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Post-covid inflammation
I don't post often, but I have been regularly reading some of the posts for the last couple of years. I really appreciate all of the knowledge that everyone is willing to share! Since my bio contains my story, I won't go into any of those details here other than to say that I have PV (JAK2+) plus
I don't post often, but I have been regularly reading some of the posts for the last couple of years. I really appreciate all of the knowledge that everyone is willing to share! Since my bio contains my story, I won't go into any of those details here other than to say that I have PV (JAK2+) plus
blue_reader
in
MPN Voice
2 years ago
Happy 1st birthday to my stent😊
This time last year i was not a well pup. Stemi in the lad and rushed to hospital with the lights flashing. Didnt know what was happening until they had inserted a stent and cleared the 100%blockage. Surgeon then says "you had a heart attack but we've inserted a stent and fixed the plumbing". At the
This time last year i was not a well pup. Stemi in the lad and rushed to hospital with the lights flashing. Didnt know what was happening until they had inserted a stent and cleared the 100%blockage. Surgeon then says "you had a heart attack but we've inserted a stent and fixed the plumbing". At the
Jules2021
in
British Heart Foundation
2 years ago
Warfarin self-doser experience
This post is for those who take warfarin, and in addition to doing their own testing they also decide on their own dose. I have been taking warfarin, and deciding my own dose, for over 28 years. I had a series of temporary contracts abroad. I became used to self-management, so when I took early retirement
This post is for those who take warfarin, and in addition to doing their own testing they also decide on their own dose. I have been taking warfarin, and deciding my own dose, for over 28 years. I had a series of temporary contracts abroad. I became used to self-management, so when I took early retirement
ILowe
in
AF Association
2 years ago
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Natural alternative to blood thinners
I’m interested to know if anyone takes anything natural to thin blood rather than blood thinners to the strength that a tablet would be. Let me know .
I’m interested to know if anyone takes anything natural to thin blood rather than blood thinners to the strength that a tablet would be. Let me know .
Electricblue1
in
AF Association
2 years ago
Teeth extraction when in AF and on Apixaban advice please
Hi all. I suffer from Af and I am on Apixaban , I need several teeth removed due to an unrelated health condition. I understand the need to stop taking Apixaban 2 days before or what the dentist recommends. However I recall reading that there is an issue with the anaesthetic can someone let me know is
Hi all. I suffer from Af and I am on Apixaban , I need several teeth removed due to an unrelated health condition. I understand the need to stop taking Apixaban 2 days before or what the dentist recommends. However I recall reading that there is an issue with the anaesthetic can someone let me know is
Davidc1075
in
Atrial Fibrillation Support
2 years ago
Blood thinner and hair loss
Hi all, has anyone had hair loss whilst being on Apixaban 5 mg , I was on them before and my hair loss was bad , I’ve been on edoxaban but they tell me it’s not doing much but I don’t understand why and is Apixaban a good one . Sorry for all the questions.
Hi all, has anyone had hair loss whilst being on Apixaban 5 mg , I was on them before and my hair loss was bad , I’ve been on edoxaban but they tell me it’s not doing much but I don’t understand why and is Apixaban a good one . Sorry for all the questions.
Electricblue1
in
AF Association
2 years ago
To antivirals or not to antivirals
ET with CALR, on warfarin and 45mcg Pegasys every 4 weeks. 3 vaccines, last one in November. Just when I started hoping I was going to remain one of the few... COVID got me. I brought my dogs on a long walk on Friday and was convinced I cought a hay fever ln Saturday... as my nose was blocked and I
ET with CALR, on warfarin and 45mcg Pegasys every 4 weeks. 3 vaccines, last one in November. Just when I started hoping I was going to remain one of the few... COVID got me. I brought my dogs on a long walk on Friday and was convinced I cought a hay fever ln Saturday... as my nose was blocked and I
flamboyant_hawking
in
MPN Voice
2 years ago
Was wondering about anemia?
I just had blood work taken by my rheumatologist, and it shows that I am getting anemic again. This happens every 6 months or so. I had all kinds of tests to see if I have cancer, but it is negative (thank goodness). I have had tests to see if I am losing blood (endoscopy and colonoscopy). Both show
I just had blood work taken by my rheumatologist, and it shows that I am getting anemic again. This happens every 6 months or so. I had all kinds of tests to see if I have cancer, but it is negative (thank goodness). I have had tests to see if I am losing blood (endoscopy and colonoscopy). Both show
Willow7733
in
LUPUS UK
2 years ago
Really heavy period after failed FET. Sorry for the TMI!
My transfer date was 25.03.2022. My test date was 13 days later 07.04.2022 which was negative. I took my morning pessaries on the 07.04.2022 because I took them earlier than my clinic was open but then spoke to my clinic afterwards who said to stop them going forward. My first full drug free day was
My transfer date was 25.03.2022. My test date was 13 days later 07.04.2022 which was negative. I took my morning pessaries on the 07.04.2022 because I took them earlier than my clinic was open but then spoke to my clinic afterwards who said to stop them going forward. My first full drug free day was
JadeH92
in
Fertility Network UK
2 years ago
New here, question on blood pressure, fatigue
Hi, great to discover this forum, and read about others' experiences! I was diagnosed with PV and the JAK2 V617F mutation in June 2021, after suffering a heart attack in March '21 due to a blocked artery. Strangely my blood counts in March were not too high, but increased rapidly thereafter, and I was
Hi, great to discover this forum, and read about others' experiences! I was diagnosed with PV and the JAK2 V617F mutation in June 2021, after suffering a heart attack in March '21 due to a blocked artery. Strangely my blood counts in March were not too high, but increased rapidly thereafter, and I was
Sewingtime
in
MPN Voice
2 years ago
Aetiology of AF and Vitamin D deficiency ? Are they related?
