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Emphysemia and celiac disease
Been having tests because of severe anemia. Just been informed i have celiac disease so going on gluten free diet. My breathing has been so much worse this past twelve months. Breathless even when walking my dog . Never used to be. Could the anemia have been making my emphysemia worse . Has anyone had
Been having tests because of severe anemia. Just been informed i have celiac disease so going on gluten free diet. My breathing has been so much worse this past twelve months. Breathless even when walking my dog . Never used to be. Could the anemia have been making my emphysemia worse . Has anyone had
natalyab
in
Lung Conditions Community Forum
2 years ago
Here's something CHEAP and EASY you can try.... Essential Oils, says Dr. Josh Axe
https://draxe.com/health/parkinsons-disease-natural-treatment-remedies/
Essential oils for Parkinson’s
: Using essential oils may effectively reduce and calm some of the symptoms associated with Parkinson’s disease such as depression, sleep trouble, skin inflammation and digestive issues.
https://draxe.com/health/parkinsons-disease-natural-treatment-remedies/
Essential oils for Parkinson’s
: Using essential oils may effectively reduce and calm some of the symptoms associated with Parkinson’s disease such as depression, sleep trouble, skin inflammation and digestive issues.
PDWarrior1900
in
Cure Parkinson's
2 years ago
Newly diagnosed with CLL and wondering what tests to request.
Hi all, I didn't feel well after partial thyroidectomy. Had some teats and was told I have cll. Was told just to watch and be retested every three months. I was tested for CBC and differential. From reading some of these posts, it looks like there is a genetic test available. I have my first appt.
Hi all, I didn't feel well after partial thyroidectomy. Had some teats and was told I have cll. Was told just to watch and be retested every three months. I was tested for CBC and differential. From reading some of these posts, it looks like there is a genetic test available. I have my first appt.
montieth
in
CLL Support
2 years ago
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Off pill causing my itchy head scalp
hey guys, i have been off pill since May for TTC. I noticed my heaf scalp is so itchy n drandruffy for like at least ⅔ weeks now. I have been using castor oil in roots every time in night time before going shower. I have used new shampoo since May and was fine until itchy scalp. My mum mentioned it
hey guys, i have been off pill since May for TTC. I noticed my heaf scalp is so itchy n drandruffy for like at least ⅔ weeks now. I have been using castor oil in roots every time in night time before going shower. I have used new shampoo since May and was fine until itchy scalp. My mum mentioned it
EDJ23
in
Women's Health
2 years ago
Aristo levo
hi, I can’t tolerate Teva levothyroxine. I usually get Mercury Pharma since telling my local pharmacy this suits me best, however, today I’ve been given Aristo 100 mcg and I’ve never had this before and don’t like changing manufacturer. I just get so annoyed by the ignorance out there that we need to
hi, I can’t tolerate Teva levothyroxine. I usually get Mercury Pharma since telling my local pharmacy this suits me best, however, today I’ve been given Aristo 100 mcg and I’ve never had this before and don’t like changing manufacturer. I just get so annoyed by the ignorance out there that we need to
Essexlil
in
Thyroid UK
2 years ago
Blood test results and thoughts on why I feel rubbish please (long post for help)
Hi folks I feel pants. I have been feeling pants for many months/probably 2 years with all of the symptoms below and it is now being made worse by the after effects of Covid which I had a month ago. The questions I have are.... What else can I do or take to feel a bit better again? Has anyone else
Hi folks I feel pants. I have been feeling pants for many months/probably 2 years with all of the symptoms below and it is now being made worse by the after effects of Covid which I had a month ago. The questions I have are.... What else can I do or take to feel a bit better again? Has anyone else
Eimear78
in
Thyroid UK
2 years ago
omega3 fish oil recommendation please
Hi all I’m a vegetarian and have been for years but after my recent heart problems I think I’m going to have to get some omega3 fish oil to h try and help my heart a bit, I won’t go back to eating fish and I’m against the oil really but if it helps me now I’ve got my new pipe work I want to look after
Hi all I’m a vegetarian and have been for years but after my recent heart problems I think I’m going to have to get some omega3 fish oil to h try and help my heart a bit, I won’t go back to eating fish and I’m against the oil really but if it helps me now I’ve got my new pipe work I want to look after
Jako999
in
British Heart Foundation
2 years ago
Blood Test Results - TPA seem strange
Hi, I have just received my Medichecks results. The result for TPA is 9 The range is <34 I know this fluctuates but was surprised to see it under range. My doctor checked it in 2007 and it was 56. It has not been checked since. So, do I still have Hashimotos? Does it fluctuate so much? I have
Hi, I have just received my Medichecks results. The result for TPA is 9 The range is <34 I know this fluctuates but was surprised to see it under range. My doctor checked it in 2007 and it was 56. It has not been checked since. So, do I still have Hashimotos? Does it fluctuate so much? I have
Conniegirl
in
Thyroid UK
2 years ago
I’ve been taking too much T3
please can someone help. I’m taking 50 mcg levo and 10 mcg lio (2x 5 mcg) daily. However I’ve just checked my meds and realised for the last month I’ve been taking 2 x 10 mcg per day T3. When I collected my prescription from the hospital I had a mix of 10 mcg and 5 mcg - I must have mixed them up.
