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Melanie Fletcher

~ Mutterings of a Tired Mind

Melanie Fletcher

Author Archives: Melanie Fletcher

So I went to Texas Frightmare Weekend…

24 Saturday May 2025

Posted by Melanie Fletcher in Cons

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A Most Malicious Murder, Jeffrey Combs, Texas Frightmare Weekend

I know, I know—I write SF and romance. Why would I go to a horror convention?

Two words: Jeffrey Combs. See, I found out from a friend that JC would be appearing at Texas Frightmare Weekend this year with his costars from RE-ANIMATOR (it’s the movie’s 40th anniversary this year and the con wanted to celebrate it). Since 1) I still have the Poe Nose Jeffrey gave me back in 2009 and wanted to get the shadow box in which it resides signed, and 2) I wanted to give him a copy of A Most Malicious Murder since it’s dedicated to him, I decided to get a day pass for today and head over to Las Colinas.

Whoo-ee. Texas Frightmare is a big con. A little smaller than A-Kon, but not by much, and it had an absolutely great vibe. The dealer’s room was packed, a lot of people had kids in tow, the costuming was fantastic, and despite the fact that it hit 94°F here today I did not smell body odor once (which gives it major points over an SF con).

After getting my day pass wristband I wandered around for awhile admiring the costuming and the dealer’s room wares, eyed the humongous signing line for Bruce Campbell, and mentally prayed that Jeffrey’s wouldn’t be as long. It wasn’t, but it was still sizeable. I got the chance to chat with some young RE-ANIMATOR fans while I waited (and yes, I may have admired him from a distance. I once told him on Twitter that he would still be hot when he was 90, and he’s proving me correct).

I finally got up to the desk and pulled out the Poe Nose shadow box (for those who don’t know or remember the story, I flew out to LA numerous times in 2009 to watch him perform as Edgar Allan Poe in the one-man show Nevermore…An Evening with Edgar Allan Poe. I wound up making a 1:12 scale reproduction of the set, including a doll of him dressed as Poe, and gave it to him on Halloween. In return, he gave me the nose he wore on stage that night, and I mounted it in a shadow box when I got home). Bless him, his face lit up and he asked, “Where did you GET that?” I explained the exchange we did and he immediately said, “I still have your shadow box! I so appreciate that you made it for me.”

We talked about Nevermore for a bit, then I then gave him a copy of A Most Malicious Murder and explained the provenance. He seemed touched and said that he’d read it. I assured him that he didn’t have to, he could just put it on his shelf as egoboo (not everyone enjoys mysteries). Then he signed my shadow box, shook my hand, and I left. Such a nice man.

And no, I didn’t get a selfie or professional photo op with him because I already have one next to my desk. But it was lovely to get a chance to speak with him again, and I may wind up going back to Texas Frightmare next year just for the fun of it.

So we won the lottery

26 Thursday Sep 2024

Posted by Melanie Fletcher in Personal

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A whole two dollars, mind you. The Brit said, “Clearly this is a sign that you have to go back and buy more tickets.”

I know just how long the odds are of winning a state lottery, I do. You don’t have to tell me that I may as well crumple up the sawbuck and toss it in the trash. And it’s not like we’re basing our retirement on this. But I like a little flutter, and I enjoy dreaming of what we’d do with that kind of money. The Brit would retire, we’d invest the bulk of it in S&P funds and live off the interest for the rest of our lives, and we’d settle down to a quiet life somewhere pleasant where the Brit would build a workshop out back and refurbish antique computers and I’d write until I dropped dead over my keyboard.

Sound kinda, well … small? Yeah, but we’re talking about the state lottery, not one of the big multi-state deals (at my age I have no interest in winning that kind of money—it would be more of a detriment than a blessing), and the store where we buy the tickets only sells the cash option AND I have to split any winnings with my editor. So we’d have about enough for a very comfortable retirement with some nice trips.

In any case, I can spare a couple of dollars a week, and hey, someone’s got to win it. So I’ll buy some more tickets with my winnings and shove them in my purse like I do, then go about my day. But if any ancestors or forces for good are listening, I would not mind winning the next Texas Two Step or Texas Lottery, just so you know. Thank you.

