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Recipe for garlic and ginger paste for RLS
This is what I'm using ..4 oz /120 grams fresh garlic, 4 oz/120 grams fresh ginger root plus runny honey to make a paste. Liquidise or mash together ..Take a teaspoonful and eat it during the afternoon/evening... My friend just takes it before bed but my RLS starts early evening so I'm starting it earlier
This is what I'm using ..4 oz /120 grams fresh garlic, 4 oz/120 grams fresh ginger root plus runny honey to make a paste. Liquidise or mash together ..Take a teaspoonful and eat it during the afternoon/evening... My friend just takes it before bed but my RLS starts early evening so I'm starting it earlier
Allyp69
in
Restless Legs Syndrome
7 months ago
A possible cure??
A friend with RLS sent me a sample of the ginger, garlic and honey mixture he makes for himself using crushed ginger and garlic...It tastes awful but I'm finding that swallowing a teaspoon a day during the early evening has stopped my RLS completely. Early days but I've not used my Therapulse etc this
A friend with RLS sent me a sample of the ginger, garlic and honey mixture he makes for himself using crushed ginger and garlic...It tastes awful but I'm finding that swallowing a teaspoon a day during the early evening has stopped my RLS completely. Early days but I've not used my Therapulse etc this
Allyp69
in
Restless Legs Syndrome
7 months ago
Parkinsons exercises
Has anyone used imagery with movement exercises? It's researched based. I'm listening to Franklin Method Fellowship | Episode 10: Parkinson's Disease on Podbean, check it out. Www.Franklinmethodfellowship.podbean.com.
Has anyone used imagery with movement exercises? It's researched based. I'm listening to Franklin Method Fellowship | Episode 10: Parkinson's Disease on Podbean, check it out. Www.Franklinmethodfellowship.podbean.com.
Biblelover
in
Cure Parkinson's
26 days ago
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Peripheral neuropathy
Hi to the CLL community , on cycle 8 of my V and O treatment and now on Venetoclax for the last 4 months. Have had the venetoclax reduced to 200mg for a few weeks to help with neutropenia, but over the last 3 weeks I have developed neuropathy particularly in my fingers which wakes me up at night as
Hi to the CLL community , on cycle 8 of my V and O treatment and now on Venetoclax for the last 4 months. Have had the venetoclax reduced to 200mg for a few weeks to help with neutropenia, but over the last 3 weeks I have developed neuropathy particularly in my fingers which wakes me up at night as
puppy43
in
CLL Support
7 months ago
burning sensation in chest and back
hi all, I’m just recently diagnosed, I was just wondering if anyone else experiences a burning sensation across there chest and there back? It seems to come and go, dr says it’s nerve pain, what do you all do to help with it?
hi all, I’m just recently diagnosed, I was just wondering if anyone else experiences a burning sensation across there chest and there back? It seems to come and go, dr says it’s nerve pain, what do you all do to help with it?
Mrs_wilkes
in
Fibromyalgia Action UK
7 months ago
Dopamine
I just read that dopamine is made in the adrenals I had not heard this in the past so I am wondering what does this all mean? So maybe there is dopamine being made but the cells can't use it properly? "Dopamine, epinephrine and norepinephrine are the main catecholamines (a label based on having part
I just read that dopamine is made in the adrenals I had not heard this in the past so I am wondering what does this all mean? So maybe there is dopamine being made but the cells can't use it properly? "Dopamine, epinephrine and norepinephrine are the main catecholamines (a label based on having part
Boscoejean
in
Cure Parkinson's
2 months ago
central sensitivity syndrome
Has anyone heard of CSS. My dr said this can cause restless legs and stems from childhood trauma. Sort of crappy to think that yes, my childhood was super traumatic and potentially from that I still need to suffer.
Has anyone heard of CSS. My dr said this can cause restless legs and stems from childhood trauma. Sort of crappy to think that yes, my childhood was super traumatic and potentially from that I still need to suffer.
