Starting Chemo Aug 09

Options
1101113151692

Comments

  • Kayel
    Kayel Member Posts: 28
    edited August 2009

    Good Morning Ladies!

    My 1st tx went well yesterday.  It took 61/2 hours which made for a long day but going yesterday my husband and I both thought we might finish our books but I do not think I even finished half a chapter, lol.  There were so many people to talk to.  It was nice to fiinely get started.  I came home nauseated and took the compazine.  By dinner time I felt better and I was really hungry.  Our sitter brought my family a crabcake dinner.  I ate it all and dessert!  Delicious.  I slept well!  Everything went well.  I go for my neulesta shot today.

     YoYo~  I am so sorry for your loss.  My thoughts and prayers are with you and your husband

    Jenn3~ Thanks so much for the tip to contact Laurie.  She is so nice and I will pick out my free scarf today.  I also got a wig the other day.

    I had a good chuckle the other night.  I was reading the messages and saw TMI mentioned a couple of times.  I could not figure out what that was.  It finally came to me in bed.  Thanks for passing that info along.  I also was not thinking about the hair "down below"

    I hope that everyone continues doing well.

  • MaineCoonKitty
    MaineCoonKitty Member Posts: 125
    edited August 2009

    Good morning, ladies!

    Yo-yo:  I'm so sorry for your loss.  I'll keep you and your family find consolation and peace.

    Kayel:  Glad your 1st tx went well.  Keep on truckin', sistah.

    Titch:  It's good to have you here.  I had a very good friend in NZ and hope to get there to visit his family in the next couple of years. Unfortunately, he was killed several years ago in an accident on a movie set in China and I never got to take him up on his offer to show me around the country he loved so much.  I'd like to get to NZ and spend some time with his wife and kids, who live outside Auckland.

  • NavyMom
    NavyMom Member Posts: 1,099
    edited August 2009

    Hi everybody,

    I am on Day #3 and feeling pretty darn good.  Slept a little better last night. And I am planning on throwing on the sneakers and the IPod and going for a walk!  Speaking of music.....if anyone out there needs some inspiration and a feeling of strength from within please listen to the song "Stand"  by Rascal Flatts. That is now my Chemo song.  DH put it on for me when the first bag of chemo started dripping in, too.  A few tears and then that feeling of let's get to it and beat this thing.  Please share if you have other music suggestions that you especially find uplifting and positive.

    And, yes this is a family of Packer Backers.  I married into it 24 years ago.  My Father and most of my friends are Bears fans of course.  But it makes for some interesting messages on our answering mahine depending on who wins on Sundays.  We have been to see the Bears play the Packers several times in Chicago and have gone to Green Bay a few times, too.  Last December we took Navy son to Jacksonville for a long weekend to see the Pack play there.  It was our last little family vacation before he went to bootcamp.  Sweet memories.  Cus ya just don't know if you get another chance so enjoy your kids while you can.  Oh shoot, now I am getting all teary.  Sorry. 

    gotta get that Ipod going.........Have a good day everyone

    Navy

  • MaineCoonKitty
    MaineCoonKitty Member Posts: 125
    edited August 2009

    Glad you are feeling better, NavyMom.  I'll have to check out that song.  I play Patty Smyth and Scandal's "The Warrior" a lot.  I've started to follow the Packers a little (even though I was born a Cleveland Brown fan).  I'm an Ohio State Buckeye nutcase and one of my favorite Buckeye players of all-time is AJ Hawk.  I loved him in Scarlet and Gray and now I follow him as a Packer.  He's a good guy.  Your Packers looked terrific against my abysmal Browns last week.  I'm very impressed with how far Aaron Rogers has come as a QB in a couple of seasons.  I believe we play you for real in Oct.  Hope your season is great!

  • gillyone
    gillyone Member Posts: 1,727
    edited August 2009

    Welcome Tania - sorry you have to be here, but you will bring a wealth of knowledge to the Amazons. (My husband and I spent from October to March in NZ - you have a great country. PM if you are interested in swapping any info).