Where did the year go?

23 Monday Sep 2024

Posted by Melanie Fletcher in Cats, Personal, Writing

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Oh, right—I was recovering from cancer surgery, my sister and BIL came to visit, then we lost Jessie, and then there was the whole run-up to the election distracting me. Never mind.

So what’s happening in Casa Fletcher right now? Well, I am currently searching for contract technical writing or instructional design work because we need a buttload of repairs done on this house, I’m doing my best to finish up another Nicola book (which will bring my total of published books to 19), and I’m trying to improve my mood. I’m very, very tired of being broke and worrying about bills all the time, and the Brit is desperately homesick and wants to see his family again, hence the search for contract work.

Apart from that, everything is pretty much all right. There’s no sign of cancer in my jaw, I’ve pretty much regained full use although parts of my jawline are still numb and may be that way permanently, I’ve lost more weight and am currently at 277, and I am developing a raging desire to do some Swedish Death Cleaning and get rid of a LOT of the stuff in this house. Only problem is, more than half of it is some form of electronics that belong to the Brit and he wants to hang onto them Just In Case. Which I cannot fault him for—his hobby is resurrecting antique computers and he does use some of the stuff he’s hoarded. But I would really like to get access to the craft room again, which is currently chocka with electronics and old computer bits. Maybe I can convince him to winnow through it this fall, who knows. I can certainly go through a lot of my stuff in the meantime and get rid of it, but where can I dispose of over 20 porcelain dolls? I don’t want to chuck them in the garbage, but do little girls even want them these days? Decisions, decisions…

Jessica Fletcher—Murder, She Purred (2012-2024)

11 Thursday Jul 2024

Posted by Melanie Fletcher in Cats

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In early June I took Jessie into the vet because she had been wheezing and coughing a lot. After an x-ray of her chest the vet opined that it was asthma (possibly seasonal or regular, she wasn’t sure) and sent me home with two weeks’ worth of cat steroids. Gave them to Jessie, and she definitely perked up and felt better. But her cough never completely disappeared.

Fast forward to this weekend, when the cough came back with a vengeance. I went in Monday to get more cat steroids and gave them to her Monday and Tuesday, but her wheezing and coughing grew worse and very wet sounding. Wednesday morning she kept throwing up her food in little foamy puddles, so I brought her back into the vet who took another chest x-ray. Apparently there was something odd in the one from June but she wasn’t sure if it had been Jessie’s arm.

This time the picture was clearer, and the upper lobes of at least one lung and most likely the other one were pretty much opaque. The vet said that this was most likely one of two things—some sort of mass on her lungs, or congestive heart failure. Since the only way to make sure would be an expensive ultrasound and a mass would mean Game Over, we decided to try treating this as CHF and start Jessie on a diuretic, with heart meds to be added if the diuretic worked.

She gave Jessie a shot of the diuretic and I took her home. She had a relatively good night—she drank lots of water and peed her brains out, had a bowl of tuna, and we loved on her every chance we got. She went to sleep in my office with a water bowl at her side. When I woke up Thursday morning, however, her breathing was still incredibly rough and she was occasionally opening her mouth to gasp. Clearly this wasn’t CHF as the diuretic would have improved her breathing, which meant it was the other thing.

So we said our goodbyes and I brought her in to our vet. Jessie relaxed with painkillers and oxygen, and passed peacefully while I stroked her and told her how much we loved her. I like to think she’s currently hanging out with Uncle JJ and Uncle Jordan while my father feeds her tuna and tells her what a pretty girl she is.

The vet said we did the right thing—she took another look at the X-rays last night since coughing isn’t a common symptom of CHF, and realized that the dark patch we saw on the x-ray was in the right place for thyroid lymphoma, which is rare in cats but does happen. One symptom is coughing, and part of the chemotherapy protocol is steroids, which is why they made her feel better in June then stopped working. If I hadn’t called them this morning, the vet was going to call me and tell me to bring Jessie in.

It isn’t fair, it isn’t right, but it is what it is. So my sweet silver girl Jessie is off on her next adventure, and we will have to get used to the hole she left in our lives.

