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diagnosed too easy...hmmm
i feel i was diagnosed too easy with lupus... I am hypothyroid since 1998.. been 3 years menopaused..that threw thyroid further crazy... then leg/knee/hip/groin pain lasting 6 months then it left there..went to my collarbone now 3 months & calve pain when trying to go for walkies. xrays revealed
i feel i was diagnosed too easy with lupus... I am hypothyroid since 1998.. been 3 years menopaused..that threw thyroid further crazy... then leg/knee/hip/groin pain lasting 6 months then it left there..went to my collarbone now 3 months & calve pain when trying to go for walkies. xrays revealed
dgleds
in
LUPUS UK
11 years ago
How can my previous positive tests come back negative after a repeat?
I had a repeat test (as requested after 6mths by lab) for my POSITIVE ANA - POSITIVE HEP 2 CELLS (which included a pattern) ..borderline positive dsDNA abs....only to have the test come back COMPLETELY NEGATIVE!!! Does anyone know if this is possible?
I had a repeat test (as requested after 6mths by lab) for my POSITIVE ANA - POSITIVE HEP 2 CELLS (which included a pattern) ..borderline positive dsDNA abs....only to have the test come back COMPLETELY NEGATIVE!!! Does anyone know if this is possible?
nannytutu
in
LUPUS UK
11 years ago
Drama queen
Yes that's what my family think is wrong with me. A drama queen. I have been ill now for at least 18 years if not longer. Been tested for lupus results came back negative. Though have a positive ANA result. Have raynards and liverdo reticulitis which breaks out into small spots which bleed like ulcers
Yes that's what my family think is wrong with me. A drama queen. I have been ill now for at least 18 years if not longer. Been tested for lupus results came back negative. Though have a positive ANA result. Have raynards and liverdo reticulitis which breaks out into small spots which bleed like ulcers
Linmur1957
in
LUPUS UK
11 years ago
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stopping medication/How long to leave your system?
Hi everyone I have had another frustrating conversation with my rhuemy nurse. Basically none of my bloods show any inflammation, I have had a positive ana on 2 occasions tested 3 months apart but were different patterns and then another ana test done which was negative. My symptoms are Joint pain
Hi everyone I have had another frustrating conversation with my rhuemy nurse. Basically none of my bloods show any inflammation, I have had a positive ana on 2 occasions tested 3 months apart but were different patterns and then another ana test done which was negative. My symptoms are Joint pain
LULU85
in
LUPUS UK
11 years ago
Lupus
My first lupus test came back positive also ANA positive. My latest lupus test was negative but ANA remains positive. Would the steroids I was on at the time affect my blood readings. Many thanks xxxxxx Also have F M and COPD.
My first lupus test came back positive also ANA positive. My latest lupus test was negative but ANA remains positive. Would the steroids I was on at the time affect my blood readings. Many thanks xxxxxx Also have F M and COPD.
Lesi
in
LUPUS UK
11 years ago
I had a borderline positive ANA test 2 years ago, and Hep2 cells were borderline positive..and the dsDNA level was very low at about 5 units
.. Mid-December 2012 I had the test repeated through a neurologist (as I was getting numb toes) and the test came back as ANA positive...Hep2 cells positive...the dsDNA level was 70 and an extra test of Crithidia came back borderline positive...The lab requested a repeat in 3 - 6 months. I have been
.. Mid-December 2012 I had the test repeated through a neurologist (as I was getting numb toes) and the test came back as ANA positive...Hep2 cells positive...the dsDNA level was 70 and an extra test of Crithidia came back borderline positive...The lab requested a repeat in 3 - 6 months. I have been
nannytutu
in
LUPUS UK
11 years ago
Can I ask if someone has had a positive ANA, and a negative DSDNA but still been diagnosed with Lupus? I have speckled pattern 1:80 titre
Im blessed with pernicious anemia, kidney problems, Ive been diagnosed with rheumatoid arthritis, bruises so eaisily, sores that just wont heal, I have flares, and dont stand the sunlight well.im totally exhausted, my eyes sting and my mouth is very dry. my joints are horrible, fingers, hands, toes,
Im blessed with pernicious anemia, kidney problems, Ive been diagnosed with rheumatoid arthritis, bruises so eaisily, sores that just wont heal, I have flares, and dont stand the sunlight well.im totally exhausted, my eyes sting and my mouth is very dry. my joints are horrible, fingers, hands, toes,
nancee
in
LUPUS UK
11 years ago
13yrs later.......
