This is so weird now it is out of control. I put 2-3 tiny water lettuce from the main pond (with fish) to the little pond that I completely drained and scrubbed out this spring. There are no rocks or any places to hide, it's small, and I got everything out of it before I filled it. So last night I'm out with my flashlight to check the tadpole I put in there (who is fine BTW thanks, sprouting little legs too) and as I see the tadpole swim under some water lettuce for cover out swims another fish! He looks like the poor little fellow I found that morning, just maybe a little smaller. A bird may cough up one dead fish but not two and not still alive! I'm wondering what killed the other guy I saw. I don't tend that pond much beyond topping off the water (with treated water) and pumping air into it, the filter & pump never really filtered out anything just kept some water flowing down the rock cascade. I did treat the water with PraziPro (as I'm treating my pond and indoor tank too) on Saturday but that is supposed to be very safe stuff. Huh! jalal: Thanks for the compliment! I'll see if I can find out a name for the grass. We got it from a friend who was chopping huge pieces out of his garden. It will grow without bounds over the years. Very hardy and comes back like clockwork every spring. I even have one clump 2 years now growing only so-so but it isn't planted! The root ball is just sitting on the ground. sleeplessinftwayne: That's a funny story. I'd love to see the fish jump from pond to pond or tank to tank. I wonder how they know which way to jump?

Were you able to get your address to Craig? If not, PM me and I will pass it on to him. Is your Privacy setting on LOW or to ACCEPT ALL COOKIES? If not, you can go to TOOLS, choose INTERNET OPTIONS, choose the PRIVACY tab, and then change your setting to LOW or ACCEPT ALL COOKIES, and then I would reboot and bring up the website again and see what happens. All this does is allow your system to accept the website's cookies. That's one option. Another option is to do all of the above, except click on SITES (another option instead of changing your privacy level), then enter the web address of Tville (I usually bring up Tville's website and just copy and paste the address in the box indicated), then click ALLOW, then OKAY. Then you don't have to allow cookies from OTHER websites, you can choose which ones you want to allow. This is the one that I chose. If you've already done either of these, the question is moot, and I don't know what to do. Maybe someone else will. I'm not that computer savvy, except to type on it, LOL! I had forgotten I had to do that, too, with Tville's website. Hope it helps, though. Susan

Want to give an long over do update.. Hubby's last treatment (chemo & radiation) were 12/23. He was supposed to finish radiation 2 days sooner but had complications with neck burns; they had to get his pain under control. I asked the radiation oncologist for the morphine pops again; this time he gave it to us but it was a 3 day wait for it to get ordered. I'd called pharmacies in both NJ & Philly; no one stocked it, not even hospitals. He ended up using a Fentynol patch for a few days; he was only able to wear it for a few hours as the Fentynol made him sick. They are supposed to be a 24 hour patch. The pain problem was a dry neck - he couldn't have the antibiotic cream on his neck for radiation because he'd fry; which meant he had to go from the shower, we'd wrap his neck in wet gauze & baby wash cloths plus an ace bandage then he'd unwrap when we crossed the bridge. He lost over 20 pounds, which he couldn't afford to lose anything. Healing was very hard on him. He did so well at 1st but his autoimmune kicked in about 2 weeks out to where his blood counts were really low. I ended up taking him to a natural Dr where he had supplements & a vitamin C drip which seemed to work; unfortunately, he needed 2 drips per week but we couldn't fit 2 into our life (it was an all day thing with ride plus waiting for the bag to drip) plus he did not like the way the girls stuck him or pulled the IV out. His body was still sore from all the needles in Philly, he didn't need more pain. Yes, we complained... He got very depressed because he wasn't healing quick enough. I could not get his mood changed. Different antidepressants were tried but nothing worked. What ended up working was our old neighbors came up from Tennessee on Valentines day (he didn't know); so that cheered him. Then we made the decision to have the feeding tube removed. The feeding tube was a huge source of pain; his intestines always hurt; he was usually found doubled up in pain. It was thought he had gas but from what I researched it could have been spasms. Any puree's that I made, he basically shut down & wouldn't eat them, nor would he eat by mouth because he had no taste buds and no saliva. To someone that likes to eat, this is very depressing. He'd tell me that the puree would sit in his stomach & not digest. We saw the radiation nurse practitioner and I was able to speak to her alone.. she backed me up that the tube needed to come out & that he needed to be able to sink or swim. Had he not started eating, they would either feed him via nose or another feeding tube. On 2/22 we saw the ENT surgeon & lied about how much he was eating by mouth; they pulled the feeding tube out.. yes, held a towel over it and yanked & out it came. 5 months after it was put in, it was taken out & he's been doing well eating. His taste buds are better; he's not complaining about the saliva as he knows he's going to have to drink water with almost every bite just to swallow it. Most food will suck up his saliva like a sponge. We knew our health insurance was going to get canceled & it did. He was going to start physical therapy 2 weeks ago when they called to say it was denied for lack of coverage. We've been on this since December, asking for Cobra forms but they never came. Thankfully I know the rep; he told me when it was sent out & when it did not arrive the following Monday & Tuesday (last week) hubby & I made the 2 hour drive to Port Newark to do it in person. We split the driving because neither of us drive that far. The insurance cost us a pretty penny until we are approved; then they will either refund the money, if hubby gets back to work before we use up our large payment or they will deduct the lower amount from my large payment until he does work. He had a PET scan on 2/4 - we were not supposed to get the results until the following week but the nurse practitioner called us the same day because she knew how depressed he was. He told me a week or 2 before the scan that he was not fighting any more nor was he doing this again if treatment did not work; so I was a basket case as well; especially since it was right before my dad's 4 year anniversary of being gone because of cancer. Had we not had my inheritance from my dad I don't know what we would have done to survive. We were very fortunate that we did move to where we are so he had better treatment options. After making the drive to North Jersey the other day, there was no way he could get treated at my original choice, where my dad had treatment; but he was able to get treated at a very large place; which I'm not sure he would have chosen had we still lived in the old house. So, everything has worked out. The next scan will be in 5 months; so we'll see. I'm not sure when he'll be able to get back into his truck to deliver cars; but hopefully he'll be able to do the yard van to drive drivers to their cars. Hopefully physical therapy will help.

I'm actually a dermatologist in my other life. First statement: you can't make a diagnosis or treat patients over the internet. He needs to see a doctor, today preferably. I don't think a GW Kitchen forum, no matter how great, is the place to get advice! Best thing which is so often neglected would have been a swab culture from the area at the initial visit, before treatment was initiated, for both bacteria, and also herpes simplex, if they really suspected "cold sores," though that's quite rare in that location. Many do what you doc did, which is to treat empirically with Bactrim, a drug that covers probably 98% of all staph including MRSA. Failure to respond certainly could indicate that this was not staph, or the incredibly rare case of Bactrim resistant staph. Equally likely, as we see this all the time, is that he's doing fine and that what you interpret as "not better" actually is improved to an expert's eye. Because of your concern, and even more so if other symptoms are present (fever, chills, red streaking, swollen lymph nodes, pus draining, etc etc) a recheck is indicated and I woudl press to get bacterial and HSV cultures if they think it's a consideration. Maybe you can guilt your derm into seeing him if he's worse. PS: staph is almost certainly acquired at school, not in the temp kitchen.