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Blood test results?
Got copy of letter to my Gp after Rheumie visit 2 weeks ago. Results are ANA positive 1.640 homogenous, IgA 4.37 increased,C4 0.39 increased, CRP<4, LFT (N) GFR 73.5, ESR 17 increased. In English please?
Got copy of letter to my Gp after Rheumie visit 2 weeks ago. Results are ANA positive 1.640 homogenous, IgA 4.37 increased,C4 0.39 increased, CRP<4, LFT (N) GFR 73.5, ESR 17 increased. In English please?
Gymbabe
in
LUPUS UK
11 years ago
More advice to help me help myself. Here's my full results from recent full bloods. Any advice please?
I've already posted a question but I am doubling up with a blog for more information.Thanks to those who already responded. I really can identify with most of the symptoms detailed on the ThyroidUK web site for Hypothyroidism, as well as a couple of weird ones (e.g. restless legs at night whenever
I've already posted a question but I am doubling up with a blog for more information.Thanks to those who already responded. I really can identify with most of the symptoms detailed on the ThyroidUK web site for Hypothyroidism, as well as a couple of weird ones (e.g. restless legs at night whenever
klicker
in
Thyroid UK
11 years ago
A confused Lupie
I ache, sometimes i really ache especially today my shoulders,upper arms and neck. but my question is, if my bloods keep showing low esr and normal ck readings then why do i ache. my doc takes my blood when i complain of hurting all over just to make sure i havent developed anything else and they
I ache, sometimes i really ache especially today my shoulders,upper arms and neck. but my question is, if my bloods keep showing low esr and normal ck readings then why do i ache. my doc takes my blood when i complain of hurting all over just to make sure i havent developed anything else and they
Hidden
in
LUPUS UK
11 years ago
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ANA "normal"
Help! I'm going to see GP in morning, ANA test normal, my symptoms ... Fatigue,hair loss,skin rash in summer,raynauds,joint pain so bad I scream in agony yet I had a fractured elbow years ago and didn't realise as my pain threshold so high!my list goes on , I took list on first visit to my GP and he
Help! I'm going to see GP in morning, ANA test normal, my symptoms ... Fatigue,hair loss,skin rash in summer,raynauds,joint pain so bad I scream in agony yet I had a fractured elbow years ago and didn't realise as my pain threshold so high!my list goes on , I took list on first visit to my GP and he
Lupdaloop
in
LUPUS UK
11 years ago
Hi to everyone I don't think I have posted before but regularly read comments and info on this site. It is very comforting and supportive
to realise that there are people out there that have similar if not exactly the same health issues and that I am not a hypochondriac as suggested by a lady consultant years ago. I was wondering if anyone can as i am now very confused. Years ago I was diagnosed with RA then about 7 years ago I was diagnosed
to realise that there are people out there that have similar if not exactly the same health issues and that I am not a hypochondriac as suggested by a lady consultant years ago. I was wondering if anyone can as i am now very confused. Years ago I was diagnosed with RA then about 7 years ago I was diagnosed
Rhodes62
in
LUPUS UK
11 years ago
has anyone ever had a positive ana test and had an xray done to find they have scolisois
i am 25 years old always had good health until about a year and a 1/2 ago when i started getting severe back pains.... was told it was spams but didnt go away... then i had 2 incidents where i became short of breathe and passed out doing light excerising ( playing iwth my kids in my yard.) at first run
i am 25 years old always had good health until about a year and a 1/2 ago when i started getting severe back pains.... was told it was spams but didnt go away... then i had 2 incidents where i became short of breathe and passed out doing light excerising ( playing iwth my kids in my yard.) at first run
ericamcnew
in
LUPUS UK
11 years ago
talked myself out of low mood.
Hi all,as you all know by now I have a phobia with taking meds,well forced myself to take half of a st johns wort tablet,last evening,felt alright for an hour,then nausea set in,felt like being sick,of course I started to panic then.felt dizzy,spacey head etc;I got really depressed.this lasted all night
Hi all,as you all know by now I have a phobia with taking meds,well forced myself to take half of a st johns wort tablet,last evening,felt alright for an hour,then nausea set in,felt like being sick,of course I started to panic then.felt dizzy,spacey head etc;I got really depressed.this lasted all night
miarose
in
Anxiety Support
11 years ago
A big Mexican wave that just keeps going ......
