LymeNet Flash: White matter lesions resolving!

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»	LymeNet Flash » Questions and Discussion » Medical Questions » White matter lesions resolving!

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Topic: White matter lesions resolving!

narrowpath
Member
Member # 15086

posted

Hi all -

Quick update for any who have white matter lesions (I seeing Flyingmom wrote something about this earlier...)

8 months ago after finally being correctly diagnosed with Lyme, I got IV antibiotics for 6 weeks then orals which continue now.

I had 4 full blown lesions on my brain and cervical MRIs and 10 additional hyperintensities.

As of several days ago, my repeat MRI reveals lesions and hyperintensities either STABLE, RESOLVING OR GONE.

My only remaing symptoms are fleeting minor, humming type twitches and scattered paresthesias on my left side. Very minor.

Still waiting to see if these will go away or if they are permanent damage. I do have MANY completely symptom free days now... Stress or eating poorly really bring the symptoms out...

I wanted to post this good news for all other who have similar issues.

And yes, I was orignally diagnosed with MS, even though I kept saying Lyme and had a PICTURE of the bite.

Keep the faith.

Allison

Posts: 43 | From Chicago | Registered: Mar 2008 | IP: Logged |

Tincup
Honored Contributor (10K+ posts)
Member # 5829

posted

Hot diggity dawgs! That is great news! Thanks so much for letting us know.

I am sure folks will be thrilled to hear of your good news and will also be looking forward to having their white matter lesions go POOF!

[Big Grin]

--------------------
www.TreatTheBite.com
www.DrJonesKids.org
www.MarylandLyme.org
www.LymeDoc.org

Posts: 20353 | From The Moon | Registered: Jun 2004 | IP: Logged |

Keebler
Honored Contributor (25K+ posts)
Member # 12673

posted

-

Wonderful. Thanks for taking the time to share hope.

-

Posts: 48021 | From Tree House | Registered: Jul 2007 | IP: Logged |

daise
Unregistered

posted

Hi narrowpath,

Wahoo! Good for you. [spinning smile]

Thank you for sharing that. I wonder how many of us who have had an MRI before treatment, have an MRI after the meds? By that time can most afford it?

I'm thinking that insurance would have no reason to approve it. That's why your story is wonderful to hear.

You're an inspiration! [Razz]

daise

IP: Logged |

Sojourner
LymeNet Contributor
Member # 9424

posted

Such great news!

My husband is MS dx'd and has seen improvement on orals, but IV might be in his future.

We are outside Chicago and am wondering who treated you. A pm would be very appreciated.

Once again, so glad to hear of your betterness [Big Grin]

Posts: 554 | From Naples, Italy | Registered: Jun 2006 | IP: Logged |

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