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neuropathy, pins, and needles in the face!! Has anyone else had this?
I have been experiencing this randomly and faintly over the past 7 months. Now I have been receiving b12 shots for 8 weeks, along with hot aching pins and needles in my feet and hands I woke this morning to way more intense pins and needles on my face. Both sides of my face and across my jaw. From what
I have been experiencing this randomly and faintly over the past 7 months. Now I have been receiving b12 shots for 8 weeks, along with hot aching pins and needles in my feet and hands I woke this morning to way more intense pins and needles on my face. Both sides of my face and across my jaw. From what
brenanddave
in
Pernicious Anaemia Society
11 months ago
sacral implant site pain for pelvic floor dysfuntion
I am on second site sacral medtronic implant after one year I have severe stabbing pain in back and front of thigh,have had si injection but made it worse,did pt, made it worse are there any thoughts out there that may help
I am on second site sacral medtronic implant after one year I have severe stabbing pain in back and front of thigh,have had si injection but made it worse,did pt, made it worse are there any thoughts out there that may help
razzle51
in
Pelvic Pain Support Network
1 year ago
HDR BT Salvage Therapy
Hello All I just completed the second BT procedure at MSK. Pain level was maybe 3 but mostly gone the next morning with some soreness. My next step I’m told is bloodwork in 3 months which I’m not concerned about. I am concerned about the 6 month MRI which could show if any cancer still remains. When
Hello All I just completed the second BT procedure at MSK. Pain level was maybe 3 but mostly gone the next morning with some soreness. My next step I’m told is bloodwork in 3 months which I’m not concerned about. I am concerned about the 6 month MRI which could show if any cancer still remains. When
Trying-Times
in
Advanced Prostate Cancer
1 year ago
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Pelvic Muscle Spasms
Ive been just diagnosed and my VJ is constantly throbbing. Using suppositories and AZO products but I dont know how to relax these muscles. Anyone else? HELP it HURTS
Ive been just diagnosed and my VJ is constantly throbbing. Using suppositories and AZO products but I dont know how to relax these muscles. Anyone else? HELP it HURTS
QueenVic1952
in
Pelvic Pain Support Network
1 year ago
Head pins and needles
Hi all, I hope you're all hanging on in there. I am newly diagnose and wanted to ask if anyone has pins and needles, especially in the head. I am having these weird sensations all over my body, difficulty walking with balance issues, plus vision problems too. Any advice greatly appreciated. Thank
Hi all, I hope you're all hanging on in there. I am newly diagnose and wanted to ask if anyone has pins and needles, especially in the head. I am having these weird sensations all over my body, difficulty walking with balance issues, plus vision problems too. Any advice greatly appreciated. Thank
bubbatetley
in
LUPUS UK
1 year ago
I’m thinking about Benfotiamine.