    I had Tx3 AC yesterday and everything went well. Then went to the look good feel better class. Lots of great makeup and I chose a wig - all free!! Make sure you sign if not already done so. One word of warning, I found the actual class times were different from those posted on the LGFB web site, so make sure you call and check.

    Hair loss - head first for me, waiting for other loss to happen.

    I got up at 5:30am today - I'd been awake for hours (steroids perhaps?). So I went on brisk 30 minute walk (felt very virtuous) and then called  my mom in England (well she's my Mum really), as the 8 hours time difference reduces the window of opportunity. So feeling great and ready to tackle the day.

    Have a good one ladies.

  • Luddy
    Luddy Member Posts: 11
    edited August 2009

    Hello all,

    Well my first tx went well on Tuesday. I must say it was easier than I anticipated.  Went for Neulast yesterday.  So far so good. Took Clartin 2 days prior to the Nuelasta as suggested on the boards.  I was constipated the first 2 days on the steriod and Zolfran. Took some over the counter stool softner and things worked out.  Monitoring now so things don't go the other way with diarrahea. Other than being a little tired, I can't complain yet.

    YoYo - Sorry for your lost. Stay strong and things will get better over time!

    Jenndogs - I too am on TCH.  There is a separate TCH thread and it looks like the window for hair lost is about 14-17 days after #1.  I purchased 2 wigs for work mostly.  I think I am going with the bald look at home and hats on casual days.

    Hugs to all until.. later.

  • MaineCoonKitty
    MaineCoonKitty Member Posts: 125
    edited August 2009

    I woke up this morning with a drippy nose and couldn't figure out why until I looked at the inside of my nose because it felt kinda weird. - no nostril hair.  Poof!  Overnight...it was gone.  Haven't started to lose it anywhere else, but assume it's coming (or going) soon.  Today is Day 8 from my 1st treatment.

  • jennsdogs
    jennsdogs Member Posts: 56
    edited August 2009

    I get my port placement this Tuesday and chemo starts on Thursday - a week from today.  Just in time for me to start back to work from summer break! UGH!   Maybe I should be in the Sept. starters but like the support here so I want to stay.

    Luddy:
      How are you feeling?  Sounds like we will be getting the same tx.  We have the same stats.  I go to look for a wig  Saturday with a good friend who will tell me how I really look! HA!  Not sure what I will do, guess I cross that bridge when I come to it.  Can't see me going without hair.  I am really hoping to keep pushing myself to exercise. I have been getting to the gym everyday and running/biking at home. Trying for 2x a day while I can, then wanting to get at least 4x/wk once school starts back and chemo starts .  Hope my motivation continues!  Keep me posted on you, that should motivate me in itself.

    Maine Cool Kitty: I had to laugh at the nose hair thing, didn't even cross my mind! 

     My ob/gyn called me today to wish me well and was so positive it almost made me tear up. Not that I am being negative but someone else who doesn't NEED to call me makes me feel good.  It's hard to accept help but I need to do it since we dont' have family around and I have two small kids.  My dentist even offered a free cleaning this week to me since my DH told him about the BC.  I am going this afternoon since I won't get one for awhile now and I am crazy about keeping my teeth clean.  What good people there are in this world!

    Sorry guys, a Cowboy fan here. Can't believe it is almost football season again.  Hear the baby crying from her nap, as Navy Mom says - spend all the time you can with them!

  • gillyone
    gillyone Member Posts: 1,727
    edited August 2009

    MCK - I have had a runny nose since starting tx. With nose hair or not, apparently it is a SE of chemo. I just checked with the onc doc yesterday.

