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Help with latest blood test results and Vit D3 advice
Hello everyone,I would really appreciate any advice regarding my latest fasting blood tests, done before taking my Levothyroxine tablet. I am still on 75mcg Levothyroxine since diagnosed with Hashimoto's in 2010. After my latest post, around Nov 2022, I followed the advice I was given and started taking
Hello everyone,I would really appreciate any advice regarding my latest fasting blood tests, done before taking my Levothyroxine tablet. I am still on 75mcg Levothyroxine since diagnosed with Hashimoto's in 2010. After my latest post, around Nov 2022, I followed the advice I was given and started taking
Griffin43
in
Thyroid UK
5 months ago
Falling platelet counts after achieving Undetectable Minimal Residual Diseaese
Hello folks I completed a course of Venetoclax & Obinituzumab (Gazyva) last March, and happily achieved UMRD (undetectable minimal residual disease). I'm part of a clinical trial, which stopped treatment once I reached UMRD (with a minimum of 6-9 months of treatment); I was treated for 9 months. Have
Hello folks I completed a course of Venetoclax & Obinituzumab (Gazyva) last March, and happily achieved UMRD (undetectable minimal residual disease). I'm part of a clinical trial, which stopped treatment once I reached UMRD (with a minimum of 6-9 months of treatment); I was treated for 9 months. Have
DinosaurDad
in
CLL Support
5 months ago
0.0 beer
Hi,I had a bleed november 2022,since then nothing untill 2 weeks ago. I have in that time drunk a couple of heineken 0.0 beers a week when out. My Doc says no soda based drinks my stomach dosnt like it. Just wondering how i managed sone 14 months with out a problem. I see him every 3 months for blood
Hi,I had a bleed november 2022,since then nothing untill 2 weeks ago. I have in that time drunk a couple of heineken 0.0 beers a week when out. My Doc says no soda based drinks my stomach dosnt like it. Just wondering how i managed sone 14 months with out a problem. I see him every 3 months for blood
Rawai
in
British Liver Trust
5 months ago
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feeling scared
Hi everyone. Im at the really really early stages. Sorry i don’t know all the acronyms yet or what they mean. If there is a glossary can anyone point me in that direction? So far ive had my blood tested while on day 3 of my period & then tested again 7 days prior to my period starting. My first blood
Hi everyone. Im at the really really early stages. Sorry i don’t know all the acronyms yet or what they mean. If there is a glossary can anyone point me in that direction? So far ive had my blood tested while on day 3 of my period & then tested again 7 days prior to my period starting. My first blood
Athena1990
in
Fertility Network UK
5 months ago
Need help
Recently diagnosed with raynauds, I have been diagnosed with autoimmune, lupus 10 years ago, I was diagnosed raynauds 2 days ago when I went to the emergency room doctors. my toes are the only area affected and the pain is unbearable!!! Feeling like big toes are going to burst! Emergency Doctors say
Recently diagnosed with raynauds, I have been diagnosed with autoimmune, lupus 10 years ago, I was diagnosed raynauds 2 days ago when I went to the emergency room doctors. my toes are the only area affected and the pain is unbearable!!! Feeling like big toes are going to burst! Emergency Doctors say
Grammi5
in
Scleroderma & Raynaud's UK (SRUK)
5 months ago
recurrence after 2 years
so I had my CRS/HIPEC operation on 21-Feb-2022 and was classed as CC1 after the op. I know it’s a 37% chance of reoccurrence but was still disappointed to be told this week that I have a recurrence of PMP in my abdomen, part of which has created a lump in the lower left side where the cancer cells have
so I had my CRS/HIPEC operation on 21-Feb-2022 and was classed as CC1 after the op. I know it’s a 37% chance of reoccurrence but was still disappointed to be told this week that I have a recurrence of PMP in my abdomen, part of which has created a lump in the lower left side where the cancer cells have
