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Cpn and specific diseases
tuftyone
13 Jun 2018

Got to get worse before getting better, right?

only been taking abx for three days and my walking is terrible. I should expect things like this? Will doing Epsom salt foot baths help get rid of toxins?

boadicea

13 Jun 2018 11:37 am

Sounds fairly typical to me. Yes, things get worse before they get better. And it tends to be a constant 'two steps forward, one step back'. We get used to reminding ourselves that here! Epsom salt baths and footbaths definitely helped me. But always start steady and build up, as even detoxing can make you feel worse at first.

 

Neuro symptoms & many health problems from 1989. NAC+all supps(04/11) CAP(05/11)

tuftyone

13 Jun 2018 11:40 am

I’m just surprised to feel like this so soon!

Diagnosed RRMS 1999. No DMDs or other meds. Have done TMJ correction, Candida protocol, CCSVI venoplasty procedure.

tuftyone

13 Jun 2018 02:55 pm

To be honest I’m not taking NAC currently as it makes my rosacea a lot worse. I know I should be taking it and this might help die off (that’s actually a question for someone ?)

Diagnosed RRMS 1999. No DMDs or other meds. Have done TMJ correction, Candida protocol, CCSVI venoplasty procedure.

katman

23 Jun 2018 04:28 pm

I am....taking my NAC, that is.  Twice a day  - every day.  Why  are you not?  Did someone tell you this is "easy as pie"?  Someone  else said it is so worth it. So...just do it.  Every day.

Rica

3/9 Symptoms returning. Began 5 abx protocol 5/9 Rifampin 600, Amox 1000, Doxy 200, MWF Azith 250, flagyl 1000 daily. Began Sept 04 PPMS EDSS 6.7 Now good days EDSS 1 Mind, like parachute, work only when open. Charlie Chan  In for the duration.&am

Sarah

23 Jun 2018 06:01 pm

Rica, I told him not to worry because it isn't  needed whilst taking the bacteristatics. I didn't start it until about 14 months, as I said just below here!

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.
Sarah

13 Jun 2018 03:44 pm

I didn't start taking it until I had started on intermittent protocol, so don't worry: if you are taking the two bacterial synthesis inhibitors you don't really need the NAC.

Completed Stratton/Wheldon regime for aggressive secondary progressive MS in June 2007, after four years, three of which intermittent.   Still improving bit by bit and no relapses since finishing treatment.
tuftyone

15 Jun 2018 05:40 pm

I really can’t believe I’m feeling this bad after only five days of abx and next week I plan to increase the dose and introduce the other one. Today I can barely put weight on my left hip. Just read another thread about die off and this appears to be quite normal and shows the abx are killing something but I’m naturally still worried

Diagnosed RRMS 1999. No DMDs or other meds. Have done TMJ correction, Candida protocol, CCSVI venoplasty procedure.

boadicea

15 Jun 2018 06:30 pm

Tuftyone - I really wouldn't rush into increasing doses or introducing the next abx until you feel you are tolerating this one at the current dose. You need to listen to your body. Remember - it's a marathon, not a sprint. 

Neuro symptoms & many health problems from 1989. NAC+all supps(04/11) CAP(05/11)

tuftyone

15 Jun 2018 06:56 pm

Thank you you’re quite right. No point in rushing things 

Diagnosed RRMS 1999. No DMDs or other meds. Have done TMJ correction, Candida protocol, CCSVI venoplasty procedure.

Barcelona

17 Jun 2018 06:24 am

Boadicea... I will take your sentence... "it's a marathon, not a sprint."

It is a beautiful way to describe it. :)

 

Gisel·la

(ONGOING PROTOCOL: 1 full year Protocol with 6 full Metro pulses)

MS Diagnosed: 21.IX.2016

 

JaneK

17 Jun 2018 10:12 am

tuftyone,

you wouldn’t be human, if this didn’t scare you. Katman gave me some good advice, when I was still early in my treatment, i was lucky, just Doxy and Roxy gave me the ability to walk  further and faster, BUT not for long, and, yes it has been 2 steps forward  and one back, ever since. And now, a year and a bit later, improvement continues in the same way, but, i’ve been able to do so much more than for years!   Keep strong and not disheartened. You’ve made the first step, and you must know how the Chinese proverb goes, this journey is long, but, you’ve begun! Congratulations!

MS symptoms from 2001, DX RRMS in 2008, following, a change of hospital who sent me for an MRI, precipitated by some sight loss. Took Interferons, on and off. Prescribed  chemo infusions to slow pro

tuftyone

1 Jul 2018 03:13 pm

Headache, nausea general malaise... die off? I felt really good last week!

Diagnosed RRMS 1999. No DMDs or other meds. Have done TMJ correction, Candida protocol, CCSVI venoplasty procedure.