LymeNet Flash: Does anyone have interpretation?

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 » Does anyone have interpretation?

UBBFriend: Email this page to someone!

Author

Topic: Does anyone have interpretation?

cigi
LymeNet Contributor
Member # 6600

posted

Does anyone know symptoms of a moderate global heteregenous hypoperfusion. They think it's from lyme because of neurological symptoms,but psych symptoms are pretty bad. Had + igm 3 bands Igenex in June, 7 bands IGG, but in november from Stony Brook 2 bands in the IGG and none in the IGM and was indetminate - low positive. I know test results aren't reliable - but it's so hard as you know to pinpoint about how long I've had this. Like everyone else, frustration because you could walk around with this for 20+ years and be recently diagnosed only 2 years ago like I was if your lucky to get a diagnosis at all.

I asked in a link earlier regarding hypoperfusion and lyme and got responses to look up and I did - thanks.

Just wondering if anyone got similar reading of their spect scan and what they're symptoms and treatment is. I'm on rocephin daily since November, but had to get off a few days since my wbc dropped.

Thanks much again for all your advice and help.

cigi

Posts: 320 | From Upstate, NY USA | Registered: Dec 2004 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Hi cigi! I don't know a thing about it. Sorry! Just popping in here to say "Don't worry about test results." You know you have Lyme, right?

So continue your treatments and chip away at it one day at a time. I hope your neuro symptoms subside with continued treatment.

------------------
oops!
Lymetutu

Posts: 96223 | From Texas | Registered: Feb 2001 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

Posts: 96223 | From Texas | Registered: Feb 2001 | IP: Logged |

MammaLyme
Frequent Contributor (1K+ posts)
Member # 1257

posted

Get tested by Bowen Research Lab so you know what you have in your blood. They cannot deny the coinfections when they see the pictures. The pictures are the same for the Pfizer pamphlet at: www.lymediseaseinformation.com

Print the pamphlet out and go to www.bowen.org and get the test. This lab just got their patent and are waiting for FDA approval. That is how accurate they are. One test will tell you many things. The best one out there. It saved my life. I had lyme, babesia, HME and HGE. Very, very sick. I kept getting different tests and they kept showing band 41. MDL nothing, BBI- babesia; LUAT-lyme (two out of three); PCR only lyme and so on. I have the white shops on my brain also and they thought I had MS with all of the symptoms. Thank GOD for this test.
It takes $250 as a donation, you get a donation letter and take the amount off of your taxes since they are a 501(c)(3).
Good luck and hope you feel better soon.

Posts: 2173 | From Maryland | Registered: Jun 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/