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Will an MRI help?
I have constant worry that I have a brain tumor and many symptoms that revolve around this. Have any others with health anxiety received MRI's did it help? Did it make it worse? Thanks
I have constant worry that I have a brain tumor and many symptoms that revolve around this. Have any others with health anxiety received MRI's did it help? Did it make it worse? Thanks
TP114
in
Anxiety Support
5 years ago
Invasive and non‐invasive brain stimulation in Parkinson's disease: Clinical effects and future perspectives
Deep brain stimulation (DBS) can improve motor symptoms in moderate to advanced PD. However, the optimal stimulation paradigm for non‐motor symptoms, freezing of gait and the optimal timing of DBS are still under investigations. The findings of pathological oscillations and abnormal frequency to amplitude
Deep brain stimulation (DBS) can improve motor symptoms in moderate to advanced PD. However, the optimal stimulation paradigm for non‐motor symptoms, freezing of gait and the optimal timing of DBS are still under investigations. The findings of pathological oscillations and abnormal frequency to amplitude
Farooqji
in
Cure Parkinson's
5 years ago
About DBS
Does anyone undergone for DBS, 1. After DBS also should take medicine 2. Any side effects 3. How long it will take to recover post surgery 4. What is the IPG machine using, which machine is good
Does anyone undergone for DBS, 1. After DBS also should take medicine 2. Any side effects 3. How long it will take to recover post surgery 4. What is the IPG machine using, which machine is good
Vishwa228
in
Cure Parkinson's
5 years ago
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Energenesis
Here is a new supplement which has most of everything that isn’t a vitamin or mineral in it. Expensive but maybe convenient if you want to try all these things at once? https://www.theenergyblueprint.com/energenesis “Energenesis is like a 5-star MEAL for your Mitochondria (LOADED with rare nutrients
Here is a new supplement which has most of everything that isn’t a vitamin or mineral in it. Expensive but maybe convenient if you want to try all these things at once? https://www.theenergyblueprint.com/energenesis “Energenesis is like a 5-star MEAL for your Mitochondria (LOADED with rare nutrients
LAJ12345
in
Cure Parkinson's
5 years ago
thyroid podcast
I found this podcast mildly interesting because this Johns Hopkins MD claims that supplemental Biotin alters thyroid test results. This guy is in favor of T3 and trials of thyroid hormone in general, but he does seem to have a problem admitting that the increase in thyroid disorders might be related
I found this podcast mildly interesting because this Johns Hopkins MD claims that supplemental Biotin alters thyroid test results. This guy is in favor of T3 and trials of thyroid hormone in general, but he does seem to have a problem admitting that the increase in thyroid disorders might be related
Eddie83
in
Thyroid UK
5 years ago
Plasma Viscosity above high ref and Hypothyroidism
Hi all experts, I'm hoping you can give me some answers. I had my Thyroid blood test on 25 April, stopping my B complex with biotin seven days before and fasting to the recommendations on HU, taking my Levo after. When I was having my test, the nurse took two phials of blood and I asked her why (thinking
Hi all experts, I'm hoping you can give me some answers. I had my Thyroid blood test on 25 April, stopping my B complex with biotin seven days before and fasting to the recommendations on HU, taking my Levo after. When I was having my test, the nurse took two phials of blood and I asked her why (thinking
Gingernut44
in
Thyroid UK
5 years ago
DBS for essential tremors?
I'm new to this site and am considering DBS. Has anyone had DBS (deep brain surgery) for essential tremors of hands, head (cervical dystonia) and voice? What result? My neurologists say it will help with my shaky head. I know DBS helps shaky hands, it's my shaky head that is annoying!
