Cpnhelp.org

Two tabs more and my first pulse is done! I've been lucky,  although I may not be, in future! I've been, a little, nauseous, I've been tired, but not horribly fatigued, as before, my remaining sight has been dreadful and my, already dodgy, leg turned to lead! And I've laughed at It all! I have also felt invincible! Doing something positive is so much more empowering than just allowing MS to do its worst! CPN is cruel, self-worth is powerful And good!

Hi.  I took 2400mg of NAC for 3.5 weeks without any symptoms, flu like or other.  Then WHAM.  I got the mac daddy of colds (and in the summer).  Major runny nose, sneezy, congestion....but no fever of any kind.  The last time I had a cold was 6 years ago.  Could this have been a delayed NAC flu reaction?  I ask, because it seems like most people noticed symptoms almost immediately after taking NAC.  It took me several weeks, and it's possible it was just a legimate (and long overdue) cold.

Half way through first pulse and stomach is unhappy... abdo pains, gas, urgent need for toilet,  softish stools(but still formed)...    Also headaches... and feeling punched in face with eyes trying to pop out(sinus?)lack of appetite, feeling poorly HR up...Def harder than tinidazole...

Well there is a country wide shortage of tinidazole... no solid eta... so... I'm starting my first metronidazole pulse...  Should be interesting...

Not sure if I missed one or plugged on...So I'm up to either 30 or 31 pulses with 26 or 27 full 5 day pulses...My excuse(poor I know) is that I caught some terrible respiratory infection in early new year... Took me weeks to stop coughing and breath well again...

it's been more than three months and I start the third ABX next week. Overall, I feel OK, but my heat intolerance and functional weakness / dropfoot.iinmy left leg, seem worse. What are other people's experiences, at this stage?

https://medicalxpress.com/news/2017-07-hidden-herpes-virus-key-role.html

One of my struggles as I worked towards wellness was that I continually 'Herxed', but actually I was really just very toxic and overloading my excretion systems.  After 3 years of trial and error and much suffering I have found the key to this toxicity.  Apparently I am a genetically super sluggish detoxer - not a good place to be.  Everything that makes you better makes you worse.  I found this presentation by Dr Chris Shade, a mercury detox specialist, who maps out the whole detox system so that you can get each part working in sequence so that you don't re-tox yourself and do more damage.https://www.youtube.com/watch?v=gITuONNWWK8&t=2091s

Hi, everyone.  Since there's nothing much going on here (though there's lots of work going on behind the scenes to update our site), I thought I'd tell you a little story.After a lifetime of fighting what I thought was chronic fatigue, a bout of optic neuritis got me an MS diagnosis in 2005.  As most of you know, I did the protocol for six or seven years.  Within months, I knew it was helping, when NOTHING had helped up til then. 

Chills yesterday afternoon.  Had to call care attendent to help me get in bed.  She left my powerchair with the front casters sticking out forward.  I felt okay when I got up around 5:30am...weak, but somewhat mobile.  Used my walker to move over to the powerchar and got my legs all tangled in the wheels.  Hit the floor.No damage done, but had to call the troups to lift me off the floor.