Melissa
Kaplan's
Chronic Neuroimmune Diseases
Information on CFS, FM, MCS, Lyme Disease, Thyroid, and more...
Last
updated December 18, 2009
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Melissa
Kaplan's |
Research on Red Blood Cell Shape & CFS
CFS Connection, 1996
| Dr.
Leslie Simpson, a CFS researcher in New Zealand, has been traveling throughout
Canada and the Northeastern US giving lectures about his theories on abnormalities
of red blood cells in CFS patients. Thanks to PWC Diane Rose who attended
a meeting in Boston for the following report on what Dr. Simpson had to
say.
Healthy people typically have six shapes of red blood cells. Healthy people usually have a higher percentage of the disc shaped blood cells, which flow easier than the other shapes. In his studies of blood from PWCs, they tend to have a higher percentage of cup-shaped and other shaped blood cells that are of a shape that is harder to get through small capillaries. Dr. Simpson's thinking is that ME/CFS is caused by having a higher percentage of the other shaped blood cells and having smaller capillaries. (He used an example of some men that had a higher percentage of cup-shaped and other shaped blood cells but were perfectly healthy - but they had large capillaries) - Most PWCs are in the lower quarter of capillary size. This might also explain the higher percentage of women that seem to get the illness. Muscles have varying sizes of capillaries, and that would explain why different people have different muscle problems. The hypothalamus has an amazingly intricate web of tiny capillaries, and that would explain all the different problems related to ME/CFS since the hypothalamus corresponds to so many different [systems in the body]. When there were higher percentages of the disc-shaped blood cells, the ME patient felt better; when their percentages of cup- and other-shaped cells was higher, they were feeling worse. Dr. Simpson's studies have shown that percentages of different blood cell shapes can vary day to day, minute to minute. It can be affected by many things, including stress and exercise. He does some muscle experiments where patients pull a trigger and shows that small muscle activity can affect blood cell shape. In his experience, there are only two or three things that can influence blood cell shape:
Note: He made a point in saying that not all EPO is as effective as the Efamol brand, possibly due to lack of careful quality control measures resulting in 500 mg capsules actually containing less than 500 mg. He also stated that borage oil was not as effective as evening primrose oil. He seemed very realistic about how no one thing helps everyone. I think he also made it pretty clear that B12 shots weren't cures, by a long shot, but rather they helped alleviate symptoms for some people. What was very clear from his studies is that he can tell from looking at people's blood samples how badly they are feeling. (And doctors in New Zealand use it to help in diagnosing ME/CFS). When he takes blood samples he has you fill in a questionnaire about how you were feeling at the time the blood was drawn, but you don't send him the questionnaire until after he sends you back the analysis of your blood. His studies to date show the percentage of how non-disc shaped blood cells corresponds to how the patient feels. Wanda Rabb, editor of the CFS Connection, found out how non-New Zealanders can have their blood tested by Dr. Simpson. Write Dr. Simpson a letter, explaining that you have CFS and would like to receive a blood sample kit. Send your letter to: Dr. L. O. Simpson You will receive, via airmail, a special tube, materials, and instructions. Send the sample back along with your check for US$ in the amount stipulated in the instructions (1996 = US$20).
In 1995, Australian researchers found a unique marker in the urine of ME/CFS patients. Now, Dr. Simpson has found a RBC marker. Why is it that other countries are funding research, and the research being done seems so much more productive, than that funded and done here in the U.S. by the NIH and other federal agencies? Besides the CDC illegally misappropriating $12.4 million of funds allocated by Congress for CFS research, that is. Tired of the status quo? Write your senators!
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http://www.anapsid.org/cnd/diagnosis/redcells.html
