nonna05
Frequent Contributor (1K+ posts)
Member # 33557
posted
and crawling ant feeling in legs and a bit in arms?? Back pain back, clogged throat.. little wheeze in chest, some sinus fullness comes and goes.. These were ALL settled down several weeks ago and did a ABX change and it came back
Could A-Bart or Cryptoleptis stir this up,,and a lot of sweats again ,but that seems to be better now
'I was to to hold back Samento./banerol and retry .'so far samento up to 7 drops .
Just don't get sleep , very well and wake up to flutters or spasms,
Usually electrolytes take care of second ,but not always.
As always thanks for the help Got a while ;till next appt.
Have other more urgent question I want to ask Dr. .
'Although it is frutrating to get a bit ahead and the symptom;s stir up again..
Posts: 2563 | From Denver,CO | Registered: Aug 2011
| IP: Logged |
posted
Those symptoms sound like Lyme to me - affecting the nerves. Clogged throat can occur for me when detoxing.
Posts: 13116 | From San Francisco | Registered: May 2006
| IP: Logged |
TF
Frequent Contributor (5K+ posts)
Member # 14183
posted
I agree. Tingles, crawling ant sensation, and insect bite sensation are all neuropathies--lyme attacking the nerves and causing false sensations.
Are you currently treating lyme? If not, you need to get back on lyme treatment.
Posts: 9931 | From Maryland | Registered: Dec 2007
| IP: Logged |
nefferdun
Frequent Contributor (1K+ posts)
Member # 20157
posted
Babesia causes sweating. I got back cramps with it. The hoarse throat, nasal congestion and insomnia can be FL1953. If you have cold hands and feet, that is FL1953. I think babesia also causes loss of voice or sore throat and coughing but you usually feel more sleepy rather than insomnia.
The creepy crawling thing I don't know. Bart hits the nerves causing tingling and twitching. So does Bb. If you don't have profound fatigue and breathlessness, then maybe it is just Bb.
-------------------- old joke: idiopathic means the patient is pathological and the the doctor is an idiot Posts: 4676 | From western Montana | Registered: Apr 2009
| IP: Logged |
Keebler
Honored Contributor (25K+ posts)
Member # 12673
posted
- Magnesium deficiency can cause tingles.
You say: wake up to flutters or spasms" - that sounds like you may need more / better magnesium, taurine, calcium and other minerals.
So can B-vitamin deficiency.
Need for more good oil in the diet, too. For the skin and for the myelin sheath to protect nerves.
Liver distress can cause the skin to feel uncomfortable in various ways. Overload of toxins can irritate the skin, as it's a major organ of detoxification, too.
Dehydration, too. You may just need more water.
In addition to addressing infection, you may need to support myelin sheath (the coating around the nerves that is attacked by lyme).
Google: Terry+Wahls
Ergonomics. Posture.
Etc.
Could be a combination of things. -
Posts: 48021 | From Tree House | Registered: Jul 2007
| IP: Logged |
nonna05
Frequent Contributor (1K+ posts)
Member # 33557
posted
Yes profound fatigue/weakness .Had 1 decent day Sunday where I could get out of bed, took a shower and bought a couch I could sleep on...
...then got home and was in so much pain When I went to bed around 12 ,I didn't get back up til next day, Tues morning at 2:30 am
Rolled over in bed a couple times, in pain left leg mostly cramping and numbness throughout, four times bathroom , and barely could drink enough to take only part of meds,
To wiped out to answer phone ,laying next to me,
Now I think ,I was in such a rush to but the stuff at furniture store , that I really bought stuff that won't fit etc.. besides spending to much.
It just so seldom I get out like that
I had to use one of their electric chairs, so I didn't walk much, or carry purse often.
Tripped a couple times
Might as well had been 10 miles,, I swear I have 2 lead suits on at times...
Keebler. I take cod liver or olive oil with Mepron, I try to watch minerals, maybe I'm doing far less than I think I am.
Neff , all those symptom's come and go.
It's just that so much was gone for a while, doc did a med change a while back and after four or so days had to stop cause a lot of this came back.. I
I thought it should have worked out of system by now,,
Kinda sounds like I went back a few steps from that point , or stirred the pot...
I keep thinking its in head or blood vessels..but I can feel it even moving around.
TF I think Lyme is being hit. maybe not enough
Robin , I did take some extra CSM lately ...
It's like I have to take a Valium to help with muscle twitching/spasms. It doesn't touch the tingles or pins and needles issue.
Like right now my throat feels phlegm, body heavy, left leg is just freaking.
Thank's for your help . Sorry to whine, just so uncomfortable. tired and can't seen to get a day straight ,except Sunday .
Posts: 2563 | From Denver,CO | Registered: Aug 2011
| IP: Logged |
nonna05
Frequent Contributor (1K+ posts)
Member # 33557
posted
What amounts of these suggestions
What about a-bart,, is it stronger than samento etc????
Can that or cryptoleptis sp? Stir tis up?
I just started those 2 about 3 weeks ago..
Posts: 2563 | From Denver,CO | Registered: Aug 2011
| IP: Logged |
nonna05
Frequent Contributor (1K+ posts)
Member # 33557
posted
any supplements to go back to?/
what about the cryptoleptis
which kill bart what kills babs.??
i Posts: 2563 | From Denver,CO | Registered: Aug 2011
| IP: Logged |
posted
I have FL1953 and the tingles in my legs and feet have been a major issue for me. In treatment at times, I can get rid of them. It's like I'm 'vibrating' at times. Like a tuning fork placed in my blood vessels. I have had nerve tests and they come back ok. It's like I say my blood is humming throughout my body.
I always thought I had babesia.... (not lyme per se') No tick bite... but blood transfusions and many other bug bites.
I do not take magnesium. I am never low with it and my dr. does not recommend it.
I am on zith, malarone,diflucan, and for me, I can get rid of them or make them very 'quiet' throughout the years.
We are all different in what we believe and what works for us. What works for me, might not you.
-------------------- Lyme, Babs, Fry Bug..... Whatever it is, may a treatment be discovered to make us all whole again! Posts: 941 | From AZ-MT | Registered: Oct 2004
| 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/