LymeNet Flash: HEPARIN

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 » HEPARIN

UBBFriend: Email this page to someone!

Author

Topic: HEPARIN

TTLav
LymeNet Contributor
Member # 33232

posted

My LLMD wants me to start heparin shots subcutaneously 2x a day -because of micro circulation in both arms caused by autonomic nervous system

-causing numbness tingling pain in arms and hands with extremely cold hands- and hands can be to painful to hold a cup.

I know it is a anti coagulant
Need any thoughts?????

Posts: 109 | From Western Massachusetts | Registered: Aug 2011 | IP: Logged |

TTLav
LymeNet Contributor
Member # 33232

posted

Also Im always cold and all lab work is normal -!!!

Posts: 109 | From Western Massachusetts | Registered: Aug 2011 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

I was like that also .. for two summers I never wore shorts because I was cold.

Now I'm on thyroid meds and I'm toasty warm! My tests never came back low .. always low normal. I'm on a very low dosage of Nature Throid and my Raynaud's is way better too!

It will be interesting to see how I do this winter!

As for the heparin, I took the shots about 12-13 years ago. I did the troches after a few months of the shots. I reacted to something in the shots.

They helped with brain fog, pain and fatigue.

but really .. look deeper into the thyroid issue. There's a Facebook group called "Stop the Thyroid Madness."

--------------------
--Lymetutu--
Opinions, not medical advice!

Posts: 96222 | From Texas | Registered: Feb 2001 | 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/