I am only 16 months into my so far confusing life journey with AF. I am 75 and otherwise healthy, and not medicated as yet for any health condition. However my latest AF event initiated a blood test which indicated a deficiency of Vitamin D. As seems commonplace these days, sadly I have received no
I am only 16 months into my so far confusing life journey with AF. I am 75 and otherwise healthy, and not medicated as yet for any health condition. However my latest AF event initiated a blood test which indicated a deficiency of Vitamin D. As seems commonplace these days, sadly I have received no
ozziebob
in
Atrial Fibrillation Support
2 years ago
prednisone side effects
Hi everybody! I would be grateful if anyone could help me with this problem .... I live with only one lung from 2018 and of course I am used to living with SOB especially under stress. I state that I am not diabetic, I have an ideal weight and good blood pressure and perfect cholesterol Unfortunately
Hi everybody! I would be grateful if anyone could help me with this problem .... I live with only one lung from 2018 and of course I am used to living with SOB especially under stress. I state that I am not diabetic, I have an ideal weight and good blood pressure and perfect cholesterol Unfortunately
pasquino
in
Lung Conditions Community Forum
2 years ago
Anticoagulation & Mental Health
Hi I was wondering if people have found anticoagulation therapy and of course the reason for anticoagulation triggers any mental health? If so what support did you access ?
Hi I was wondering if people have found anticoagulation therapy and of course the reason for anticoagulation triggers any mental health? If so what support did you access ?
KivetonGuy
in
Anticoagulation Support
2 years ago
Surgery when suffering from AF and on blood thinners
Can anyone help, I need to have my gall bladder removed. I'm I'm persistent AF going from 40 to 140 bpm in a minute or so. This is bought on on when I have pains in my stomach and have also suffered from.IBS most of my adult life. Has anyone else had experience of having an operation whilst being in
Can anyone help, I need to have my gall bladder removed. I'm I'm persistent AF going from 40 to 140 bpm in a minute or so. This is bought on on when I have pains in my stomach and have also suffered from.IBS most of my adult life. Has anyone else had experience of having an operation whilst being in
Davidc1075
in
Atrial Fibrillation Support
2 years ago
Having a tooth out
I am going to have a tooth extraction the dentist was worried that I am still on blood thinners to help with my stent fitted in April 2021 ( coming off these tablets which I take twice a day end of this month) The tooth is a large tooth at the back as I said the dentist was worried about the bleeding
I am going to have a tooth extraction the dentist was worried that I am still on blood thinners to help with my stent fitted in April 2021 ( coming off these tablets which I take twice a day end of this month) The tooth is a large tooth at the back as I said the dentist was worried about the bleeding
Chelsea55
in
British Heart Foundation
2 years ago
Any risks when going to the dentist while on Imbruvica?
As I heard that Imbruvica works as a blood thinner
As I heard that Imbruvica works as a blood thinner
AshGS
in
CLL Support
2 years ago
BB on the road
Ok lets get the tabs out of the way, Stilton 40mg Pred, also statins and blood thinners, done. Been noticing recently ( by the way I have flat foot ) which is on my left which is also the same leg as my total knee replacement. Apart from walking round looking like Michael Flattly ( river dance man)
Ok lets get the tabs out of the way, Stilton 40mg Pred, also statins and blood thinners, done. Been noticing recently ( by the way I have flat foot ) which is on my left which is also the same leg as my total knee replacement. Apart from walking round looking like Michael Flattly ( river dance man)
Burnley1959
in
PMRGCAuk
2 years ago
Update
My wife Stage 4 lung cancer, spread to liver and bones. Was admitted to hospital yesterday in terrible pain for days. NO treatments (radiation for bones, chemo for the lungs) to start before 2 weeks. CT results now show blood clots in the lungs. Giving her blood thinners by needle in her stomach, and
My wife Stage 4 lung cancer, spread to liver and bones. Was admitted to hospital yesterday in terrible pain for days. NO treatments (radiation for bones, chemo for the lungs) to start before 2 weeks. CT results now show blood clots in the lungs. Giving her blood thinners by needle in her stomach, and
Enair
in
The Roy Castle Lung Cancer Foundation
2 years ago
Esophageal thrush
I would be grateful for any information,I had an endoscope and was diagnosed with esophageal thrush I am on warfarin and all of the medication is contraindicated with warfarin.My GP is concerned as the consultant didn't recommend anything and yet it has to be treated as to leave it could be determental
I would be grateful for any information,I had an endoscope and was diagnosed with esophageal thrush I am on warfarin and all of the medication is contraindicated with warfarin.My GP is concerned as the consultant didn't recommend anything and yet it has to be treated as to leave it could be determental
charlie007
in
LUPUS UK
2 years ago
Advice
or to take me off warfarin altogether and use one of the newer
anticoagulants
I take high dose warfarin to protect my nervous system I have a demyelinating disease cause by an underlying vascular disorder Has anyone heard of the vitamin K treatment for fluctuating INR ?Thanks
or to take me off warfarin altogether and use one of the newer
anticoagulants
I take high dose warfarin to protect my nervous system I have a demyelinating disease cause by an underlying vascular disorder Has anyone heard of the vitamin K treatment for fluctuating INR ?Thanks
mully
in
Hughes Syndrome APS Forum
2 years ago
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