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Side effects of baby aspirin
I currently take a white
willow
bark
supplement instead of aspirin for blood thinning. I take a supplement of hawthorn to stabilize my blood pressure, and a supplement of burdock root and vitamin D3 to support overall health and the immune system. All of this is working well at the moment.
I currently take a white
willow
bark
supplement instead of aspirin for blood thinning. I take a supplement of hawthorn to stabilize my blood pressure, and a supplement of burdock root and vitamin D3 to support overall health and the immune system. All of this is working well at the moment.
Softy125
in
MPN Voice
10 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
4 months ago
Swallowing problems
HiDoes anyone have an issue with swallowing. I've been told my muscles in my throat spasm causing me to vomit 2/3 times a week. I am hardly eating anything and what I get down is a liquid diet and 8 months on I'm fed up. This has caused a pharyngeal pouch. I've seen an ENT specialist for this and I've
HiDoes anyone have an issue with swallowing. I've been told my muscles in my throat spasm causing me to vomit 2/3 times a week. I am hardly eating anything and what I get down is a liquid diet and 8 months on I'm fed up. This has caused a pharyngeal pouch. I've seen an ENT specialist for this and I've
Loobyloo1966
in
FND Action
1 day ago
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Ginkgo - possible adverse side effect: Nervous anxiety
It's me again. On about Ginkgo as usual... Having taken Ginkgo for over 6 months, and having planned relief from Tinnitus by doing so, I may have experienced a side effect. Recent bouts of nervous anxiety. This is not the kind of anxiety you might experience in a dentist waiting room. No, this is
It's me again. On about Ginkgo as usual... Having taken Ginkgo for over 6 months, and having planned relief from Tinnitus by doing so, I may have experienced a side effect. Recent bouts of nervous anxiety. This is not the kind of anxiety you might experience in a dentist waiting room. No, this is
Ray200
in
Tinnitus UK
2 days ago
Malaria tablets
Hi everyone, am I the process of looking at a holiday. I know yellow fever vaccine is a big no no. Am on hydroxycarbamide and daily aspirin with a diagnosis of ET. Has anyone taken malaria tablets with such a condition? TIA.
Hi everyone, am I the process of looking at a holiday. I know yellow fever vaccine is a big no no. Am on hydroxycarbamide and daily aspirin with a diagnosis of ET. Has anyone taken malaria tablets with such a condition? TIA.
SazzaC
in
MPN Voice
1 month ago
I've finally reached a milestone
I quit teaching due to hyperacusis. The classroom was the only place that used to keep me going in that job. So I finished last week and started doing a couple of days at my new job this week. Day two in the office and I managed all day with no hearing protection.Its a small quiet office with only a
I quit teaching due to hyperacusis. The classroom was the only place that used to keep me going in that job. So I finished last week and started doing a couple of days at my new job this week. Day two in the office and I managed all day with no hearing protection.Its a small quiet office with only a
daverussell
in
Tinnitus UK
14 days ago
Hello everyone, question about gluten and globus (feeling of lump in throat) ?
Hello everyone, question about gluten and globus (feeling of lump in throat) I also have painful tongue, chronic constipation, bouts of diarrhoea, I've had rashes that look like little spots/patches over the years, burning mouth, tongue, oesophagus, sore stomach, and tingling/vibrating in stomach and
Hello everyone, question about gluten and globus (feeling of lump in throat) I also have painful tongue, chronic constipation, bouts of diarrhoea, I've had rashes that look like little spots/patches over the years, burning mouth, tongue, oesophagus, sore stomach, and tingling/vibrating in stomach and
Suffering_sunny
in
Gluten Free Guerrillas
1 month ago
Next instalment
Before I start my next task, either proofreading or, dread the thought, cleaning the car, here`s the next instalment. Chris. One of mum's best friends from childhood was, without a doubt, Lydia, a confident who in later life became Aunty Lyds to all of us. Their friendship through their teenage years
Before I start my next task, either proofreading or, dread the thought, cleaning the car, here`s the next instalment. Chris. One of mum's best friends from childhood was, without a doubt, Lydia, a confident who in later life became Aunty Lyds to all of us. Their friendship through their teenage years
LissacFrance
in
Lung Conditions Community Forum
1 month ago
Impact of brief CBT on chronic pain and anxiety
Hello, My name is Audrey and I am a student at Pepperdine University. I am doing a research study about the impact of brief Cognitive Behavioral Therapy on people with chronic pain and anxiety. I would appreciate it if you could take a few minutes to complete both parts. It will also expose you to a
Hello, My name is Audrey and I am a student at Pepperdine University. I am doing a research study about the impact of brief Cognitive Behavioral Therapy on people with chronic pain and anxiety. I would appreciate it if you could take a few minutes to complete both parts. It will also expose you to a
audreycosta
in
Pain Concern
2 months ago
Patients with higher apolipoprotein A-I levels at greater risk for giant cell arteritis
https://www.healio.com/news/rheumatology/20240315/patients-with-higher-apolipoprotein-ai-levels-at-greater-risk-for-giant-cell-arteritis
https://www.healio.com/news/rheumatology/20240315/patients-with-higher-apolipoprotein-ai-levels-at-greater-risk-for-giant-cell-arteritis
perceptual63
in
PMRGCAuk
2 months ago
Side effects of nefopam sweats
Recently been put on nefopam due to night pains because of hip and back pain. Does anyone else suffer sweats from nefopam? I'm trying to rule them out as on other meds too.