Hello all of you HU people ~ I am the wife of a PwP, dx 12/29/2020. Our history ( very briefly) ~ left sides tremors and anxiety, mostly. We tried B1 HCL ~ didn’t work. Tried Thiamine mononitrate and that seemed to work for a while Recently I took hubby off all B1. None of them seemed to work
Hello all of you HU people ~ I am the wife of a PwP, dx 12/29/2020. Our history ( very briefly) ~ left sides tremors and anxiety, mostly. We tried B1 HCL ~ didn’t work. Tried Thiamine mononitrate and that seemed to work for a while Recently I took hubby off all B1. None of them seemed to work
Lizzy9
in
Cure Parkinson's
1 year ago
Homeopathic treatment
I've lived with ataxia for around ten years and its grown progressively worse. Contemporary straightforward here's your prescription' medicine seems to have no place in its treatment. What about homeopathic medicine? Has anyone out there found a homeopathic treatment which has any effect on this debilitating
I've lived with ataxia for around ten years and its grown progressively worse. Contemporary straightforward here's your prescription' medicine seems to have no place in its treatment. What about homeopathic medicine? Has anyone out there found a homeopathic treatment which has any effect on this debilitating
Piero
in
Ataxia UK
1 year ago
Pycnogenol® supplementation alleviates symptoms of Parkinson's disease with mild cognitive impairment
Recent article 2022. Not sure if it was posted. I was going to take it to lower my BP which has started to creep up. I worried because I had read [i]Their pharmacodynamic action primarily consists of antioxidant properties and possible anti-inflammatory effects. Pycnogenol may also influence the release
Recent article 2022. Not sure if it was posted. I was going to take it to lower my BP which has started to creep up. I worried because I had read [i]Their pharmacodynamic action primarily consists of antioxidant properties and possible anti-inflammatory effects. Pycnogenol may also influence the release
Sydney75
in
Cure Parkinson's
1 year ago
Auto injector advice please
I SI B12, but my daughter is needle phobic so I have to do her injections regularly for her. She would like to try an auto injector... Where do I begin? Any advice welcome as to where to purchase and tips on how to use (especially if you are needle phobic). How did you find it? Did it help? is it painless
I SI B12, but my daughter is needle phobic so I have to do her injections regularly for her. She would like to try an auto injector... Where do I begin? Any advice welcome as to where to purchase and tips on how to use (especially if you are needle phobic). How did you find it? Did it help? is it painless
Hidden
in
Pernicious Anaemia Society
1 year ago
Caffeine and progression of Parkinson’s disease: A deleterious interaction with Creatine
So I was thinking of adding Creatine to my stack based on a VERY positive video I watched from a "doctor" who it turns out graduated from an unimpressive medical school within the last 10 years and has already surrendered his license. So then I thought I should research his claims about Creatine and
So I was thinking of adding Creatine to my stack based on a VERY positive video I watched from a "doctor" who it turns out graduated from an unimpressive medical school within the last 10 years and has already surrendered his license. So then I thought I should research his claims about Creatine and
Bolt_Upright
in
Cure Parkinson's
1 year ago
Hypothyroidism and Quercetin
Hello i've recently posted about my subclinical hypothyroidism results and i'm having some confirmatory tests next week. I've been looking at my supplement regime and i've been taking Quercetin with Bromelain regularly for about the last 15 years only 500mg a day. There have been a few papers recently
Hello i've recently posted about my subclinical hypothyroidism results and i'm having some confirmatory tests next week. I've been looking at my supplement regime and i've been taking Quercetin with Bromelain regularly for about the last 15 years only 500mg a day. There have been a few papers recently
ockerdoc
in
Thyroid UK
1 year ago
Reducing Nifedipine dose for the warmer months?
I am on 20mg x 2 daily Nifedipine for secondary Raynauds, I started in the Autumn last year. I know I need to consult my Rheumatologist about this but wondered if others do the same ? Now the weather is warming up, I'm finding it's very easy to go into overheat mode, in that my hands start to swell
I am on 20mg x 2 daily Nifedipine for secondary Raynauds, I started in the Autumn last year. I know I need to consult my Rheumatologist about this but wondered if others do the same ? Now the weather is warming up, I'm finding it's very easy to go into overheat mode, in that my hands start to swell
andy7551
in
Scleroderma & Raynaud's UK (SRUK)
1 year ago
Rough in heat
My Fibromyalgia and neuropathy has been crazy lately. That happens for me when it gets hot. The burning sensation is annoying. My meds do help. But, what things do you do to help with the pain from the flareups?
My Fibromyalgia and neuropathy has been crazy lately. That happens for me when it gets hot. The burning sensation is annoying. My meds do help. But, what things do you do to help with the pain from the flareups?
Cecethat
in
Neuropathy Support
1 year ago
Gabapentin
I am currently taking 5 300mg Gabapentin a day. I'm also taking 0.5 mg of pramipexole 5 times a day and hydrocodone 3 times a day which helps. Gabapentin alone didn't help me but I hope it does you.
