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Results from blood tests ... eex help understanding
Thanks for replying to my previous post guys. It prompted me to ask for copies of the tests rather than accepting ... "They've come back normal." When I said that I had been prescribed vitamin d ... That is over a number of years. The last time being in February following blood tests then. I'm listing
Thanks for replying to my previous post guys. It prompted me to ask for copies of the tests rather than accepting ... "They've come back normal." When I said that I had been prescribed vitamin d ... That is over a number of years. The last time being in February following blood tests then. I'm listing
Jo444
in
Thyroid UK
6 years ago
Feels Like so Much Waiting and Worrying
I'm really trying to go day to day with what's been happening to me. When this all started with stomach problems I didn't really expect to end up here. I keep worrying about things like scleroderma, even though I don't seem to have any of the symptoms of it. I've made a little progress on the gastro
I'm really trying to go day to day with what's been happening to me. When this all started with stomach problems I didn't really expect to end up here. I keep worrying about things like scleroderma, even though I don't seem to have any of the symptoms of it. I've made a little progress on the gastro
eirinym
in
LUPUS UK
6 years ago
Adalat retard
Please could anyone let me know if they are on adalat retard 20 mg I have been on adalat la for a few years now the chemist can't get them , I feel very anxious and exhausted on these Meds l have no colour very pale , also muzzy headed .i also have underactive thyroid which is not helping .as my THS
Please could anyone let me know if they are on adalat retard 20 mg I have been on adalat la for a few years now the chemist can't get them , I feel very anxious and exhausted on these Meds l have no colour very pale , also muzzy headed .i also have underactive thyroid which is not helping .as my THS
Harrispat
in
Thyroid UK
6 years ago
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New and Confused
Good morning. I have tests coming up that according to my hepatologist, will confirm what she is 95% sure of: PBC. As background, I am 64 years old. I have had Hashimoto's Thyroiditis for 40 years, Crohn's for 12 years, on and off suffering from psoriasis. The Crohn's has been in remission for the
Good morning. I have tests coming up that according to my hepatologist, will confirm what she is 95% sure of: PBC. As background, I am 64 years old. I have had Hashimoto's Thyroiditis for 40 years, Crohn's for 12 years, on and off suffering from psoriasis. The Crohn's has been in remission for the
Chefess
in
PBC Foundation
6 years ago
Endo Fighting Diet - non medical
Hi guys, I have been diagnosed with endometriosis 2 years ago and i had a laparoscopy about a year ago. Symptoms improved after lap but eventually came back after about 6 months. Since then i was put on different pills which had adverse effects so my gynocologist put me on the evra patch so it bypasses
Hi guys, I have been diagnosed with endometriosis 2 years ago and i had a laparoscopy about a year ago. Symptoms improved after lap but eventually came back after about 6 months. Since then i was put on different pills which had adverse effects so my gynocologist put me on the evra patch so it bypasses
Jaas1
in
Endometriosis UK
6 years ago
Positive ANA and history of tests.
