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Finger prick testing from Horizon advice please ☺️
Hi I have received my blood kit from horizon but we tried to draw blood and my blood barely comes out - either it's too thick or whatever. My daughter pricked hers and it poured out mine didn't even bleed at all 😕 If I go to my local hospital blood clinic with the form and ( I do have a nhs one for
Hi I have received my blood kit from horizon but we tried to draw blood and my blood barely comes out - either it's too thick or whatever. My daughter pricked hers and it poured out mine didn't even bleed at all 😕 If I go to my local hospital blood clinic with the form and ( I do have a nhs one for
Peaches71
in
Thyroid UK
7 years ago
Creatine with CoQ10
Has anyone tried these together? I've read that together, they could be neuroprotective. However, mixing coffee with creatine is really bad and could enhance progression. I'm confused. I though coffee was beneficial for PD.?
Has anyone tried these together? I've read that together, they could be neuroprotective. However, mixing coffee with creatine is really bad and could enhance progression. I'm confused. I though coffee was beneficial for PD.?
Jamielee1
in
Cure Parkinson's
7 years ago
Creatine and leg pain
Hi all. I've been on levo since April. 75mg then 100mg for the last few weeks. I have leg and hip pain with muscle weakness. Doc says I should have creatine checked. It's been getting slowly worse since diagnosed with autoimmune hypo in April. Can anyone shed a light on my leg issues? Thanks so much
Hi all. I've been on levo since April. 75mg then 100mg for the last few weeks. I have leg and hip pain with muscle weakness. Doc says I should have creatine checked. It's been getting slowly worse since diagnosed with autoimmune hypo in April. Can anyone shed a light on my leg issues? Thanks so much
Hidden
in
Thyroid UK
7 years ago
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Pins & needles in hands & feet, PBC or peripheral neuropathy?
Hi all I'd thought for a week that the very unpleasant new 'prickling' sensation that I'd developed was PBC itch, but now believe after visit to GP that it's probably peripheral neuropathy. Been diagnosed with PBC 14 yrs and only ever had mild-moderate skin irritation. Weird thing is, this pins & needles
Hi all I'd thought for a week that the very unpleasant new 'prickling' sensation that I'd developed was PBC itch, but now believe after visit to GP that it's probably peripheral neuropathy. Been diagnosed with PBC 14 yrs and only ever had mild-moderate skin irritation. Weird thing is, this pins & needles
Skypony
in
PBC Foundation
7 years ago
Cramp
Does anyone know how to ease severe cramp? I have really painful attacks (calf muscles) in the night in bed. Waken in agony and pain felt for sometime in the day.
Does anyone know how to ease severe cramp? I have really painful attacks (calf muscles) in the night in bed. Waken in agony and pain felt for sometime in the day.
foxglove
in
Pain Concern
7 years ago
Peripheal neuropathy
Greg, after months of searching I finally came across a web-site with other people that have non- diabetic neuropathy and for a while I thought I was the only one with neuropathy not being a diabetic. I know there are so many types of neuropathy mine is poly neuropathy in my lower exetremities ( leg's
Greg, after months of searching I finally came across a web-site with other people that have non- diabetic neuropathy and for a while I thought I was the only one with neuropathy not being a diabetic. I know there are so many types of neuropathy mine is poly neuropathy in my lower exetremities ( leg's
Kclrgtj
in
Foggy's "Invisible Illness" Support
7 years ago
Premotor Symptoms of Parkinson’s Disease - EHP 2013
Developing methods for researching Premotor symptoms in PD seems so very important. Here's an excerpt from a well-focused review. Research on the Premotor Symptoms of Parkinson’s Disease: Clinical and Etiological Implications Environ Health Perspect 2013 Nov-Dec; 121(11
Developing methods for researching Premotor symptoms in PD seems so very important. Here's an excerpt from a well-focused review. Research on the Premotor Symptoms of Parkinson’s Disease: Clinical and Etiological Implications Environ Health Perspect 2013 Nov-Dec; 121(11
aspergerian
in
Cure Parkinson's
7 years ago
Donepezil - has anyone tried this med for brain fog and to help with walking? does it affect your sleep?
