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Genetic variation unlikely to influence COVID-19 morbidity and mortality.
African Americans and Latinos in the United States and ethnic minorities in the United Kingdom are disproportionately affected by COVID-19. They are more likely to develop severe symptoms and also show significantly higher mortality compared with other regional and ethnic groups. To investigate if
African Americans and Latinos in the United States and ethnic minorities in the United Kingdom are disproportionately affected by COVID-19. They are more likely to develop severe symptoms and also show significantly higher mortality compared with other regional and ethnic groups. To investigate if
2greys
in
Lung Conditions Community Forum
4 years ago
Horrendous Tinnitus
Really bad in the evenings seems to spike at the same time for no apparent reason, sleeping is proving difficult, nytol doesn’t seem to work. I also suffer with hyperacusis so using headphones for sound therapy might be good for the tinnitus but not so good for the hyperacusis. Any positive thoughts
Really bad in the evenings seems to spike at the same time for no apparent reason, sleeping is proving difficult, nytol doesn’t seem to work. I also suffer with hyperacusis so using headphones for sound therapy might be good for the tinnitus but not so good for the hyperacusis. Any positive thoughts
catman68
in
British Tinnitus Association
4 years ago
My husband is refusing his meds
John has finally been diagnosed with PSP. It's only been 4 years! But he is starting to refuse his anti depressants, saying they are causing his headaches. He doesn't seem to realize the PSP effects both of us, and has become very self-centered. Any suggestions?
John has finally been diagnosed with PSP. It's only been 4 years! But he is starting to refuse his anti depressants, saying they are causing his headaches. He doesn't seem to realize the PSP effects both of us, and has become very self-centered. Any suggestions?
ladydog255
in
PSP Association
4 years ago
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Bronchiectasis and mesalazine
Hi I have just been given some medication for my Crohn's but have read that it could make my bronchiectasis worse....has anyone had any experience with this, the medication is mesalazine
Hi I have just been given some medication for my Crohn's but have read that it could make my bronchiectasis worse....has anyone had any experience with this, the medication is mesalazine
Lebod
in
Lung Conditions Community Forum
4 years ago
Living in a maisonette/flat
Hello I have spinal ataxia and live in a maisonette on the 2nd floor (no lift). I have been using home delivery services for my supermarket shopping. Today me and my 8yr old had to go and collected the shopping from the delivery driver as she said they are no longer allowed to enter the communal area
Hello I have spinal ataxia and live in a maisonette on the 2nd floor (no lift). I have been using home delivery services for my supermarket shopping. Today me and my 8yr old had to go and collected the shopping from the delivery driver as she said they are no longer allowed to enter the communal area
Eveie78
in
Ataxia UK
4 years ago
Elavil causing brain fog ? Treatment for fibromyalgia needed
My fibromyalgia started after a viral infection (viral labyrinthitis- an inner ear infection). My head felt very heavy and then my generalized muscle aches started. 30 years later my body is very stiff and sore all over which causes me difficulty sleeping. I have found no medication that helps- Elavil
My fibromyalgia started after a viral infection (viral labyrinthitis- an inner ear infection). My head felt very heavy and then my generalized muscle aches started. 30 years later my body is very stiff and sore all over which causes me difficulty sleeping. I have found no medication that helps- Elavil
Stimmy
in
Fibromyalgia Action UK
4 years ago
Supplements for endometriosis, detoxification and immune health
Vitex
Cramp
Bark
(Viburnum opulus), Pine Bark Extract (Pycnogenol) Black Haw (Viburnum prunifolium), Black Cohosh (Actaea racemosa), Dong Quai (Angelica sinensis), and California Poppy (Eschscholzia californica) Raspberry Leaf (Rubus idaeus), Nettles (Urtica dioica), Violet (Viola spp), and Red
Vitex
Cramp
Bark
(Viburnum opulus), Pine Bark Extract (Pycnogenol) Black Haw (Viburnum prunifolium), Black Cohosh (Actaea racemosa), Dong Quai (Angelica sinensis), and California Poppy (Eschscholzia californica) Raspberry Leaf (Rubus idaeus), Nettles (Urtica dioica), Violet (Viola spp), and Red
ScarletBlossom
in
Endometriosis UK
4 years ago
Ankyolosing Spondylitis and Adalimumab
I have Ankyolosing Spondylitis with a number of spinal fusions already. I started on Adalimumab at the end of April but it's not really helping. I have just had a phone appointment with the specialist nurse who told me that I can't expect to be pain free as I have a lot going on. I told her I don't
