Charleston Bound, part 2
Comments
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That is so kind of you Marty. We are staying in a condo at the Abermarle. Great local for DH golf tourney. Not as great for me but it's very nice. I'd love to meet you for lunch if you are close. Let me know. I think I sent you my cell pm.
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Jamie - I didn't know if you got my PM from this morning. I so wish I could come get you for lunch. You are only about 40 min away (not far around here), but I am booked for lunch until Friday. And, I think you are otherwise tied up on Friday. Wednesday is bridge at my home and Thursday is my nuclear stress test. Do you think I should study? I know all will go well for you. If you want to try for Thursday evening??? Husbands included. Marty
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Hi Marty, So sorry I didn't get back to you yesterday. We could try for Thursday night and meet in the middle? It would be great to meet you. Just let me know and any restaurant selections. Thanks so much. Jamie
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Jamie - Yes! Chuck & I would love to get together with y'all. Restaurant suggestions: Slightly North of Broad (on East Bay); Lana (corner Rutledge & Cannon); or anything you would like as you are having surgery the next day! Name your time. Marty
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Hey Jamie! Don't be nervous, great Dr, great hospital and nurses. Great city to visit and people to meet! Your butt will probably hurt more than when they took the flap, at least mine did, and the lipo is painful but it dissipates pretty quickly and pain killers do their job. (c: You'll do wonderfully and be so happy. The end is near! Tell Marga howdy. Text or call me any time. Enjoy dinner with Marty and dh.
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Adey, my surgery buddy......thanks for the pep talk. I can see a little light at the end of this long tunnel. I'll tell Marga howdy for you. I had Rick take the car to the golf course today so I am just puttering around the condo. I still have my PJs on. Never do this at home.
Marty, I'll look forward to meeting you both. You make the restaurant choice since you know way more about them than we do.
Hugs, Jamie
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Go to the pool or hot tub! Drains and holes in the bod are coming. (c: Enjoy a peaceful day.
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Will be thinking of you Downey. Hope all goes well. Give Dr. M a big hug and tell her I wish I were there. (sniff, sniff) Let us all know how things go. Should be an easier go around this time.
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Downey-warm wishes for surgery on friday and to easy recovery and great results. Enjoy dinner with marty too--that's fun that you were able to connect. Good luck to your dh too.
Gma-how's your hbot going? Hope you are able to relax and enjoy all those movies.
Cascader- it's almost time for your hbot too and hope logistics going smoothly for you. I read in my East Cooper hospital brochure that they have a wound care center and two hbot chambers there. I almost wish i had rented the tiny cottage on sullivans island and done my therapy there at ec.
Sherry--thinking of you and hope you have turned the corner and healing so you can get on with next surgery as planned. Are you doing okay now? -
Jamie and Marty, wish I could join Y'all for dinner in SC. Such great restaurants. I especially love SNOB!
Marty, a little over a month for your surgery. Keep us posted.
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Jamie, wishing you an easy surgery and a swift recovery. You are in good hands. Let us hear from you soon!!
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Jamie and I had a wonderful dinner last night with our DH. She is wonderful and very helpful. Right about now, she should be peacefully snoozing as Dr. M gets to work. Yesterday I did my nuclear stress test and passed with flying colors. Next week blood and x-ray. Packing lists getting put together. Five weeks out. WooHoo! Can't wait to get real ones back.
BTW, I will be cooking at Hope Lodge again on October 22 if any of our girls are there please say hi.
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Prayers Jamie.
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Prayers too, Downey. Hope this one is much easier and speedy recoup.
Pinkheart, I am 12 down, 8 to go and then 10 after surgery. Not so bad now. I was getting donor site pain and wrist pain about 45 minutes into the HBOT treatments. We decided I would take an aspirin one hour prior (but I forgot and took it just before), either way today didn't have that pain. I also bought season 1 of a tv series Emily of New Moon? And that has kept me interested without worrying I was perverting the HBOT tech (had some pretty racy stuff from the library at first)(even a movie called Bananas!) now is see 2 episodes each dive and works out just fine. The back donor site really hurt prior to the aspirin.
Marty, truly so appreciated at Hope Lodge! The men would be talking about and speculating what the dinner fare would be while sitting in the screen porch early in the day. Truly a blessing.
Sherry- hoping all is going better? So interested in your Seroma condition. I have 2, one on each side. Was told they would be addressed when I get to the stage 2.
I'm looking at Jan. 3 for re doing the left breast that failed in April. Woo hoo! 3 months to get this body working! -
Hi everyone, I left the hospital about noon today. I could have stayed another night but it is very difficult to get much rest there. Dr. M fixed my shark bites, fat grafting, revisions on breasts, and fixed some dog ears on abdomen. I'm pretty sore but know it will resolve soon. I have four drains but they are not putting out all that much.
It was realy great meeting Marty and her husband Chuck. SNOB's was fabulous and so was the conversation.
