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Some advice please
I had my oblation back in November 2016, I was taking 80mg of sotalol and 150mg of Irbesartan, two weeks ago my doctor suggested that I come off the sotalol and move to rivaroxaban. For the past week, every evening I have had AF for a couple of hours. What has gone wrong ? It feels that I have gone
I had my oblation back in November 2016, I was taking 80mg of sotalol and 150mg of Irbesartan, two weeks ago my doctor suggested that I come off the sotalol and move to rivaroxaban. For the past week, every evening I have had AF for a couple of hours. What has gone wrong ? It feels that I have gone
Between68and148
in
AF Association
7 years ago
Cold cap worked for me
I just thought I'd say that I have finished treatment with weekly taxol, and still have my hair. I had the cold cap all through. While I was walking to the loo with it on a woman said 'I've heard that doesn't work' and I know it doesn't for some people but I wanted to say it's worked for me. I wasn't
I just thought I'd say that I have finished treatment with weekly taxol, and still have my hair. I had the cold cap all through. While I was walking to the loo with it on a woman said 'I've heard that doesn't work' and I know it doesn't for some people but I wanted to say it's worked for me. I wasn't
LesleyGreengran
in
My Ovacome
7 years ago
Hereditary Neuropathy
I was diagnosed with PN 10 years ago. It initially started in my hands with tingling and numbness in my index fingers and thumbs. After having the carpel tunnel operation three times on each hand it was decided that I should see a neurologist who after several tests diagnosed hereditary neuropathy.
I was diagnosed with PN 10 years ago. It initially started in my hands with tingling and numbness in my index fingers and thumbs. After having the carpel tunnel operation three times on each hand it was decided that I should see a neurologist who after several tests diagnosed hereditary neuropathy.
Gigforgig
in
Neuropathy Support
7 years ago
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Docetaxel not taxol
Hi lovely ladies, In my last post I asked if weekly Taxol at 50gms was low and from your replies it seems to be, I have had 3 dose and it 's going up so I was stressing out thinking that I was on too low a dose. I called my clinic nurse she was great called me back with in a couple hours to let me know
Hi lovely ladies, In my last post I asked if weekly Taxol at 50gms was low and from your replies it seems to be, I have had 3 dose and it 's going up so I was stressing out thinking that I was on too low a dose. I called my clinic nurse she was great called me back with in a couple hours to let me know
lorraine71-Australia
in
My Ovacome
7 years ago
Phew!🙃 Latest round of tests is complete!
So I had the MRI and I haven't got the official report but I don't think there's anything concerning there. Blood tests all came back normal except plasma free metanephrines were high so will call the doc and see what he says. The tilt table test I had today....... And the cardiologist stopped it after
So I had the MRI and I haven't got the official report but I don't think there's anything concerning there. Blood tests all came back normal except plasma free metanephrines were high so will call the doc and see what he says. The tilt table test I had today....... And the cardiologist stopped it after
1985mum
in
LUPUS UK
7 years ago
plant based foods
naturopathy
doctor says if we follow only plant based foods(vegetables and fruits) and oil free foods can definetly reverse all lifestyle diseases within three months.that means vegan diet.fruits replaces the dairy products.there are many instenses of reversing according to DR.PRAMOD TRIPATY of poona.he
naturopathy
doctor says if we follow only plant based foods(vegetables and fruits) and oil free foods can definetly reverse all lifestyle diseases within three months.that means vegan diet.fruits replaces the dairy products.there are many instenses of reversing according to DR.PRAMOD TRIPATY of poona.he
matru13-ashram
in
Diabetes India
7 years ago
Post- thoracotomy and peripheral neuropathic pain
I have been diagnosed with post- thoractomy syndrome and peripheral neuropathic pain which is a horrendous condition. My issue that I am struggling with the most lately is mobility. Everytime I walk it literally feels like my insides are tearing with every step I take.The pain feels like an open
