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Burning Muscle Pain

Freddd

Senior Member
Messages
5,184
Location
Salt Lake City
In the list of symptoms I have approximate 10 specific and different muscle pains described. They are each connected to a separate combination of nutrients, possibly even with different layers of healing despite being all in the muscles. One of them specifically is what feels like lactic acid burn that went on for 17 years for me. This is of specific interest in Salt Lake since our resident FMS/CFS researchers, Drs Light (both of them). As they work up at the U of U my pain docs follow their work carefully. One of the things that they are involved with is what causes that pain and how to get rid of it. In my discussion with my doc we discussed the role of exercise and lack there of. It appears that the burn sensors proliferate during non use of muscles, the inactivity forced on all of us. I wonder if there is a failure of mitochondria to proliferate when these sensors do proliferate? They sure seem to go together. For me, the pain faded, but that wasn't sufficient for exercise tolerance to return. That took both AdoCbl and LCF to restore the tolerance to exercise to then rebuild the mitochondria and muscles.

My experiences was that the burning pain of 17 years duration actually decreased to almost zero in 10 days following the start of MeCbl and the return of some energy. However, it took AdoCbl and LCF to restore exercise tolerance, mitochondria proliferation and muscle growth. He was interested in how I went from essentially housebound and able to do a few steps up the stairs at a time to being able to do 2000-4000 feet of vertical up AND down each day with 3 to 5 miles or more of walking distance, at least during the summer. The doc I started with at the pain clinic had retired from the clinic so I was reassigned and he hadn't watched from the beginning. I had 99% of my total healing while still having paradoxical folate insufficiency symptoms. These slowly squeezed down to a very few "signal" symptoms. While keeping these minimized, at least other layers of healing can be going on.

As usual, this doc watches and agrees that I am doing well and that treatment should continue. I sure don't look like or have affect like the rest of the patients there. The thing about the pain clinic which they tell us up front is that they are not there for finding a cure to our problems. They are there to manage the pain that in itself has become the problem, regardless of underlying problems.

With most of my nerves functioning adequately to have nerves to muscles, most of my muscles have come back except for those having nerves that were damaged by the car wreck, showing the asymmetries quite strongly.
 

aprilk1869

Senior Member
Messages
294
Location
Scotland, UK
Fred, I've been reading up on the effects of pulsed EMFs such as those from mobile phones, cordless phones, Wifi and electrical items in general.

Decades ago Dr Frey found that using pulsed EMFs caused the BBB to open up to allow a blue tracer dye into the brains of rats.

More recent research by Henrietta Nittby showed that albumin can leak out of rat brains when exposed to pulsed EMFs. This is not supposed to happen.

Question: If albumin can leak out of the brain when exposed to pulsed EMFs, can this cause B12 to also leak out? Is this why you need so much B12?

You can see more of her research here: http://lib.bioinfo.pl/auid:8179037
 

Freddd

Senior Member
Messages
5,184
Location
Salt Lake City
HI Aprilk,

I don't know that it does or doesn't have anything to do with it EMFs. Whatever the cause it has been around apparently unchanged for 60 + years. Also my maternal grandfather had the same problems for 50 years before I was even born. Neurological pain will return if the vitamins are discontinued for several reasons. One doc with experience at healing neuropathy said it takes 5 years of uninterrupted b12 etc to permanently heal the nerves. If it can't be healed 100% it appears to require b12 for the rest of the life to maintain benefit. Nerve damage is very difficult to fully heal. The neurological pain I had following the car wreck went away and seems permanently gone. It didn't come back when the CNS problems did with the two crashes.
 

