ok, so I wanted to give update on progress at hale clinic, london.
I have been treated there just over 3 weeks.
To give you idea where I was when I started I was started my Vo2Max was 12.9ml/min with maximum ventilation 30/l/min. I was somewhere around 30-40% of normal function.
Today, i would say i have improved quite dramatically to maybe a 70-80 on Bells CFS scale. I much..much more cardiovascular ability, stamina and overall feeling of well being. Its been quite a dramatic turnaround in a short period of time. Pulse feels strong, tingling and numb extremities has vanished.
I attach 2 blood slides, the first from initial meeting and the latter from the latest session after 3 IV infusions.
As you can see quite substantial difference, slide 1 RBC clogged on top of each other, slide 2 free and easy moving.
Huge reduction in fibrin....something
@Eeyore touched on. I had borderline low fibrogen @ 169 (x1000 / uL)....which meant possibly high blood fibrin.
Additionally, the analysts suggested improvement in WBC functionality from slide 1 to 2. (shape and movement)
As there is lower blood congestion now,,,improved circulation and so forth.
I was drawn to Hale originally as a follower of Dr Les Simpson old work on RBCS:
http://cfidsreport.com/Articles/researchers/lessimpson.htm
Onto the treatments...I have had 4 treatments now each time consisting;
1. IV alkalising mix
2. IV Vitamin C (23g per dose)
3. A central nervous system injection (not sure of active drug...makes your saliva glands open fully,,body flushing and double vision for 30 secs)
4. Ozone Therapy
5. Gluatathione injections
Bioresononce machine still detecting streptoccus active infection in spleen.
They believe the strep is making spleen overworked and thus issue with immune cells...
When there is issue with immune cells....it is turning on and off AMPK..hence cycles of wellness (in cfs context h ) and crashes.
So the plan to continue with immune targeting and cell function improvement,,,,increase to nk cell count also.
Supplement protocol is fibrin dissolvers, alkaline drink mixes, amoxicillan (for strep), High dose vit D (50,000ui Day) to stabilise immune system. (similar protocol to the brazil doc:
http://www.vitamindwiki.com/Video by Dr. Coimbra – 95 percent of auto-immune cured with vitamin D in high doses - April 2014)
Also, paleo diet to keep AMPK boosted as they operate better in starve mode which body thinks its in under ketosis.
Other supplements include silvercillan, quercetin, reservatrol, pine bark extract.
Most the supplements are german,,,hale clinic suggest CFS supplements and treatments vastly superior there.
So, so far so good...I hope to build on the excellent start.
They say in past experience it takes 2-3 months for immune system to restore complete functionality.
Going by the start i had i dont have any reasons to disbelieve them at this point.