So, I’m Losing Weight…

06 Wednesday Mar 2024

Posted by Melanie Fletcher in Personal

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Which bemuses me. See, I’ve been heroically sized for most of my childhood and all of my adult life. I won’t get into the complicated reasons behind all that, but I’ve been dealing with excess weight for a good fifty years or so.

Until last year, which had a number of medical things happen. For one, I officially entered menopause in April. With most women, that means that their estrogen level drops precipitously and they start putting on weight. With me, it meant that my cysted-up malfunctioning ovaries finally shut down and stopped dumping estrogen into my system at random times, also stopping the random water retention that would occur no matter what part of my cycle I was at. As I wasn’t constantly bloating up anymore, I slowly dropped from 334 pounds to 321 pounds.

Then I got cancer. The surgery required to remove it left me with a relatively torn up mouth for months. Biting into anything tough or chewy was challenging due to my numb lower lip so I switched out my breakfast bagel for oatmeal. Anything crisp or sharp like chips threatened to damage the healing gumline so those got deleted from my diet as well. My surgeon said no working out for six weeks minimum, so I switched over from 15 minutes of walking a day to 30 minutes.

And I lost more weight. Mind you, I’m sure that the increased exercise and ditching the chips helped with that. But I went from my average breakfast of a Lender’s onion bagel with regular cream cheese and a serving of Frito’s chili cheese corn chips (488 calories) to three bags of Quaker Oats instant oatmeal, a splash of heavy cream, and two heaping spoons of brown sugar (454 calories). Calorie-wise, that’s not much of a change. My calorie intake for lunch and dinner remained pretty much the same, and may have even increased a bit.

Nevertheless, I continued to lose weight. At my 01/24 oncologist’s appointment I officially weighed 301.4 pounds (with clothes and shoes on—I was 299.6 that morning naked). As of this morning, I weigh 289.6 pounds.

According to medical science this weight loss doesn’t make sense. I haven’t made that many changes to my eating habits, and I’ve been walking every day for years. Hell, this last weekend I was eating fast food and store-bought pizza like it was going out of style because Lyndon and I both had con crud and I was too sick to cook. And I still lost weight.

But. My paternal grandmother, who also had Hashimoto’s and I suspect had PCOS as well, was a large woman for much of her life until she hit her fifties. Suddenly she lost all her excess weight. She said it was due to a diet, but I think what really happened was that she went into menopause and stopped getting hit with estrogen storms. Not having to deal with constant bouts of inflammation, her body shed the excess weight and settled at what should have been her normal baseline. That seems to be what’s happening with me.

Which … is nice? I mean, I’ve been going shopping in my closet and finding all kinds of clothes that I haven’t been able to wear for years because I’d outgrown them or they were bought on the dream of, “Well, someday…” I had to throw out a bunch of my capris because they were simply too big and baggy, and I’m getting to the point where I need to go through my t-shirts and consider which ones to save for a t-shirt quilt because they’re too big. When I step out of the shower I can see the actual outline of my shoulders and upper arms, and my collarbones are slowly emerging. When I’m in bed I can feel my xiphoid process (the lower tip of the sternum) and the curve of my ribs.

And yes, I have sagging skin. I’ve got an increasingly impressive set of batwings, and pretty much everything on my torso is drooping. By the end of this I’m going to need a tummy tuck at minimum, and a tummy tuck, butt/breast/thigh lift, and brachioplasty at maximum. But my neck skin seems to be tightening up (I’m using Vaseline on my lymph node removal scar every day so maybe that’s helping) and my calves look fabulous.

So, yeah, I’m getting smaller. It’ll be interesting to see if there are any changes in my vitals at my physical in April, especially since I may well be in the 270s by then.

Renovations Look A Lot Easier On TV

02 Tuesday Jan 2024

Posted by Melanie Fletcher in Personal

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home renovation

I have to give credit to all those people on HGTV home reno shows—this shit is HARD.

