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11-23-2009, 05:17 PM
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New Member
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Just joined Neuro Talk. I find this CCSVI discovery amazing. Is there suggested methods towards fast tracking this procedure?
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11-23-2009, 07:02 PM
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Magnate
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Quote:
 I called my GP today and made an appointment, but the secretary said that to see a vascular doc will require referral. I'm not sure the waiting list here for vascular specialists.Won't see my GP till Dec. 18 as it is.. I may call offices of vascular doctors regardless of GP and run it by several secretaries. I'm skipping my neuro on this and letting HIM call me if he catches on, since my last words in his office were "contact me if there's a big breakthrough or orals become available". We'll give him time though  Welcome to Neurotalk Kazzman, nice to meet you 
__________________
2004 to present - Trigeminal Neuralgia 2007 to present - Burning Mouth Syndrome March 2008 - Multiple Sclerosis DX 05/2008 - Relapse 05/2008 to 02/2009 - Copaxone 10/2011 - Relapse - Optic Neuritis developed 9/2012 - Relapse - Balance issues 1 sided 8/2012 - Erythema Nodosum - diagnosed 10/2012, reaction to Topiramate (Topamax) April 7/14 - Raynaud's Syndrome DX |
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11-23-2009, 07:25 PM
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Wise Elder
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Not sure about the fast tracking. I would think the pharmaceutical companies would put up a pretty good fight against that since they may lose lots of $$$$'s. Sadly, it's not about the patient. |
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