Bb does look to trigger "self destruction" - to its own advantage.
Posts: 9424 | From Sunshine State | Registered: Mar 2001
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joalo
Frequent Contributor (1K+ posts)
Member # 12752
posted
-------------------- Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006. Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007
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joalo
Frequent Contributor (1K+ posts)
Member # 12752
posted
My husband had plamapharesis in 2007 and again in 2009 for CIDP. Which is the chronic form of GB. He had five sessions. One every other day for ten days, both times.
He also had five days of IVIG in 2007 and again in 2009.
He still has lyme, bart and possibly babs.
-------------------- Sick since January 1985. Misdiagnosed for 20 years. Tested CDC positive October 2005. Treating since April 2006. Posts: 3228 | From Somewhere west of the Mississippi | Registered: Aug 2007
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Marnie
Frequent Contributor (5K+ posts)
Member # 773
If you want to go the Rx route to deal with the inflammatory component:
The Food and Drug Administration has approved a medicine, Lovaza, which can deliver higher doses of EPA and DHA--but only with a doctor's prescription.
Posts: 9424 | From Sunshine State | Registered: Mar 2001
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Tracy9
Frequent Contributor (1K+ posts)
Member # 7521
posted
I am looking into this for treatment of small fiber neuropathy. I have had some problems with IVIG with my body possibly rejecting the donor plasma. I thought that plasmapheresis also involves donor plasma, doesn't it?
13 years Lyme & Co.; Small Fiber Neuropathy; Myasthenia Gravis, Adrenal Insufficiency. On chemo for 2 1/2 years as experimental treatment for MG. Posts: 4480 | From Northeastern Connecticut | Registered: Jun 2005
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