Recently been put on nefopam due to night pains because of hip and back pain. Does anyone else suffer sweats from nefopam? I'm trying to rule them out as on other meds too.
Jackieginger44
in
Pain Concern
2 months ago
Aortitis
I was diagnosed with non cranial Giant Cell Arteritis in September last year. So far I haven't managed to find anyone else with this condition because most people have the temporal version with the headaches.Mine is Aortitis which apparently is rare. I'd love to share experiences with someone else
I was diagnosed with non cranial Giant Cell Arteritis in September last year. So far I haven't managed to find anyone else with this condition because most people have the temporal version with the headaches.Mine is Aortitis which apparently is rare. I'd love to share experiences with someone else
Dance62
in
PMRGCAuk
3 months ago
PMR and brachial neuritis
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
It looks like I have developed a fairly rare condition called Parsonage-Turner syndrome (PTS), also called brachial neuritis. It started with terrible pain in the shoulder, so initially I thought it would appear in the other shoulder and be the beginning of a PMR relapse. But it is taking a different
dmart7
in
PMRGCAuk
3 months ago
Question to the collective
As mentioned previously, I was diagnosed (Prof H/Sheffield) as having the SCA7 version of Ataxia in 2014. I was put on a tablet,( DANTROLENE) that has been gradually increased from 1 X 25mg capsule to the current 3 X 25mg Just had a phone call about some physio I saw last year, and it was then kind
As mentioned previously, I was diagnosed (Prof H/Sheffield) as having the SCA7 version of Ataxia in 2014. I was put on a tablet,( DANTROLENE) that has been gradually increased from 1 X 25mg capsule to the current 3 X 25mg Just had a phone call about some physio I saw last year, and it was then kind
Butcherpete
in
Ataxia UK
3 months ago
Oesophagus/Stomach issues - where to start?
My complaint has been going on for at least 10 years now and the symptoms get worse every year but I am unsure of how to proceed. My symptoms. Every intake of breath seems to increase the pressure in my oesophagus and every few seconds I have to either break the seal by flexing my throat to intake
My complaint has been going on for at least 10 years now and the symptoms get worse every year but I am unsure of how to proceed. My symptoms. Every intake of breath seems to increase the pressure in my oesophagus and every few seconds I have to either break the seal by flexing my throat to intake
hankpym
in
IBS Network
3 months ago
Hi I’m dory10. I was diagnosed inDec2019 but had it for 27 years. I fall over a lot now I’m having tests to find out why.
I fell down stairs expecting my 3rd child at 37 weeks . She was fine a genius infact but I was left in muscle spasms and so much pain. I was told I was so close to being a paraplegic. I put up with all the little things that went wrong, I was fortunate not to be paraplegic. In 2016 I had a minor car
I fell down stairs expecting my 3rd child at 37 weeks . She was fine a genius infact but I was left in muscle spasms and so much pain. I was told I was so close to being a paraplegic. I put up with all the little things that went wrong, I was fortunate not to be paraplegic. In 2016 I had a minor car
Dory10
in
Fibromyalgia Action UK
3 months ago
Loss of voice!
Anybody with asthma + bronchiectasis combo ever suffer with total loss of voice? Ihave the odd croaky days, but it doesn't last long, now I've lost my voice ccompletely.....had loads of hot drinks, nothing working. Tips please!! Thanks.
Anybody with asthma + bronchiectasis combo ever suffer with total loss of voice? Ihave the odd croaky days, but it doesn't last long, now I've lost my voice ccompletely.....had loads of hot drinks, nothing working. Tips please!! Thanks.
Tiggertheterrier
in
Asthma Community Forum
3 months ago
Desperate need answers
Good morning I'm a 45 year old female who back 2021 I had contracted COVID after that went away after eight days I started having a phlegm ok then the phlegm stated getting thicker it has been four your since the change now I can't hold food don't get me wrong I can chew the food swallow but when the
Good morning I'm a 45 year old female who back 2021 I had contracted COVID after that went away after eight days I started having a phlegm ok then the phlegm stated getting thicker it has been four your since the change now I can't hold food don't get me wrong I can chew the food swallow but when the
Hikeemah
in
Lung Conditions Community Forum
3 months ago
Royal Free visit
Hi all, I just thought I would give a quick update. I attended the Royal Free Hospital last Thursday ,I was seen in the Scleroderma clinic by a member of the team. She asked questions and examined me, she then went and got a senior colleague,(not Prof Denton) unfortunately can’t remember their names
Hi all, I just thought I would give a quick update. I attended the Royal Free Hospital last Thursday ,I was seen in the Scleroderma clinic by a member of the team. She asked questions and examined me, she then went and got a senior colleague,(not Prof Denton) unfortunately can’t remember their names
Buttsy
in
Scleroderma & Raynaud's UK (SRUK)
3 months ago
Pseudomonas colonised.
Morning all, l have been on nebulised Colomycin since last August. Although it has kept infections at bay, l am more breathless than l used to be and energy levels are very low. I have told that l will be on this medication for a long time as my lungs are very badly damaged. I cannot walk any length
Morning all, l have been on nebulised Colomycin since last August. Although it has kept infections at bay, l am more breathless than l used to be and energy levels are very low. I have told that l will be on this medication for a long time as my lungs are very badly damaged. I cannot walk any length
falcon68
in
Lung Conditions Community Forum
3 months ago
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