Petrolhead276
in
Pseudomyxoma Survivor
5 months ago
Back pain
Hi I have for several months a good deal of back pain also radiating down the top half of both legs. I have prostate Mets in these areas but I am beginning to wonder if this pain which is similar to sciatica could be caused by something other than the mets. Any comment’s appreciated. My consultant hasn
Hi I have for several months a good deal of back pain also radiating down the top half of both legs. I have prostate Mets in these areas but I am beginning to wonder if this pain which is similar to sciatica could be caused by something other than the mets. Any comment’s appreciated. My consultant hasn
Rogersw
in
Advanced Prostate Cancer
5 months ago
trying to get a diagnosis
Hi my name is Jane I am new to this site. I've had whole body aches for 20 years I am now 65. I have seen my GP on countless occasions regarding this but to date nothing has been done. I had a disectomy 2014 due to severe sciatica, and an operation for a prolapse bowel. I have arthritis in my thumb
Hi my name is Jane I am new to this site. I've had whole body aches for 20 years I am now 65. I have seen my GP on countless occasions regarding this but to date nothing has been done. I had a disectomy 2014 due to severe sciatica, and an operation for a prolapse bowel. I have arthritis in my thumb
CarrGomm
in
Fibromyalgia Action UK
5 months ago
Excruciating pain
Woke up a week ago with excruciating pain in shoulder neck and arm. Contacted 111 was seen at out of hours and given a pain injection and 350g tramadol and diazepam. 2 days still in agony ,saw gp got another pain injection, give it time .On Wednesday saw doc again ,she increased tramadol gave me naproxen
Woke up a week ago with excruciating pain in shoulder neck and arm. Contacted 111 was seen at out of hours and given a pain injection and 350g tramadol and diazepam. 2 days still in agony ,saw gp got another pain injection, give it time .On Wednesday saw doc again ,she increased tramadol gave me naproxen
Dipkin1962
in
Fibromyalgia Action UK
5 months ago
Help please with blood test results
Hi Everyone, Would appreciate some help on some blood test results please. I’m asking on behalf of my niece who was diagnosed with ME when she was a teenager. She is in her forties now and has had a range of health issues over her life. She has suffered many tummy issues and she believes she now has
Hi Everyone, Would appreciate some help on some blood test results please. I’m asking on behalf of my niece who was diagnosed with ME when she was a teenager. She is in her forties now and has had a range of health issues over her life. She has suffered many tummy issues and she believes she now has
Bookworm63
in
Thyroid UK
2 months ago
Fatigue.. bloods good. Is remission over and SLL back?
SLL 2016 - bloods good, bulky lymph nodesBR x6 rounds 2019 Remission 2024: bloods all good - bad fatigue is back Is remission over, or is it something else? Had a thought: if I took steroids, that would typically 'flush' the CLL cells out of hiding in my lymph nodes.. then a blood test would better
SLL 2016 - bloods good, bulky lymph nodesBR x6 rounds 2019 Remission 2024: bloods all good - bad fatigue is back Is remission over, or is it something else? Had a thought: if I took steroids, that would typically 'flush' the CLL cells out of hiding in my lymph nodes.. then a blood test would better
Shedman
in
CLL Support
5 months ago
High FSH & LH but normal oestrogen - aged 37 still having periods
Has any one else had a high FSH and LH blood result? Oestrogen normal. I’m 37 years old, I have very severe stage 4 Endo and adeno with a lot of bowel involvement, multiple surgeries and excisions but disease continues to return within months. Disease causes infertility so I’ve never had children.
Has any one else had a high FSH and LH blood result? Oestrogen normal. I’m 37 years old, I have very severe stage 4 Endo and adeno with a lot of bowel involvement, multiple surgeries and excisions but disease continues to return within months. Disease causes infertility so I’ve never had children.
