LymeNet Home LymeNet Home Page LymeNet Flash Discussion LymeNet Support Group Database LymeNet Literature Library LymeNet Legal Resources LymeNet Medical & Scientific Abstract Database LymeNet Newsletter Home Page LymeNet Recommended Books LymeNet Tick Pictures Search The LymeNet Site LymeNet Links LymeNet Frequently Asked Questions About The Lyme Disease Network LymeNet Menu

LymeNet on Facebook

LymeNet on Twitter




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.

LymeNet Flash Discussion
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 Post New Topic  New Poll  Post A Reply
my profile | directory login | register | search | faq | forum home

  next oldest topic   next newest topic
» LymeNet Flash » Questions and Discussion » Medical Questions » Heparin anyone?

 - UBBFriend: Email this page to someone!    
Author Topic: Heparin anyone?
jarjar
LymeNet Contributor
Member # 8847

Icon 1 posted      Profile for jarjar     Send New Private Message       Edit/Delete Post   Reply With Quote 
I tried Heparin before diagnosed with Lyme for 1 month and didn't feel any difference. My LLMD is big on working with it and I was curious if people that took it long term started noticing difference.
I have one friend that was bed ridden and heparin was what got her out of bed. But I'm not in the bed ridden stage.

Jay

Posts: 805 | From Utopia | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
DR. Wiseass
LymeNet Contributor
Member # 6777

Icon 1 posted      Profile for DR. Wiseass   Author's Homepage     Send New Private Message       Edit/Delete Post   Reply With Quote 
Jay -

If you're not bed ridden - no wonder you're living in "Utopia"! ha!

I've been on heparin 2 separate times.

One time for 9 months and I think it did make a differene.

I just started it again this past month as I supposedly had a TIA and doc wants my blood to be thin. Immediately after starting it, I felt better. Placebo effect? Don't know -- but if you've ever had a TIA or a TIA-like experience, you'd be happy to inject heparin or whatever -- no questions asked!

Did you doc perform a hypercoagulation test on you? Do you have air hunger? Did the doc tell you WHY s/he wanted you on heparin?

I think if you understand WHY you're on various drugs/supplements - it helps with issues of compliance.

Good luck with it - I hope it helps you.

Hugs & [kiss]

--------------------
DR. Wiseass
NOT a real doc - just a real wise  -
 -

Posts: 792 | From USA | Registered: Jan 2005  |  IP: Logged | Report this post to a Moderator
jarjar
LymeNet Contributor
Member # 8847

Icon 1 posted      Profile for jarjar     Send New Private Message       Edit/Delete Post   Reply With Quote 
My first doc checked my fibrogen {sp} and sed rate and thought I would benefit from heparin.

My current LLMD says 90% of his Lyme patients test positive for hypercoagulation and claim patients feel better on it.

At times I do have shortness of breath after exertion if thats what you mean by air hunger.

Posts: 805 | From Utopia | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
Healing in Santa Cruz
LymeNet Contributor
Member # 7798

Icon 9 posted      Profile for Healing in Santa Cruz     Send New Private Message       Edit/Delete Post   Reply With Quote 
I became allergic to it. Its made out of pork. Tests confirmed it.
Posts: 905 | From Santa Cruz,Calif | Registered: Aug 2005  |  IP: Logged | Report this post to a Moderator
karatelady
LymeNet Contributor
Member # 7854

Icon 1 posted      Profile for karatelady     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been on Heparin for almost 9 months. I didn't notice any difference one way or the other (except for the lovely black and blue marks on my tummy and the bumps -- yuck)

I do feel it helps with the thinning blood so the lyme can more easily be rooted out.

Sandy

Posts: 686 | From Northeast Georgia | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
SForsgren
Frequent Contributor (1K+ posts)
Member # 7686

Icon 1 posted      Profile for SForsgren         Edit/Delete Post   Reply With Quote 
I opted not to use Heparin and instead to use the German enzyme formula Rechts Regulat which I feel has done a nice job. www.BioPureUS.com

--------------------
Be well,
Scott

Posts: 4617 | From San Jose, CA | Registered: Jul 2005  |  IP: Logged | Report this post to a Moderator
jarjar
LymeNet Contributor
Member # 8847

Icon 1 posted      Profile for jarjar     Send New Private Message       Edit/Delete Post   Reply With Quote 
Thanks guys for your responses. I appreciate anyone that takes the extra effort to chime in their 2 cents about a treatment.

Jay

Posts: 805 | From Utopia | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
Cate
Member
Member # 8787

Icon 1 posted      Profile for Cate     Send New Private Message       Edit/Delete Post   Reply With Quote 
I've been doing very low dose sublingual heparin for about 3 months and it has given interesting results. I have less muscle stiffness when I'm taking it.

Also, after the first month, I started running low-grade fevers and having lots of lymph symptoms. When I stopped the herparin, the symptoms went away, only to come back again when restarted. Over time, both symptoms got less intense, but haven't yet disappeared.

Besides helping your body access hidden infections, there is also a theory that heparin is a TH1-shifter -- that is, helps the immune system fight intra-cellular infections. See
http://www.anapsid.org/cnd/diagnosis/cheneyis.html

Posts: 47 | From California | Registered: Feb 2006  |  IP: Logged | Report this post to a Moderator
liz28
Unregistered


Icon 1 posted            Edit/Delete Post   Reply With Quote 
If you don't mind "two cents" treatments, you could take a look at vinpocetine. Both Source Naturals and Jarrow market it, and there are probably more versions on the way. It's a derivative of the periwinkle plant that increases oxygen flow in the brain, is given to stroke victims in Europe, and has a good rep in the smart drug community as one of the safer, cheaper products of its kind on the market. You don't have to take more than 5mg per day.