Hugocfs

Senior Member
Messages
121
Location
U.S.A.
To me, methylators are speaking a different language and this thread is no different. I need a translation. I assume MeCbl is methylcobalamin, but what are AdoCbl and LCF? Can you provide a link that explains methylation is simple english? I would like to learn more about it, but need a place to start. Thanks.
 

aprilk1869

Senior Member
Messages
294
Location
Scotland, UK
According to Dr Jack Kruse, the problems with EMFs go back many decades when homes were getting electricity, artificial light, radios, TVs and so on. Technology has been growing exponentially along with disease since then.
 

triffid113

Day of the Square Peg
Messages
831
Location
Michigan
To me, methylators are speaking a different language and this thread is no different. I need a translation. I assume MeCbl is methylcobalamin, but what are AdoCbl and LCF? Can you provide a link that explains methylation is simple english? I would like to learn more about it, but need a place to start. Thanks.
MeCbl = methylcobalamine (I just say mB12)
AdoCbl is adenosylcobalamine (I just say aB12)
LCF = L-carnitine-fumarate

LCF is involved in energy metabolism and protection of nerve cells from damage by sugar via the polyol pathway.
(Don't know anything about the polyol pathway but it is the name of the pathway should you desire to research it...gotta have the right buzz word to effectively search).

You can go to these sites for a brief orientation on methylation...the rest you get by reading here and asking questions.
http://www.enzymestuff.com/methylation.htm
http://www.heartfixer.com/AMRI-Nutrigenomics.htm
http://www.lef.org/protocols/heart_circulatory/homocysteine_reduction_01.htm
http://www.lef.org/magazine/mag2001/june2001_report_homocysteine.html
http://drmyhill.co.uk/wiki/CFS_-_The_Methylation_Cycle

*NOTE: Life Extension (and heartfixer and possibly enzymestuff) take the view that most people do not need active forms of the B vitamins...they feel that genetic defects are rare and the only reason to require active B's. We, here, know that is not true. Unfortunately there is no source of info that necessarily possesses the whole truth in the matter. You have to read with your own critical reasoning skills and make your own decisions. Although the info on the above sites is consolidated and well written and an easy IN to understaning methtylation, phoeniz rising has more information on it than any of the above sources.
 

triffid113

Day of the Square Peg
Messages
831
Location
Michigan
http://www.lef.org/magazine/mag2000/may00-cover2.htm
The Antiaging Effects of Acetyl-L-Carnitine ...By facilitating the youthful transport of fatty acids into the cell's mitochondria, acetyl-L-carnitine better enables dietary fats to be converted to energy and muscle. Carnitine is approved as a drug in the United States to protect against muscle wasting diseases, including heart muscle weakness and low energy levels....

(article contains the following headers, read if interested):
Reversing heart aging
Brain protection
Emergency use of acetyl-L-carnitine (for stroke)
Regenerating nerves
Suggested dosage
Summary
References

Velha recovered from CFS using Freddd's protocol and 4-5g/day of LCF (She said only 2 brands were potent, Drs Best and some other I cannot recall). The article above shows benefits from ALC, but the only CFS benefit I have heard was from LCF. I suspect the overlap somewhat in benefits, but LCF is clearly the one you want if you reached this site.

http://www.lef.org/protocols/abstracts/abstr-082.html
Polyol pathway hyperactivity is closely related to carnitine deficiency in the pathogenesis of diabetic neuropathy of streptozotocin-diabetic rats.
Nakamura J, Koh N, Sakakibara F, Hamada Y, Hara T, Sasaki H, Chaya S, Komori T, Nakashima E, Naruse K, Kato K, Takeuchi N, Kasuya Y, Hotta N. The Third Department of Internal Medicine, Nagoya University School of Medicine, Nagoya, Japan.
J Pharmacol Exp Ther 1998 Dec;287(3):897-902
To investigate the relationship between polyol pathway hyperactivity and altered carnitine metabolism in the pathogenesis of diabetic neuropathy, the effects of an aldose reductase inhibitor, [5-(3-thienyl) tetrazol-1-yl]acetic acid (TAT), and a carnitine analog, acetyl-L-carnitine (ALC), on neural functions and biochemistry and hemodynamic factors were compared in streptozotocin-diabetic rats. Significantly delayed motor nerve conduction velocity, decreased R-R interval variation, reduced sciatic nerve blood flow and decreased erythrocyte 2, 3-diphosphoglycerate concentrations in diabetic rats were all ameliorated by treatment with TAT (administered with rat chow containing 0.05% TAT, approximately 50 mg/kg/day) or ALC (by gavage, 300 mg/kg/day) for 4 weeks. Platelet hyperaggregation activity in diabetic rats was diminished by TAT but not by ALC. TAT decreased sorbitol accumulation and prevented not only myo-inositol depletion but also free-carnitine deficiency in diabetic nerves. On the other hand, ALC also increased the myo-inositol as well as the free-carnitine content without affecting the sorbitol content. These observations suggest that there is a close relationship between increased polyol pathway activity and carnitine deficiency in the development of diabetic neuropathy and that an aldose reductase inhibitor, TAT, and a carnitine analog, ALC, have therapeutic potential for the treatment of diabetic neuropathy.
 