I was given this med by my dr. to help with my brain fog and my gait in walking. He started me on a very low dose 5mg, and i have only been on it a few days. However, i seem to be sleeping in a deeper(stranger) sleep, but my mind feels awake. i know it sound crazy, but sometimes I will think to myself
I was given this med by my dr. to help with my brain fog and my gait in walking. He started me on a very low dose 5mg, and i have only been on it a few days. However, i seem to be sleeping in a deeper(stranger) sleep, but my mind feels awake. i know it sound crazy, but sometimes I will think to myself
moparkie715
in
Cure Parkinson's
7 years ago
9 days & nights with no RLS or withdrawal symptoms--ahh!
After suffering through over a month of DAWS or Dopamine Agonist Withdrawal Syndrome when I went cold turkey off Ropinerole, I transitioned into Lyrica. It has been 9, no now 10 wonderful days -- I feel like a normal person again. No RLS symptoms at all!!! I'm taking 100 mgs 3x/day. Going cold turkey
After suffering through over a month of DAWS or Dopamine Agonist Withdrawal Syndrome when I went cold turkey off Ropinerole, I transitioned into Lyrica. It has been 9, no now 10 wonderful days -- I feel like a normal person again. No RLS symptoms at all!!! I'm taking 100 mgs 3x/day. Going cold turkey
Bganim1947
in
Restless Legs Syndrome
7 years ago
Anyone tried using Creatine ?
I am not medically trained . So do not undertake any of my suggestions without consulting your doctor or PD nurse. As running and general fitness is the main reason for my always " looking for help and assistance" I came across Creatine. It's useful in maintaining muscle strength in sports and also
I am not medically trained . So do not undertake any of my suggestions without consulting your doctor or PD nurse. As running and general fitness is the main reason for my always " looking for help and assistance" I came across Creatine. It's useful in maintaining muscle strength in sports and also
Mike1942
in
Cure Parkinson's
7 years ago
Help - Advice G-CSF Injections Filgrastim
Hi All, Had 8 R-CVP Chemo in January competed in July, fortunately had very little side effects, main problem being very low neutropenia, had G CSF injections which worked quickly, only side effect is bad pain in spine (throbbing). PET scan in July found another problem and i have now 6 R CHOP Chemo
Hi All, Had 8 R-CVP Chemo in January competed in July, fortunately had very little side effects, main problem being very low neutropenia, had G CSF injections which worked quickly, only side effect is bad pain in spine (throbbing). PET scan in July found another problem and i have now 6 R CHOP Chemo
Blueb
in
Non Hodgkin's Lymphoma Friends
7 years ago
Medication overload?
My husband has PD for 20 years. He is on Madapor 250mg x 5 daily plus Comtess 200mg x 5 daily. His mobility is poor, uses rolator most of the time, but occasionally gets up and walks without it. Has had a few falls. Not much stamina, sleeps a lot. Voice low, some memory loss but OK mentally 95% of
My husband has PD for 20 years. He is on Madapor 250mg x 5 daily plus Comtess 200mg x 5 daily. His mobility is poor, uses rolator most of the time, but occasionally gets up and walks without it. Has had a few falls. Not much stamina, sleeps a lot. Voice low, some memory loss but OK mentally 95% of
Winann
in
Cure Parkinson's
7 years ago
Hello from Australia
Hello Robyn from Australia. Good to read about many different issues regarding PD. I was diagnosed 2014 and imediately got two more opinions from two of the top neurologists in the country who gave me the same diagnosis. I am now about to turn 57 in October. I was on azelect , sifrol er, and madapar
Hello Robyn from Australia. Good to read about many different issues regarding PD. I was diagnosed 2014 and imediately got two more opinions from two of the top neurologists in the country who gave me the same diagnosis. I am now about to turn 57 in October. I was on azelect , sifrol er, and madapar
moonel60
in
Cure Parkinson's
7 years ago
Severe idiopathic neuropathy pain
The best help with my severe nerve pain I have found is Liv/Relief cream...a Canadian product, I have used it for a couple of years and it does take a lot of the burning and pain away...all natural and Gabapentin 1500 mg a day (a lot) Jackie Orr
The best help with my severe nerve pain I have found is Liv/Relief cream...a Canadian product, I have used it for a couple of years and it does take a lot of the burning and pain away...all natural and Gabapentin 1500 mg a day (a lot) Jackie Orr
jackieorr
in
Neuropathy Support
7 years ago
My poor before and after hair...