morning fellow bloggers :) Newbies might find this interesting. It is nearly a month since I started blogging, I was consumed by fear, always anxious and lived in nerves of something bad happening. I have suffered from anxiety and depression for many years but sometimes can go months without even
morning fellow bloggers :) Newbies might find this interesting. It is nearly a month since I started blogging, I was consumed by fear, always anxious and lived in nerves of something bad happening. I have suffered from anxiety and depression for many years but sometimes can go months without even
Tara67
in
Anxiety Support
11 years ago
Professor Graham Hughes' March blog
Another record! The coldest March for 50 years! It's nearly a year since the UK's drought warning and it hasn't stopped raining since. Let's hope Easter brings a change! Earlier this week, my colleague Professor Munther Khamashta excitedly showed me a report taken from a recent American Academy of
Another record! The coldest March for 50 years! It's nearly a year since the UK's drought warning and it hasn't stopped raining since. Let's hope Easter brings a change! Earlier this week, my colleague Professor Munther Khamashta excitedly showed me a report taken from a recent American Academy of
Hidden
in
Hughes Syndrome APS Forum
11 years ago
Help with blood test results
Hi I am 59 and for 15 years have been hypothyroid and autoimmune. For all of those 15 years I have suffered with constant fatigue my life is one long battle against it do a bit have a rest carry on. Doctors not interested and I gave up for a couple of years not even going after trying for many to get
Hi I am 59 and for 15 years have been hypothyroid and autoimmune. For all of those 15 years I have suffered with constant fatigue my life is one long battle against it do a bit have a rest carry on. Doctors not interested and I gave up for a couple of years not even going after trying for many to get
JanW
in
Thyroid UK
11 years ago
ANA Test
Just got off the phone to my GP my blood test were abnormal, and the doctor has accepted my telephone request for the ANA test, form awaiting me at the local hospital! I have an appointment then to see GP on 24th April. I'm hoping this is going to result in a referral to a specialist, not bad considering
Just got off the phone to my GP my blood test were abnormal, and the doctor has accepted my telephone request for the ANA test, form awaiting me at the local hospital! I have an appointment then to see GP on 24th April. I'm hoping this is going to result in a referral to a specialist, not bad considering
Lupdaloop
in
LUPUS UK
11 years ago
Something is working !
Morning everyone, my positive good mood seems to be lasting :) I really think the St Johns Wort has taken the edge of my anxiety/ depression. I am also taking Omega complex capsules and I really good multi vitamin. Of course blogging here is really keeping me focused, and I am putting some of my
Morning everyone, my positive good mood seems to be lasting :) I really think the St Johns Wort has taken the edge of my anxiety/ depression. I am also taking Omega complex capsules and I really good multi vitamin. Of course blogging here is really keeping me focused, and I am putting some of my
Tara67
in
Anxiety Support
11 years ago
Blood tests
Anyone have an idea how long I'm likely to wait for my results, I understand that some tests take time to "culture" or something like that, but I just asked the doctor to add on a ANA test as I've read it's result is a good indicator of Lupus,I've not heard back from him yet with an answer. Fingers crossed
Anyone have an idea how long I'm likely to wait for my results, I understand that some tests take time to "culture" or something like that, but I just asked the doctor to add on a ANA test as I've read it's result is a good indicator of Lupus,I've not heard back from him yet with an answer. Fingers crossed
Lupdaloop
in
LUPUS UK
11 years ago
So far so good
It's Saturday and I have survived so far, my parents were ok about me not staying for easter, so that anxiety has passed. Stepdaughter has been and gone without any teenage mood swings and no noise from next door all week. I am sure saturday night will bring some noise but I don't mind too much as the
It's Saturday and I have survived so far, my parents were ok about me not staying for easter, so that anxiety has passed. Stepdaughter has been and gone without any teenage mood swings and no noise from next door all week. I am sure saturday night will bring some noise but I don't mind too much as the
Tara67
in
Anxiety Support
11 years ago
Has anyone tried a spinal cord stimulator?
LadyPink
in
Functional Neurological Disorder - FND Hope
11 years ago
St Johns Wort and knitting
Just wondering if any takes St Johns Wort, I took it years ago but can't remember if it made any difference. I have started taking them again and wonder how long it takes before you notice any difference. I have noticed the brand I buy has been repackaged with 'help with low mood' not mentioning depression
Just wondering if any takes St Johns Wort, I took it years ago but can't remember if it made any difference. I have started taking them again and wonder how long it takes before you notice any difference. I have noticed the brand I buy has been repackaged with 'help with low mood' not mentioning depression
Tara67
in
Anxiety Support
11 years ago
Just want to say hello
My journey began about 6 months ago when after a 10 day course of Augmentin I noticed that my urine was a bright orange and I was itching all over my body. I also had incredibly bad indigestion along with constipation. This lasted about a week and I went in to see my physician. The labs came back with
My journey began about 6 months ago when after a 10 day course of Augmentin I noticed that my urine was a bright orange and I was itching all over my body. I also had incredibly bad indigestion along with constipation. This lasted about a week and I went in to see my physician. The labs came back with
bbobb55
in
PBC Foundation
11 years ago
lupus tests
I have had so many over the years some neg some positive this time ena positive ana negative and anti Ro positive Anyone know what this means
I have had so many over the years some neg some positive this time ena positive ana negative and anti Ro positive Anyone know what this means
katepscot
in
LUPUS UK
11 years ago
Blood Test Update
Well had load more bloods take last week and consultants meeting etc. Yesterday I got back the lastest. Based upon a positive ANA test I had to have several other tests. Doctor rung me up yesterday to inform me that my ESR is very high at 56 when in range is below 10. Based on this I have further
Well had load more bloods take last week and consultants meeting etc. Yesterday I got back the lastest. Based upon a positive ANA test I had to have several other tests. Doctor rung me up yesterday to inform me that my ESR is very high at 56 when in range is below 10. Based on this I have further
Bigplanet
in
British Liver Trust
11 years ago
Tiny red dots on skin
I've just come back from beach holiday and while I was there staying in the shade on our deck, while hubby was sunning himself, I've noticed I now have some tiny red dots on my skin. They are not raised, don't itch and look like pinpricks. They are not in a particular pattern, and are spread out on
I've just come back from beach holiday and while I was there staying in the shade on our deck, while hubby was sunning himself, I've noticed I now have some tiny red dots on my skin. They are not raised, don't itch and look like pinpricks. They are not in a particular pattern, and are spread out on
Purpletop
in
LUPUS UK
11 years ago
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