I have been diagnosed with post- thoractomy syndrome and peripheral neuropathic pain which is a horrendous condition. My issue that I am struggling with the most lately is mobility. Everytime I walk it literally feels like my insides are tearing with every step I take.The pain feels like an open
jaybrody
in
Pain Concern
7 years ago
Help with peripheral Neoropathy
I am currently having tests for Peripheral neuropathy - awaiting a MRI scan and Nerve conducting test. They have done all the blood tests and they have all come back normal. The doctor I seen has done lots of tests that proves there is a difference in my nerves above my knee to below and change between
I am currently having tests for Peripheral neuropathy - awaiting a MRI scan and Nerve conducting test. They have done all the blood tests and they have all come back normal. The doctor I seen has done lots of tests that proves there is a difference in my nerves above my knee to below and change between
Sheltie3
in
Foggy's "Invisible Illness" Support
7 years ago
Burning Feet
Hi there, I'm hoping someone may have some thoughts on one of my symptoms. Before I was diagnosed with PA, one of my symptoms was severe burning soles of my feet. After 2 months of self injecting daily, this symptom improved hugely. I've noticed now I've decreased injections, that before my soles start
Hi there, I'm hoping someone may have some thoughts on one of my symptoms. Before I was diagnosed with PA, one of my symptoms was severe burning soles of my feet. After 2 months of self injecting daily, this symptom improved hugely. I've noticed now I've decreased injections, that before my soles start
AnnaKatrina
in
Pernicious Anaemia Society
7 years ago
Introduction
I have suffered with what I called 'leapy legs' for 35 years. it manifests during rest times but, thankfully not when sleeping. I ;have found that if I keep my hands busy with craft or cards I can keep symptoms at bay. I no longer visit the cinema or theatre, watching tv does not bring relief but
I have suffered with what I called 'leapy legs' for 35 years. it manifests during rest times but, thankfully not when sleeping. I ;have found that if I keep my hands busy with craft or cards I can keep symptoms at bay. I no longer visit the cinema or theatre, watching tv does not bring relief but
leapylegs
in
Restless Legs Syndrome
7 years ago
Sensory Neuropathy
Having been diagnosed with this title 2 years ago and not R.L.S i am still no farther forward in obtaining relief on a daily basis. Having tried numerous medications prescribed by my Doctor the discomfort i am experiencing affects my quality of life. I am a 67 male fairly fit exercise 3 times a week
Having been diagnosed with this title 2 years ago and not R.L.S i am still no farther forward in obtaining relief on a daily basis. Having tried numerous medications prescribed by my Doctor the discomfort i am experiencing affects my quality of life. I am a 67 male fairly fit exercise 3 times a week
Hidden
in
Restless Legs Syndrome
7 years ago
Severe reactions to RLS prescriptions.
Oh Kim what a truly revealing article. I wish I had written it because it is exactly what I am going through now. Thank you Kim and I wish you all that I wish for myself and more for your bravery. I did not want to reveal all, especially 'the electric shock sensations'. I am 76 this year and didn't
Oh Kim what a truly revealing article. I wish I had written it because it is exactly what I am going through now. Thank you Kim and I wish you all that I wish for myself and more for your bravery. I did not want to reveal all, especially 'the electric shock sensations'. I am 76 this year and didn't
dojen
in
Restless Legs Syndrome
7 years ago
Hot tub use during chemo and neuropathy
So in 2015 I used my hot tub following taxotere. I have severe peripheral neuropathy since getting chemo. Now I'm wondering if I did this to myself by using the hot tub, I thought it was a good thing to get the circulation, but I've read here that cold packs on feet and hands "during" chemo reduces
So in 2015 I used my hot tub following taxotere. I have severe peripheral neuropathy since getting chemo. Now I'm wondering if I did this to myself by using the hot tub, I thought it was a good thing to get the circulation, but I've read here that cold packs on feet and hands "during" chemo reduces
Jashelby
in
Advanced Prostate Cancer
7 years ago
homeopathic medicine for tinnitus
I am 57 year old suffering from bi-lateral tinnitus from the last ten years with roaring sound in my both ears and severe deafness. Presently I am on high power hearing aid. My disease increased gradually from the last ten years. I am symptomatically emotional. Kindly prescribe appropriate homeopathic
