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Side effects of baby aspirin
I want to talk about the side effects of taking baby aspirin. I had been taking aspirin daily for more than a year on doctor's orders, and at the end of last year, I experienced eye problems and almost constant slight fatigue, especially after breakfast. In the eyes, especially in the right, strong
I want to talk about the side effects of taking baby aspirin. I had been taking aspirin daily for more than a year on doctor's orders, and at the end of last year, I experienced eye problems and almost constant slight fatigue, especially after breakfast. In the eyes, especially in the right, strong
Softy125
in
MPN Voice
10 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
anyone used myovvii device ?
hello everyone, curious to find out if any of you have used the myovvii device that is promoted on instagram for period pain and endo pains? Apparently it sends signals to your brain to change where the pain is being detected. A little bit like acupuncture which I have also read about. I’m currently
hello everyone, curious to find out if any of you have used the myovvii device that is promoted on instagram for period pain and endo pains? Apparently it sends signals to your brain to change where the pain is being detected. A little bit like acupuncture which I have also read about. I’m currently
Virginia10
in
Endometriosis UK
4 months ago
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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
weird prickling
hi everyone. Hope you all had a good Christmas. My doctor has been trying me on different medication to help with anxiety. It’s mainly in the mornings Im anxious. I’ve tried sertraline, which kept me awake and made me feel worse. Then they tried Mirtazapine, which seemed to help with sleep and the anxiety
hi everyone. Hope you all had a good Christmas. My doctor has been trying me on different medication to help with anxiety. It’s mainly in the mornings Im anxious. I’ve tried sertraline, which kept me awake and made me feel worse. Then they tried Mirtazapine, which seemed to help with sleep and the anxiety
Lakeshiker
in
Tinnitus UK
4 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
2 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
2 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
2 months ago
Dead down below. Asexual?
I am feeling a deep sense of loss, although maybe, or at least at one time, and maybe now, it may be what I want or perhaps need. For the last 30 years, I have had a very high libido, and while my partnered life has been vanilla, I had been curious about and interested in just about everything. Since
I am feeling a deep sense of loss, although maybe, or at least at one time, and maybe now, it may be what I want or perhaps need. For the last 30 years, I have had a very high libido, and while my partnered life has been vanilla, I had been curious about and interested in just about everything. Since
Hidden
in
Anxiety and Depression Support
5 months ago
Pain diminishing
Hi All Wanted to post an update and share what I'm doing with my diet: I was diagnosed on 20th October 2023, put on 15mg Pred, 1 month later reduced to 12.5mg then Saturday 16th Dec reduced to 10mg, at first all the pain and stiffness reappeared and I was gutted but it was "only" 6/10 and after taking
Hi All Wanted to post an update and share what I'm doing with my diet: I was diagnosed on 20th October 2023, put on 15mg Pred, 1 month later reduced to 12.5mg then Saturday 16th Dec reduced to 10mg, at first all the pain and stiffness reappeared and I was gutted but it was "only" 6/10 and after taking
MalloryMoss
in
PMRGCAuk
5 months ago
Tamoxifen v Acid Reflux
Hi All I have been clear from hormone related breast cancer for 3 years now. I am 62 & post menapausal . I changed medication from anastrozole to tamoxifen last month to try to help slow my osteopenia, as I do not get on with bisphosphonates. Unfortunately it appears to have aggravated my hiatus
Hi All I have been clear from hormone related breast cancer for 3 years now. I am 62 & post menapausal . I changed medication from anastrozole to tamoxifen last month to try to help slow my osteopenia, as I do not get on with bisphosphonates. Unfortunately it appears to have aggravated my hiatus
Calamintha
in
My Breast Cancer Community
5 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
Ant-inflammatory
I have chronic pancreatitis treated with Creon but I just discovered why and that I had additional issues. I has an MRI/MRCP, which disclosed I have 4 cysts on my pancreas and I have autoimmune cirrhosis. The cysts are just under a cc so nothing can be done but wait and watch. I wanted him to treat cirrhosis
I have chronic pancreatitis treated with Creon but I just discovered why and that I had additional issues. I has an MRI/MRCP, which disclosed I have 4 cysts on my pancreas and I have autoimmune cirrhosis. The cysts are just under a cc so nothing can be done but wait and watch. I wanted him to treat cirrhosis
Joanhappy21
in
Chronic Pancreatitis Support
5 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
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
connective tissues & lupus flare
Can I ask, what other supplements are others taking and has any one ever tried pycnogenol
pine
bark
extract
to help with inflammation? Seems lots of good reports on net. I am taking Vitamin d due to not going out in sun due to sensitivity and omega three.
Can I ask, what other supplements are others taking and has any one ever tried pycnogenol
pine
bark
extract
to help with inflammation? Seems lots of good reports on net. I am taking Vitamin d due to not going out in sun due to sensitivity and omega three.
Geeforce99
in
LUPUS UK
2 years ago
how soon after stopping prog/estro did you get period?
Found out today that our first fet failed. I already took my progesterone shot and morning estrace today but will not take it tomorrow. Wondering, if you've had a fet that didn't work, when did you get your period after stopping progesterone and estrogen?
Found out today that our first fet failed. I already took my progesterone shot and morning estrace today but will not take it tomorrow. Wondering, if you've had a fet that didn't work, when did you get your period after stopping progesterone and estrogen?
Rjfguitfg
in
Fertility Network UK
3 months ago
Ginkgo trials - something different
I don't know if anyone is following my posts on Ginkgo, but if there be... Once a week I take 3 x 30mg the day before I would like a guaranteed (?) break from tinnitus for a few hours the afternoon of the following day. It didn't happen yesterday. Instead, it happened today. T in the morning (as usual
I don't know if anyone is following my posts on Ginkgo, but if there be... Once a week I take 3 x 30mg the day before I would like a guaranteed (?) break from tinnitus for a few hours the afternoon of the following day. It didn't happen yesterday. Instead, it happened today. T in the morning (as usual
Ray200
in
Tinnitus UK
5 months ago
Getting bombarded with ads for RA treatment Honey bee venom cream?.
Amazing too good to be true claims for this but there seems to be a few bits of research on it being anti inflammatory. Anyone tried it ? Still taking the meds....
Amazing too good to be true claims for this but there seems to be a few bits of research on it being anti inflammatory. Anyone tried it ? Still taking the meds....
welsh12
in
NRAS
4 months ago
MGUS and PMR/GCA
If true, this is a little unsettling... MGUS can be a precursor to Multiple Myeloma. Quote from article: "A study of United States veterans suggested that subjects with autoimmune conditions where autoantibodies are detectable are at increased risk of developing MGUS [46]. Furthermore, a recent
If true, this is a little unsettling... MGUS can be a precursor to Multiple Myeloma. Quote from article: "A study of United States veterans suggested that subjects with autoimmune conditions where autoantibodies are detectable are at increased risk of developing MGUS [46]. Furthermore, a recent
kp60
in
PMRGCAuk
4 months ago
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