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Coagulation factor IX
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Intrinsic factor
Hi should have asked this question before but does pa mean u have no intrinsic factor or you have but it doesn't work?
Hi should have asked this question before but does pa mean u have no intrinsic factor or you have but it doesn't work?
mummytina
in
Pernicious Anaemia Society
12 years ago
NutrEval Plus and FACT Test results!
Hi people, i have had a NutrEval Plus Fact test done, and my results have returned. It did cost an awful lot of money, but it could possibly be the best money ever spent. This shows everything at root level, Minerals, amino acids,vitamins, antioxidants, essential fatty acids, neurotransmitters, malabsorption
Hi people, i have had a NutrEval Plus Fact test done, and my results have returned. It did cost an awful lot of money, but it could possibly be the best money ever spent. This shows everything at root level, Minerals, amino acids,vitamins, antioxidants, essential fatty acids, neurotransmitters, malabsorption
paulb44
in
Gluten Free Guerrillas
12 years ago
NutrEval Plus and FACT Test results! Could it be Anemia?
Hi people, i have had a NutrEval Plus Fact test done, and my results have returned. It did cost an awful lot of money, but it could possibly be the best money ever spent. This shows everything at root level, Minerals, amino acids,vitamins, antioxidants, essential fatty acids, neurotransmitters, malabsorption
Hi people, i have had a NutrEval Plus Fact test done, and my results have returned. It did cost an awful lot of money, but it could possibly be the best money ever spent. This shows everything at root level, Minerals, amino acids,vitamins, antioxidants, essential fatty acids, neurotransmitters, malabsorption
paulb44
in
Pernicious Anaemia Society
12 years ago
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Not a good day today
Have just had 2 fairly good days wont say I was painfree but was less stiff and slept abit better but just had a dreadful nights sleep with pain and stiffness in hands. Thanks for your answers to my question on Rheumatoid factor. Only 2 weeks now till see Rheumy and hope to get a diagnosis. Then can
Have just had 2 fairly good days wont say I was painfree but was less stiff and slept abit better but just had a dreadful nights sleep with pain and stiffness in hands. Thanks for your answers to my question on Rheumatoid factor. Only 2 weeks now till see Rheumy and hope to get a diagnosis. Then can
cris1728
in
NRAS
12 years ago
Blood test results and DR visit update.
Hi everyone, Thanks for all you help on my previous post. Just got back from Dr, she seems very nice. Went with a possitive attitude this time. Got a printout of my last blood test results, did a lot of chatting and before she refers me to anybody she want's some more bloods taken first, so have to
Hi everyone, Thanks for all you help on my previous post. Just got back from Dr, she seems very nice. Went with a possitive attitude this time. Got a printout of my last blood test results, did a lot of chatting and before she refers me to anybody she want's some more bloods taken first, so have to
LittleDragon
in
NRAS
12 years ago
Charcot joint??
