I got the partial report for the blood work from last Friday. As a result, I am taking new medication for the chronic fatigue and fibromyalgia (more on that later). Because I haven't been able to gain control over the Type II Diabetes, I am now taking Insulin via a pre-loaded injection pen instead of medication.

Some good news. I don't have Multiple Sclerosis, which my immunologist had feared, nor do I have Lupus. The concern had arisen from the fibro and chronic fatigue, which pretty much mirror symptomatically Lupus and MS, but to a much lesser and temporary degree.

The real problem lies with my immune system. The chronic fatigue arises from an increased percentage of the presence of the HHV-6 virus, which is in the same family as herpes, chickenpox, and shingles. The results from that portion of the test haven't been completed yet, but the lack of any relief from the symptoms already indicate no improvement at best. The new medication is supposed to help with sleep, which in turn will help the immune system fight off the virus. That is a symptomatic treatment only; I have already taken valtrex as an anti-viral course, but it didn't do much good. At this point, it's diet, exercise, and rest that will ultimately make or break it.

For those of you who may have been required to receive inoculations while traveling abroad, you may be familiar with the following. My IGG - Immunogammaglobulin is very low, and may require a supplement.

The bottom line is that I am tired and very achy all the time; imagine having the flu 24/7. But the good news is that as I get stronger, my own system will ultimately be what gets things back in control. And please remember that I'm doing so much better than I was. I have the best medical and therapeutic help anyone could ask for. I have a supportive and loving family. And I have you folks, for which I am supremely grateful and filled with hope. i do so treasure your support and encouragement and I'm blessed by your thoughts and prayers. So thank you once again. Love you! Andrea