I have Ankyolosing Spondylitis with a number of spinal fusions already. I started on Adalimumab at the end of April but it's not really helping. I have just had a phone appointment with the specialist nurse who told me that I can't expect to be pain free as I have a lot going on. I told her I don't
Stephanie6637
in
NRAS
4 years ago
Job
Hi guys. I had treatment for endo last August, I also had a IDU inserted during this procedure. Everything was great until December when the pain started to return, I saw my consultant again in February who suspected Adenomyosis-the treatment plan for this is not something I am ready for being only 29
Hi guys. I had treatment for endo last August, I also had a IDU inserted during this procedure. Everything was great until December when the pain started to return, I saw my consultant again in February who suspected Adenomyosis-the treatment plan for this is not something I am ready for being only 29
DisneyP
in
Endometriosis UK
4 years ago
Cerzatte AND lexapro?
Hi! I've had endo for years but in Jan 2020 found out I'd two big cyst. One on the left was 8cm and wouldn't shrink with the Syrenal I was taking. I just had surgery 2 weeks ago to remove them (after waiting for months due to covid) and I'm down a fallopian tube and my ovary is damaged too, all on the
Hi! I've had endo for years but in Jan 2020 found out I'd two big cyst. One on the left was 8cm and wouldn't shrink with the Syrenal I was taking. I just had surgery 2 weeks ago to remove them (after waiting for months due to covid) and I'm down a fallopian tube and my ovary is damaged too, all on the
Doggymomma92
in
Endometriosis UK
4 years ago
Langerhans cell histiocytosis
I was diagnosed last year and would like to hear from anyone else diagnosed with lch
I was diagnosed last year and would like to hear from anyone else diagnosed with lch
Mrsclh
in
Lung Conditions Community Forum
4 years ago
No medication
So I finished my meeting with the endo, she said my symptoms were mainly due to anxiety and depression and so she prescribed me Cipralex (Lexapro). She said as I was subclinical, if she were to prescribe me with thyroid medication, it will make my anxiety worse. I have another meeting with her in 2
So I finished my meeting with the endo, she said my symptoms were mainly due to anxiety and depression and so she prescribed me Cipralex (Lexapro). She said as I was subclinical, if she were to prescribe me with thyroid medication, it will make my anxiety worse. I have another meeting with her in 2
borahae
in
Thyroid UK
4 years ago
Meds
Hi. Many of the T patients that write in this Forum, are taking meds to deal with the side effects of T, like stress, anxiety, and perhaps they don´t realise that there are other ways that can help without resorting to meds, and that is by uncluttering your mind of negative thoughts. Some of these
Hi. Many of the T patients that write in this Forum, are taking meds to deal with the side effects of T, like stress, anxiety, and perhaps they don´t realise that there are other ways that can help without resorting to meds, and that is by uncluttering your mind of negative thoughts. Some of these
bailongo
in
British Tinnitus Association
4 years ago
OVERCOMING GVHD AFTER ASCT
Post by MPN-MATE Admin » Thu Jul 16, 2020 9:56 am Morning all... :D For some of us here, (but hopefully not all...?), some may eventually have to travel down the path of having an Allogenic Stem Cell Transplant (ASCT), when and if it becomes necessary... ... If, and when that occurs, one of the known
Post by MPN-MATE Admin » Thu Jul 16, 2020 9:56 am Morning all... :D For some of us here, (but hopefully not all...?), some may eventually have to travel down the path of having an Allogenic Stem Cell Transplant (ASCT), when and if it becomes necessary... ... If, and when that occurs, one of the known
socrates_8
in
MPN Voice
4 years ago
St John's wort
Hi all, I'm looking for some advice. I've been really struggling with anxiety, feeling like I can't cope and feeling low, all due to my pain levels. I have been on antidepressants before and have a prescription to start them again but I'm hesitant. I have tried supplements before with no help but have
Hi all, I'm looking for some advice. I've been really struggling with anxiety, feeling like I can't cope and feeling low, all due to my pain levels. I have been on antidepressants before and have a prescription to start them again but I'm hesitant. I have tried supplements before with no help but have
Emseykins
in
NRAS
4 years ago
New article on designing proper trials for T4/T3 combination therapy
New article has appeared in full discussing how to design trials for determining use of combination therapy. Naturally, being US based, it makes no mention of our work whatsoever.
