Oral lipid supplements for treating pain and fibromyalgia
A method of oral delivery of phospholipid/inulin compositions comprising capsules, tablets, chewable wafers or powdered material in a liquid carrier in quantities effective for treating systemic pain from fibromyalgia. The compositions further including effective amounts of caffeine also reduces fatigue and enhances alertness and focus.
1. A method of treating an individual diagnosed as having fibromyalgia wherein the individual is provided
a) a liquid for drinking, the liquid having a powder dissolved or suspended therein, or
b) an ingestible tablet or capsule the powder, tablet, or capsule comprising a combination of inulin, and phospholipids in therapeutically effective amounts for relieving the symptoms of fibromyalgia, or
c) a chewable wafer comprising:
i) a base composition comprising a combination of inulin, and phospholipids in therapeutically effective amounts for relieving the symptoms of fibromyalgia, and
ii) a carrier for the base composition comprising xylitol, a flavoring agent, stearic acid and/or vegetable stearate, and
wherein the phospholipids comprise about 19-29% phosphatidylcholine (PC), 15-25% phosphatidylethanolamine (PE), 3.5%-10% phosphatidic acid (PA), 10-18% phosphatidylinositol (PI), 2-10% phosphatidylglycerol (PG), 10-20% glycolipids and phosphatidylserine (PS).
2. The method of claim 1 wherein an effective unit dose comprises at least about 1 g of the phospholipids.
3. The method of claim 2 wherein an effective daily dosage is 4 g of the phospholipids, said daily dosage comprising four unit dosages delivered approximately every 6 hours over a 24-hour period.
4. The method of claim 3 wherein the daily dosage is delivered for about 14 days.
5. The method of claim 2 wherein the unit dosage also includes an amount of caffeine effective to reduce fatigue and enhance alertness and/or focus.
6. The method of claim 1 wherein an effective unit dose comprises at least 1.2 g of the phospholipids.
7. The method of claim 6 wherein an effective daily dosage is 4.8 g of the phospholipids, said daily dosage comprising four unit dosages delivered approximately every 6 hours over a 24-hour period.
8. A method of treating an individual diagnosed as having fibromyalgia while also reducing fatigue and enhancing alertness comprising orally delivering to said individual:
a) a liquid having a powder dissolved or suspended therein,
b) an ingestible tablet or capsule,
wherein the powder, the tablet, or the capsule comprises a combination of inulin and phospholipids in therapeutically effective amounts for relieving the symptoms of fibromyalgia and caffeine in therapeutically effective amounts for reducing fatigue and enhancing alertness and/or focus, or
c) a chewable wafer comprising:
i) a base composition comprising a combination of inulin, and phospholipids in therapeutically effective amounts for relieving the symptoms of fibromyalgia,
ii) a carrier for the base composition comprising xylitol, a flavoring agent, stearic acid and/or vegetable stearate, and
iii) caffeine,
wherein the phospholipids comprise phosphatidylcholine, phosphatidylethanolamine, phosphatidic acid, phosphatidylinositol, phosphatidylglycerol, glycolipids and phosphatidylserine.
9. The method of claim 8 wherein an effective unit dose comprises about 1 g of the phospholipids and about 1 gm of caffeine.
10. The method of claim 8 wherein an effective unit dose comprises about 1 g of the phospholipids and about 1.75 gm of caffeine.
11. The method of claim 8 wherein an effective daily dosage is four 1 g dosages of the phospholipids and four 1 g dosages of caffeine, said 1 g dosages delivered approximately every 6 hours in a 24-hour period.
12. The method of claim 8 wherein an effective daily dosage is at least about 4 g of the phospholipids and at least about 4 g of caffeine delivered over a 24-hour period.
13. The method of claim 11 wherein the daily dosage is delivered for about 14 consecutive days.
14. The method of claim 12 wherein the daily dosage is delivered for about 14 consecutive days.
15. The method of claim 8 wherein the phospholipids comprises about 19-29% phosphatidylcholine (PC), 15-25% phosphatidylethanolamine (PE), 3.5%-10% phosphatidic acid (PA), 10-18% phosphatidylinositol (PI), 2-10% phosphatidylglycerol (PG), 10-20% glycolipids and phosphatidylserine (PS).