please can someone help. I’m taking 50 mcg levo and 10 mcg lio (2x 5 mcg) daily. However I’ve just checked my meds and realised for the last month I’ve been taking 2 x 10 mcg per day T3. When I collected my prescription from the hospital I had a mix of 10 mcg and 5 mcg - I must have mixed them up.
Simba53
in
Thyroid UK
2 years ago
ADVICE ??
I’ve had celiac disease for ever it seems like but only went gluten free the beginning of this year. All my symptoms were always blamed on not eating a controlled gluten free diet. Now that I am GF, the stomach issues are worse and they say it’s IBS-C. I’ve had a lot of problems with constipation, trying
I’ve had celiac disease for ever it seems like but only went gluten free the beginning of this year. All my symptoms were always blamed on not eating a controlled gluten free diet. Now that I am GF, the stomach issues are worse and they say it’s IBS-C. I’ve had a lot of problems with constipation, trying
IBSsucksallthetime
in
IBS Network
2 years ago
Going it alone but hit a snag
Hi all Since my post from June, after initially trying to increase the T3, I had massive heart palps and sweating, phone endo on 12th July who said to leave T3 at 2.5 mcg per day and leave levo at 91.07mcg per day. He informed me the symptons I was talking about, hip pain, muscle aches etc where not
Hi all Since my post from June, after initially trying to increase the T3, I had massive heart palps and sweating, phone endo on 12th July who said to leave T3 at 2.5 mcg per day and leave levo at 91.07mcg per day. He informed me the symptons I was talking about, hip pain, muscle aches etc where not
AleB
in
Thyroid UK
2 years ago
Thyroid Hormone Transporters in a Human Placental Cell Model
There has long been the received wisdom that T3 does not cross the placenta. I am not aware this has been proved in any level of detail. This paper appears to make that look wrong. Indeed, it appears to identify specific pharmaceutical agents which directly and significantly affect T3 transport
There has long been the received wisdom that T3 does not cross the placenta. I am not aware this has been proved in any level of detail. This paper appears to make that look wrong. Indeed, it appears to identify specific pharmaceutical agents which directly and significantly affect T3 transport
helvella
Thyroid UK
in
Thyroid UK
2 years ago
WARNING about 'wheat' ... !
"Could gluten's toxicity extend to the nervous system, producing symptoms identical to classical Parkinson's disease? A remarkable case study adds to a growing body of research indicating that [i]
wheat's neurotoxicity is greatly underestimated
[/i]." "A remarkable case report describing the[i]
"Could gluten's toxicity extend to the nervous system, producing symptoms identical to classical Parkinson's disease? A remarkable case study adds to a growing body of research indicating that [i]
wheat's neurotoxicity is greatly underestimated
[/i]." "A remarkable case report describing the[i]
PDWarrior1900
in
Cure Parkinson's
2 years ago
Blood test results
Hi I have had a Medichecks blood test before having my Endo appointment next week. I’m on 50 mcg levothyroxine and 10 mcg Liothyronine (taken as 5 mcg twice daily). My TSH levels are low and TPA very high. Is this normal on combination therapy? While I feel better on this regime I cannot lose the
Hi I have had a Medichecks blood test before having my Endo appointment next week. I’m on 50 mcg levothyroxine and 10 mcg Liothyronine (taken as 5 mcg twice daily). My TSH levels are low and TPA very high. Is this normal on combination therapy? While I feel better on this regime I cannot lose the
Simba53
in
Thyroid UK
2 years ago
Counteracting the negative effects of ADT on the CV system?