Yesterday it took me a good two hours to get all the tools up to my room, attempt to install the blind, realize I’d screwed the pooch, and fill all the holes with spackle in preparation for paint. Today I went to Home Depot to pick up a quart of Glidden Diamond paint in Commercial White (I’m guessing this is the American equivalent of Magnolia in England) and some painter’s tape. My desk is now strewn with drills, power screwdrivers, bits, a hammer, screws, anchors, and all the hardware for the blind. I have paper taped down on the base of the window inlet and painter’s tape going around the base of the inset top and along the opening (with no way to do touch-ups I can’t risk drips).

Then and only then did I climb on the stepladder and very, very carefully start painting over my spackled screw-ups. To my amazement I got pretty much all of it in one coat. When I pulled off the tape I did find a couple of drips on the left side and wiped those away with a damp rag, but on the whole it looks damned good. Tomorrow after the paint dries I’ll retape the left side and repair the swipes I made when I wiped away the drips, and then once that’s dried I’ll try putting the blind up. Again.

I would also like to note that climbing on a stepladder and painting an 18″ x 47″ swatch of inset top made me sweat like a whore in church. I was literally dripping onto the paper I’d taped down to catch any paint. Watching people painting a room on Bargain Block or Fixer to Fabulous is one thing; actually doing it yourself is a whole ‘nother kettle of fish.

Onward 2024

01 Monday Jan 2024

Posted by Melanie Fletcher in Personal

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Yeah, I know, I’ve been quiet since October 24th. In my defense I was 1) still recovering from the cancer surgery, 2) cleaning the house for guests (and that took a whole month in itself), then 3) decorating the place for Christmas.

On the upside I’ve managed to keep the house relatively clean and I hope that can continue once I find some contract work. We are in desperate need of a new air handler for downstairs, foundation repair, and a bunch of other expensive repairs, and until I start making more money with the books the only way to do that is for me to pick up contract tech writing/instructional designer work. Meh—it is what it is.

On the plus side I finished a knitting project today (a Doctor Who scarf) and I think I can knock out a second one in the next two days (a coordinating beanie), which is a good way to kick off the year. I also decided to try and put the blinds up again in my office window, which has been a saga in itself. They’re cordless, which means you have to install two or three clips that the blind bar snaps into, and when I tried doing it before my knee surgery I completely screwed up the placement. To make matters worse my then-bad knee started screaming at me so I just left the blinds standing next to the window until, well, today.

So, yeah, guess what I screwed up again? Yup, the clip placement (you have to position them so that they don’t hit the flywheel innards in the blind bar), and now there are a bunch of holes in the top of the window inset. I’ve repaired everything with spackle and I’m going to pick up some plain white paint tomorrow (since the 15-year-old can of paint I used to paint the office is completely dried up) and paint the ceiling of the inset, then try again.

By the way, this burst of DIY may or may not have something to do with the fact that I binge watched Bargain Block and Fixer to Fabulous over the Christmas break. Ahem.

And Now, Some Good News

26 Thursday Oct 2023

Posted by Melanie Fletcher in Personal

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Tuesday I had an appointment with my chemo oncologist. According to the path results my squamous cell cancer is Stage Two and the surgeon got everything. There is no evidence of cancer in the jawbone, nerves, or lymph nodes; apparently the tumor was wide (35mm) but only 2mm deep (or as Lyndon put it, “You just had a bit of surface rust.” Dr. T says I don’t need chemo and he strongly doubts I need radiation, either, but I need to confirm that with my radiation oncologist next week.

Dr. T has officially recommended that I continue to recover and we monitor with scans in January and April, then another one in October, then go to yearly checkups. This is, without a doubt, the best damn early Christmas present I could have asked for. Phew.

I’m Home

12 Thursday Oct 2023

Posted by Melanie Fletcher in Personal

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I’m missing four teeth, gum tissue, a strip of jawbone, and all the lymph nodes in the left side of my neck, but the surgeon said he got all of the cancer and nice clean margins. We’ll get path reports in a week, at which time I find out what further treatment is required, but my chemo oncologist was visiting someone else and stopped in to see me, and said that the prelim path reports are good. Right now I feel majorly relieved more than anything. And I’m gonna have a really cool scar on my neck from the lymph node removal.