HYPOTHESIS AND THEORY ARTICLE
Front. Endocrinol., 08 July 2020 | https://doi.org/10.3389/fendo.2020.00371
[
New article has appeared in full discussing how to design trials for determining use of combination therapy. Naturally, being US based, it makes no mention of our work whatsoever.
HYPOTHESIS AND THEORY ARTICLE
Front. Endocrinol., 08 July 2020 | https://doi.org/10.3389/fendo.2020.00371
[
diogenes
in
Thyroid UK
4 years ago
Newbie
Hi everyone New here. I’ve had fibromyalgia for at least 8/9 years. I’ve just recently been referred to rheumatology and the want to do test for spondylitis. From what I’ve read on the nhs website it’s quite scary! Can’t talk to my partner just in case it turns out not to be spondylitis. Saves the both
Hi everyone New here. I’ve had fibromyalgia for at least 8/9 years. I’ve just recently been referred to rheumatology and the want to do test for spondylitis. From what I’ve read on the nhs website it’s quite scary! Can’t talk to my partner just in case it turns out not to be spondylitis. Saves the both
LostPain
in
Fibromyalgia Action UK
4 years ago
Colomycin
I have put in colomycin inhalant with nebuliser. But been on for two weeks now and feel so much worse. Been taken off of it my breathing is no where near as bad as it was. Within a day or so. Not sure what they will do now also on steroids. Had pseudomonas infections on and off since last October. Always
I have put in colomycin inhalant with nebuliser. But been on for two weeks now and feel so much worse. Been taken off of it my breathing is no where near as bad as it was. Within a day or so. Not sure what they will do now also on steroids. Had pseudomonas infections on and off since last October. Always
patj
in
Lung Conditions Community Forum
4 years ago
tinnitus due to acoustic neuroma
have an acoustic neuroma diagnosed in january and havent seen any doctors yet, i had appointment in march which was cancelled due to the corona virus. my tinnitus is getting worse, and this morning had a new echo vibration noise everytime i touched my head or brushed my hair...
have an acoustic neuroma diagnosed in january and havent seen any doctors yet, i had appointment in march which was cancelled due to the corona virus. my tinnitus is getting worse, and this morning had a new echo vibration noise everytime i touched my head or brushed my hair...
karenm1
in
British Tinnitus Association
4 years ago
Experience of neurology during the coronavirus crisis. Asking for your help!
Dear all We have a virtual meeting of the Medical Advisory Panel of Ataxia UK in a couple of weeks. One of the topics we will be discussing is how neurology appointments have been affected by the coronavirus climate that we unfortunately find ourselves in. I would be so grateful if you could let me
Dear all We have a virtual meeting of the Medical Advisory Panel of Ataxia UK in a couple of weeks. One of the topics we will be discussing is how neurology appointments have been affected by the coronavirus climate that we unfortunately find ourselves in. I would be so grateful if you could let me
HarryB
Administrator
in
Ataxia UK
4 years ago
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