Hi girls, Been feeling really poorly this week with the neuropathy and also had lots to do so haven't seen a lot of your posts so much to catch up with. Monday night, after a party, and a few glasses of lemonade, my dear friend, Joy, gave me a trim as it started to fall out that morning. I photographed
Hi girls, Been feeling really poorly this week with the neuropathy and also had lots to do so haven't seen a lot of your posts so much to catch up with. Monday night, after a party, and a few glasses of lemonade, my dear friend, Joy, gave me a trim as it started to fall out that morning. I photographed
Kryssy
in
My Ovacome
7 years ago
Fibromyaligia keep on moving check out all your options.
I hope you are feeling well today. You were asking about exercise. Try exercising in water even the bath or pool will be better. Start simple the water will help movement and if it is warm feels so good. There are a lot of rehabs around that maybe covered by you insurance or the YMCA. Start slow and
I hope you are feeling well today. You were asking about exercise. Try exercising in water even the bath or pool will be better. Start simple the water will help movement and if it is warm feels so good. There are a lot of rehabs around that maybe covered by you insurance or the YMCA. Start slow and
Whonbarger1
in
Fibromyalgia Action UK
7 years ago
What is my arm pain (at mainly at night)?
My first post: I have a dull pain in my upper arms, mainly at night though more recently in the daytime too (though less). By morning the pain has extended down to my hands which feel weak and I find it difficult to hold my toothbrush. After a shower, the pain seems less but now doesn't completely go
My first post: I have a dull pain in my upper arms, mainly at night though more recently in the daytime too (though less). By morning the pain has extended down to my hands which feel weak and I find it difficult to hold my toothbrush. After a shower, the pain seems less but now doesn't completely go
Herrylaw
in
Fibromyalgia Action UK
7 years ago
DRUG INTERACTIONS?
Hi. Steff here. I'm a 68 year old female who has been fairly healthy all my life apart from problems with depression. I now have a range of awful symptoms which have come on suddenly around March of this year. My rheumatologist says I have 'lupus like symptoms' and suspects this could have been caused
Hi. Steff here. I'm a 68 year old female who has been fairly healthy all my life apart from problems with depression. I now have a range of awful symptoms which have come on suddenly around March of this year. My rheumatologist says I have 'lupus like symptoms' and suspects this could have been caused
Orchard1
in
LUPUS UK
7 years ago
7534
Hi....my outer of palms....are red.... and swollen....and are really painful 😖.....not in the middle.....my fingers do not hurt or tingle.....I have 3 nodes of arthritis in lower fingers......I also have Planta Fasciitis too !!!!!! to my feet !!!! That to is so painful. !!! Are the two related?.....
Hi....my outer of palms....are red.... and swollen....and are really painful 😖.....not in the middle.....my fingers do not hurt or tingle.....I have 3 nodes of arthritis in lower fingers......I also have Planta Fasciitis too !!!!!! to my feet !!!! That to is so painful. !!! Are the two related?.....
7534
in
Pain Concern
7 years ago
Ablation update 3 days later
Hi guys Well it's been 3 days since my ablation and I've only just found out that my procedure was only partially done, The right hand side was cut easily but the left hand side wouldn't take so they had to burn around the veins in a pearl necklace way,or spot welded which makes more sense to me,with
Hi guys Well it's been 3 days since my ablation and I've only just found out that my procedure was only partially done, The right hand side was cut easily but the left hand side wouldn't take so they had to burn around the veins in a pearl necklace way,or spot welded which makes more sense to me,with
Spearof66
in
AF Association
7 years ago
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