Thanks, David. I'll look for that Super Troopers comedy.

Nope. No aspertame in the ingredients. Just rice, vitamins, and 45mg of sodium and good old sugar.

I'm certain that the people of Tennessee appreciate your comment, but I'm afraid I live on the west coast not that far from Xheli/Nitroplanes. But the state one is in doesn't have much bearing when the complaint is with the vendor company. I bought a fair amount of stuff from Xheli: V200D02, V370D01, Falcon 40, the ugh! Eagle, and a couple of vanilla 450 clones. From Nitroplanes I picked up a number of fixed wing aircraft. But that business stopped because I couldn't get reply one from their support email. I'[m glad that you obviously had a different experience than I. But I don't have any warm and fuzzy experiences to relate because my requests for support were just plain ignored.

The Eagle was sold as a plane suitable for beginners. It was supposed to be RTF, test flown at the factory. So if the gyro was on backwards or the belt too loose, one would think that would be something a fair and honest vendor would want to know about and make good on. You can go ahead and flip out insults all you like, but it is interesting that I have gotten emails from a number of people who say they had terrible support experiences with Xheli as well. Your response is so negative it makes me think you work there or something.

Thanks David, I appreciate the compliment!

Thanks for your kind words. It is hard to explain things to family, especially kids between 8 and 14. They seem to have a more difficult time rationalizing positives like your few symptoms and lack of need for treatment. You can bring them up to speed slowly, letting them know, for instance, that you are having headaches on and off. It allows them to get used to the idea of needing a doctor's care. If the time comes for aggressive treatment, it's not so much a shock. Plus, with Multiple Myeloma, it's entirely possible, depending on your subtype, that you'll never really need disabling therapy. Personally, I'm in the group that believes that therapy should be avoided until such time as paraproteins are at threatening levels or lesions become problematic. Research shows that delaying treatment doesn't harm the efficacy of the drugs we currently have to treat the cancer with. I find it encouraging that your doctor isn't rushing to get you on a regimen.

I'm glad you stopped by and again, appreciate your kind words. My best to you and your family!
Bob K

I can be reached as bk here at my website's domain.

You're back among the swaying fronds of the jungle? Wow, you get around quickly. Good to hear from you and my regards to South America!

I'd like to hear a bit of first person description about the subcutaneous Velcade. Any reaction to the injection site? Will you update to one of the new analog polyamines when they're available? If you'd like to write a personal experience piece, I'd be happy to post it here. Maybe 300 words? Let me know!

Thank you Ron. Yep, it's a heck of a thing and I'm really glad to hear about you apparent success (remission!). My best wishes and hopes that you will stay in remission permanently!

High praise coming from you Pat. Thanks. I hope things are going well for you too!