I am 57 year old suffering from bi-lateral tinnitus from the last ten years with roaring sound in my both ears and severe deafness. Presently I am on high power hearing aid. My disease increased gradually from the last ten years. I am symptomatically emotional. Kindly prescribe appropriate homeopathic
gilkar
in
Diabetes India
7 years ago
Father diagnosed after 20 years
20 years ago my father presented with peripheral neuropathy in his hands (in his early 40's). He would wake up with numb hands that felt like balloons and have pins and needles and loss of sensation. He was diagnosed at the time with peripheral neuropathy, but with no cause of this investigated! His
20 years ago my father presented with peripheral neuropathy in his hands (in his early 40's). He would wake up with numb hands that felt like balloons and have pins and needles and loss of sensation. He was diagnosed at the time with peripheral neuropathy, but with no cause of this investigated! His
CMonkey
in
Charcot-Marie-Tooth UK
7 years ago
Which B12
Hello all I have Hashi's, Candida and gut bacterial overgrowth problems. When I had my 23andme test last year it came back that I was MTHFR etc., and my then FD said I needed to take Hydroxycobalmin, not the methyl that I was taking. My levels are all in my profile,arn't too bad so I cut down on taking
Hello all I have Hashi's, Candida and gut bacterial overgrowth problems. When I had my 23andme test last year it came back that I was MTHFR etc., and my then FD said I needed to take Hydroxycobalmin, not the methyl that I was taking. My levels are all in my profile,arn't too bad so I cut down on taking
Jefner
in
Pernicious Anaemia Society
7 years ago
ironic pain
On behalf of my wife in to much pain to come on at the moment,a few days ago she had a Lumbar epidural injection to relieve back pain it seems to have made things worse.She has suffered for 20 years with pain sometimes a lot worse than others,so the injection was done through the N.H.S.has anyone else
On behalf of my wife in to much pain to come on at the moment,a few days ago she had a Lumbar epidural injection to relieve back pain it seems to have made things worse.She has suffered for 20 years with pain sometimes a lot worse than others,so the injection was done through the N.H.S.has anyone else
olliemo
in
Pain Concern
7 years ago
Moskowitz Plasticity: Brain Maps
My 30 year old son is suffering from severe nerve pain following misdiagnosed compartment syndrome in his right arm. The pain is all but paralytic and his life has done a 180 degree turn. He is on high morphine dose, and has monthly lidocaine infusion which have become less effective over time. He has
My 30 year old son is suffering from severe nerve pain following misdiagnosed compartment syndrome in his right arm. The pain is all but paralytic and his life has done a 180 degree turn. He is on high morphine dose, and has monthly lidocaine infusion which have become less effective over time. He has
Zedman
in
Pain Concern
7 years ago
Allergic reaction
I read previous post about the alleric reactions to the electrode pads, gel or the nickel inside of them ...well I had a sleep study done and the first over night study when removing the pads I had red patches that itched for 5-6 days I used neosporin, nowI had the second study done,this time my skin
I read previous post about the alleric reactions to the electrode pads, gel or the nickel inside of them ...well I had a sleep study done and the first over night study when removing the pads I had red patches that itched for 5-6 days I used neosporin, nowI had the second study done,this time my skin
dcc1t4
in
AF Association
7 years ago
Filter needles for self injecting
Hi Folks, I'm after a bit more advice - now I've decided to SI I'm nervous about using. The correct procedure regarding needles. I've already been given some great advice here, but my issue is regarding the use of a filter needle when drawing hydro up from an ampoule. All the reading I have done suggests
Hi Folks, I'm after a bit more advice - now I've decided to SI I'm nervous about using. The correct procedure regarding needles. I've already been given some great advice here, but my issue is regarding the use of a filter needle when drawing hydro up from an ampoule. All the reading I have done suggests
Ree2705
in
Pernicious Anaemia Society
7 years ago
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