropathy and I suffer with bad muscle spasms and neuropathic pain, I've tried loads of medication but they just make me feel like a zombie! the best thing I have found is Vitamin D3 with Magnesium, however vitamin d uses magnesium to be converted to it's active
Hi, I have a rare disease Adrenomyeloneuropathy and I suffer with bad muscle spasms and neuropathic pain, I've tried loads of medication but they just make me feel like a zombie! the best thing I have found is Vitamin D3 with Magnesium, however vitamin d uses magnesium to be converted to it's active
StevenSims
in
Pain Concern
12 years ago
Vitamin D3 and Himalayan Salt
Hi, I have a rare disease Adrenomyeloneuropathy and I suffer muscle spasms in my arms and legs and I have found that Vitamin D3 stops them! however vitamin d uses magnesium to be converted to it's active form in the bloodstream and after taking it for 2 months it has caused Magnesium dificiency! so
Hi, I have a rare disease Adrenomyeloneuropathy and I suffer muscle spasms in my arms and legs and I have found that Vitamin D3 stops them! however vitamin d uses magnesium to be converted to it's active form in the bloodstream and after taking it for 2 months it has caused Magnesium dificiency! so
StevenSims
in
Restless Legs Syndrome
12 years ago
ZMA + VITAMIN D3 = NO SPASM'S + LESS PAIN!
Hi, Since the end of last year I have been suffering with very bad neuropathic pain and muscle spasm's. Last Friday I got some ZMA, it's a bodybuilding supplement containing: Zinc Sulphate 240mg, Chelated Zinc 40mg, Chelated Magnesium 426mg and, Vitamin B6 24mg, I have been taking these along with 4000iu
Hi, Since the end of last year I have been suffering with very bad neuropathic pain and muscle spasm's. Last Friday I got some ZMA, it's a bodybuilding supplement containing: Zinc Sulphate 240mg, Chelated Zinc 40mg, Chelated Magnesium 426mg and, Vitamin B6 24mg, I have been taking these along with 4000iu
StevenSims
in
AMN EASIER
12 years ago
Red Skin Syndrome and Topical Steroid Addiction
Many people have never heard of Red Skin Syndrome. in fact, it is a condition with many names: Steroid Rosacea, Perioral dermatitis, steroid rebound phenomenon and many more. The term "Red Skin Syndrome" was coined by Dr Marvin Rapaport MD, an American dematologist who has worked with many patients
Many people have never heard of Red Skin Syndrome. in fact, it is a condition with many names: Steroid Rosacea, Perioral dermatitis, steroid rebound phenomenon and many more. The term "Red Skin Syndrome" was coined by Dr Marvin Rapaport MD, an American dematologist who has worked with many patients
Hidden
in
MY SKIN
12 years ago
The importance of vitamin D
I have been extremely tired and getting worse over the past few months, in fact so bad that I was threatened with a sleep study. However my consultant decided to test my vitamin D levels and it was low. I am now taking 250mcg/10,000 iu vitamin D3 a day for a month. I certainly feel as though I have more
I have been extremely tired and getting worse over the past few months, in fact so bad that I was threatened with a sleep study. However my consultant decided to test my vitamin D levels and it was low. I am now taking 250mcg/10,000 iu vitamin D3 a day for a month. I certainly feel as though I have more
alanjudy
in
Lung Conditions Community Forum
12 years ago
MEN WITH GENITAL SYMPTOMS OUT THERE?
Hi, have had BD for at least ten years but only now getting genital symptoms. Can get cracked skin, sores and ulcers down there, which seems exacerbated by 'certain activity' involving the area. I have a steroid cream but am increasingly looking to avoid and 'activity'. Whole thing can get quite painful
Hi, have had BD for at least ten years but only now getting genital symptoms. Can get cracked skin, sores and ulcers down there, which seems exacerbated by 'certain activity' involving the area. I have a steroid cream but am increasingly looking to avoid and 'activity'. Whole thing can get quite painful
GUEVARA
in
Behçet's UK
12 years ago
Topic of the Month: March - Itchy Rashes
There are many different skin manifestations in lupus, which vary from person to person. The ‘classical’ skin problem in lupus is the [i]butterfly rash[/i]. This is a red rash, sometimes no more than a mild blush that occurs across the bridge of the nose and on the cheeks. This type of rash tends to
There are many different skin manifestations in lupus, which vary from person to person. The ‘classical’ skin problem in lupus is the [i]butterfly rash[/i]. This is a red rash, sometimes no more than a mild blush that occurs across the bridge of the nose and on the cheeks. This type of rash tends to
Paul_Howard
LUPUS UK
in
LUPUS UK
12 years ago
Asthma Drugs ?