Highlights from the hospital stay:

  • Zofran is a godsend for opioid-induced nausea, but it doesn’t do bubkes for blood-induced nausea. And I swallowed a lot during surgery, apparently, so I spent a fair amount of Monday vomiting. Whee.
  • Doing my prehab routine and getting into as good a shape as possible for the surgery paid benefits in that I was able to do three rounds of the floor on Tuesday, got cleared by speech and physical therapy, and was untethered from the DVT calf sleeves so that I could get up and wheel my IV stand into the bathroom unassisted. The only reason I had to stay for one more night is that my surgeon wanted me to get a few more rounds of IV antibiotics.
  • There is a phlebotomist out there who is damn lucky I didn’t punch him in the nads when he startled me awake at 3 AM this morning and proceeded to use a regular blood draw needle on the back of my hand while saying, “Huh—I should use a baby needle for this. Oh, well.”
  • My GOD, hospitals are noisy places at night. But my nurses and CNTs were lovely people so many thanks go out to them.
  • A diet of clear liquids gets really, really dull after awhile. But I can start eating soft foods tomorrow so I’m looking forward to pudding, overcooked pasta, and soup instead of broth.
  • Pain-wise, it’s being handled nicely with Tylenol (granted, I still have a lot of opioids from the surgery in my system). Right now the most annoying thing is the sensation of having the world’s biggest canker sore under the left side of my tongue from the stitches poking said tongue.
  • I still have a drain in my neck from the lymph node removal, as well as some swelling that is giving me an impressive double chin, and I’m getting rather good at decanting the vacuum bulb and recording the output. The fluid is going from red to straw, which is expected and means that things are healing well.
  • I’m tired, happy to be home, and will be taking it easy for the rest of the week under direct orders from Lyndon. I am not to clean, cook, do laundry, or any other chores. That will be a challenge, but I also know I really do need to rest and heal. The cats will just have to live with being locked out of the bedroom until my drain gets removed on Monday.

So I’m Having Surgery

04 Wednesday Oct 2023

Posted by Melanie Fletcher in Personal

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Why am I having surgery, you ask? Welp, I found out in August that I have a patch of oral squamous cell cancer on my lower left gum. Let me say first that it is eminently treatable, I have a top rate team taking care of me, I have an excellent prognosis of recovery, and nobody should be freaking about about this. I’ve got it handled.

The Background:

In 2001 my dentist put a crown on a molar in my lower left jaw (Molar 19 if you grok dentistspeak) that had been root canal-ed in Sweden. Shortly after the crown was installed a small patch of inflammation appeared on the gum directly under the crown. The dentist checked it, didn’t see anything concerning, told me to use salt water rinses, and said that he would monitor it.

The inflammation continued over the next twenty years, never really hurting or anything, just there. In July 2021 I had the bicuspid next to the molar crowned. The inflammation began to get a bit puffy. I was supposed to have it biopsied but the periodontist I was sent to … let’s just say that he didn’t inspire confidence. Fast forward to this spring’s dental cleaning when my dentist said, “This is growing. You really need to get this biopsied—I’m making an appointment for you with an oral surgeon.” The OS turned out to be the same one who took out Lyndon’s wisdom teeth so I knew he was good.

I went there, he looked at the inflammation and opined that I was having some kind of reaction to the dental cement in the crowns, but that we’d take samples and send them off to pathology anyway just to confirm. He numbed me up, snipped out five bits of gum, and sent me on my way.

A week later, he called. To his shock, it was oral squamous cell cancer, the most common form of oral cancer. Since I don’t smoke at all or use any tobacco products he really didn’t expect this diagnosis. But it needed to come out tout de suite so my August and September suddenly became filled with medical visits.