I'm new to this site and am considering DBS. Has anyone had DBS (deep brain surgery) for essential tremors of hands, head (cervical dystonia) and voice? What result? My neurologists say it will help with my shaky head. I know DBS helps shaky hands, it's my shaky head that is annoying!
piano_gal
in
National Tremor Foundation
5 years ago
Stopping vitamin supplements before a thyroid test
I am due for an annual thyroid test as my medication needs reviewing. I take vitamin D, omega 3 (fish oil), magnesium glycinate and vitamin B complex supplements. I know that I should stop taking the vitamin B tablets as they contain biotin but what about the other supplements? Should I stop taking them
I am due for an annual thyroid test as my medication needs reviewing. I take vitamin D, omega 3 (fish oil), magnesium glycinate and vitamin B complex supplements. I know that I should stop taking the vitamin B tablets as they contain biotin but what about the other supplements? Should I stop taking them
Happywalker
in
Thyroid UK
5 years ago
Acute exacerbation of Hashimoto's thyroiditis in a patient treated with dimethyl fumarate for multiple sclerosis: A case report
Another one to add to the list of medicines which potentially cause problems in those with thyroid issues. (We already have biotin on the list due to its interference will many blood tests - ironically, high dose biotin is also use in multiple sclerosis.) [i]Medicine (Baltimore). 2019 Apr;98(17):e15185
Another one to add to the list of medicines which potentially cause problems in those with thyroid issues. (We already have biotin on the list due to its interference will many blood tests - ironically, high dose biotin is also use in multiple sclerosis.) [i]Medicine (Baltimore). 2019 Apr;98(17):e15185
helvella
Thyroid UK
in
Thyroid UK
5 years ago
Losing hope
Dx 2003 aged 46. until about 6 months ago i refused to be beaten. Now I am utterly beaten. For years I’ve taken madopar every 90 mins . I have always had sudden swings between off and on but was able to make them bearable – with the odd blip - with extra madopar. I worked out years ago that protein interferes
Dx 2003 aged 46. until about 6 months ago i refused to be beaten. Now I am utterly beaten. For years I’ve taken madopar every 90 mins . I have always had sudden swings between off and on but was able to make them bearable – with the odd blip - with extra madopar. I worked out years ago that protein interferes
pen1
in
Cure Parkinson's
5 years ago
Playing with the settings of my brain
Hi all This is a link to my vlog about DBS and speech issues. https://www.youtube.com/watch?v=Sn4IP7-px0w Cheers, Ian
Hi all This is a link to my vlog about DBS and speech issues. https://www.youtube.com/watch?v=Sn4IP7-px0w Cheers, Ian
Ianfrizell
in
Cure Parkinson's
5 years ago
Anxious I have a brain tumour
I'm 19, and I'm so anxious I have a brain tumour. About five months ago, I saw bright lights all over my room for a couple of seconds and it was gone. A few days later, I developed an odd feeling in my head - like a tingling, slight pressure in my head, all over my scalp and ears. It's so bad it feels
I'm 19, and I'm so anxious I have a brain tumour. About five months ago, I saw bright lights all over my room for a couple of seconds and it was gone. A few days later, I developed an odd feeling in my head - like a tingling, slight pressure in my head, all over my scalp and ears. It's so bad it feels
Hidden
in
Anxiety Support
5 years ago
Raynaud’s help please new to site they kept telling me I had gout , nope now doctor says Raynaud’s
So for years they said I had gout with normal Uric acid results now they finally say Raynaud’s I feel like I have been walking on blisters on the bottom of my toes red spots I t’s very painful any suggestions on a cream none rx that would help with that ? I’m taking fish oil and just started taking
So for years they said I had gout with normal Uric acid results now they finally say Raynaud’s I feel like I have been walking on blisters on the bottom of my toes red spots I t’s very painful any suggestions on a cream none rx that would help with that ? I’m taking fish oil and just started taking
Brendab7869
in
Scleroderma & Raynaud's UK (SRUK)
5 years ago
DBS, has anyone considered this procedure to help with tremors?