  • yasminv1
    yasminv1 Member Posts: 238
    edited August 2009

    Hi Ladies,

    I hope all of you are doing well. I am feeling pretty good today. Sunday-Tuesday were my worst days but I managed to make it to work anyway. My sore throat and thrush made it difficult to eat and drink. By yesterday my throat was better and I had a tiny bit of energy and was able to workout. Right now food has no taste and my tongue feels burnt all the time. This has been the most irritating SE for me because I will crave something and then I'll eat it and I feel disappointed because I can't taste it very well. I still have diarrhea and I have developed an acne like rash on my face and parts of my upper body. I went to see my Onc today. He said the rash is from the Taxotere and the mouth issues I have are normal. He is a tiny bit concerned about my diarrhea. So tomorrow morning I need to produce a stool sample and take it into the office for them to test. He wants to make sure I don't have "C. diff," (Clostridium difficile) which is a bacteria in your intestines. The stool sample has to be carefully handled. It has to stay cool because if I do have C. Diff the sample will explode if it gets warm. You can only imagine the laughter my husband was having when the nurse was explaining all this to us. She luckily had a great sense of humor. Laughing

    Kayel and Luddy- I am glad your first tx went well.

    MaineCoonKitty - I hope your Runny nose gets better. How crazy your lost the hair nose already.

    jennsdogs - great idea on seeing the dentist before chemo. Sounds like you have a great Dentist and OB.

    Take Care Everyone!

    Yasmin

  • Titch
    Titch Member Posts: 141
    edited August 2009

    Thanks for the welcome...Hi to everyone,,,,,

    Gill: It will be the steroids keeping you up, for me it was usually up to 4 days after the tx.  Fatigue will set in cause you are so tired, I hated waking up at 2 am and brain going non stop, when all I wanted was to go back to sleep, was very productive writing lists of things by 4 am. especially cause I was working during the day, I was really tired. Most of my SE were from the steroids, on my final tx I mucked around with steroids and had a worst experience.  Lesson learnt, take the steroids at exactly the same time as prescribed.  In NZ we have our first steroids whilst on chemo, and have steroids for 3 days after tx.  I have had no probs with nausea the whole time of chemo. It sounds like you had a nice long stay here in NZ.

    Abit of advice on this site I read which I now live for, if you are working thru your treatments, have your tx on a Thursday, Fri you will be running around with lots of energy, Sat and Sun are fatigue days, then Monday you are ready for action.

    Yasmin:  I hated the taste bud changing, thankfully it was only on my first treatment.  The steroids made me extremely hungry, wanted to eat.  There were some foods/drinks I could not stomach at all, one was any dairy food and the other was coffee.  Thankfully it was only for the first 3 weeks.  I don't normally drink ginger beer / ginger ale but started drinking lots during my treatments, it really soothed everything.  Another thing I seem to drink alot of was Orange juice and apple juice......  This also help minimise constipation which is a very common SE. 

    Jenns:I can relate to the hair loss, mine started falling out on Day 12, and it came out all day in clumps, I already had my wig ready, so that evening my hubby shaved it to a number one, I had really long hair and it was getting everywhere.  It was initially very strange having no hair.  I wore my wig everywhere and many people thought I had a haircut.  But I found the wigs very hot and very uncomfortable, I was also concerned it was not on properly so forever adjusting it, not a good look when people don't know u have no hair.  So I started wearing hats and now I very seldom wear my wigs.  I also now tend to take all headgear off and do the oh natural look, like when driving, or when at home or even at friends, I would rather be uncomfortable. 

    I also have a port, they are brilliant.  I had my first tx without it, and all others with it, definitely recommend getting one.

    Maine:  Hope u get here one day, you will love it, NZ is very beautiful.  I have travelled around abit overseas but only been to LA in the US and enjoyed it, it is very different to NZ (next time I will travel further).

    Yo-yo thoughts are with you and your family.....

    I am currently of work for a month (been 3 weeks already) recovering from my masectomy surgery, long posts for me are not the norm, cause normally I don't have the time, but I normally pop in and read many of the posts and add small messages.  But at the mo I have lots of time........

