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Does biotin affect saliva test results?
I'm aware that biotin supplementation interferes with blood test results and wondering if the same is true for saliva tests?
Is it necessary to suspend biotin supplementation prior to saliva tests?
I'm planning to do the Adrenal Function Profile (saliva test of cortisol and DHEA) tomorrow so
I'm aware that biotin supplementation interferes with blood test results and wondering if the same is true for saliva tests?
Is it necessary to suspend biotin supplementation prior to saliva tests?
I'm planning to do the Adrenal Function Profile (saliva test of cortisol and DHEA) tomorrow so
Venus77
in
Thyroid UK
6 years ago
New Boston Scientific DBS machine, anyone tried it?
I've been doing research on the BOSTON SCIENTIFIC DBS machine. 400 people in the US have gotten it installed since Jan. 2018. 4000 in Europe. It sounds pretty interesting - less side effects. I'm a bit scared to get it done. Hoping someone out there has had experience with it. Love to hear about
I've been doing research on the BOSTON SCIENTIFIC DBS machine. 400 people in the US have gotten it installed since Jan. 2018. 4000 in Europe. It sounds pretty interesting - less side effects. I'm a bit scared to get it done. Hoping someone out there has had experience with it. Love to hear about
ktbate
in
Cure Parkinson's
6 years ago
1St rheumatology appt
HI everyone. Have my first rheumatology appt tomorrow. Have written all my symptoms down cause I will forget and I now have new symptoms. For the last 3 weeks I have pain in my wrists and stiff fingers and ankles are now hurting. Also feels like tingling like when you come in from the cold. Not pins
HI everyone. Have my first rheumatology appt tomorrow. Have written all my symptoms down cause I will forget and I now have new symptoms. For the last 3 weeks I have pain in my wrists and stiff fingers and ankles are now hurting. Also feels like tingling like when you come in from the cold. Not pins
Keiraleigh07
in
LUPUS UK
6 years ago
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New results after Levo increase
Thought I’d start a new post as my update on the original thread hasnt been responded to so think it’s got lost. Just had my 6 weeks after increase of 25mcg a day & results as follows; TSH - 0.03 (0.35-5) FT3 - 4.8 (3.5-6.5) FT4 - 20.5 (9-24) On top of the increase in Levothyroxine to 100mcg from 75mcg
Thought I’d start a new post as my update on the original thread hasnt been responded to so think it’s got lost. Just had my 6 weeks after increase of 25mcg a day & results as follows; TSH - 0.03 (0.35-5) FT3 - 4.8 (3.5-6.5) FT4 - 20.5 (9-24) On top of the increase in Levothyroxine to 100mcg from 75mcg
Kateefc
in
Thyroid UK
6 years ago
HELP! Hairloss despite normal thyroid/vitamin levels
Ever since I started taking levothyroxin in Feb 2017, post ROI treatment for hyperthyroidism, I have had hairloss issues although my hair was perfectly fine before. At first it seemed like just an intense bought of acute TE due to starting the medication and sudden hormone level changes. After loosing
Ever since I started taking levothyroxin in Feb 2017, post ROI treatment for hyperthyroidism, I have had hairloss issues although my hair was perfectly fine before. At first it seemed like just an intense bought of acute TE due to starting the medication and sudden hormone level changes. After loosing
Bobsy1
in
Thyroid UK
6 years ago
anyone had a nerve block procedure done?
my son had an accident 18 months ago boxing. His recovery has been slow , recent mri scans are good and now his neuro has told him he has "nerve damage" . He is on amitripyline and gabapetin . On monday he is having a "nerve block" procedure which will be injected into the base of his skull , has anyone
my son had an accident 18 months ago boxing. His recovery has been slow , recent mri scans are good and now his neuro has told him he has "nerve damage" . He is on amitripyline and gabapetin . On monday he is having a "nerve block" procedure which will be injected into the base of his skull , has anyone
joben45
in
Headway
6 years ago
Anyone out there who had DBS for 10 years or more
I'm hearing different views about the longevity of DBS. has this been covered before and can anyone out there who had DBS for more than 10 years comment / share his or her views?
