LymeNet Flash: My headaches are gone!!

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»	LymeNet Flash » Questions and Discussion » General Support » My headaches are gone!!

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Topic: My headaches are gone!!

savebabe
Frequent Contributor (1K+ posts)
Member # 9847

posted

Yup...after years of fighting this disease I finally got rid of my headaches. I found that aggressive treatment, rest and stopping all pains meds, especially the ones that included caffeine, has done the trick.

I just wanted to post this success story for others who are disabled from head pain.

Feel better everyone.

Posts: 1603 | From ny | Registered: Aug 2006 | IP: Logged |

Lymetoo
Moderator
Member # 743

posted

That's cool!! Mine are gone too after years and years of migraines.

I think mine are gone due to treatment of babesia.. not sure.

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

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

laurie sm
LymeNet Contributor
Member # 14584

posted

That's great news.

I am treating for babesia now but basically feel like I am ready to die from neuropathic pain and nausea.

I had the worst headaches of my life 2 weeks ago and now thankfully they are somewhat better

The burning pain is the worst!!

How long did you treat for?

Posts: 256 | From long island, new york | Registered: Feb 2008 | IP: Logged |

bettyg
Unregistered

posted

...

babe...WAY TO GO FINALLY!! please copy this post to SUCCESS STORIES at top of page.

this is what others need to learn too and give them HOPE! [group hug]

IP: Logged |

savebabe
Frequent Contributor (1K+ posts)
Member # 9847

posted

I had headaches for years and years. I found that aggressive abx treatment including babs treatment helped, and stopping all pain meds.

It seems that I was medicating my pain for so long that I caused rebound headaches that I thought were lyme headaches.

As for the burning sensations, levaquin reduced all my neuropathy. I never tested positive for bart, but I would suggest to treat this infection as well.

FYI- bart is found on long island more than lyme disease, so if you were bitten in NY I would recommend get testing and start treating bart.

Posts: 1603 | From ny | Registered: Aug 2006 | IP: Logged |

laurie sm
LymeNet Contributor
Member # 14584

posted

savebabe- How did you treat for Bart? What were your symptoms of Bart?

Is neuropathic pain one of its symptoms? Mine is very bad as is my brain haze.

I was originally diagnosed with bart tru Fry but only been treated for 6 months with zithromax.

New LLMD has found Babesia w-1 and is treating that now. He is not sure I have Bart as he doesn't believe in Fry testing.

I tend to disagree with him.

Laurie

Posts: 256 | From long island, new york | Registered: Feb 2008 | IP: Logged |

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