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Did Cortisol Ruin Your Gut?
Hashimoto's is an autoimmune condition often due to leaky gut. Low or high cortisol can cause gut infections and therefore the stomach may not be able to produce enough acid to digest our food. High cortisol shuts down the valves in the gut. If the food doesn't move through the small intestine well
Hashimoto's is an autoimmune condition often due to leaky gut. Low or high cortisol can cause gut infections and therefore the stomach may not be able to produce enough acid to digest our food. High cortisol shuts down the valves in the gut. If the food doesn't move through the small intestine well
Hidden
in
Thyroid UK
7 years ago
BUTTER VERSUS NON BUTTER
BUTTER VERSUS NON BUTTER While the decision of whether to choose butter or margarine is dependent on the individual and their specific dietary needs.,maintaining proper nutrition is a personal undertaking. What makes sense for one person might not be in the best interest of the next. Trans fat raises
BUTTER VERSUS NON BUTTER While the decision of whether to choose butter or margarine is dependent on the individual and their specific dietary needs.,maintaining proper nutrition is a personal undertaking. What makes sense for one person might not be in the best interest of the next. Trans fat raises
rvmasalvad
in
Healthy Eating
7 years ago
Is there any help for health anxiety?
I'm new to this page. I have had anxiety and panic disorder for almost 8 years. Initially it was so bad that I could barely function. I spent most of the time looking for answers. Why is this happening? What can I do to stop it? How long will it last? I've sought help from countless doctors and
I'm new to this page. I have had anxiety and panic disorder for almost 8 years. Initially it was so bad that I could barely function. I spent most of the time looking for answers. Why is this happening? What can I do to stop it? How long will it last? I've sought help from countless doctors and
BB106
in
Anxiety Support
7 years ago
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Glutamate
I recently followed a link on here which led me to a forum on ME. 'Phoenix rising.me' I've tried to find the article since without success but I remember the word glutamate and the phrase 'wired but tired' came up. It suggested krill oil as it 'crosses the brain barrier, unlike fish oil'. It also suggested
I recently followed a link on here which led me to a forum on ME. 'Phoenix rising.me' I've tried to find the article since without success but I remember the word glutamate and the phrase 'wired but tired' came up. It suggested krill oil as it 'crosses the brain barrier, unlike fish oil'. It also suggested
2everett
in
Restless Legs Syndrome
7 years ago
Adrenal or Thyroid treatment, which to do first?
Hi there - please see my test results attached. I have finally found a decent doctor a d she prescribed me pregnenolone (100mg, which seemed very high, so I have reduced to 50mg), 15mg DHEA, 20mg levoxy and also 1IU HGH per day. Levels are: Free T4: 16.8 pmol/L TSH: 2.4 mIU/L Free T3 5.7 pmol/L RT3
Hi there - please see my test results attached. I have finally found a decent doctor a d she prescribed me pregnenolone (100mg, which seemed very high, so I have reduced to 50mg), 15mg DHEA, 20mg levoxy and also 1IU HGH per day. Levels are: Free T4: 16.8 pmol/L TSH: 2.4 mIU/L Free T3 5.7 pmol/L RT3
slimecity
in
Thyroid UK
7 years ago
Getting started on Gluten-Free (GF)
Hi Recently diagnosed with Coeliac's disease I am now on a GF diet; at least probably. I'm looking for confirmation that my medication Actavis (now, think it was something else before) Levothyroxine and Atorvastatin is GF. Can anyone help please? Also, can I go further and ask if anyone has any gluten
Hi Recently diagnosed with Coeliac's disease I am now on a GF diet; at least probably. I'm looking for confirmation that my medication Actavis (now, think it was something else before) Levothyroxine and Atorvastatin is GF. Can anyone help please? Also, can I go further and ask if anyone has any gluten
laurencehalliwell
in
Gluten Free Guerrillas
7 years ago
On levothyroxine for 7 months but nothing's changed
Hi friends! I just want to have some insights. I was diagnosed with hypothyroidism 7 months ago, since then Im taking levothyroxine, I started with 50mg and then increased to 75mg. i thought taking the meds would make me feel ok but its the reverse. I feel as if im not a normal person. I still feel
Hi friends! I just want to have some insights. I was diagnosed with hypothyroidism 7 months ago, since then Im taking levothyroxine, I started with 50mg and then increased to 75mg. i thought taking the meds would make me feel ok but its the reverse. I feel as if im not a normal person. I still feel
angelindisguise
in
Thyroid UK
7 years ago
What helps me during flares...
