Being I am a thrombofeliac this interests me.
I have had three DVT's and four pulmonary embolisms and one renal embolisms and suffer from post thrombotic syndrome in both legs.
Having gone through some secondary complications due to long term Coumadin therapy (rat posion), in which I got severe Osteoporosis and had a collapes
fracture of T12 with a wedge deformity in Nov 06.
The adverse effect on Vit K is the culprit although two doctors knew nothing of severe bone loss and long term coumadin therapy or heparins. Vit K
plays many roles in the body, one being clotting, another being bone growth.
This too was not something I had ever seen in the compendium and sure enough its not there but it is in the literature I found on the web. The amount
was around 15% based on different studies on women, men and children, which is clincal significant and should be under the adverse effects for
coumadin, but it is not!
Thats not right.
Be that as it may, it just goes to show u, now matter how much you know (I am a registered medical professional in ontario) and how much your doctors
know and no matter what you think you may know.....
we all know so little.
I decided against the advice of my medical team to quit coumadin last month and tried 8 natural alternatives together for a month.
Well that did not work.
DOOH!
I have been put on Low Molecular Weight Heparin again via stomach injectioins as I have my third DVT in my left common femoral and the Illiac vein.
The clot goes from my hip to just above my knee.
I am requesting life time LMW Heparin for my condition vs Coumadin.
The compendium info on coumadin is not good.
This is about even lower weight Heparins, 4 chain molecules and some promising studies
www.hinduonnet.com...
There was another drug in FDA trials for blood clotting but it caused some liver failure and it was stopped.
Bummer.
What is your experinece with long term blood thinners?
[edit on 23-5-2007 by junglelord]