Search
Search
About
Log in
Join
Experiences with
Alna
Posts
Communities
945 public posts
Filter results
Ana test
Just wondering if anyone has a negative ana but still has scleroderma? My hands have started showing symptoms but my ana test a couple months ago was negative..
Just wondering if anyone has a negative ana but still has scleroderma? My hands have started showing symptoms but my ana test a couple months ago was negative..
Katie2333
in
Scleroderma & Raynaud's UK (SRUK)
3 years ago
Awaiting diagnosis (fibromyalgia)
I’ve recently had a letter saying I’ve had a weakly Positive ANA blood test result with an anticentromere pattern. Does anyone know what this means. I’ve not got my appointment until 24th December when I go back to see the rheumatologist. Any help or advice would be really appreciated in lots of pain
I’ve recently had a letter saying I’ve had a weakly Positive ANA blood test result with an anticentromere pattern. Does anyone know what this means. I’ve not got my appointment until 24th December when I go back to see the rheumatologist. Any help or advice would be really appreciated in lots of pain
Larma
in
Fibromyalgia Action UK
3 years ago
How to prepare for Rheumatology Appointment
Hello, I'm new here. I have an appointment with rheumatology on Saturday, and would love some advice on how to prepare for it fully. I've been referred because a recurrent miscarriage clinic picked up a positive ANA test- the repeat test was also positive (a weak positive.) I have struggled with joint
Hello, I'm new here. I have an appointment with rheumatology on Saturday, and would love some advice on how to prepare for it fully. I've been referred because a recurrent miscarriage clinic picked up a positive ANA test- the repeat test was also positive (a weak positive.) I have struggled with joint
natmitch
in
LUPUS UK
3 years ago
Want to take advantage of all our features? Just log in!
Log in
or
Join
ANA positive patients needed for a new research study
Hi everyone, I have received a request from researchers at University of Nottingham for a project about whether antinuclear antibodies (ANA) can be predictive of disease.
[u]Lay summary[/u]
[i]Patients with rare diseases frequently describe a long path to diagnosis. ANA-associated diseases are
Hi everyone, I have received a request from researchers at University of Nottingham for a project about whether antinuclear antibodies (ANA) can be predictive of disease.
[u]Lay summary[/u]
[i]Patients with rare diseases frequently describe a long path to diagnosis. ANA-associated diseases are
Paul_Howard
LUPUS UK
in
LUPUS UK
3 years ago
I'm a little scared with my cbc
I had some blood work done it shows low wbc at 3.4, rbc at 4.24 and abnormal mpv 11.6 most worrisome results is NEUTROPHILS 34.7 %LYMPHOCYTES 49.5 What could this mean? I got to the doctor tomorrow but I've just been so nervous. I also have a few enlarged lymph nodes in my neck that have been there
I had some blood work done it shows low wbc at 3.4, rbc at 4.24 and abnormal mpv 11.6 most worrisome results is NEUTROPHILS 34.7 %LYMPHOCYTES 49.5 What could this mean? I got to the doctor tomorrow but I've just been so nervous. I also have a few enlarged lymph nodes in my neck that have been there
19ashley89
in
CLL Support
3 years ago
Struggling to get any doctors to listen to me.
I’m having an extremely difficult time getting any doctors to listen to me. I have been struggling with my joints now for around 6-7 years. I have been seeing GPs and the like for all of this time and the answers have always been the same, there’s a potential I have arthritis but because my Rheumatoid
I’m having an extremely difficult time getting any doctors to listen to me. I have been struggling with my joints now for around 6-7 years. I have been seeing GPs and the like for all of this time and the answers have always been the same, there’s a potential I have arthritis but because my Rheumatoid
SadGirlRaceClub
in
LUPUS UK
3 years ago
Overview of the Ataxias
🙂 This is lengthy, but it does have useful, interesting information. Overview of Adult Onset Cerebellar Ataxia Pravin Khemani, MD The ataxias are clinically heterogenous disorders caused by pathological processes affecting the cerebellum and cerebellar pathways resulting in impaired coordination. The
🙂 This is lengthy, but it does have useful, interesting information. Overview of Adult Onset Cerebellar Ataxia Pravin Khemani, MD The ataxias are clinically heterogenous disorders caused by pathological processes affecting the cerebellum and cerebellar pathways resulting in impaired coordination. The
wobblybee
in
Ataxia UK
3 years ago
Need help with readings
Hi there! Over the last year I've been experiencing lots of weird health issues which may be related to hormones. Hot flushes on my cheeks, but very cold hands and feet, extremely dry hair. I've also had shingles many times and very low cholesterol. Because my GP ran a few blood tests but nothing unusual
Hi there! Over the last year I've been experiencing lots of weird health issues which may be related to hormones. Hot flushes on my cheeks, but very cold hands and feet, extremely dry hair. I've also had shingles many times and very low cholesterol. Because my GP ran a few blood tests but nothing unusual
Smiekie_t
in
Thyroid UK
3 years ago
Ouch !!!!!