Just had my first Rhuemy appointment ! Only taken 13 years to get there! The last few months I've been on a serious mission to get to the bottom of my condition/s Been backwards and forwards to Gp with all my various symptoms over the last 13 years,finally when I moved I changed Gp and I think I made
Just had my first Rhuemy appointment ! Only taken 13 years to get there! The last few months I've been on a serious mission to get to the bottom of my condition/s Been backwards and forwards to Gp with all my various symptoms over the last 13 years,finally when I moved I changed Gp and I think I made
Lupdaloop
in
LUPUS UK
11 years ago
Anyone had oral thrush and small blisters on fingers?
I have raynauds and a strongly positive ANA marker in my bloods but not yet been diagnosed with a particular connective tissue disorder. I feel my raynauds has been worse the last week or so and have also randomly developed oral thrush and small little bubble type blisters on the side of my finger. Doctor
I have raynauds and a strongly positive ANA marker in my bloods but not yet been diagnosed with a particular connective tissue disorder. I feel my raynauds has been worse the last week or so and have also randomly developed oral thrush and small little bubble type blisters on the side of my finger. Doctor
Dancingc21
in
Scleroderma & Raynaud's UK (SRUK)
11 years ago
Help and value your advice friends .
I was off Hydroxy and MTX as had a face rash and coldsore and was given antibiotics. I went back on Hydroxy and felt great..no joint pain and actually felt human and guess what had 'knuckles' and no 'swollen knees' and thought this was a breakthrough. An ANA test has been sent off and no results yet
I was off Hydroxy and MTX as had a face rash and coldsore and was given antibiotics. I went back on Hydroxy and felt great..no joint pain and actually felt human and guess what had 'knuckles' and no 'swollen knees' and thought this was a breakthrough. An ANA test has been sent off and no results yet
Rockpool60
in
NRAS
11 years ago
Feeling worse again :(
Can you help? Was off MTX for 3 weeks due to cold sore / rash on face so getting ANA test for other connective tissue diseases. First injection and feel more swollen and stiff and mood down than when I was just on hydroxy..very confused. Feel that since diagnosed exactly 1 year ago I am no better forward
Can you help? Was off MTX for 3 weeks due to cold sore / rash on face so getting ANA test for other connective tissue diseases. First injection and feel more swollen and stiff and mood down than when I was just on hydroxy..very confused. Feel that since diagnosed exactly 1 year ago I am no better forward
Rockpool60
in
NRAS
11 years ago
Endo wants me to trial T3
i had my first visit today with an Endo and I had a positive outcome...Wow ..you all might say lol. He wants me to trial T3 for 6 weeks and start taking Vit D. Do you take this with your normal dosage of Levo, I'm currently on 100mcg and have Hashi's. i'm sure my Gp will advice but it's good to get
i had my first visit today with an Endo and I had a positive outcome...Wow ..you all might say lol. He wants me to trial T3 for 6 weeks and start taking Vit D. Do you take this with your normal dosage of Levo, I'm currently on 100mcg and have Hashi's. i'm sure my Gp will advice but it's good to get
angelharley
in
Thyroid UK
11 years ago
Go home and have a baby !