cph13

Senior Member
Messages
221
Location
USA
In the list of symptoms I have approximate 10 specific and different muscle pains described. They are each connected to a separate combination of nutrients, possibly even with different layers of healing despite being all in the muscles. One of them specifically is what feels like lactic acid burn that went on for 17 years for me. This is of specific interest in Salt Lake since our resident FMS/CFS researchers, Drs Light (both of them). As they work up at the U of U my pain docs follow their work carefully. One of the things that they are involved with is what causes that pain and how to get rid of it. In my discussion with my doc we discussed the role of exercise and lack there of. It appears that the burn sensors proliferate during non use of muscles, the inactivity forced on all of us. I wonder if there is a failure of mitochondria to proliferate when these sensors do proliferate? They sure seem to go together. For me, the pain faded, but that wasn't sufficient for exercise tolerance to return. That took both AdoCbl and LCF to restore the tolerance to exercise to then rebuild the mitochondria and muscles.

My experiences was that the burning pain of 17 years duration actually decreased to almost zero in 10 days following the start of MeCbl and the return of some energy. However, it took AdoCbl and LCF to restore exercise tolerance, mitochondria proliferation and muscle growth. He was interested in how I went from essentially housebound and able to do a few steps up the stairs at a time to being able to do 2000-4000 feet of vertical up AND down each day with 3 to 5 miles or more of walking distance, at least during the summer. The doc I started with at the pain clinic had retired from the clinic so I was reassigned and he hadn't watched from the beginning. I had 99% of my total healing while still having paradoxical folate insufficiency symptoms. These slowly squeezed down to a very few "signal" symptoms. While keeping these minimized, at least other layers of healing can be going on.

As usual, this doc watches and agrees that I am doing well and that treatment should continue. I sure don't look like or have affect like the rest of the patients there. The thing about the pain clinic which they tell us up front is that they are not there for finding a cure to our problems. They are there to manage the pain that in itself has become the problem, regardless of underlying problems.

With most of my nerves functioning adequately to have nerves to muscles, most of my muscles have come back except for those having nerves that were damaged by the car wreck, showing the asymmetries quite strongly.
I've been experiencing burning (warmer than expected) feet lately. Is this a folate issue so I should increase it. I'm @ 3mg mB12 8.6mg cB12 2,000 mcg folate....do I hear a 2,400????? On another NOTE:
I had lactic acid BURN in my shins after doing a marathon (shopping trip that is) in NYC for Thanksgiving. I suffered for 3 weeks saying, "oh it's shin splints" Took some Potassium and I was good to go.... This coudn't be potassium again????
 

Phred

Senior Member
Messages
141
cph13 I had burning feet too. I had problems with a degraded adb12 I had. I switched to Anabol and that helped. I also reduced my zinc. That seemed to reduce any residual burning I had.
 

Freddd

Senior Member
Messages
5,184
Location
Salt Lake City
As regards the warm feeling of feet with these nutrients it is a change that happens at certain "stages". Sometimes things are getting better and sometimes worse. However, when it is a response to these nutrients it is favorable generally and all stages are gone through in reverse order. If it is going in the right direction then changes slowly happen towards feeling more normal. So my feet may burn with neurology but I haven't had any lactic acid burn on a prolonged basis in 10 years. I don't overdo exercise. That is individual because most all summer I'll be walking 3-5 miles a day and 2000 feet of vertical up and down, but I don't jog and push the speed to the edge as I used to until the muscle pain became too much. Moving my pace from 5 miles in 45 minutes to 5 miles in 40 minutes took considerable effort. I don't jog anymore, too much strain on the joints. I work up to things at a speed that doesn't make me sore.

The chronic lactic acid type burn lasted 17 years in all the muscles in my body. Just hold up my head and body was enough to do it.