Any advice for recovery from CDS enema?

Hello,

Sorry for any note of desperation in my message here, it's not like me, but 25 years of ebbing and flowing chronic illness can really mess with you...

I recently discovered ClO2 and immediately resonated with what I was hearing, quite convinced of having Lyme coinfections, not least because I had tick bites when my immune system was already compromised from you know what.

I started working towards Kalcker's protocol C on 28th of February, starting with 1mL and adding 1mL each day. My immediate response was incredibly positive: better energy, cognition, even having a feeling of energy and vitality through my core when I woke up in the morning, which I know may not sound like a lot to some, but to me was an absolute revelation.

I was eager to push on and when I reach 7mL per day, I also added in my very first enema. I had heard it was important to attack the situation from both ends. The enema went well enough. I did 10mL CDS in 1L of water, but only used around 250mL of it and held for around a minute on each side. I evacuated almost immediately after that and felt good.

But then things went very south around 30mins to an hour later. I started getting horrible gut sensations: nausea, pulling through my gut, my entire nervous system feeling like it was being scrunched up, loss of sensation in my feet and hands, tingling, pounding pulse through my head and body, etc. It seems like any time anything moves in my gut - whether from food intake or from a bowel movement - that movement triggers waves of these sensations. And because my gut motility is so poor (I assume due to a lack of energy) it severely disrupts my sleep, causing me to wake frequently with all these symptoms.

I feel like I've taken a gigantic step backwards here and don't know how to course correct. I'm worried because it's been 5 days now and no sign of significant improvement. I've stopped all CDS intake of course, including oral ingestion. I've added some probiotics and some mineralized water.

Is this as bad as it seems? Does anyone have any suggestions on how to navigate this?

Thanks for any advice.

gauche wrote:

Hello,

Sorry for any note of desperation in my message here, it's not like me, but 25 years of ebbing and flowing chronic illness can really mess with you...

I recently discovered ClO2 and immediately resonated with what I was hearing, quite convinced of having Lyme coinfections, not least because I had tick bites when my immune system was already compromised from you know what.

I started working towards Kalcker's protocol C on 28th of February, starting with 1mL and adding 1mL each day. My immediate response was incredibly positive: better energy, cognition, even having a feeling of energy and vitality through my core when I woke up in the morning, which I know may not sound like a lot to some, but to me was an absolute revelation.

I was eager to push on and when I reach 7mL per day, I also added in my very first enema. I had heard it was important to attack the situation from both ends. The enema went well enough. I did 10mL CDS in 1L of water, but only used around 250mL of it and held for around a minute on each side. I evacuated almost immediately after that and felt good.

But then things went very south around 30mins to an hour later. I started getting horrible gut sensations: nausea, pulling through my gut, my entire nervous system feeling like it was being scrunched up, loss of sensation in my feet and hands, tingling, pounding pulse through my head and body, etc. It seems like any time anything moves in my gut - whether from food intake or from a bowel movement - that movement triggers waves of these sensations. And because my gut motility is so poor (I assume due to a lack of energy) it severely disrupts my sleep, causing me to wake frequently with all these symptoms.

I feel like I've taken a gigantic step backwards here and don't know how to course correct. I'm worried because it's been 5 days now and no sign of significant improvement. I've stopped all CDS intake of course, including oral ingestion. I've added some probiotics and some mineralized water.

Is this as bad as it seems? Does anyone have any suggestions on how to navigate this?

Thanks for any advice.

Here is a reply from a friend on your CDS enema problem: 

"I would take glycine nightly, as it helps to repair the gut lining. I would be taking a good probiotic. I would consume slippery elm, bark tea. I would work on exercises to calm my vagus nerve." 

www.quantamagazine.org/how-our-longest-nerve-orchestrates-the-mind-body-connection-20240826/