  • jenn3
    jenn3 Member Posts: 3,316
    edited August 2009

    Good afternoon - Yesterday was tx #2, it went and is going much better than #1.  The dr added Emend and Ativan and took away the Dexamethasone because I had too many bad SE's from it, sleep issues, heart racing, etc.  However, if I struggle with nausea he said he would have to add it back.  I had no nausea during treatment and only a mild headache.  The nurse also slowed the time I received the chemo drugs to help with the SE.  I got home and was mildly nauseated, took phenergan ate soup and slept for 12 hours - it was wonderful.  I did shave my head to the GI Jane look, now all of the stubbles are now falling out like crazy.  I've learned to tie scarves!!!!  Oh with that said I received my scarf from Laurie, it is beautiful!! She also sent a silky band to accent or hold the scarf on.  I was feeling well enough today to attend my daughter's candelight ceremony where the Seniors hand the "torch" to the Freshman.  One of my biggest upsets when I got my dx was that I wouldn't be able to do or attend things during her final year of high school - so I was really excited that I was well enough to go.

    Titch - Sorry you have to go through this again, but welcome to the August Amazons!!! 

    YoYo- I am so sorry for the loss of your FIL.  I will have you and your family in my prayers. 

    Paulingmom/mnikityger - good idea on the scarves, I never thought of making my own.  However, I'm going to have to get LSU and Saints material..........

    Yasmin - sorry you're having a rough couple days - wishing you luck that you don't have an infection. I hear ya' on the sore throat and thrush - frustrating!

    Mainecoonekitty-sorry you couldn't get treatment. Apparently my WBC was really low and they gave me the heads up that I may have to wait an extra week for treatment next round. I don't want to delay this mess!!!!!

    Manue - sounds like the port placement is just what you need with bad veins, but glad to hear the placement went well.

    Kayel-glad you got the first tx done  - now you're on count down.

    Gill- glad you had fun at the class too!  Lots of good makeup.

    Jennsdogs - We're avid Saints fains, but I do have a soft spot for the Cowboys and end up routing for both teams when we play each other. 

    Well - it's seems I've rambled again, off to dinner and probably become a couch potato the rest of the night.  Talk to y'all later.

  • Kim09
    Kim09 Member Posts: 100
    edited August 2009

    Had my 2 tx today.  Was a little worried about the blood tests since I was in the hospital last week for my WBC's being to low.  But there was no problem.  I go in tomorrow to get my neulasta shot.

    PauldingMom - I didn't think to check with my doctor regarding going into the pool (it was a private not public pool).  I didn't have a probelm and it felt great to be able to have fun with my friends.  I did put on 30 sunscreen with UVA/UVB protection.  There is no way I wanted to take a chance with sunburn.

    Jennsdogs - I did not have a problem my port when I went swimming but the port is under my skin and the two surgical scars had healed.

    In reading about everyone's experiences with getting ports it appears that there are a varity of ways the doctor's do it.  For me, it was considered outpatient surgery and the surgeon knocked me out. He may have done that since the port is connected to a vein in my neck and maybe he didn't want me to flinch.

  • karina_il
    karina_il Member Posts: 29
    edited August 2009

    Hi ladies.I had yesterday my first tretment of AC.On evening I was mess,this morning so far I'm fine I hope this filling will not chage for worse.

    I wish for everyone fest recovery.

    Karina

  • MaineCoonKitty
    MaineCoonKitty Member Posts: 125
    edited August 2009

    Yesterday, the nostril hair....today the arm hair!  It's Day #10 for me and my arms felt strangly smooth when I put my body lotion on after my shower this morning.  Look Ma...no arm hair!  I've never had dark or very coarse arm hair, just a little blonde fuzz, but it's gone!  And the really fine blonde hair on my face is gone too.  I noticed how shiny my face was this morning when I was putting on my makeup.

    I suspect I'll be bald by next weekend if this keeps up.  So far, haven't lost any "down there" hair or anything on my head.

  • sheila888
    sheila888 Member Posts: 25,634
    edited August 2009

    Hi Kitty, What a  organized way to loose your hair. Lets all try to keep our sense of humor. Thats how i survived those difficult days. Next will be the arm pit shining. The hair down there gets thinner but not completely out. LOL.! ! ! ! ! ! !