I’m 66. I started Orgovyx in Oct. of ‘21, then completed sbrt in Nov.. My MO wants me on adt for 2 yrs.. That’s fine as I’ve tolerated the physical effects pretty well. I exercise regularly (walking ever day, weights every other day). But, my bloodwork is coming back with high triglycerides & cholesterol
I’m 66. I started Orgovyx in Oct. of ‘21, then completed sbrt in Nov.. My MO wants me on adt for 2 yrs.. That’s fine as I’ve tolerated the physical effects pretty well. I exercise regularly (walking ever day, weights every other day). But, my bloodwork is coming back with high triglycerides & cholesterol
Scooter22
in
Prostate Cancer Network
2 years ago
Latest Consensus on Omega-3, Aspirin & Curcumin?
So in finishing up my deep dive into supplements, these were the three I had the most trouble making any definitive personal conclusions about so I wanted to do a review before putting them to bed to get any last input. My general feeling is without well-designed long-term studies (not retrospective
So in finishing up my deep dive into supplements, these were the three I had the most trouble making any definitive personal conclusions about so I wanted to do a review before putting them to bed to get any last input. My general feeling is without well-designed long-term studies (not retrospective
jazj
in
Advanced Prostate Cancer
2 years ago
Mild pins and needles..
Hi..I’ve been on strict gluten-free diet since my celiac diagnose in august 2021 I’ve started my strict gouten free diet in December and so have on and off situations. Before diagnose I had body ache,hand tingling,dizziness,fatigue,achy feet. I know celiac cause malnutrition. My B12 was at 173 units
Hi..I’ve been on strict gluten-free diet since my celiac diagnose in august 2021 I’ve started my strict gouten free diet in December and so have on and off situations. Before diagnose I had body ache,hand tingling,dizziness,fatigue,achy feet. I know celiac cause malnutrition. My B12 was at 173 units
Saba82
in
Pernicious Anaemia Society
2 years ago
Rosemary oil for hair loss.
Hi all, hope you are all good. For anyone interested I’ve been using rosemary oil for hair loss , my hair loss has eased , not stopped yet but only done about 10 treatments, my hair is glossy, softer and darker. I put it on my scalp with carrier oil and also lavender oil and also put it in my shampoo
Hi all, hope you are all good. For anyone interested I’ve been using rosemary oil for hair loss , my hair loss has eased , not stopped yet but only done about 10 treatments, my hair is glossy, softer and darker. I put it on my scalp with carrier oil and also lavender oil and also put it in my shampoo
Electricblue1
in
AF Association
2 years ago
Pins and needles..
Hi..I’ve been on strict gluten-free diet since December and so have on and off situations. I see improvement. My iron level and vitamin deficiencies got improved a little bit. I used to have light tingling in my right hand before the diagnose and B12 shots helped me a lot. I’ve never had crazy GI symptoms
Hi..I’ve been on strict gluten-free diet since December and so have on and off situations. I see improvement. My iron level and vitamin deficiencies got improved a little bit. I used to have light tingling in my right hand before the diagnose and B12 shots helped me a lot. I’ve never had crazy GI symptoms
Saba82
in
Gluten Free Guerrillas
2 years ago
Very confused - should I change treatment or continue trying different Levothyroxine doses
Hi – I am new to the forum (in fact not used a forum before!), am very confused and really need some advice! I am 64 and was diagnosed with hypothyroidism (Hashimoto’s) 15 years ago and have been taking Levothyroxine but I don’t seem to be able to find the right dose. When I was first diagnosed,
Hi – I am new to the forum (in fact not used a forum before!), am very confused and really need some advice! I am 64 and was diagnosed with hypothyroidism (Hashimoto’s) 15 years ago and have been taking Levothyroxine but I don’t seem to be able to find the right dose. When I was first diagnosed,
Goldfinch7
in
Thyroid UK
2 years ago
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