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ginkgo biloba - safe to take??
Does anyone know if ginkgo biloba is safe to take when taking Levo? If so what benefits do you find from it?
Does anyone know if ginkgo biloba is safe to take when taking Levo? If so what benefits do you find from it?
Henson1980
in
Thyroid UK
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
7 months 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
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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
7 months 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
7 months ago
HELP! Firmagon reaction?
Hi - yesterday I had my 3rd monthly (80mg) injection of Firmagon. For all my previous injections, including the 2 initial loading doses, I did not have any major side effects, just some minimal soreness at the injection site which resolved in less than 2 days. Yesterday's injection was a little bit
Hi - yesterday I had my 3rd monthly (80mg) injection of Firmagon. For all my previous injections, including the 2 initial loading doses, I did not have any major side effects, just some minimal soreness at the injection site which resolved in less than 2 days. Yesterday's injection was a little bit
LongevityAT
in
Advanced Prostate Cancer
1 year 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
10 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
10 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
10 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
10 months ago
Dupuytrens contracture and PMR
This may seem a silly question but is the condition of Dupuytrens contracture linked in any way to PMR ? I have done a bit of research and it would seem both conditions are linked to genetics particularly in the northern Hemisphere . Some medical staff even call this 'The Viking disease' !!!!! I
This may seem a silly question but is the condition of Dupuytrens contracture linked in any way to PMR ? I have done a bit of research and it would seem both conditions are linked to genetics particularly in the northern Hemisphere . Some medical staff even call this 'The Viking disease' !!!!! I
larkthebark
in
PMRGCAuk
1 year ago
From a Gleason 9 to a clean CT scan in 18 mos.
18 mos ago, my husband was told by his dr. that he "most likely had two or three good years left." (WHY do they say stupid things like that?) I think that a lot of people believe whatever the dr. says and subconsciously program themselves accordingly. I, on the other hand, thought to myself, "We'll
18 mos ago, my husband was told by his dr. that he "most likely had two or three good years left." (WHY do they say stupid things like that?) I think that a lot of people believe whatever the dr. says and subconsciously program themselves accordingly. I, on the other hand, thought to myself, "We'll
jtango
in
Advanced Prostate Cancer
9 months ago
Fibromyalgia help! Please
Hiya, I was wondering if anyone knows of anything that can help symptoms from fibromyalgia, anything that isn't hard medication, I have heard cod liver oil, tumeric and magnesium. I want to know any thoughts on this or anything else that people have found that works. Anything and information at all
Hiya, I was wondering if anyone knows of anything that can help symptoms from fibromyalgia, anything that isn't hard medication, I have heard cod liver oil, tumeric and magnesium. I want to know any thoughts on this or anything else that people have found that works. Anything and information at all
sunflower022
in
Fibromyalgia Action UK
11 months ago
Prednisone tapering
I've been tapering off prednisone which initially was 30 mg daily by 1 mg every 3 days on dr's and rheumatologist advice. (Was diagnosed with PMR then changed to fibromyalgia). I was also taking tumeric supplements which i stopped on saturday. As of today I am on 7 mg. My question is: the last 2 days
I've been tapering off prednisone which initially was 30 mg daily by 1 mg every 3 days on dr's and rheumatologist advice. (Was diagnosed with PMR then changed to fibromyalgia). I was also taking tumeric supplements which i stopped on saturday. As of today I am on 7 mg. My question is: the last 2 days
Monkey321
in
PMRGCAuk
11 months ago
Vitamins/supplements for cll?
I found out AFTER I was diagnosed with CLL that low vitamin D is a risk factor for getting CLL. I have had chronically low vitamin D even though I worked outside for half my working life. I was haphazard in supplementing the past 30 years. With recent research, I'm seeing all kinds of supposedly helpful
I found out AFTER I was diagnosed with CLL that low vitamin D is a risk factor for getting CLL. I have had chronically low vitamin D even though I worked outside for half my working life. I was haphazard in supplementing the past 30 years. With recent research, I'm seeing all kinds of supposedly helpful
Vivikaye1
in
CLL Support
9 months ago
Radiation after Radical Prostatectomy with Lymph Node Removal in Non Metastatic and Metastatic Men. Need some answers.
For anyone following this post, just asking for clarity on the differences and to share your individual experiences. I had a radical prostatectomy with lymph node removal only 8, negative for pca. But, found with positive EPE margins, bladder wall, and microscopic bladder neck. A RO mentioned radiation
For anyone following this post, just asking for clarity on the differences and to share your individual experiences. I had a radical prostatectomy with lymph node removal only 8, negative for pca. But, found with positive EPE margins, bladder wall, and microscopic bladder neck. A RO mentioned radiation
Shorehousejam
in
Advanced Prostate Cancer
1 year ago
CBD Capsules
Can I take this while on the Pred My anxiety is through the roof and this used to help Also are we allowed Tumeric capsules to help with immflamation?
Can I take this while on the Pred My anxiety is through the roof and this used to help Also are we allowed Tumeric capsules to help with immflamation?
Northernnugget
in
PMRGCAuk
1 year ago
Experience with lupron
Well brother I was on lupron for about a year couldn't tolerate the side effects went on firmagon could not tolerate side effects finally went and had a orchiectomy it was the best thing I've ever had done don't have to deal with the pain and the side effects of the injections and the only thing I take
Well brother I was on lupron for about a year couldn't tolerate the side effects went on firmagon could not tolerate side effects finally went and had a orchiectomy it was the best thing I've ever had done don't have to deal with the pain and the side effects of the injections and the only thing I take
Startanew
in
Advanced Prostate Cancer
1 year ago
Aspergillus fumigatus
Both my wide and self have recently had Covid. symptoms seem to be dragging on and wife`s doctor told her to get a sputum test done. Finally after 2 weeks the results have arrived and she has Aspergillus fumigatus, a fungal infection in her lungs. Does anyone, with bronchiectais have any experience
Both my wide and self have recently had Covid. symptoms seem to be dragging on and wife`s doctor told her to get a sputum test done. Finally after 2 weeks the results have arrived and she has Aspergillus fumigatus, a fungal infection in her lungs. Does anyone, with bronchiectais have any experience
LissacFrance
in
Lung Conditions Community Forum
5 days ago
Doxycycline long term use
Hi, I’m 11 months into my 15 month treatment for CLL. I’m on Ibrutinib with Venetoclax and it’s suited me well, and I’m really pleased that my bloods now appear to be normal. I’m also on Co-Trimoxazole antibiotic and Aciclovir antiviral to deal with any infections should they arise during my treatment
Hi, I’m 11 months into my 15 month treatment for CLL. I’m on Ibrutinib with Venetoclax and it’s suited me well, and I’m really pleased that my bloods now appear to be normal. I’m also on Co-Trimoxazole antibiotic and Aciclovir antiviral to deal with any infections should they arise during my treatment
Smiley60
in
CLL Support
15 days ago
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