    I even named my port as an electrical outlet because it looked like one.

    Good luck with your journey.

    Smile Sheila Smile

  • Reni
    Reni Member Posts: 81
    edited August 2009

    Wow I didnt check the boards for 4/5 days and now I'm sooo dizzy just trying to remember who what where...

    Yo-yo sorry for your loss...

    Everyone else I hope your all doing better..... Sooo funny about the hair below....

    For those exercising I really recommend it. I'm day 12 from Tx 1 and feel like the old me (with the exception of the furry tongue and the no appetite. However I've been riding my bike for more than an hour and its really made a difference... kinda put a pep in my step.

    I am still having a hard time sleeping which is wierd cos i'm on no meds right now.

    My next treatment is Aug 31 and I'm hoping to be like Jenn3 with it being better than #1 Tongue out For now I'm just grateful that the hair is intact and I'm living a semi normal life.

  • MaineCoonKitty
    MaineCoonKitty Member Posts: 125
    edited August 2009

    Yep, Seyla....it's so bizarre!  It's like every hair on my body is starting to jump ship like an organized lifeboat drill on the Titanic!  I think pretty soon, I'll hear a tiny band on my head start playing "Nearer My God To Thee".  Wink

    "Attention.....attention.......arm hairs and nostril hairs, please get in the lifeboats and abandon ship.  Pubic hairs........please move forward and prepare to leave next."

  • sheila888
    sheila888 Member Posts: 25,634
    edited August 2009

    Kitty, with that kind of sense of humor you'll do just fine.

    PauldingMom from chemo July 09 made me a honorary member for Triple J's.

    Cool Sheila

  • Luddy
    Luddy Member Posts: 11
    edited August 2009

    Jennsdog,

    So far so good.  Today, day 4, has been the worst so far but very tolerable.  I woke up feeling achy all over.  Ate & took some Tylenol and I was feeling better. I took my last Zolfran last evening, so today I did take compazine as I was feeling a little queasy.   I slept most of the afternoon. I was not really sure why, as I was not tired, but perhaps the stress of the past 4 days just caught up to me.  I have been walking and it has definitely boosted my energy levels.  I suggest you just do not push it and take your meds.   

  • Titch
    Titch Member Posts: 141
    edited August 2009

    In my first session of chemo, I lost most of my hair on my head (I had shaved it to a number one when my hair loss started), but not all fell out.  I was definitely more bald than not though. I maintained my eyebrows, nose hair and eyelashes, but they thinned heaps, and if I shaped eyebrows, hair did not grow back where they were removed.  My arm hairs also thinned. Anywhere I shaved normally, legs, underarms and pubic hair, did not grow at all whilst on chemo, it was great.  Pubic hair went away totally.

    A positive, I have saved lots of money in hair products, haircuts and hair removal since being on chemo.  :)

    I also did the look good feel better course here in NZ and that is wonderful for giving ideas on managing hair loss in the face (eg eyebrows and eyelashes).

  • Titch
    Titch Member Posts: 141
    edited August 2009

    Just to add though......

    Chemo does throw your life into a turmoil, losing hair, you don't sleep, taste buds, feel yuk, long treatments, etc.... But I saw the results of chemo.... My cancer was very agressive(growing 1 cm every 2 weeks), hence why I was put on a chemo regime before surgery.  My lump in my breast was 5.5 cm (ultrasounds and by touch)  when I started chemo (the first time).  I was clinical Grade 3.  It was also in my nodes since feb.  After 2 weeks of chemo I felt differences in my lump, which I thought was too soon.  It stopped growing and started shrinking, after 12 weeks the lump had shrunks heaps. 

