posted
Has anynone experienced this? It happened after I used CSM for a while to address biotoxins. I was doing fine for a while... pain going.. then BAM.
This will not go away. Well, it did stabalize on 50 mg toprol (up from my usual 12.5-25 mg) and the I took 1/4 tsp then 1/2 tsp of csm and BAM again.
I was at one point up to 1 TBS 4 times a day, though briefly and I backed down because my intestines felt sluggish, possibly inflamed, though my stool were moving fine.
Im guessing that toxins started moving and or my intestines were inflammed and "blood pooling" developed there which would logically lead to POTs symptoms.
I tend to run hyadrenergic but this is nuts.
Any thoughts, experience?? Thank you!
Posts: 861 | From USA | Registered: Dec 2008
| IP: Logged |
posted
I see an autonomic specialist week following next. Beta blockers may help bring pulse down but and address further exacerbating adrenaline surges but sheesh.. I can still feel the adrenaline and it is driving me insane.. my gut feels horrible and continual loose stools and just nervousnes.
I would love to use an intestinal mopper but I am afraid that anyting that is worthwhile will interfere with this extended release beta blocker.
Posts: 861 | From USA | Registered: Dec 2008
| IP: Logged |
posted
Hi i have suffered from these too. I use a calcium beta blocker. But please read Stop The Thyroid Madness book first. It addresses adrenal fatigue first . You cannot fix Thyroid without fixing your adrenals first. i am convinced that POTS and dysautonomia are failed or failing adrenals. I have started with Dr. Lam on his website and he is one of the three top adrenal docs in the World. He does consults on the phone and works with your dr. I am already about 30% better. Please read the book and go to his site. There is a wealth of info on both adrenals/thyroid and the adrenalin rushes.
[ 01-01-2011, 06:19 PM: Message edited by: sk8ter ]
Posts: 871 | From orange county, ca. | Registered: Jan 2006
| IP: Logged |
posted
Thank you, sk8ter. I will get the book. i keep looking on line at info and its all becoming mush in my brain.. thanks for the insight. Good to hear that much improvement so far.. very encouraging!
Posts: 861 | From USA | Registered: Dec 2008
| IP: Logged |
The Lyme Disease Network is a non-profit organization funded by individual donations. If you would like to support the Network and the LymeNet system of Web services, please send your donations to:
The
Lyme Disease Network of New Jersey 907 Pebble Creek Court,
Pennington,
NJ08534USA http://www.lymenet.org/
UBBFriend: Email this page to someone!
Printer-friendly view of this topic