Good morning all ! First time posting on here …. But need some advice if poss . Will attempt to post pic of my hand , but this is the 5 th time it has happened in exactly the same place . I have no diagnosis , but have had positive ANA , and rheumatoid factor high . I do have pernicious anaemia and folate
Good morning all ! First time posting on here …. But need some advice if poss . Will attempt to post pic of my hand , but this is the 5 th time it has happened in exactly the same place . I have no diagnosis , but have had positive ANA , and rheumatoid factor high . I do have pernicious anaemia and folate
SarahLou2
in
LUPUS UK
3 years ago
What exactly is needed for a Lupus diagnosis?
Looking for some advice from people who have been diagnosed with Lupus… In July I went to my GP due to severe joint pain, along with other symptoms. Pain started in my wrists but has moved to my other joints now and is making day to day very difficult. The GP took some bloods, but was so sure it was
Looking for some advice from people who have been diagnosed with Lupus… In July I went to my GP due to severe joint pain, along with other symptoms. Pain started in my wrists but has moved to my other joints now and is making day to day very difficult. The GP took some bloods, but was so sure it was
AFrances
in
LUPUS UK
3 years ago
Positive ANA, negative ENA?
Hi all!.Within the past year I've been experiencing fatigue, burning muscle and joint aches, skin rashes, hives, hair loss, weight loss, easy bruising, dry mouth, dry eyes, swollen glands etc I recently had an ANA test which came back positive at 1:320 titre with homogenous and speckled pattern. My
Hi all!.Within the past year I've been experiencing fatigue, burning muscle and joint aches, skin rashes, hives, hair loss, weight loss, easy bruising, dry mouth, dry eyes, swollen glands etc I recently had an ANA test which came back positive at 1:320 titre with homogenous and speckled pattern. My
Hidden
in
LUpus Patients Understanding and Support
3 years ago
Positive ANA, negative ENA?
Hi all!.Within the past year I've been experiencing fatigue, burning muscle and joint aches, skin rashes, hives, hair loss, weight loss, easy bruising, dry mouth, dry eyes, swollen glands etc I recently had an ANA test which came back positive at 1:320 titre with homogenous and speckled pattern. My ENA
Hi all!.Within the past year I've been experiencing fatigue, burning muscle and joint aches, skin rashes, hives, hair loss, weight loss, easy bruising, dry mouth, dry eyes, swollen glands etc I recently had an ANA test which came back positive at 1:320 titre with homogenous and speckled pattern. My ENA
Hidden
in
LUPUS UK
3 years ago
Fnd or lupus?
Hi just wondering if anyone can help me I started having symptoms after the birth of my second child last year. Then i was seen by a neurologist who diagnosed fnd (functional neurological disorder) however my gastronolgist and a gp has said they believe it to be autoimmune disease underlying and not
Hi just wondering if anyone can help me I started having symptoms after the birth of my second child last year. Then i was seen by a neurologist who diagnosed fnd (functional neurological disorder) however my gastronolgist and a gp has said they believe it to be autoimmune disease underlying and not
Haylz2109
in
LUPUS UK
3 years ago
Followup to my post 8 months back, sudden jaundice and hemolytic anemia
I had posted 8 months back about sudden onset of jaundice and hemolytic anemia. So my brother was tested with ANA and complement factors for SLE and was diagnosed as questionable lupus but hematolgist believed it was lupus although my brother didn't have any physical symptoms or manifestations of lupus
I had posted 8 months back about sudden onset of jaundice and hemolytic anemia. So my brother was tested with ANA and complement factors for SLE and was diagnosed as questionable lupus but hematolgist believed it was lupus although my brother didn't have any physical symptoms or manifestations of lupus
Akam
in
Hughes Syndrome APS Forum
3 years ago
Could I have Myasthenia Gravis, please help!