Hi everyone...I havent been on this site in a while, but i think of all of you and appreciate all the help and support that you all give even when not feeling well. My feet always had poor circulation. I am not overweight and i exercise,dont drink or smoke. However, three of my drs. think i have charcot
Hi everyone...I havent been on this site in a while, but i think of all of you and appreciate all the help and support that you all give even when not feeling well. My feet always had poor circulation. I am not overweight and i exercise,dont drink or smoke. However, three of my drs. think i have charcot
lovemyheart
in
Hughes Syndrome APS Forum
12 years ago
ANA tests
Hello everyone I have never posted on this forum before, only in the Lupus and Fibromyalgia ones. I just wanted to ask for a bit of general advice on your diagnosis. I have not yet had a diagnosis but have been ill all year. I have pains in my back, neck, fingers, knees, and feet. Some days are
Hello everyone I have never posted on this forum before, only in the Lupus and Fibromyalgia ones. I just wanted to ask for a bit of general advice on your diagnosis. I have not yet had a diagnosis but have been ill all year. I have pains in my back, neck, fingers, knees, and feet. Some days are
natal1a
in
NRAS
12 years ago
Newbie hear to pick your brains
Hi all, I have found this group by browsing the communities here as I have Polymyalgia Rheumatica and on their group. After going to the docs for a few years I was finally diagnosed with PMR at the end of June. However I have tremendous pain in one hand and fingers and now my knees are hurting. I
Hi all, I have found this group by browsing the communities here as I have Polymyalgia Rheumatica and on their group. After going to the docs for a few years I was finally diagnosed with PMR at the end of June. However I have tremendous pain in one hand and fingers and now my knees are hurting. I
Sue8
in
NRAS
12 years ago
The painful opening of the eyes
Not mine - although the associated 'getting out of bed' is generally not a pain-free experience - but my boss'. I had a brief chat with her yesterday, as she was trying to arrange my final stage 2 sickness meeting (about time it was my final one, as I returned to work in February, and haven't had a
Not mine - although the associated 'getting out of bed' is generally not a pain-free experience - but my boss'. I had a brief chat with her yesterday, as she was trying to arrange my final stage 2 sickness meeting (about time it was my final one, as I returned to work in February, and haven't had a
SootyB
in
Fibromyalgia Action UK
12 years ago
A BRIEF HISTORY OF RA AND ITS TREATMENT
I thought it would be interesting to delve into the history of RA. It goes back pretty far; farther than I thought it would. Some skeletal remains in what is now Tennessee (USA) date back to 4500 BC and have shown some signs of Rheumatoid Arthritis. So far, that’s been the earliest appearance of this
I thought it would be interesting to delve into the history of RA. It goes back pretty far; farther than I thought it would. Some skeletal remains in what is now Tennessee (USA) date back to 4500 BC and have shown some signs of Rheumatoid Arthritis. So far, that’s been the earliest appearance of this
mike7748
in
Arthritis Foundation of South Africa
12 years ago
Diagnosed in December and learning to live with the ghost that hides in my body
So this is my first post. I am somewhat hesitant about opening a window on my life, but having spent some time reading the posts over a few weeks, and discovering the real sense of community on this blog, I thought I would share my story with you, having found comfort that I am far from alone in my diagnosis
So this is my first post. I am somewhat hesitant about opening a window on my life, but having spent some time reading the posts over a few weeks, and discovering the real sense of community on this blog, I thought I would share my story with you, having found comfort that I am far from alone in my diagnosis
Aliced
in
NRAS
12 years ago
doctors today most un helpful you have had an mri etc etc
could not get an xray on me back to see if it had gone worse or enything for that matter the pople i payed to see sendiing me for these blood tests B12 CK CRP EPS ESR FBC LFT UE SAN ANTI NEUTROPHIL SRA CYTOPLASMIC ANTIBODIES RHEUMATOID FACTOR WILL THESE THEST SHOW IF IF GOT RUMATOID OR
could not get an xray on me back to see if it had gone worse or enything for that matter the pople i payed to see sendiing me for these blood tests B12 CK CRP EPS ESR FBC LFT UE SAN ANTI NEUTROPHIL SRA CYTOPLASMIC ANTIBODIES RHEUMATOID FACTOR WILL THESE THEST SHOW IF IF GOT RUMATOID OR
minka
in
NRAS
12 years ago
The light at the end of the tunnel is sometimes an oncoming train ...
Well, I had my appointment with my 'second opinion' rheumy on Tuesday, and - after prodding me, listening to my chest front and back, and quizzing me on my pain, lifestyle, history, and bowel movements - decided that, pending some blood tests for vitamin D, antibodies, rheumatoid factor, and inflammatory
Well, I had my appointment with my 'second opinion' rheumy on Tuesday, and - after prodding me, listening to my chest front and back, and quizzing me on my pain, lifestyle, history, and bowel movements - decided that, pending some blood tests for vitamin D, antibodies, rheumatoid factor, and inflammatory
SootyB
in
NRAS
12 years ago
What does "negative for antibodies" mean?