I'm hearing different views about the longevity of DBS. has this been covered before and can anyone out there who had DBS for more than 10 years comment / share his or her views?
Xabojuro2
in
Cure Parkinson's
6 years ago
Mom of triplets, spouse with Parkinson’s
Hi, I literally just found this place. It’s a bit of a relief. I’m in a place in my mind that is confusing, because I can’t predict what’s going to happen next, I can’t figure out if it’s him or the disease. One day it’s one thing, then a couple days later it’ll be something else. He’s had this disease
Hi, I literally just found this place. It’s a bit of a relief. I’m in a place in my mind that is confusing, because I can’t predict what’s going to happen next, I can’t figure out if it’s him or the disease. One day it’s one thing, then a couple days later it’ll be something else. He’s had this disease
3Fishies
in
Cure Parkinson's
6 years ago
Biotin while on Ibrutinib and rituximab.
Hi just wondering if anyone on Ibrutinib and rituximab is using increased doses of biotin to help with brittle nails and dry skin? I have just seen my consultant today and was told it was ok but just wondered if anyone out there has any experience they can share? Thanks in advance Ann
Hi just wondering if anyone on Ibrutinib and rituximab is using increased doses of biotin to help with brittle nails and dry skin? I have just seen my consultant today and was told it was ok but just wondered if anyone out there has any experience they can share? Thanks in advance Ann
annmcgowan
in
CLL Support
6 years ago
Shingles
Oh wise ones - please give me some advice. I am due to spend my usual Wednesday with my almost 98 year old mother tomorrow but I’ve just phoned her to confirm arrangements only to be told she has developed shingles, poor thing. Now, I’ve just been reading up about it and it seems to me that you can’t
Oh wise ones - please give me some advice. I am due to spend my usual Wednesday with my almost 98 year old mother tomorrow but I’ve just phoned her to confirm arrangements only to be told she has developed shingles, poor thing. Now, I’ve just been reading up about it and it seems to me that you can’t
LizzieGuinn
in
PMRGCAuk
6 years ago
Vitamin B3 and PD
Helpful post today on this topic from Science of Parkinson's https://scienceofparkinsons.com/2018/05/27/niacin/ Supports previous comments on this (eg Sylvestrov). Just popped a Niacin (non flush) tablet :-)
Helpful post today on this topic from Science of Parkinson's https://scienceofparkinsons.com/2018/05/27/niacin/ Supports previous comments on this (eg Sylvestrov). Just popped a Niacin (non flush) tablet :-)
Kevin51
in
Cure Parkinson's
6 years ago
DBS or : No DBS : Please share your story by taking part in this survey https://surveyhero.com/c/9147d280
results will be published here https://tinyurl.com/yaqkvjlk I'm lined up for DBS and I'm going through a period they call 'working up' which will test my readiness and ability to live with electrodes in my head and a battery buried into my chest. my family, colleagues and friends are divided on what
results will be published here https://tinyurl.com/yaqkvjlk I'm lined up for DBS and I'm going through a period they call 'working up' which will test my readiness and ability to live with electrodes in my head and a battery buried into my chest. my family, colleagues and friends are divided on what
Xabojuro2
in
Cure Parkinson's
6 years ago
Wow, this Inversion Table is interesting! New member here!
Diagnose with PD in 2004. Had DBS surgery in 2016 and it was literally a Godsend! Totally eliminated the hand tremors which had become significant! Hit the gym EVERY morning 7 days a week with emphasis on cardio-vascular! Now my problem is "freezing of gate." However after getting my Teeter Inversion
Diagnose with PD in 2004. Had DBS surgery in 2016 and it was literally a Godsend! Totally eliminated the hand tremors which had become significant! Hit the gym EVERY morning 7 days a week with emphasis on cardio-vascular! Now my problem is "freezing of gate." However after getting my Teeter Inversion
boydbill
in
Cure Parkinson's
6 years ago
DBS SURGERY
i am now celebrating six months since my DBS surgery. This surgery for me has truly been a gift of life renewed. If you are thinking about exploring this option and would like to hear more about it or have specific fears or questions, I would love to help. I, too, was afraid of having the surgery,
i am now celebrating six months since my DBS surgery. This surgery for me has truly been a gift of life renewed. If you are thinking about exploring this option and would like to hear more about it or have specific fears or questions, I would love to help. I, too, was afraid of having the surgery,
annmariebaird
in
Cure Parkinson's
6 years ago
Why one should be wary of biotin.