As far as boosting the immune system, you'd probably do just as well on a good zinc/copper supplement for $5.

IP: Logged | Report this post to a Moderator
FoggyLikeLA
Member
Member # 8170

Icon 1 posted      Profile for FoggyLikeLA     Send New Private Message       Edit/Delete Post   Reply With Quote 
My doc uses heparin, he's found that more lyme and CFS patients have a high fibrin count. If your fibrin is too high things have a hard time getting though to your veins for absorbtion including ABX. Plus the fibrin traps nutrience(can't spell..damn lyme), hormones and anything and everything else, including the lyme bacteria. I actually got worse at first when i first started to use it. It helped my brain fog though.
Posts: 31 | From Los Angeles, Ca | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
I had great results on it. I took it for three years and now take the Bolouke, or lumbrokinase instead.

It helped my brain fog, pain, and fatigue....alot.

You can indeed feel worse on it for awhile because if you're on abx, the heparin makes it easier for the abx to get to the cells.

If the blood vessels are clogged with fibrinogen, the abx can't get deep into the cells. That's another reason this therapy helps Lyme patients get well.

I had trouble with the injectable form, but after switching to the sublingual, I did fine.

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
karatelady
LymeNet Contributor
Member # 7854

Icon 1 posted      Profile for karatelady     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lymetoo,

I've been on Heparin about 9 months. If I remember correctly, you're not supposed to be on it any longer than that? Yet you did okay for 3 years?

My doc also puts all us lymies on Lumbrokinase along with the Heparin. I guess I'll find out on my next visit whether she will keep me on both.

The thought that its made out of pork isn't exactly inviting.

Sandy

Posts: 686 | From Northeast Georgia | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
cantgiveupyet
Frequent Contributor (1K+ posts)
Member # 8165

Icon 1 posted      Profile for cantgiveupyet     Send New Private Message       Edit/Delete Post   Reply With Quote 
hmm i find this interesting. After my bladder procedure this is one of the drugs used to irigate my bladder.....might be why i felt better...who knows.

I didnt realize this was used in LD treatment.

--------------------
"Say it straight simple and with a smile."

"Thus the task is, not so much to see what no one has seen yet,
But to think what nobody has thought yet, About what everybody sees."

-Schopenhauer

pos babs, bart, igenex WB igm/igg

Posts: 3156 | From Lyme limbo | Registered: Oct 2005  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hey can't ... I used to instill heparin in my bladder daily [or was it twice a day??]. It really did help with the pain. However, the catheter part kind of caused "more" pain so it sometimes was offset by the heparin.

Karate...Yes, I took it that long. LLMD wanted me to go off but I always whined and said I couldn't take the pain!

I'd skipped doses before and knew what would happen when I stopped the heparin! UGH! Once I got on Xango, I was able to get off the heparin.

I'd never heard of anyone taking lumbrokinase AND heparin at the same time. Guess it doesn't matter as long as you're being monitored.

Sure gets expensive though.

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
karatelady
LymeNet Contributor
Member # 7854

Icon 1 posted      Profile for karatelady     Send New Private Message       Edit/Delete Post   Reply With Quote 
Lymetoo,

One more question - how long were you on the XanGo before you stopped the Heparin.

I guess my question is how would you know when to stop?

Sandy

Posts: 686 | From Northeast Georgia | Registered: Sep 2005  |  IP: Logged | Report this post to a Moderator
pq
Frequent Contributor (1K+ posts)
Member # 6886

Icon 1 posted      Profile for pq     Send New Private Message       Edit/Delete Post   Reply With Quote 
heparin + other blood thinners, of any kind = real bad idea.
Posts: 2708 | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
Lymetoo
Moderator
Member # 743

Icon 1 posted      Profile for Lymetoo     Send New Private Message       Edit/Delete Post   Reply With Quote 
Hmmmm.... I'm not sure. Maybe 6 months?

pq....If you're thinking Xango is a blood thinner, it's not. Mangosteen has anti-inflammatory actions, so I was able to get off the heparin. But I then switched to lumbrokinase for the hypercoagulation. I just wanted to go the natural route.

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

Posts: 96239 | From Texas | Registered: Feb 2001  |  IP: Logged | Report this post to a Moderator
pq
Frequent Contributor (1K+ posts)
Member # 6886

Icon 1 posted      Profile for pq     Send New Private Message       Edit/Delete Post   Reply With Quote 
Tutu,

just caught your post.
i didn't have xango on mind; actually, some how i missed your statement on stopping heparin and going on lumbrokinase.

never did xango, but have it on mind. approx. a year ago, i read a lot on it and looked at one or more molecular structures of some of the ingredients.
looks like good ancillary stuff.
if xango has blood thinning properties,i'm unaware of this.

Posts: 2708 | Registered: Feb 2005  |  IP: Logged | Report this post to a Moderator
   

Quick Reply
Message:

HTML is not enabled.
UBB Code� is enabled.

Instant Graemlins
   


Post New Topic  New Poll  Post A Reply Close Topic   Feature Topic   Move Topic   Delete Topic next oldest topic   next newest topic
 - Printer-friendly view of this topic
Hop To:


Contact Us | LymeNet home page | Privacy Statement

Powered by UBB.classic™ 6.7.3


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


| Flash Discussion | Support Groups | On-Line Library
Legal Resources | Medical Abstracts | Newsletter | Books
Pictures | Site Search | Links | Help/Questions
About LymeNet | Contact Us

© 1993-2020 The Lyme Disease Network of New Jersey, Inc.
All Rights Reserved.
Use of the LymeNet Site is subject to Terms and Conditions.