Saw my consultant yesterday and he mentioned that my blood tests show negative for antibodies and that this means I have a less aggressive form of RA. I know I test positive for Rheumatoid Factor (and have since I first went to the doctor about joint pain) so what does the consultant mean. It
Saw my consultant yesterday and he mentioned that my blood tests show negative for antibodies and that this means I have a less aggressive form of RA. I know I test positive for Rheumatoid Factor (and have since I first went to the doctor about joint pain) so what does the consultant mean. It
Nikk
in
NRAS
12 years ago
What does "negative for antibodies" mean?
Saw my consultant yesterday and he mentioned that my blood tests show negative for antibodies and that this means I have a less aggressive form of RA. I know I test positive for Rheumatoid Factor (and have since I first went to the doctor about joint pain) so what does the consultant mean? It
Saw my consultant yesterday and he mentioned that my blood tests show negative for antibodies and that this means I have a less aggressive form of RA. I know I test positive for Rheumatoid Factor (and have since I first went to the doctor about joint pain) so what does the consultant mean? It
Nikk
in
NRAS
12 years ago
"Emphysema and airways disease COPD GOLD class 1. Mild fibrotic subpleural changes on CT scan".
Can anyone please explain the following quote which is the Diagnosis title on my latest hospital letter: "Emphysema and airways disease COPD GOLD class 1. Mild fibrotic subpleural changes on CT scan". I have also
Can anyone please explain the following quote which is the Diagnosis title on my latest hospital letter: "Emphysema and airways disease COPD GOLD class 1. Mild fibrotic subpleural changes on CT scan". I have also
Hidden
in
Lung Conditions Community Forum
12 years ago
Rituximab,Toxilizumab,and the Scleroderma Conference in Texas!
Hello everyone! It has been a while since my last blog,all my best intentions went out of the window with a downhill turn in health.I remember reading some questions about Rituximab and thought I'd let you know my situation. Very briefly: I have diffuse systemic sclerosis,severe lung fibrosis
Hello everyone! It has been a while since my last blog,all my best intentions went out of the window with a downhill turn in health.I remember reading some questions about Rituximab and thought I'd let you know my situation. Very briefly: I have diffuse systemic sclerosis,severe lung fibrosis
Alexandra-M
in
Scleroderma & Raynaud's UK (SRUK)
12 years ago
Anyone else have Low Factor VIII Levels???
I has occurred to me that I may be alone with this - so am asking, for it has made my APS quite difficult. Because my Factor VIII Levels are low (which is hemophilia) I was not a candidate for warfarin and heparin did not agree with me either. In other words, I have both the sticky blood of APS and
I has occurred to me that I may be alone with this - so am asking, for it has made my APS quite difficult. Because my Factor VIII Levels are low (which is hemophilia) I was not a candidate for warfarin and heparin did not agree with me either. In other words, I have both the sticky blood of APS and
Leigha
in
Hughes Syndrome APS Forum
12 years ago
Do many of you have scleritis with your RA.
Mine started about 18 months before I was diagnosed with RA. 4 months before my RA diagnosis I was also diagnosed with type 2 diabetes and hypertension(2 1/2 year ago now).18 months ago I was having palpitations and tests showed I had SVT. A cardiologist told me I had a conduction disorder probably caused
Mine started about 18 months before I was diagnosed with RA. 4 months before my RA diagnosis I was also diagnosed with type 2 diabetes and hypertension(2 1/2 year ago now).18 months ago I was having palpitations and tests showed I had SVT. A cardiologist told me I had a conduction disorder probably caused
thekeys46
in
NRAS
12 years ago
Could this suggest PA..?
Hello people, I'm new here so please forgive what's probably going to be lots of words to ask a silly question. (I seem to talk forever these days and make no sense!) I had B12 deficiency in Summer 2010 (169) and was told by GP to buy standard B12 supplements. I took Jarrow's sublinguals as I'd
Hello people, I'm new here so please forgive what's probably going to be lots of words to ask a silly question. (I seem to talk forever these days and make no sense!) I had B12 deficiency in Summer 2010 (169) and was told by GP to buy standard B12 supplements. I took Jarrow's sublinguals as I'd
CathyT
in
Pernicious Anaemia Society
12 years ago
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