Does anyone else feel like they can't get a full breath? I think it's anxiety but it scares me every time. I feel like it's hard work to breath and the back of my throat feels like when i have been exercising hard. (Don't know if that makes sense?)
Does anyone else feel like they can't get a full breath? I think it's anxiety but it scares me every time. I feel like it's hard work to breath and the back of my throat feels like when i have been exercising hard. (Don't know if that makes sense?)
Sometimes I can sneak a deeper breath by suddenly inhaling. Lying down is the best remedy since the breathing problems are a sign that my body needs to lie down so the blood can circulate properly.
I know I have POTS, but when I lie down I feel worse, like I'm fighting against a weight on my chest. (Sounds like congestive heart failure, I know. But so obv not!) It does seem to get better when I'm less active, though. When it was worst, I'd go lie down, but propped up on a bunch of pillows.
Could your BP have risen when lying down to cause that effect? Some people can't lie down when they take too much of certain BP raising meds because their BP rises too much when they lie down.
Whenever I have the "asthma" feeling (and I don't have asthma) I know it is from salicylates / phenols / nitrates. Estradiol is a phenol... I think Vitex inhibits aromatase and lowers estradiol production.Eventually, I also figured out this was related to:
...particularly milk. Dropped milk and the issue didn't drop off my radar, but it became so much easier to breathe! Apart from that, it may well be a cell metabolism issue for me.
- food allergies!
I take Vitex agnus-castus to help regulate hormones, but it's also reputed to be a mitochondrial protectant, and an anti-inflammatory specific to the lungs. It is one of those supplements I (maybe literally) can't live without. If I drop it a few days in a row, the problem has 100% returned.
Whenever I have the "asthma" feeling (and I don't have asthma) I know it is from salicylates / phenols / nitrates.
Estradiol is a phenol... I think Vitex inhibits aromatase and lowers estradiol production.
The only things that help me with salicylates (plant hormones)
Phenols deplete B1
I don't think anyone should avoid them, but must be careful if deficient in nutrients that help to process them.How would it be possible to avoid such a thing?
Cite!
https://medlineplus.gov/druginfo/natural/965.html
Are there interactions with herbs and supplements?
Areca
Areca (betel) nuts change thiamine chemically so it doesn't work as well. Regular, long-term chewing of betel nuts may contribute to thiamine deficiency.
Horsetail
Horsetail (Equisetum) contains a chemical that can destroy thiamine in the stomach, possibly leading to thiamine deficiency. The Canadian government requires that equisetum-containing products be certified free of this chemical. Stay on the safe side, and don't use horsetail if you are at risk for thiamine deficiency.
Are there interactions with foods?
Coffee and tea
Chemicals in coffee and tea called tannins can react with thiamine, converting it to a form that is difficult for the body to take in. This could lead to thiamine deficiency. Interestingly, thiamine deficiency has been found in a group of people in rural Thailand who drink large amounts of tea (>1 liter per day) or chew fermented tea leaves long-term. However, this effect hasn't been found in Western populations, despite regular tea use. Researchers think the interaction between coffee and tea and thiamine may not be important unless the diet is low in thiamine or vitamin C. Vitamin C seems to prevent the interaction between thiamine and the tannins in coffee and tea.
Seafood
Raw freshwater fish and shellfish contain chemicals that destroy thiamine. Eating a lot of raw fish or shellfish can contribute to thiamine deficiency. However, cooked fish and seafood are OK. They don't have any effect on thiamine, since cooking destroys the chemicals that harm thiamine.
http://www.medicalnewstoday.com/articles/219545.php
Interactions with vitamin B1
Tea and coffee contain tannins, chemicals that may interact with thiamin, making it harder to absorb.
Some of the chemicals in raw shellfish and fish can destroy thiamin, potentially leading to a deficiency if eaten in large quantities. Cooking destroys these chemicals, but it destroys thiamin too.
Foods containing vitamin B1 should not be overcooked.
Thiamine deficiency and its prevention and control in major emergencies WHO (page 28)
Thiamine is water soluble and is susceptible to destruction by several factors including:
Thiamine is stable at low pH (pH under 7), but decomposes when heated particularly under nonacidic
- neutral and alkaline conditions
- heat
- oxidising and reducing agents
- ionizing radiation
conditions. Protein-bound thiamine, as found in animal tissues, is more stable. Thiamine is
stable when stored frozen; however, substantial losses occur during thawing.