I am currently taking 5 300mg Gabapentin a day. I'm also taking 0.5 mg of pramipexole 5 times a day and hydrocodone 3 times a day which helps. Gabapentin alone didn't help me but I hope it does you.
Blu34
in
Restless Legs Syndrome
1 year ago
What is the first symptom you notice when your B12 is low......?
Hi, I don't mean the first symptom you noticed. What I am asking is, for those who SI regularly, what is the first symptom you notice when you have maybe pushed yourself to do too much, or are unwell with an infection, or drink too much alcohol, or are stressed, etc? Mine is a return of neuropathy, which
Hi, I don't mean the first symptom you noticed. What I am asking is, for those who SI regularly, what is the first symptom you notice when you have maybe pushed yourself to do too much, or are unwell with an infection, or drink too much alcohol, or are stressed, etc? Mine is a return of neuropathy, which
BeachArt
in
Pernicious Anaemia Society
1 year ago
Restless leg cure
Well I hope it is for some of you. I've been down all the various medication routes and magnesium cream and jels and nothing still the same getting worse by the week. Until someone suggested what worked for them and it's worked for me, I'll also add I've suffered with constipation for decades and nothing
Well I hope it is for some of you. I've been down all the various medication routes and magnesium cream and jels and nothing still the same getting worse by the week. Until someone suggested what worked for them and it's worked for me, I'll also add I've suffered with constipation for decades and nothing
Cottylotty
in
Restless Legs Syndrome
1 year ago
Drug interaction
I have neuropathy of the motor nerves,I am in my 23 rd year of this illness and for the last 6 months have been on BuTec 10 mg for severe burning pain in legs and feet and overall body pain,I have also been on Citalopram 20mg for 10 years my concern is that the interaction between the two drugs is
I have neuropathy of the motor nerves,I am in my 23 rd year of this illness and for the last 6 months have been on BuTec 10 mg for severe burning pain in legs and feet and overall body pain,I have also been on Citalopram 20mg for 10 years my concern is that the interaction between the two drugs is
Shihtz6
in
Neuropathy Support
1 year ago
Allodynia
many contributors say that because of the different symptoms it is difficult to diagnose the exact Problem.this is because medical science isn’t yet quite up with the many problems of the body. Our Doctor advises that my wife no longer has Fibromyalgia. I’m not sure about that.one of the associated
many contributors say that because of the different symptoms it is difficult to diagnose the exact Problem.this is because medical science isn’t yet quite up with the many problems of the body. Our Doctor advises that my wife no longer has Fibromyalgia. I’m not sure about that.one of the associated
Vivtom
in
Fibromyalgia Action UK
1 year ago
walking problems on Olaparib
Does anyone have any suggestions to help walking problems on Olaparib, please? My legs are stiff and are sort As if I have slight cerebral palsy in that I can’t fine control where they are going to land when I walk andthat disturbs my balance, so now I walk with a stick. Am Ithe only one? Onc, says it
Does anyone have any suggestions to help walking problems on Olaparib, please? My legs are stiff and are sort As if I have slight cerebral palsy in that I can’t fine control where they are going to land when I walk andthat disturbs my balance, so now I walk with a stick. Am Ithe only one? Onc, says it
Trickysite
in
My Ovacome
1 year ago
PD and B1
I have had PD Symptoms for 7 years but only diagnosed three years ago. I am taking carbidopa/levodopa for three years now. I have read ”Parkinson’s and the B1 therapy“ on Amazon and am evaluating my next steps. At my last visit to the Neurologist, she mentioned something that could put the cabidopa
I have had PD Symptoms for 7 years but only diagnosed three years ago. I am taking carbidopa/levodopa for three years now. I have read ”Parkinson’s and the B1 therapy“ on Amazon and am evaluating my next steps. At my last visit to the Neurologist, she mentioned something that could put the cabidopa
Hidden
in
Cure Parkinson's
1 year ago
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