LymeNet Flash: Fibrin and long COVID

LymeNet on Facebook

LymeNet on Twitter

Follow @LymeDiseaseNet

The Lyme Disease Network receives a commission from Amazon.com for each purchase originating from this site.

When purchasing from Amazon.com, please
click here first.

Thank you.

Dedicated to the Bachmann Family

LymeNet needs your help:
LymeNet 2020 fund drive

The Lyme Disease Network is a non-profit organization funded by individual donations.

»	LymeNet Flash » Questions and Discussion » Medical Questions » Fibrin and long COVID

UBBFriend: Email this page to someone!

Author

Topic: Fibrin and long COVID

mlg
LymeNet Contributor
Member # 35383

posted

Fibrin and Long COVID

https://www.nature.com/articles/s41586-024-07873-4?fbclid=IwZXh0bgNhZW0CMTEAAR1e3q7hCJnlZvoaJ7wQsrLqHEnNALSeLLJcVN_TtClMwU5Vl_l3Wr-DmXI_aem_bQrTHQNSiTvLEqukVBnVNg

Posts: 722 | From CA | Registered: Dec 2011 | IP: Logged |

hiker53
Moderator
Member # 6046

posted

thanks, mlg.

--------------------
Hiker53

"God is light. In Him there is no
darkness." 1John 1:5

Posts: 10168 | From Illinois | Registered: Aug 2004 | IP: Logged |

kgg
Frequent Contributor (1K+ posts)
Member # 5867

posted

People can have high levels of fibrin from Lyme as well. It is an immune response. Years ago they called it hypercoagulation. And had a heparin protocol for it. People who couldn't get Heparin used Bromelain on an empty stomach.

Thank you for posting.

Posts: 1844 | From Maine | Registered: Jun 2004 | IP: Logged |

mlg
LymeNet Contributor
Member # 35383

posted

Does anyone know of a doctor that treats with heparin. I am on my 3rd FLCC doctor. They all have small contributions but I think this is a major info. I’d like to try Heparin again. I used Heparin like 10 years ago when I had Lyme, bart, babesia, etc.

Posts: 722 | From CA | Registered: Dec 2011 | IP: Logged |

kgg
Frequent Contributor (1K+ posts)
Member # 5867

posted

I wish I knew. I felt great while on Heparin. But the doc took me off of it after 3 months. Said it was not safe to be on it longer. I was not happy.

David Berg of Hemex labs (now sold, not sure what it is called or exists now) and Dr. Joseph Brewer of Missouri, were the ones that studied it years ago.

I believe they use Proteolytic enzymes now. If at all.

Posts: 1844 | From Maine | Registered: Jun 2004 | IP: Logged |

Printer-friendly view of this topic

The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:

The Lyme Disease Network of New Jersey
907 Pebble Creek Court, Pennington, NJ 08534 USA
http://www.lymenet.org/