Table B, Annex 3, shows examples of thiamine losses in food processing. Losses of thiamine
during the commercial baking of white bread, which is between 15 to 20%, is partly due to the yeast
fermentation which can convert thiamine to co-carboxylase which is less stable than thiamine (Berry
Ottoway,1993). According to a study reported by Marks (1975), the loss in the crust was 30% and
that in the rest 7%; rusks, baked twice, lost 40–50%.
Thiamine is very sensitive to sulphites and bisulphites, especially at a high pH. Consequently there
are large losses of the vitamin in vegetables blanched with sulphite, and in meat products where
sulphites and bisulphites are used as preservatives. Berry Ottoway (1993) reported a thiamine loss
in cabbage of 45% in sulphite-treated blanching water compared with 15% in untreated water.
Where the pH is low, such as in citrus fruit juices, thiamine losses are considerably less. The
practice of adding sodium bicarbonate to peas or beans for retention of their colour in cooking or
canning results in large losses of the vitamin due to the alkaline environment.
Thiamine is also decomposed both by oxidizing and reducing agents eg. in the presence of copper
ions. A comprehensive study of heat processing in tin and glass containers showed significant
losses of thiamine; 50% of thiamine was retained after processing and the levels reduced to between
15–40% after 12 months storage (Berry Ottoway,1993). Prolonged dehydration of fruits and
vegetables resulted in a loss of 30–50% of thiamine (WHO, 1967).
Thiamine is also cleaved by residual chlorine in proportion to the rise in temperature, rise in pH and
...
p. 31
Heat-stable thiamine antagonists occur in several plants; ferns, tea, betel nut. They include polyphenols; these and related compounds are found in blueberries, red currants, red beets, brussel sprouts, red cabbage, betel nuts, coffee and tea (Hilker and Somogyi, 1982). They react with thiamine to yield the non-absorbable thiamine disulfide. In addition, some flavonoids have been reported to antagonize thiamine as well as haemin in animal tissues. (See Table 15).
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I just don't see how a human could avoid polyphenols in the diet.
Food for thought.https://www.ncbi.nlm.nih.gov/pubmed/27695291
In a diet devoid of carbohydrates (bread, pasta, fruit, and rice), free from goitrogenic food, and based on body mass index, the distribution of body mass and intracellular and extracellular water conducted for 3 weeks gives the following results: patients treated as above showed a significant reduction of antithyroid (-40%, P<0.013), anti-microsomal (-57%, P<0.003), and anti-peroxidase (-44%, P<0,029) Abs.
It is worth to note that 83% of patients with a high level of autoantibodies are breath test positive to lactase with a lactase deficit higher than 50% (personal communication). All these support our results, because the reduction of simple and complex carbohydrates in the diet, as we have done in our dietary plan, probably reduces the translocation of the ChREBP protein, a phenomenon necessary to induce transcription of genes involved in lipogenesis. In fact, a recent study reported that ChREBP is necessary to induce L-PK and ACC glucose-dependent genes, suggesting the probable existence of other transcriptional regulators in the liver different from LXR.30–36
After all, glucose is not only a primary carbon source for anabolic and catabolic purposes, but also serves as a signal in the regulation of metabolic gene expression. In this sense, ChREBP is a transcriptional factor that responds to glucose signaling.37,38
ChREBP mRNA is most abundant in tissues in which lipogenesis is highly active.39–42 In hepatocytes and adipocytes, ChREBP-α expression is induced by glucose.42–46
ChREBP regulates a high number of genes encoding glycolytic enzymes, most of the genes involved in NADPH generation, and genes that play roles in regulating metabolic and energy homeostasis.47,48 In summary, ChREBP/Mlx represents the principal transcription factor in the upregulation (in a glucose-dependent manner) of genes involved in glucose uptake, glycolysis, and lipogenesis in metabolic tissues such as the liver and brown and white adipose tissues.
Understanding the role of ChREBP in the various tissues will provide important insight into the pathogenesis of metabolic syndrome.