Lily1986
in
Endometriosis UK
5 months ago
ESR blood test
just wondering whether anyone knows if Thyroxine affects ESR blood test results. Having taken higher dose of thyroxine for a few weeks now my TSH has reduced considerably from 4.62 to 1.6 but an ESR blood test was done at the same time and is now above the reference range and registered at 24. My previous
just wondering whether anyone knows if Thyroxine affects ESR blood test results. Having taken higher dose of thyroxine for a few weeks now my TSH has reduced considerably from 4.62 to 1.6 but an ESR blood test was done at the same time and is now above the reference range and registered at 24. My previous
Thirtyone
in
Thyroid UK
5 months ago
Update to last post.
As suggested I wrote a request, via Patches, asking for a Gp to refer me to a private endo. I got an appointment for Today to speak to a clincian, who turned out to be a paramedic. He informed me that 'They' do not write referrals to private endos. I would need to approach one myself and if He/She wanted
As suggested I wrote a request, via Patches, asking for a Gp to refer me to a private endo. I got an appointment for Today to speak to a clincian, who turned out to be a paramedic. He informed me that 'They' do not write referrals to private endos. I would need to approach one myself and if He/She wanted
PurpleOliver
in
Thyroid UK
5 months ago
What exclusionary tests should I ask my doctor for? IL-6 inflammation tests? + other random PMR questions
I'm a 44-year old woman fairly confident I have PMR due to the symptoms I've experienced & the dramatic success of prednisone in treating them. (I put a longer backstory in my profile - which I'm assuming you can access.) I worry somewhat about GCA involvement because when my symptoms have been strong
I'm a 44-year old woman fairly confident I have PMR due to the symptoms I've experienced & the dramatic success of prednisone in treating them. (I put a longer backstory in my profile - which I'm assuming you can access.) I worry somewhat about GCA involvement because when my symptoms have been strong
MizDiana
in
PMRGCAuk
5 months ago
EGFR drop
My egfr 4 months ago was 72 now 60, i am fasting since two weeks, i did my blood test during fasting. Does fasting causing egfr drop or something else it could be?
My egfr 4 months ago was 72 now 60, i am fasting since two weeks, i did my blood test during fasting. Does fasting causing egfr drop or something else it could be?
Viky45
in
Kidney Disease
5 months ago
SCT journey update No.2
Hi all, following on from my last post, have just heard from my clinical nurse that they have found three very good donor matches on the registers!! Have been somewhat impatient waiting but as this situation is so new and different for everyone, has been difficult to gauge what is right or wrong. Anyway
Hi all, following on from my last post, have just heard from my clinical nurse that they have found three very good donor matches on the registers!! Have been somewhat impatient waiting but as this situation is so new and different for everyone, has been difficult to gauge what is right or wrong. Anyway
LFCLove
in
MPN Voice
5 months ago
Diagnosing
Has anyone been diagnosed with MS but when they did blood tests there was no inflammation in the blood?
Has anyone been diagnosed with MS but when they did blood tests there was no inflammation in the blood?
ChronicJazzHands
in
MS Society
5 months ago
Diagnosing
My neurologists suspects MS or another auto immune condition based on my symptoms history. Has anyone been diagnosed with MS even of your blood tests did not show inflammation in your body?
My neurologists suspects MS or another auto immune condition based on my symptoms history. Has anyone been diagnosed with MS even of your blood tests did not show inflammation in your body?
ChronicJazzHands
in
My MSAA Community
5 months ago
t3 Monotherapy
Hello everyone, I have been a reader of the forum for a while now and it is nice to know so many other people are struggling with un-resolved thyroid problems. This forum was the first place where I thought wow, these guys get it. I have hypermobile ehlers danlos syndrome, I was diagnosed with MS
Hello everyone, I have been a reader of the forum for a while now and it is nice to know so many other people are struggling with un-resolved thyroid problems. This forum was the first place where I thought wow, these guys get it. I have hypermobile ehlers danlos syndrome, I was diagnosed with MS
Jimjamio
in
Thyroid UK
5 months ago
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