Hi My attacks are becoming more frequent and am having to use prednisolone more often. I have had spirometry tests which were not too bad considering I have been asthmatic for all my life and a heart scan which was fine.I have had some great help from members regarding my absences from work and pressure
Hi My attacks are becoming more frequent and am having to use prednisolone more often. I have had spirometry tests which were not too bad considering I have been asthmatic for all my life and a heart scan which was fine.I have had some great help from members regarding my absences from work and pressure
Hidden
in
Asthma Community Forum
12 years ago
hi... i am on fentanyl patches 75mg,
i take fentanyl patches 75mg. also i take oral morphine.. i am on amitrypline. paracentomol. lansoprasol, vitamin d3 at 5000 units... i also take diclofencic and diazpam when needed... i have tried lots of pain killers in the past and been on those tablets for about 2 years now.. i feel they work the
i take fentanyl patches 75mg. also i take oral morphine.. i am on amitrypline. paracentomol. lansoprasol, vitamin d3 at 5000 units... i also take diclofencic and diazpam when needed... i have tried lots of pain killers in the past and been on those tablets for about 2 years now.. i feel they work the
diane63
in
Fibromyalgia Action UK
12 years ago
Vitamin D's Impact on Autoimmunity
Taken from Dr. Jack Kruse's website (www.jackkruse.com). I think this guy is on to something. In fact, I think this guy is on to a lot of somethings. He's not waiting for air-tight, double-blind clinical trials, and at my age, neither am I. I believe that the keys to autoimmune disorders lie in the
Taken from Dr. Jack Kruse's website (www.jackkruse.com). I think this guy is on to something. In fact, I think this guy is on to a lot of somethings. He's not waiting for air-tight, double-blind clinical trials, and at my age, neither am I. I believe that the keys to autoimmune disorders lie in the
TheKid
in
Hughes Syndrome APS Forum
12 years ago
Being given the run around with diagnosis and other gripes
Finally at age 46 I am beginning to make sense of the endless health problems I have had since childhood, and in particular teenage years. However from one medic to another with one complaint thrown in, (forced upon us by the local PCT so it could defend itself), has made my life for myself and family
Finally at age 46 I am beginning to make sense of the endless health problems I have had since childhood, and in particular teenage years. However from one medic to another with one complaint thrown in, (forced upon us by the local PCT so it could defend itself), has made my life for myself and family
MaryF
Administrator
in
Hughes Syndrome APS Forum
12 years ago
Hair condition
Put on preventer inhaler in Feb. Since then its as if my scalp is producing more oil than usual. I have white flakes beneath my hair and it feels for all the world like the cradle cap my children had as a baby. I'm loathe to go to the GP as a few years ago, I had a similar thing on my legs and was
Put on preventer inhaler in Feb. Since then its as if my scalp is producing more oil than usual. I have white flakes beneath my hair and it feels for all the world like the cradle cap my children had as a baby. I'm loathe to go to the GP as a few years ago, I had a similar thing on my legs and was
Hidden
in
Asthma Community Forum
15 years ago
Brittle asthma medication help!
Hi all, I hardly ever post on here but I do read here from time to time and have always had great experiences and help in the past. I am a brittle asthmatic - diagnosed feb 2000 am under the brompton under prof durham and debbie and under my local hospital - broomfield where i'm currently in reidence
Hi all, I hardly ever post on here but I do read here from time to time and have always had great experiences and help in the past. I am a brittle asthmatic - diagnosed feb 2000 am under the brompton under prof durham and debbie and under my local hospital - broomfield where i'm currently in reidence
yaf_user681_26872
in
Asthma Community Forum
15 years ago
Vitamin D/Calcium or Alendronate (Fosamax)
Because this has sort of come up on the Pred Thread, I thought I would ask who is prescribed what for their anti Pred bone thinning med regimen. Have you been put on AdCal D3, Fosamax, Calci-Chew or anything else. It is always good to know what the current trend is. If you know your T score and degree
Because this has sort of come up on the Pred Thread, I thought I would ask who is prescribed what for their anti Pred bone thinning med regimen. Have you been put on AdCal D3, Fosamax, Calci-Chew or anything else. It is always good to know what the current trend is. If you know your T score and degree
Hidden
in
Asthma Community Forum
18 years ago
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