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Confused
I have just been diagnosed with PBC. My AMA was double and my alk phos was elevated with the lab work my family doctor ordered. She then referred me to a GI dr who ordered more blood work and put me on ursoliol... I just received my lab work on line....everything that he ordered was normal !! Except
I have just been diagnosed with PBC. My AMA was double and my alk phos was elevated with the lab work my family doctor ordered. She then referred me to a GI dr who ordered more blood work and put me on ursoliol... I just received my lab work on line....everything that he ordered was normal !! Except
Blessed123
in
PBC Foundation
6 years ago
I’d like to introduce myself
New here and want to share my history with you. On Dec 2015 went to primary doctor due to sore throat and while there told him “oh by the way, my index finger is swollen and really hurts.” Sent me to a rheumatologist who thought I had psoriatic arthritis ( I have2 brothers with that) and started me
New here and want to share my history with you. On Dec 2015 went to primary doctor due to sore throat and while there told him “oh by the way, my index finger is swollen and really hurts.” Sent me to a rheumatologist who thought I had psoriatic arthritis ( I have2 brothers with that) and started me
sara1215
in
NRAS
6 years ago
Final Test Results in including Free Thyroxine.... am I converting efficiently??
My Doctor sent me for tests (see results below) and which very helpful and knowledgeable Seaside Susie commented upon. Unfortunately the doctor did not ask for my Free Thyroxine to be tested so I had to get that done via Medichecks. My suspicion is that I am not converting very well. Medichecks TSH 1.99
My Doctor sent me for tests (see results below) and which very helpful and knowledgeable Seaside Susie commented upon. Unfortunately the doctor did not ask for my Free Thyroxine to be tested so I had to get that done via Medichecks. My suspicion is that I am not converting very well. Medichecks TSH 1.99
Dotty1340
in
Thyroid UK
6 years ago
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Spike in RBC. What does it mean?
I am 56. Diagnosed straight to advanced stage 4 in July 2017. PSA 11 and discovered due to severe nerve back pain. Extensive spine Mets. I started ADT within days and chemo within a week. Did 10 rounds and ended in february 2018. End of chemo my PSA was 0.01 and scans showed no remaining visible Mets
I am 56. Diagnosed straight to advanced stage 4 in July 2017. PSA 11 and discovered due to severe nerve back pain. Extensive spine Mets. I started ADT within days and chemo within a week. Did 10 rounds and ended in february 2018. End of chemo my PSA was 0.01 and scans showed no remaining visible Mets
BigM62
in
Advanced Prostate Cancer
6 years ago
Fibromyalgia: A Primary Care Approach
Fibromyalgia: A Primary Care Approach
Veronica Hackethal, MD Jun 26, 2018
Fibromyalgia
Patient resources include the University of Michigan FibroGuide and the Arthritis Foundation patient information page. Fibromyalgia is a controversial condition. There is no clear cause, no definitive
Fibromyalgia: A Primary Care Approach
Veronica Hackethal, MD Jun 26, 2018
Fibromyalgia
Patient resources include the University of Michigan FibroGuide and the Arthritis Foundation patient information page. Fibromyalgia is a controversial condition. There is no clear cause, no definitive
lupus-support1
Administrator
in
LUpus Patients Understanding and Support
6 years ago
Second opinion?
Hi This is my first post so please bare with me. Can anybody help me with symptoms I’m having and test results. I saw a rhuematologist yesterday who didn’t listen at all and completely dismissed my test results, diagnosed me with fibromyalgia within 5 mins - I’ve been unwell for over 3 years and seen
Hi This is my first post so please bare with me. Can anybody help me with symptoms I’m having and test results. I saw a rhuematologist yesterday who didn’t listen at all and completely dismissed my test results, diagnosed me with fibromyalgia within 5 mins - I’ve been unwell for over 3 years and seen
Littlemisssunshine87
in
LUPUS UK
6 years ago
Advice please on latest Test Results
Dear All, I had a telephone consultation with my doctor recently as I have started to feel very tired again and not myself. He reluctantly agreed to the full range of tests including T3. I had to quote Thyroid UK in order to argue my case for testing T3. The results are as below...please can someone
Dear All, I had a telephone consultation with my doctor recently as I have started to feel very tired again and not myself. He reluctantly agreed to the full range of tests including T3. I had to quote Thyroid UK in order to argue my case for testing T3. The results are as below...please can someone
Dotty1340
in
Thyroid UK
6 years ago
Xtandi
My husband was diagnosed with stage 4 prostate cancer 2 1/2 years ago. He was on casodex 18 months and then switched to Xtandi one year ago. His PSA was never more than 4 but alk phos was 4000. His PSA has been < .1 for two years but last month it was .2. Doctor doesn’t think it’s significant but articles
My husband was diagnosed with stage 4 prostate cancer 2 1/2 years ago. He was on casodex 18 months and then switched to Xtandi one year ago. His PSA was never more than 4 but alk phos was 4000. His PSA has been < .1 for two years but last month it was .2. Doctor doesn’t think it’s significant but articles
Bball
in
Advanced Prostate Cancer
6 years ago
blood results
High have been recently diagnosed with under active thyroid and am doing six weekly blood tests, and level is going down last result was Serum TSH level 3.8 miu/L [0.2 - 5.5] taking 75 Levothyroxine but feeling rubbish at the moment tender neck rough dry throat and shortness of breath. may not be connected
High have been recently diagnosed with under active thyroid and am doing six weekly blood tests, and level is going down last result was Serum TSH level 3.8 miu/L [0.2 - 5.5] taking 75 Levothyroxine but feeling rubbish at the moment tender neck rough dry throat and shortness of breath. may not be connected
Dianejackson
in
Thyroid UK
6 years ago
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
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
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