___________________________________________________________
Prague, The Czech Republic, on CAPi from December, 2005. Diagnosis before the treatment: chronic fatigue syndromeii, chronic glandular fever and Epstein-Barr virus (EBVii), cHSP60 (chlamydia heat schock proteinii) + 4,8.
Driving a car while being on the CAP?
Submitted by Zdenicka on Sat, 2008-07-05 11:42. Dear all,
even I am 3 years on the CAPi, I am not sure, if I can give an answer on one question.
Is it possible to drive a car everyday while being on the CAP? I know that many people had not so strong reactions as I had for example, but .... anyway, they might come later, am I right? Is there anybody, who started the CAP and was not limited in his activity by the treatment? My friend drives almost everyday of about hundreds of km and I am afraid how it would be on pulses for example .... I am afraid (according to my experiences) that it would be dangerous .... but I would like to hear your opinions. Thanks a lot.
»
- Login or register to post comments
- Email this page
- Printer-friendly version
Zdenicka, about four months
___________________________________________________________
98% well and going for 100! CAPi since 8-05 for Cpni and Mycoplasma P. for MSi and/or CFSi Also EBVi and HHV6 My grateful thanks to all the CAP docs!!!
I didn't drive the first
___________________________________________________________
The difference between what we do and what we are capable of doing would suffice to solve most of the world’s problems. Mohandas Gandhi
Zdenika, In my opinion it
Zdenika, In my opinion it would be hard to tell prior to treatment how a person will react or be able to tolerate treatment and preform complex activities such as driving. Personally, early on Brain Fog was a factor in my choosing not to drive at times. I was taking bateriocidal dosage of Doxycycline (high dose, 400 mg/day per order of MD) and die-off and porphria were both contributing to my situation. For me at times it seemed unsave to drive.
My observation, after reading these pages for the past year is that the type of presentation of chronic illness that one has been dealing with has some relevance in the downtime one experiences. For me the first 4 months were the most difficult. And changing from high dose mono abxi (high dose doxy alone) to Doxy/Roxi CAPi was much easier on me. When I started Tinidazole pulses I also started cholestyramine with the pulse so cannot say how it would have been for me had I not had that anti-porphrin measure in place. I continue to use cholestryamine intermittently as needed with or without pulse when I begin to feel signs of increasing brain fog and the other porphria symptoms.
Thanks for asking this question and nice to hear from you again. Louise
___________________________________________________________
Louise-CFSi, CPN+/Bb+ Wheldon CAPi 6/07, Cholestyramine1-2pksHSforPorphoria& Endotoxinsi, Doxy100daily,Roxi300BID,Tini500mgBIDpulses,VitD3-4000IU,MagnascentIodine,{S.O.D.3/QD[KAL Brand],+Pyruvate3.75G+SAM-eForEnergy}
I know, I only wanted to
___________________________________________________________
Prague, The Czech Republic, on CAPi from December, 2005. Diagnosis before the treatment: chronic fatigue syndromei, chronic glandular fever and Epstein-Barr virus (EBVi), cHSP60 (chlamydia heat schock proteini) + 4,8.