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01-27-2019, 11:40 AM | #11 | |||
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Senior Member
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i take slo mag which is available at walmart if you have one near you. it has really cut down on my muscle cramping, especially while sleeping. i still cramp up from time to time, but much less than in the past.
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"Thanks for this!" says: | janieg (01-27-2019) |
01-27-2019, 11:55 AM | #12 | |||
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I took a generic version of Slo Mag for a long time before switching to threonate to give it a try. Maybe I'll switch back and increase the amount...just to try.
One thing I've learned in this journey that you can ingest all the nutrient-rich food and supplements that you want, but if your body can't process and make use of them, it's pointless. I learned that with my biotinidase problem. I have low levels of the enzyme necessary to unbind biotin from protein sources. When tested, my biotin levels are fine, but without adequate levels of the enzyme, I couldn't make use of it. I have to take a supplement in a freely bioavailable form to circumvent the enzyme problem. What if my body can't process magnesium, or calcium, or whatever? The levels show as normal, but it doesn't mean the proper processing is taking place. I can't help but wonder if something like that is going on. Posting these here for future reference: Renal Control of Calcium, Phosphate, and Magnesium Homeostasis Electrolyte Balance | Boundless Anatomy and Physiology _______ Last edited by janieg; 01-27-2019 at 12:15 PM. |
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"Thanks for this!" says: | echoes long ago (01-27-2019) |
01-27-2019, 12:52 PM | #13 | ||
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Newly Joined
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Yes, I have a lot of pain in my hands when I retain water as a result of eating salt. I think the swelling (even minor) must put some pressure on the small fiber sensory nerves.
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"Thanks for this!" says: | ger715 (01-31-2019) |
01-27-2019, 09:36 PM | #14 | |||
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Senior Member
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Quote:
it can get quite maddening after a while....even the tests cant be trusted to be accurate for your individual case. i have another illness now, diagnosed in June 2018 via biopsy....sarcoidosis. less is known about the causes, and process than even peripheral neuropathy. testing is limited to imagining, cat and pet or biopsy. none of the blood tests are accurate. treatments are also limited, either prednisone, or methotrexate. prognosis is there is none, it can stay active, it can become less active, it never leaves your body so there is no remission. to complicate matters, im sure i have had sarcoidosis since at least 2006, which was my first chest cat scan that picked up lung nodules, which was finally diagnosed to be sarcoidosis in 2018. now the complexity of did sarcoidosis cause my peripheral neuropathy which first presented in 2001, or did sarcoidosis and peripheral neuropathy develop independently from the same toxic exposures. i am sure that i will never know. like i said it can get maddening |
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01-30-2019, 07:42 PM | #15 | |||
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Gads, sorry to hear about the sarcoidosis. That's just downright rude to have TWO disorders that aren't well understood!
Interestingly, I had two inflammatory spots in my lungs show up. My PCP had nothing to say about them, and when I showed my neuro the report, she wanted to know what my PCP had to say. When I told her that my PCP had nothing to say, she looked a little surprised and said, "Well, that is interesting to me," but nothing more. I didn't know whether to laugh or cry. She did refer me to another neurologist/neuromuscular specialist at the Univ. of MD just to see if he has any thoughts. Quote:
Last edited by janieg; 01-30-2019 at 08:43 PM. |
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"Thanks for this!" says: | echoes long ago (01-30-2019) |
01-30-2019, 09:36 PM | #16 | |||
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Senior Member
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you might want to have a pulmonary doctor take a look at those two inflammatory spots.
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02-03-2019, 02:40 PM | #17 | ||
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Quote:
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It ain't what it used to be... . It ain't what it's gonna' be... . It is what it is!... . |
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03-29-2021, 05:07 PM | #18 | ||
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New Member
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Quote:
I've been lurking for a few months trying to get some insight into solving my neuropathy. It started about 6 months ago as a burning sensation in my feet, which spread to my arms and torso and face. It's mostly pressure related at this point, so always worse at night. I am not diabetic. The neuropathy started after I developed hyperthyroidism. Anyway, I also noticed that salty foods like salted cashews or corn chips seemed to worsen the pain. I tried an experiment with baking soda (1/4 tsp in 8 oz water) and also saw an increase in pain. I'm just now looking into sodium-related neuropathy and came across an article that talks about a sodium pump defect in diabetic neropathy. A sodium-pump defect in diabetic peripheral nerve corrected by sorbinil administration: relationship to myo-inositol metabolism and nerve conduction slowing Not enough posts for a direct link but it's a pubmed NIH document 2421135. I'm wondering if anyone has already looked at this or has some experience with sorbinil. |
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03-29-2021, 08:01 PM | #19 | |||
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Grand Magnate
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Hi B_MC
Welcome to NeuroTalk . Sorbinil is an aldolase reductase inhibitor which may prevent the peripheral neuropathy in diabetes. See this Wikipedia link for references: Sorbinil - Wikipedia
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03-30-2021, 11:09 AM | #20 | ||
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Grand Magnate
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Welcome B_MC.
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Kitt -------------------------------------------------------------------------------------------------------- "It is what it is." |
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