At 25 I started with joint pain. First Rheumy I saw asked me how many children I had given birth to. (None, as I have antiphosolipid syndrome and couldn't get full term). He told me there was nothing wrong with me and to go home and have a baby to "take my mind off my imaginary illnesses". He then
At 25 I started with joint pain. First Rheumy I saw asked me how many children I had given birth to. (None, as I have antiphosolipid syndrome and couldn't get full term). He told me there was nothing wrong with me and to go home and have a baby to "take my mind off my imaginary illnesses". He then
MadMatilda
in
LUPUS UK
11 years ago
Blood tests
Hi, My rheumy sent me a letter about recent blood tests. She said that it had shown up something that causes APS and Raynards. But I can't find a particular result that would diagnose the two. I did have a positive ANA which could apply to the Raynards but does it apply to APS as well? Regards
Hi, My rheumy sent me a letter about recent blood tests. She said that it had shown up something that causes APS and Raynards. But I can't find a particular result that would diagnose the two. I did have a positive ANA which could apply to the Raynards but does it apply to APS as well? Regards
rosiemay
in
Hughes Syndrome APS Forum
11 years ago
Can having PA give a positive ANA blood test result OR can a positive ANA possibly be PA(if you have many of the symptoms too of course)?
melodypond
in
Pernicious Anaemia Society
11 years ago
Blood test results
Female 47 and Hashimoto's. Recently been very unwell, signed off sick. I had Mri scans, ct scans and blood tests. Bloods revealed ANA positive 1:80 with nucleolar pattern, Peroxidase Ab 500 Gast. Parietal cell Abs positive ALT 8 TSh 2.14 FreeT4 18.7 FreeT3 4.1 Should I be concerned?
Female 47 and Hashimoto's. Recently been very unwell, signed off sick. I had Mri scans, ct scans and blood tests. Bloods revealed ANA positive 1:80 with nucleolar pattern, Peroxidase Ab 500 Gast. Parietal cell Abs positive ALT 8 TSh 2.14 FreeT4 18.7 FreeT3 4.1 Should I be concerned?
angelharley
in
Thyroid UK
11 years ago
Hydroxychloroquine help
Hi all Hope everyone is well. I just wanted to check something about hydroxychloroquine. I started taking it just over two months ago and in the past two weeks have started experiencing tingling in my arms and hands. I did used to get some tingling in my fingertips before starting it, it just seems
Hi all Hope everyone is well. I just wanted to check something about hydroxychloroquine. I started taking it just over two months ago and in the past two weeks have started experiencing tingling in my arms and hands. I did used to get some tingling in my fingertips before starting it, it just seems
natal1a
in
LUPUS UK
11 years ago
New here - any help/advice would be very gratefully accepted!
hello there I apologise in advance and say thank you to anyone who takes the trouble to read this. My history is quite a long one going back around four years. But in essence after many symptoms and an ANA test that came back positive (and I asked for) I was sent to a rheumy who investigated me
hello there I apologise in advance and say thank you to anyone who takes the trouble to read this. My history is quite a long one going back around four years. But in essence after many symptoms and an ANA test that came back positive (and I asked for) I was sent to a rheumy who investigated me
melodypond
in
Pernicious Anaemia Society
11 years ago
Why dark circles will appear under eyes even though i used to drink water regularly?
My ANA speckled positive[2+] from the past 1.5 years. my lupes is negative. i have auto immune heamolytic anemia and auto immune antithyrodities previously. i used medicines for 1.2 years. Doctors advised me to stop all the medicines and come back for regular check up after 3 months as my CBC, thyroid
My ANA speckled positive[2+] from the past 1.5 years. my lupes is negative. i have auto immune heamolytic anemia and auto immune antithyrodities previously. i used medicines for 1.2 years. Doctors advised me to stop all the medicines and come back for regular check up after 3 months as my CBC, thyroid
bindhu
in
LUPUS UK
11 years ago
Going round in circles! Help with blood tests please.
Hi there Sorry is this is a little long, I appreciate anyone who reads on. Hard to know where to begin but have been feeling ill for around 4 years with lots of varied symptoms some of which come and go, some which hang around. But they include severe fatigue, muscle weakness/pain, hair loss on head
Hi there Sorry is this is a little long, I appreciate anyone who reads on. Hard to know where to begin but have been feeling ill for around 4 years with lots of varied symptoms some of which come and go, some which hang around. But they include severe fatigue, muscle weakness/pain, hair loss on head
melodypond
in
LUPUS UK
11 years ago
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