I am scheduled to have this procedure next month. I have heard some good things from some PD patients and would like to hear other PD patient’s prospective. My diagnosis was in early 2018. Right hand tremor, now taking 25/100 x 3 (3 times/day), my procedure will be on my left side. Meds work, but tire
I am scheduled to have this procedure next month. I have heard some good things from some PD patients and would like to hear other PD patient’s prospective. My diagnosis was in early 2018. Right hand tremor, now taking 25/100 x 3 (3 times/day), my procedure will be on my left side. Meds work, but tire
PHN001
in
Cure Parkinson's
5 years ago
Hair loss
How many girls have had there hair falling out, I called my neurologist and spoke to her nurse and she stated it’s from the steroids they give before the Ocrevus I’m having a little hard time believeing this. How about you guys what do you think??? And I like to know will my hair come back I’m not into
How many girls have had there hair falling out, I called my neurologist and spoke to her nurse and she stated it’s from the steroids they give before the Ocrevus I’m having a little hard time believeing this. How about you guys what do you think??? And I like to know will my hair come back I’m not into
Horse714
in
My MSAA Community
5 years ago
Limited vasculitus I
Hi there all. Im throwing a party tomorrow and my neice has informed me she has shingles on the end stages of the illness. She is worried about passing the disease onto me if she comes she has been informed not to mix with people with low immune systems.. Has anyone had experience of shingles and
Hi there all. Im throwing a party tomorrow and my neice has informed me she has shingles on the end stages of the illness. She is worried about passing the disease onto me if she comes she has been informed not to mix with people with low immune systems.. Has anyone had experience of shingles and
foweraker
in
Vasculitis UK
5 years ago
Long term after effects of viral meningitis
I was diagnosed with VM in April 2011. So 8 years later and I still suffer from daily headaches. Some days are easier than others but I go through "spells" where the headaches get really bad for weeks at a time. I also still suffer from extreme fatigue and now have anxiety. I was on Amitriptyline for
I was diagnosed with VM in April 2011. So 8 years later and I still suffer from daily headaches. Some days are easier than others but I go through "spells" where the headaches get really bad for weeks at a time. I also still suffer from extreme fatigue and now have anxiety. I was on Amitriptyline for
Moranmom85
in
Meningitis Now
5 years ago
B1 Intolerance
My husband has tried taking B1 twice. Firstly with powder then recently with Solgar capsules as recommended. He started on 500mg capsule in the morning then 500mg late afternoon. After 7 days he felt it was making his symptoms worse and had to stop.I read how so many people are benefitting from B1 and
My husband has tried taking B1 twice. Firstly with powder then recently with Solgar capsules as recommended. He started on 500mg capsule in the morning then 500mg late afternoon. After 7 days he felt it was making his symptoms worse and had to stop.I read how so many people are benefitting from B1 and
JeanieBeanie
in
Cure Parkinson's
5 years ago
Test results interpretation and advice please
Hi again all, I finally have some new test results back, as follows. I welcome any comments/guidance etc. please :-) For those of you that already "know" me, I posted a very long associated history a couple of weeks ago over at https://healthunlocked.com/thyroiduk/posts/140448758/my-test-results-and-symptoms-interpretation-request-please
Hi again all, I finally have some new test results back, as follows. I welcome any comments/guidance etc. please :-) For those of you that already "know" me, I posted a very long associated history a couple of weeks ago over at https://healthunlocked.com/thyroiduk/posts/140448758/my-test-results-and-symptoms-interpretation-request-please
tomranson85
in
Thyroid UK
5 years ago
Should be better?
It's been nearly 12 months since my brain haemorrhage it's been a very hard road without my partner's support I don't know where I would be now we've had to fight for support professional help I'm only just now getting any professional help my mental health and anxiety levels are at a very very low
It's been nearly 12 months since my brain haemorrhage it's been a very hard road without my partner's support I don't know where I would be now we've had to fight for support professional help I'm only just now getting any professional help my mental health and anxiety levels are at a very very low
Gym1bunny
in
Headway
5 years ago
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