Hello, I want to provide a clear history of facts. Last December, I experienced joint pain, my hands were burning for no reason, and my joints were cracking. I felt really run down as well. I ordered my GP (where I had to pay for private referral to rheumy...) to send me there and test me for Sjogren's
Hello, I want to provide a clear history of facts. Last December, I experienced joint pain, my hands were burning for no reason, and my joints were cracking. I felt really run down as well. I ordered my GP (where I had to pay for private referral to rheumy...) to send me there and test me for Sjogren's
darkknightlt
in
LUPUS UK
6 years ago
Positive ANA 1:80
I am currently in the process of doing something about my fatigue, and weird symptoms I had for years. January 2018, I was tested by a rheumy because I was afraid of having Sjogren's. My symptoms were dry mouth at night. I had a lot of antibodies tests then and all of them said negative. I got a referral
I am currently in the process of doing something about my fatigue, and weird symptoms I had for years. January 2018, I was tested by a rheumy because I was afraid of having Sjogren's. My symptoms were dry mouth at night. I had a lot of antibodies tests then and all of them said negative. I got a referral
darkknightlt
in
Thyroid UK
6 years ago
Thyroid issues
Good morning! I am struggling to find some answers about my health as all I can hear from my GP is all blood test are in the range. The most recent blood test I have had done was in April 2018 and the results are as follow: TSH 2.36 mu/L (0.35-5.50mu/L) free T4 13 pmol/L (9.00-22.70pmol/L) free T3 4.2
Good morning! I am struggling to find some answers about my health as all I can hear from my GP is all blood test are in the range. The most recent blood test I have had done was in April 2018 and the results are as follow: TSH 2.36 mu/L (0.35-5.50mu/L) free T4 13 pmol/L (9.00-22.70pmol/L) free T3 4.2
Felly35
in
Thyroid UK
6 years ago
CRPS
i have crps which was caused originally by a cyst on my spinal cord and has given me peripheral pain in both my legs i have had this for over 8 years now and it has been life changing, i have been offered a spinal cord stimulator trial and wanted to know if anyone has had this done and if so what is
i have crps which was caused originally by a cyst on my spinal cord and has given me peripheral pain in both my legs i have had this for over 8 years now and it has been life changing, i have been offered a spinal cord stimulator trial and wanted to know if anyone has had this done and if so what is
vivikin
in
Pain Concern
6 years ago
VATS BIOPSY RESULTS FINALLY
Hi, I have posted a few times. I had a VATS lung biopsy and have a general diagnosis FINALLY. They first told me they were almost sure I had constrictive Bronchiolitis (thanks for those that have it who were so kind and helpful). The biopsy showed Cellular Interstitial Pneumonitis and most likely Hypersensitivity
Hi, I have posted a few times. I had a VATS lung biopsy and have a general diagnosis FINALLY. They first told me they were almost sure I had constrictive Bronchiolitis (thanks for those that have it who were so kind and helpful). The biopsy showed Cellular Interstitial Pneumonitis and most likely Hypersensitivity
rottiro1
in
Lung Conditions Community Forum
6 years ago
CRPC survey
Howdy, I am fairly new here but have gained some very valuable knowledge from lots of folks here sharing their experiences. I became "castrate resistant" just 5 months after being initialky diagnosed with stage 4 PC. I have done many things since then to beat down the constantly rising PSA and even more
Howdy, I am fairly new here but have gained some very valuable knowledge from lots of folks here sharing their experiences. I became "castrate resistant" just 5 months after being initialky diagnosed with stage 4 PC. I have done many things since then to beat down the constantly rising PSA and even more
Grandude58
in
Advanced Prostate Cancer
6 years ago
Hello everybody, this my first post
Well a little about myself first , I'm 44 i was officially under weight as a child until i had my tonsils out when i 4 or 5 then i got to the weight i should be for my age now fast forward to when i was about 8 and I was diagonsed with eczema and the thing that is any good is betnovate but as it is steriods
Well a little about myself first , I'm 44 i was officially under weight as a child until i had my tonsils out when i 4 or 5 then i got to the weight i should be for my age now fast forward to when i was about 8 and I was diagonsed with eczema and the thing that is any good is betnovate but as it is steriods
Northener73
in
Thyroid UK
6 years ago
Blog: July 2018 by Professor Graham R V Hughes MD FRCP
Wonderful. Wall to wall sunshine. Temperatures in the high 80’s and low 90’s. (How deceitful I feel advising my patients to avoid the sun!). This month our monthly medical journal LUPUS, now in its 27th year, received news of its rising ‘impact factor’. The annual ‘impact factor’ is a slightly imperfect
Wonderful. Wall to wall sunshine. Temperatures in the high 80’s and low 90’s. (How deceitful I feel advising my patients to avoid the sun!). This month our monthly medical journal LUPUS, now in its 27th year, received news of its rising ‘impact factor’. The annual ‘impact factor’ is a slightly imperfect
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
6 years ago
Spinal cord stimulator experiences
Hi folks, I am 37 years old and slipped on ice last year, twisted back and my injury was made far worse following physio intervention in which I was asked to lift 5kg weight repetively as quick as I could in a minute. I had an instant flare up resulting in numbness lower back, groin, lower legs ext
Hi folks, I am 37 years old and slipped on ice last year, twisted back and my injury was made far worse following physio intervention in which I was asked to lift 5kg weight repetively as quick as I could in a minute. I had an instant flare up resulting in numbness lower back, groin, lower legs ext
Kerrycop
in
Pain Concern
6 years ago
Advice on blood results anyone?