I thought I'd take this opportunity to share what helps me with this community. When I have a bad canker sore outbreak there are usually 2-4 directly on my tonsils. Tonsillitis is essentially inflammation and irritation so I think I get that too on top of a flare. When I get mouth ulcers like that..
I thought I'd take this opportunity to share what helps me with this community. When I have a bad canker sore outbreak there are usually 2-4 directly on my tonsils. Tonsillitis is essentially inflammation and irritation so I think I get that too on top of a flare. When I get mouth ulcers like that..
justbr34the
in
Behçet's UK
7 years ago
Any New News on Xolair? How essential oils have helped me be calmer.
Hi there I have just been reading some posts about xolar. I am 62 years old and have been an asthma sufferer all of my life. I'm getting my first jab tomorrow but I am apprehensive to say the least because of the frightening stories I have read. I am 62 and because of being poorly most of my life,
Hi there I have just been reading some posts about xolar. I am 62 years old and have been an asthma sufferer all of my life. I'm getting my first jab tomorrow but I am apprehensive to say the least because of the frightening stories I have read. I am 62 and because of being poorly most of my life,
lindanut
in
Asthma Community Forum
7 years ago
Out of no where
Hi there, new to the community, suffered with IBS for over 4 years now and had taken Colofac Mebeverine.. I stopped taking this around 2 years ago and take a daily peppermint oil tab, up until around 2 months ago I have been mostly ibs free for over a year and one day around a couple of months ago the
Hi there, new to the community, suffered with IBS for over 4 years now and had taken Colofac Mebeverine.. I stopped taking this around 2 years ago and take a daily peppermint oil tab, up until around 2 months ago I have been mostly ibs free for over a year and one day around a couple of months ago the
Sk1nnerB
in
IBS Network
7 years ago
PVC's and PAC's Drastically Reduced/Stopped after years of terror and diminished life quality....? I'm not sure, but this is what I did..
Well, over the past couple of weeks my life has turned around for the positive and I cannot believe it!!!! I am so happy, but don't want to get too excited until more time has passed. After literally starting to plan my demise (that's right...having up to 13,000 + PVC's and hundreds of PAC's and not
Well, over the past couple of weeks my life has turned around for the positive and I cannot believe it!!!! I am so happy, but don't want to get too excited until more time has passed. After literally starting to plan my demise (that's right...having up to 13,000 + PVC's and hundreds of PAC's and not
CatAnn
in
AF Association
7 years ago
IBS: Advice about travel care, and about other people ...
Hi I am new to the Forum. I have a long term but very intermittent spastic colon problem, and as it's tending to get more frequent (and worse, less warning) as I get older, I'm seeking advice on two things. One is, is there anything you can take when you are travelling to reduce the risk of having a
Hi I am new to the Forum. I have a long term but very intermittent spastic colon problem, and as it's tending to get more frequent (and worse, less warning) as I get older, I'm seeking advice on two things. One is, is there anything you can take when you are travelling to reduce the risk of having a
FicusElastica
in
IBS Network
7 years ago
RLS or not??
The neurologist I had been under for three years ( who has now signed me off!), insisted I had RLS . However, I don't have ANY jerking or thrashing of my legs at all my symptoms are: numbness in all my toes, although I can feel touch on them!!burning painful feet and lower legs. Often during the
The neurologist I had been under for three years ( who has now signed me off!), insisted I had RLS . However, I don't have ANY jerking or thrashing of my legs at all my symptoms are: numbness in all my toes, although I can feel touch on them!!burning painful feet and lower legs. Often during the
Hidden
in
Restless Legs Syndrome
7 years ago
Lasting relief from the Low Chemical Diet
Diet News. Sorry if you are tired of hearing about this. As you know I have been lucky to get relief through diets. I adopted the FODMAP diet and got (say) 80% relief. Tried the Low Chemical diet and have had 100% relief when I have stuck to it. In both diets I have had trouble expanding the types of
Diet News. Sorry if you are tired of hearing about this. As you know I have been lucky to get relief through diets. I adopted the FODMAP diet and got (say) 80% relief. Tried the Low Chemical diet and have had 100% relief when I have stuck to it. In both diets I have had trouble expanding the types of
Graham3196
in
Restless Legs Syndrome
7 years ago
Ground Flaxseed, Flaxsee Oil & Flaxseed Oil.