Several people have mentioned taking biotin. Here’s a few reasons why one might want to think carefully about doing so... https://www.bustle.com/p/7-unexpected-dangerous-side-effects-of-taking-biotin-9205383
Several people have mentioned taking biotin. Here’s a few reasons why one might want to think carefully about doing so... https://www.bustle.com/p/7-unexpected-dangerous-side-effects-of-taking-biotin-9205383
fbirder
in
Pernicious Anaemia Society
6 years ago
Advice B vitamins
Hi everyone, I have just finished my 6 loading doses of B12 injections. I gather I should have taken Folic Acid once started with them but I didn't realise at the time. I have in the cupboard some Vitamin B tablets and I wonder of you could advise whether they are suitable to take. Each tablet contains
Hi everyone, I have just finished my 6 loading doses of B12 injections. I gather I should have taken Folic Acid once started with them but I didn't realise at the time. I have in the cupboard some Vitamin B tablets and I wonder of you could advise whether they are suitable to take. Each tablet contains
Tanzanite55
in
Pernicious Anaemia Society
6 years ago
My trip to Viterbo to see Dr. Antonio Constantini -Sharing info
I will use this post to share information about my recent Dr Antonio Constantini 's visit. I am a little bit busy at work and will not have the time to write it all up on in one session. so bear with me, please. in the meantime please ask questions and I will do my first answer. sections of this post
I will use this post to share information about my recent Dr Antonio Constantini 's visit. I am a little bit busy at work and will not have the time to write it all up on in one session. so bear with me, please. in the meantime please ask questions and I will do my first answer. sections of this post
Xabojuro2
in
Cure Parkinson's
6 years ago
Depression/Loneliness after brain surgery.
I am four years post operation from having a brain tumour removed when I was 17. I developed epilepsy and lost half my eyesight as side effects to the operation. Although very lucky to be here, I feel guilt that I have been given a second shot at life and I am not enjoying it. I have seeked help with
I am four years post operation from having a brain tumour removed when I was 17. I developed epilepsy and lost half my eyesight as side effects to the operation. Although very lucky to be here, I feel guilt that I have been given a second shot at life and I am not enjoying it. I have seeked help with
BethVictoria
in
Headway
6 years ago
Feeling worried ... brain tumour?
Head feels tight when I bend down and get up kind of like a head rush and ears feel muffled and also when I jump in bed and lay straight down on my stomach and look up I get the same thing but it only lasts for like 10 seconds. I’m worried I have POTS disease or a brain tumour
Head feels tight when I bend down and get up kind of like a head rush and ears feel muffled and also when I jump in bed and lay straight down on my stomach and look up I get the same thing but it only lasts for like 10 seconds. I’m worried I have POTS disease or a brain tumour
butterflyz01
in
Anxiety Support
6 years ago
If it's not Chickenpox or Shingles...
I was diagnosed with phoritic RA ( as well as all the other arthritis ) put on a high dose of mexitrate by injection . Anyhow, broke out in a horrible rash on my hands and arms. Went to the chemist, they said heat rash and flogged me antihistamines. Rash continued to be really painful and incredibly
I was diagnosed with phoritic RA ( as well as all the other arthritis ) put on a high dose of mexitrate by injection . Anyhow, broke out in a horrible rash on my hands and arms. Went to the chemist, they said heat rash and flogged me antihistamines. Rash continued to be really painful and incredibly
Mcdebz
in
NRAS
6 years ago
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