15 Years of Warfarin: Been on warfarin... - Hughes Syndrome A...

Hughes Syndrome APS Forum

10,443 members10,641 posts

15 Years of Warfarin

petert223hkj profile image
5 Replies

Been on warfarin which has always been up and down but am blessed with a great group of Phlebotomists at beacon medical in Plymstock who have all been very caring. To answer to the pain problems as we cannot use Voltarol but have been prescribe 5% ibuprofin gel which helps but not totally. Still have to thank God ,all the medics and my wife's care that I am still alive with my metal heart valve which ticks away thankfully

A good saying is you lay down and die or get up and fight!

Written by
petert223hkj profile image
petert223hkj
To view profiles and participate in discussions please or .
Read more about...
5 Replies
Lure2 profile image
Lure2

Hi,

I wonder if you fight against a diagnosed Antiphospholipidsyndrome?

petert223hkj profile image
petert223hkj in reply toLure2

HI

I am not familiar with you problem but a quick read shows it is very serious. My comment about get up and fight is about trying to encourage a positive attitude to life's problems which when you are down can be helpful

Lure2 profile image
Lure2 in reply topetert223hkj

Why I asked is because this is a site which focus on Antiphospholipidsyndrom which we all have here. Before diagnosed and also afterwards we have to fight hard to be believed and to get a Specialist of autoimmun illnesses who understands that we all have too thick blood which has to be thinned to avoid a lot of dangerous symptoms and further trouble.

APS is a rare illness and that is the tragic thing for us, as so very few Doctors know about it. Exercise for example is one of the best ways to feel better. That makes the blood flow easier.

You are quite wright a positive attitude to life´s problems are always helpful!

Best wishes from Kerstin in Stockholm

Fra22-57 profile image
Fra22-57

Don't know if this might help you but you can get 10% ibuprofen gel

MaryF profile image
MaryFAdministrator

Have you got a Hughes Syndrome/APS specialist helping with your care? MaryF

Not what you're looking for?

You may also like...

Warfarin andBleeding

I was taken into hospital 3 days ago with a PR bleed, first they did was stop my warfarin....
Sue2803 profile image

the bugbears of warfarin

Looks like my biopsy for tomorrow which I have geared myself up to isn't going to happen as my inr...
panda60 profile image

Triple Positive/Warfarin

Hi, I am confused and wanted to see if anyone who is triple positive without a clot is on blood...
rottiro profile image

Aneurysm and Warfarin

Hi all, I was diagnosed with APS in January and am on warfarin now. My INR rarely gets above 2 and...
minnime63 profile image

Warfarin

I have been on Warfarin for the last 10 years and was told I will be on it for life. My INR,...
Kentish_Man profile image

Moderation team

See all
KellyInTexas profile image
KellyInTexasAdministrator
MaryF profile image
MaryFAdministrator
lupus-support1 profile image
lupus-support1Administrator

Content on HealthUnlocked does not replace the relationship between you and doctors or other healthcare professionals nor the advice you receive from them.

Never delay seeking advice or dialling emergency services because of something that you have read on HealthUnlocked.