This is a follow-on from my Fred Kummerow post - in response to some questions. Flaxseed contains two elements that might affect PCa progression: lignans that might impede it & alpha-linolenic acid [ALA] that might accelerate it. A tablespoon of flaxseed oil contails a lot of ALA with little or none
This is a follow-on from my Fred Kummerow post - in response to some questions. Flaxseed contains two elements that might affect PCa progression: lignans that might impede it & alpha-linolenic acid [ALA] that might accelerate it. A tablespoon of flaxseed oil contails a lot of ALA with little or none
pjoshea13
in
Advanced Prostate Cancer
7 years ago
Fred Kummerow & Flaxseed oil.
Fred Kummerov, biochemist, died on Wednesday at 102 [1]. At age 99, frustrated by the continued presence of trans fats in the food supply, he sued the FDA. This led to a ban, which comes into effect next year - 60 years after his research on trans fats began. But I was interested to see his paper on
Fred Kummerov, biochemist, died on Wednesday at 102 [1]. At age 99, frustrated by the continued presence of trans fats in the food supply, he sued the FDA. This led to a ban, which comes into effect next year - 60 years after his research on trans fats began. But I was interested to see his paper on
pjoshea13
in
Advanced Prostate Cancer
7 years ago
Vitamins with ckd
So just wondering are vitamins ok to take having ckd? I usually take vitamin c in the winter months And a daily cod liver oil capsul Does anyone know if vitamins or cod liver oil or any other vitamins are good/bad for ckd? I take vitamin c to boost immune system over winter and cod liver oil daily
So just wondering are vitamins ok to take having ckd? I usually take vitamin c in the winter months And a daily cod liver oil capsul Does anyone know if vitamins or cod liver oil or any other vitamins are good/bad for ckd? I take vitamin c to boost immune system over winter and cod liver oil daily
Stevo99
in
Early CKD Support
7 years ago
Is increasing Levo dose a good idea?
Hi, I have been taking 50mcg of levothyroxine for about 8 weeks. I went back to my GP after a thryoid function blood test 2 weeks ago. I didn't ask for specific numbers but she told me my results were now normal. But I haven't been feeling any better - still exhausted all the time, unexplained pain
Hi, I have been taking 50mcg of levothyroxine for about 8 weeks. I went back to my GP after a thryoid function blood test 2 weeks ago. I didn't ask for specific numbers but she told me my results were now normal. But I haven't been feeling any better - still exhausted all the time, unexplained pain
EmsW
in
Thyroid UK
7 years ago
Anybody use Essential Oils?
I was wondering if anybody uses them for pain?I have PBC plus Endometriosis.I have no symptoms of PBC but Endo I do.I was diagnosed with PBC last month and Endo last July.I get frequent Sinus Headaches and Cramps
I was wondering if anybody uses them for pain?I have PBC plus Endometriosis.I have no symptoms of PBC but Endo I do.I was diagnosed with PBC last month and Endo last July.I get frequent Sinus Headaches and Cramps
PBCTracy
in
PBC Foundation
7 years ago
Little update
A little update to people who follow my challenging stay in the UK. I have found a therapist so Im tryong to process different things connected to my injury and surgery. It has been around 5-6 sessions and I see the direction of it which is good. I also managed to negotiate a contract with my old
A little update to people who follow my challenging stay in the UK. I have found a therapist so Im tryong to process different things connected to my injury and surgery. It has been around 5-6 sessions and I see the direction of it which is good. I also managed to negotiate a contract with my old
Iwona084
in
Headway
7 years ago
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