Jenevewill
in
Restless Legs Syndrome
7 months ago
ADT therapy and breast enlargement
Hello, any feedback on outlook for breast enlargement with ADT therapy ..currently taking Lupron and Bicalutmide? Diagnosed in Japan this June , 56, Gleason 7 , 4+3, PSA18, most likely no metastasis..was fairly fit…165, 5’10 but gaining weight and some man boobs. I generally was working out 4 days a
Hello, any feedback on outlook for breast enlargement with ADT therapy ..currently taking Lupron and Bicalutmide? Diagnosed in Japan this June , 56, Gleason 7 , 4+3, PSA18, most likely no metastasis..was fairly fit…165, 5’10 but gaining weight and some man boobs. I generally was working out 4 days a
Yokohama2023
in
Advanced Prostate Cancer
7 months ago
Just a touch away: CT-optimal touch perception and its influence on pain and itch
Psychologist Larissa Meijer has discovered that gentle caresses from a partner can provide relief from chronic pain. This treatment has no side effects and can be done at home. It should normally be free too 🙂 Meijer has demonstrated the effect of light stroking on pain and itchiness in Parkinson's
Psychologist Larissa Meijer has discovered that gentle caresses from a partner can provide relief from chronic pain. This treatment has no side effects and can be done at home. It should normally be free too 🙂 Meijer has demonstrated the effect of light stroking on pain and itchiness in Parkinson's
Esperanto
in
Cure Parkinson's
3 months ago
Help in understanding drugs in Parkinsons
I've recently been diagnosed with Parkinsons and have been prescribed LevaDopa -1/2 tablet (125mg) 4 times per day. I understand that there are complimentary drugs such MAO-B Inhibitors (such as Selegiline, Rasagiline, and Safinamide) I've done some cursory reseach which indicates that MAO-B inhibitors
I've recently been diagnosed with Parkinsons and have been prescribed LevaDopa -1/2 tablet (125mg) 4 times per day. I understand that there are complimentary drugs such MAO-B Inhibitors (such as Selegiline, Rasagiline, and Safinamide) I've done some cursory reseach which indicates that MAO-B inhibitors
Mezmerric
in
Cure Parkinson's
3 months ago
Too much B12??
Can high serum and active B12 levels (above recommended levels) cause the nerve damage? I recently had to visit my GP clinic and couldn’t get my favourite doctor so, agreed to seeing another doctor. Upon looking at my file he was shocked to see my apparently ‘very high B12’ results. In his opinion, too
Can high serum and active B12 levels (above recommended levels) cause the nerve damage? I recently had to visit my GP clinic and couldn’t get my favourite doctor so, agreed to seeing another doctor. Upon looking at my file he was shocked to see my apparently ‘very high B12’ results. In his opinion, too
GoneWithTheWind1972
in
Pernicious Anaemia Society
7 months ago
pigment dispersion syndrome
Hi lovely people 😀 I have EDS, not lupus, but many of my symptoms are similar I’ve recently been dxd with pigment dispersion syndrome by an ophthalmologist at our regional eye hospital. It happens when pigment from the iris sheds onto other parts of the eye, causing inflammation and vision problems
Hi lovely people 😀 I have EDS, not lupus, but many of my symptoms are similar I’ve recently been dxd with pigment dispersion syndrome by an ophthalmologist at our regional eye hospital. It happens when pigment from the iris sheds onto other parts of the eye, causing inflammation and vision problems
MEGS53
in
LUPUS UK
3 months ago
question about macuna
hi Few questions. 1. Does macuna capsule must take with benserazide or carbidopa? 2. If so, i am taking 100mg levodopa/25mg benserazide(Madopar) if I want to add 400mg mucuna15% levodopa ; so I need to take extra benserazide? thx
hi Few questions. 1. Does macuna capsule must take with benserazide or carbidopa? 2. If so, i am taking 100mg levodopa/25mg benserazide(Madopar) if I want to add 400mg mucuna15% levodopa ; so I need to take extra benserazide? thx
limcheeese22
in
Cure Parkinson's
3 months ago
Scientists say mystery of how red wine headaches occur may be solved