Thanks to everyone for your good wishes. Hugs, Jamie
P.S. It's nap time
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Jamie, what a trooper, don't know if I could be online and out of the hospital so quickly! An inspiration for me for sure, congrats! Did you have the crab soup at SNOB? There is another restaurant just across or down from SNOB that is fantastic too. Chef Is wonderful.
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Finished my first 2 HBOT sessions today. All went well but BORING. Read some and just closed my eyes to relax. 8 of us in the chamber today. Tonight feeling congested and like I am getting sick. Not sure it is related, but back again in the am. Hope you are all good and enjoying the fall
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Cascader~
I got congested and then pain and pressure in ears because of it and then the tech would have to lower pressure slowly. Did the doc or tech suggest nasal spray? Mine did and it definitely helped. My ears would stay plugged up for about 6 hours after I got out of chamber. Everything sounded muffled, and then my ears would pop open around dinnertime.
Yes, BORING is the word. I never want to watch another episode of HGTV!
Hope Dr. K doesn't have 10 more sessions in my future like GMA
Thinking of you and hope you feel lots better soon.
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Cascader, I'm now only 6 from being done this go round. I agree with Pinkheart, congested ears right after, then tired about 2-3 hours later, which I mostly just plowed through, and then by dinner or bedtime I'm feeling normal ish, but not totally.
I tired tv but have to get the tech to change channels, then tried movies from the library, now engrossed in Emily of New Moon. The latter keeps me really forgetting about the fact that I'm in the chamber and goes quickly. I have another tv series to watch when I'm done with these dvd's. wondering if my vision will go wonky as I hit my 15th session tomorrow.
Cascader, you are really plowing through the sessions with 2 at a time! I would also like to be in a different position than on the gurney. Donor site hurts sometimes. I've been taking an aspirin 1 hour prior to entering, and it seems to help. By the time I'm done ill figure it out!
I do get super hungry at mid point though, but subsides after I get out.
Are you able to chat with other patients?
I'm not sure Dr Kline is requiring or suggesting the extra 10 but more so the HBOT wound care doc. -
Going to Marga's seminar in Chicago on Nov 17, anyone else?
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Had originally planned to but having lymph node transfer with dr kline.
My insurance just approved!
Will have it at same time as stage 2.
My old pt may be going to her seminar though. -
Congrats on the approval!
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Pinkheart, wow anxious to read how the lymphnode transfer went. Addey where is the Chicago seminar with Marga? Would like to see her but going into surgery again.
I was trying to set up a consult with Marga and met also with Dr. Song UofC to fix a botched TE and capsular. Then bombshell hit, I was told I have kidney cancer. So instead of having a DIEP procedure I Am going in for Nephrectomy surgery instead.
Seem to just keep getting bad news and can't stand these hard tissue expanders in me anymore, one side breast lymphadema, other side hard scar tissue, I am a mess and llosing faith. I have had to advocate heavily and fight to get the proper scans. -
Oh my Bogie that sucks. What day is your surgery, at what hospital? I will add you to my prayers. Here is the link for "The Doctor Is In" seminars. Sent PM.
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Bogie, I am so sorry to hear about your kidney cancer on top of breast cancer reconstruction complications. You have much to bear and prayers r n my heart for you. Have you been to Cancer Treatment Centers of America in Chicago. Do u have surgery date yet?
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Bogie, you are in my thoughts and prayers.
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Sherry...did you ever hear what your cultures showed? How did they treat the abscess? Hoping it is resolving!
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For those people about to have a Stage 1...
I'm getting rid of my surplus surgery supplies and I'll be glad to send someone a care package (if you chip in 5 bucks for shipping). I have:
- about 50 ABD pads
- 2 boxes of 4x4 gauze pads (soft ones), 50-count each (25 packages w/2 in each)
- a box of alcohol wipes for stripping drains
- huge stack of measuring cups for measuring drain output
- latex gloves (as many as you want, I have a box + extras)
- a lanyard for hanging drains in the shower
I also have 2 extra doms in size XL that I wore once, but I'm guessing no one really wants those.
If you're interested, send me a PM and we'll make arrangements to ship.
-Brenda
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Adey,Pink and Downey, thank you for your kind words and I'm glad you are all on the mend. My Nephrectomy surgery is on 10/23 at University of Chicago.
Pink, do you recommend the cancer treatments of America?
I did email and they were so nice, but don't typically take HMO BCBS insurance they told me. I may have to add another insurance through my work if allowed to. I use my husbands only right now. We have no idea where this came from and I'm still fairly young and working full time. -
Bogie,
I haven't been to Cancer Treatment Center of America, but my husband's cousin switched from UofC to CTCA. His wife had breast cancer and went to UofC and wasn't happy either, but haven't heard if she switched yet too. Her husband is late stage prostrate and she is Stage 0 BC. Her reconstruction (implants) is messed up, but she is waiting to take care of it because her husband's health is unfortunately failing. When I talked to her at family reunion in Chicago this summer, she said there was an overwhelming amount of compassion shown toward her husband, and more true "teamwork" involved with his care between types of therapy, doctors and staff at CTCA vs. UofC.
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