Hi everyone, I wonder if you could help me out. Could my symptoms be related to Myasthenia Gravis? I've been very sick for some time, which has got progressively worse over the years (7 years now, the last 2 have been very bad). I've started to attach my symptoms to acetylcholine as when I eat foods
Hi everyone, I wonder if you could help me out. Could my symptoms be related to Myasthenia Gravis? I've been very sick for some time, which has got progressively worse over the years (7 years now, the last 2 have been very bad). I've started to attach my symptoms to acetylcholine as when I eat foods
LPLx
in
Myasthenia Gravis Association
3 years ago
Confused
So had my appt with Rheumatologist and even though my RA factor and ANA test was positive and my joint pain is in both sides he says seeing I don’t have inflammation I don’t have rheumatoid arthritis
So had my appt with Rheumatologist and even though my RA factor and ANA test was positive and my joint pain is in both sides he says seeing I don’t have inflammation I don’t have rheumatoid arthritis
Hurting2012
in
NRAS
3 years ago
A little advice would be most welcome...
Hi everyone, I was wondering if anyone can give me some advice. My mother had PBC. I have NAFLD but am also Strongly Positive ANA, moderately positive Anti SMA , and Anti SP100 Multiple Nuclear Dot pattern. But I am AMA negative. I was recently seen by a dermatologist for severe itching, and she has
Hi everyone, I was wondering if anyone can give me some advice. My mother had PBC. I have NAFLD but am also Strongly Positive ANA, moderately positive Anti SMA , and Anti SP100 Multiple Nuclear Dot pattern. But I am AMA negative. I was recently seen by a dermatologist for severe itching, and she has
InkyTrickle
in
British Liver Trust
3 years ago
Feedback very much appreciated.
I am writing to see if anyone is in the same boat, and can shed some light on what is going on. I hate the waiting game, as everyone knows, it can take weeks, or months to get answers. Here is my experience. I am 38 years old (F) and would consider myself to be healthy overall. For the last two years
I am writing to see if anyone is in the same boat, and can shed some light on what is going on. I hate the waiting game, as everyone knows, it can take weeks, or months to get answers. Here is my experience. I am 38 years old (F) and would consider myself to be healthy overall. For the last two years
aataalak
in
Kidney Disease
3 years ago
Exercise and weight gain
I'd be grateful for advice. I've recently been diagnosed with lupus, but have had the symptoms and indeed many of the signs for at least 5 years. I've now got positive ANA and RNP antibodies, plus a stubbornly low iron, low C3 and C4, neutropenia, plus painful joints, fatigue, brain fog and other physical
I'd be grateful for advice. I've recently been diagnosed with lupus, but have had the symptoms and indeed many of the signs for at least 5 years. I've now got positive ANA and RNP antibodies, plus a stubbornly low iron, low C3 and C4, neutropenia, plus painful joints, fatigue, brain fog and other physical
Ophelia1
in
LUPUS UK
3 years ago
Elf score
Hi, I'm very worried about some results I've had this week, my lft were raised last yr inflamed liver to drink but returned to normal 7 week later no drink since, asked for scan referral fibrscan Dr would do not refer but did a lft tests again and elf test, lft still normal, elf score 10.1 they said
Hi, I'm very worried about some results I've had this week, my lft were raised last yr inflamed liver to drink but returned to normal 7 week later no drink since, asked for scan referral fibrscan Dr would do not refer but did a lft tests again and elf test, lft still normal, elf score 10.1 they said
Poe2012
in
British Liver Trust
3 years ago
1
...
6
7
8
...
48
Next page
10
20
30
40
Filter results
Clear filters
Posted in
All communities
LUPUS UK
499 results
Thyroid UK
77 results
Scleroderma & Raynaud's UK (SRUK)
47 results
View top 10 communities
Sort by
Most Relevant
Newest