Thought this could be relevant on at least two grounds: First, so many members say they have issues tolerating alcoholic drinks, especially red wine. And it is specifically in this respect that I am posting. Not ordinary excessive drinking. Second, there are numerous posts here which advocate taking
Thought this could be relevant on at least two grounds: First, so many members say they have issues tolerating alcoholic drinks, especially red wine. And it is specifically in this respect that I am posting. Not ordinary excessive drinking. Second, there are numerous posts here which advocate taking
helvella
Thyroid UK
in
Thyroid UK
7 months ago
Vagus nerve stimulation'
I've posted here a few times to discuss gut health for those of you suffering from PA who also have gut issues. In my quest to find some relief from visceral hypersensitivity and massive intolerances (leading to malabsorption) I began acupuncture treatment this year. I am very lucky to have an anethesist
I've posted here a few times to discuss gut health for those of you suffering from PA who also have gut issues. In my quest to find some relief from visceral hypersensitivity and massive intolerances (leading to malabsorption) I began acupuncture treatment this year. I am very lucky to have an anethesist
expatkerry
in
Pernicious Anaemia Society
7 months ago
pending CABG
I’m so inspired by the stories people have shared, and photos! This is my first post so apologies if not all relevant. Being a fit 58 year old male recently diagnosed with angina to just hearing I need a double bypass has terrified me. But the wealth of information on here as well has people’s first
I’m so inspired by the stories people have shared, and photos! This is my first post so apologies if not all relevant. Being a fit 58 year old male recently diagnosed with angina to just hearing I need a double bypass has terrified me. But the wealth of information on here as well has people’s first
Mancunian1
in
British Heart Foundation
1 day ago
Ejection Fraction and CABG?
Whats the lowest EF that people here have been operated on please?
Whats the lowest EF that people here have been operated on please?
Burnley1
in
British Heart Foundation
3 days ago
11 months post quadruple CABG (25/07/23) after Nstemi heart attack (13/07/23)
Wow , what a month. Enjoyed that one 🤣👊🏻. Passed my module 2 motorbike test and got my full A license to ride unrestricted motorcycles. Passed in the Monday , picked up my 2019 Harley Davidson Sportster 883 on the Tuesday 🙌🏻. A couple of little issues meant that it went back to the dealer for some
Wow , what a month. Enjoyed that one 🤣👊🏻. Passed my module 2 motorbike test and got my full A license to ride unrestricted motorcycles. Passed in the Monday , picked up my 2019 Harley Davidson Sportster 883 on the Tuesday 🙌🏻. A couple of little issues meant that it went back to the dealer for some
DWizza
in
British Heart Foundation
3 days ago
Concerned I have PAD
Hello All, I used to be on this forum as Judge Dredd but I had to drop out due to some issues on another chat group unfortunately. Had long-term (20 plus years) hypertension and was diagnosed with CAD approx 5 years ago. Underwent a double CABG in Feb 2020 and then angioplasty with stent in Mar 2023
Hello All, I used to be on this forum as Judge Dredd but I had to drop out due to some issues on another chat group unfortunately. Had long-term (20 plus years) hypertension and was diagnosed with CAD approx 5 years ago. Underwent a double CABG in Feb 2020 and then angioplasty with stent in Mar 2023
GrumpyYorkshireman
in
British Heart Foundation
5 days ago
CTO of AV circumflex
I had CABG just over a year ago. Continued to have same symptoms as before after discharge from hospital. Angiography revealed that CABG had failed. MRI revealed CTO of AV circumflex. Now been referred to interventionist to “risk assess” procedure. This I take to mean they will likely go nothing
I had CABG just over a year ago. Continued to have same symptoms as before after discharge from hospital. Angiography revealed that CABG had failed. MRI revealed CTO of AV circumflex. Now been referred to interventionist to “risk assess” procedure. This I take to mean they will likely go nothing
Bergid65
in
British Heart Foundation
8 days ago
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