Hi All. Thank you for letting me join. I'm not actually diagnosed with lupus yet. I have so many medical mysteries that have been going on for so long I that it will be a relief to know what exactly is going on. I've just picked up some latest blood results. Make sense to anyone? ANA Positive. Nucleolar
Hi All. Thank you for letting me join. I'm not actually diagnosed with lupus yet. I have so many medical mysteries that have been going on for so long I that it will be a relief to know what exactly is going on. I've just picked up some latest blood results. Make sense to anyone? ANA Positive. Nucleolar
missmolly55
in
LUPUS UK
6 years ago
Fibroscan liver test report mean 5.69kpa, in LFT SGOT 105 & SGPT 166
Fibroscan liver test report mean 5.69kpa, in LFT SGOT 105 & SGPT 166. Is it normal or something dangerous. what should i do. Thanks in Advance !
Fibroscan liver test report mean 5.69kpa, in LFT SGOT 105 & SGPT 166. Is it normal or something dangerous. what should i do. Thanks in Advance !
Saiyyad
in
British Liver Trust
6 years ago
lengthy struggle to get a diagnosis.
Hi I'm Rachael, 26 from Gloucestershire. I'm currently in the lengthy process of trying to get a definitive diagnosis for Lupus. I've been suffering with symptoms for the past 6 years ranging from extreme fatigue, pains in my lower back, abdomen and many joints, hemiplegic migraines, skin rashes, reactive
Hi I'm Rachael, 26 from Gloucestershire. I'm currently in the lengthy process of trying to get a definitive diagnosis for Lupus. I've been suffering with symptoms for the past 6 years ranging from extreme fatigue, pains in my lower back, abdomen and many joints, hemiplegic migraines, skin rashes, reactive
lovesmoo91
in
LUPUS UK
6 years ago
Latest blood test results
Good Afternoon. I have just picked up these results for my daughter and would be grateful if anyone can give me any idea as to what is going on. The first page of results are in the photo the rest are typed below. I hope this is ok to post them this way as am not really good on the computer. My daughter
Good Afternoon. I have just picked up these results for my daughter and would be grateful if anyone can give me any idea as to what is going on. The first page of results are in the photo the rest are typed below. I hope this is ok to post them this way as am not really good on the computer. My daughter
Catlover3
in
Thyroid UK
6 years ago
Where do I go from here?
Do I just take my Dr's diagnosis? If I had more faith in her I'd be happy, but I'm not so sure. I've had dry eye since very young (maybe since birth but not sure). Diagnosed as a young child. Every singe eye specialist would tell me I'd grow out of it as a child, then as and adult in their expertise
Do I just take my Dr's diagnosis? If I had more faith in her I'd be happy, but I'm not so sure. I've had dry eye since very young (maybe since birth but not sure). Diagnosed as a young child. Every singe eye specialist would tell me I'd grow out of it as a child, then as and adult in their expertise
Eeve
in
The Australian Sjögren's Syndrome Association
6 years ago
Blood Test Results-Confused!
Hi all This is my first post and I will try to keep in brief. I suffered from hair loss and and fatigue which started some months ago, I went to the doctor and the hair loss on my head they believed was stress, when I lost more hair (several patches on my face) I was diagnosed with alopecia. The fatigue
Hi all This is my first post and I will try to keep in brief. I suffered from hair loss and and fatigue which started some months ago, I went to the doctor and the hair loss on my head they believed was stress, when I lost more hair (several patches on my face) I was diagnosed with alopecia. The fatigue
MMHGA
in
Thyroid UK
6 years ago
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