The Medical Visits:

The Oncology Surgeon: Doctor E (nice guy, very competent) x-rayed my jaw, palpated my neck (nobody, by the way, has been able to feel any swollen lymph nodes, nothing has ever shown up on my blood tests, and all the x-rays of my teeth including the ones taken at my dentist show no sign of cancer in the bone), scoped my nose and throat, and laid out a surgical plan. He would surgically remove the two molars and two bicuspids on my lower left jaw, remove the cancerous gum tissue and a strip of jawbone to make sure nothing had gotten in there, do some reconstruction on my jawbone, then wrap everything up by taking out the lymph nodes under that side of the jaw. Everything would be sent off to pathology, at which point it would be decided whether or not I needed radiation, chemo, both, or neither. In about six months or so I could be fitted with a partial denture or implants, depending on how well the jawbone healed.

Pre-surgery physical: That was done at my GP’s office and was a standard physical with an additional EKG and chest x-ray. Everything came back okay (I have a little bit of opacity at the bottom of my lungs, but so do 90% of people in the United States who had COVID so…) and I was cleared for surgery.

The Radiation Oncologist: Dr. D (very nice guy, also extremely competent, with a great scheduler and nurse) took my history, palpated my neck, and felt around in my mouth. He told me I would most likely need radiation and what I could expect from it. Treatment would take six weeks; every week day I would drive to their office where I’d lie on a table and a mask that had been fitted to my face would hold me in place while I got hit with radiation. I could expect loss of taste, a drop in saliva production, and increased soreness and pain in my jaw and throat as the treatments proceeded. It would become painful to swallow during the second half of the treatments and I’d probably go on liquids, at which point I would need to make sure that I was taking in 2000 calories a day as the pain and lack of taste would affect my interest in eating. That being said, they have good painkillers that are very effective for this sort of thing, and I have a Ninja blender that could turn a brick into soup.

Long term effects would be a permanent drop in my saliva production (he said I’d probably need to have a water bottle next to my bed, which I already do), but it wouldn’t affect my ability to swallow or speak, and my sense of taste would eventually come back. I can live with that.

The Chemotherapy Oncologist: Dr. T (also a very nice guy—really, everyone I met at the cancer center was a doll) had spent a rotation at the University of Chicago Medical Center so we commiserated on Chicago winters. He didn’t think that I would need chemo, but it would depend on the PET scan and the path results of the excised tissue. We talked a little bit about the effects of chemo and what I could expect from that. He also asked me when I was supposed to get the PET scan. When I said it was two weeks out he said, “That’s unacceptable,” made some calls, and got it for me the next morning.

The PET-CT scan: I showed up after not eating anything since midnight, got a shot of radioactive glucose, waited for an hour for it to make the rounds of my body, then spent a half hour with my arms over my head while the scanner did its thing. A PET scan finds areas of high metabolic activity, which can include cancer, incisions, infections, and recent bone breaks. Unsurprisingly, it picked up on some low-level activity in my jaw, more apparent on the side with the cancer and much spottier on the other side. The doctor who wrote the report said that the other side might be due to an infection; since I had an URI/sinus infection complete with sore throat, coughing, etc. at the time, that could explain it. Oh, and apparently I have a large mass on my right ovary, but it didn’t react to the tracer so it’s either a cyst or a fibroid. Quelle surprise, said the woman with PCOS. I’ll get that dealt with once the jaw is done.

The Surgery:

The surgery was scheduled to happen on last Monday but there was a scheduling miscommunication between my surgeon’s office and the hospital so the event has been moved to 7:30 AM on Monday, October 9. Once I’m out of surgery I’ll spend between 2-5 days in the hospital (I’m hoping for two but it’ll be whatever they recommend), then go home to recuperate and heal for 2-3 weeks before they start the radiation and/or chemo.

Pretty much every medical professional I have spoken to has gone out of their way to reassure me that they can handle this and I have an excellent prognosis. I choose to believe them, so I’ve been doing my best not to panic. I probably won’t be bringing my laptop to the hospital but I’ll load my login details into my phone and hopefully I can update you tomorrow. Think good thoughts for me, please, and if you would like to support me in a more material way you can always join my Patreon. The most basic tier gets a free short story from me every month for $3, plus updates on my work and sneak peeks at the current WIP. Higher tiers will get bonus material, a free ebook, print book, or hardcover book, and all proceeds will go towards paying off my medical bills. And if you can’t swing that, totally cool—I will be happy with prayers, healing vibes, and any good thoughts you can shoot my way.

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