    I then had my masectomy and lymphs taken out, and got my pathologist report.  I had 2 cancer lumps 1.5 cm and 2.5 cm, they suspect my cancer had shrunk and broken into 2 lumps as a result of the chemo.  There was also no cancer in the tissues surrounding the lumps.  The cancer was only in 2 nodes, it had not spread.  Cancer had not spread anywhere else.

    Chemo had definitely made a difference in my cancer and I have no regrets of having it.  So no matter what it does throw me physically, being cancer free and not having in spread is more important............

  • Reni
    Reni Member Posts: 81
    edited August 2009

    Titch - I loved reading your post... it really makes it all worthwhile and reminds us of the positives!!!

  • lindal52809
    lindal52809 Member Posts: 25
    edited August 2009

    Hello August Amazons,

    I'm just poppin in to let you all know, i've been reading all you're posts. Makes me dizzy trying to sort out who's who as it has from the beginning, so I wish you ALL the very best whatever stage you are in.  I've been out of it all day today(day7), I'd have to say it was my worst day so far. Luckly I was home from work. My first friday off this summer without a dr appt. and i'm sick. Go figure. oh well, I've been sleeping alot, and the mouth is sore. Controling my diarreha and trying to eat, little snacks thru-out the day. This morning that wasn't the case. This evening I'm doing better. Thank goodness. Felt like I had the flu since last nite. Even had the chills at one point. I can't tell you how many times I've thought of your posts and what you are going thru and said to myself I can get thru this. I am strong, as I drift off to sleep again.  I'll take it, as long as this thing is working. I can get thru it.  Thanks for your posts -  be well all.  Linda 

  • manue
    manue Member Posts: 34
    edited August 2009

    Went shopping for a wig with my sister yesterday... I was trying to have fun with the all process but it was hard. Got my schedule with my oncologist on Wednesday and I should start chemo next Thursday if my plastic surgeon give me the green light! Reading all the posts I'm sometimes overwhelmed with so many feelings - I hope I can be as brave as all of you, AUGUST  AMAZONS.

    Titch - You have quite a story 

  • smore
    smore Member Posts: 16
    edited August 2009

    I guess this is the group that I am now a member of.  I had my first Chemo, August 13.  I am on the Taxatere/Carboplatin/Herceptin every three weeks cycle,Herceptin weekly. It wiped me out, spent the three days after that sleep the majority of the time. But was able to go back to work.  Half day on Monday, all day Wed, after Herceptin Thurs and all day Friday.  I was very encouraged about that. Side effects lost of taste buds, touch of thrush that cleared up quickly with magic mouthwash, first the constipation, then of course the opposite right after the first was cleared  up. One down, five to go.

  • yasminv1
    yasminv1 Member Posts: 238
    edited August 2009

    Good Morning All,

    I hope all of you are doing well. I am doing ok. I have been having some stomach issues the past 2 days but other than that I am doing OK. I am still waiting to hear if I have a stomach infection. I noticed last night my nose was runny and irritated. I took a look in the mirror and realized about 75% of my nose hair is gone. I haven't noticed hair loss anywhere else although my leg hairs aren't growing as fast as normal. My legs are super soft and smooth and generally I have to shave every day. My throat is so much better as well as my tongue. My tongue is still a bit irritated and I still don't have my taste buds back. I long for the day when I can taste food again. My acne like rash is beginning to heal up a bit..thank goodness! I was starting to get embarrassed with the way my face looked. Tomorrow my friends and family are throwing me a hat party. It was so thoughtful of them to plan something like that for me. I was not very excited about it when they first mentioned it to me but now I am looking forward to it.

    I hope all of you have a wonderful weekend. Hugs and Take Care All!

    Yasmin

    Titch - You are an inspiration. Thanks for sharing your story.

    Jenn3 - I hope you are feeling well after TX #2. So happy to hear you were able to make it to your daughter's event. I need to figure out how to tie scarves. I am sure sometime in the next couple of weeks I will likely have a shaved head too.

    Kim09 - I hope you too are feeling well after second tx.

    Karina - How are you feeling after first treatment? I hope all is well.

    Reni - So glad you are working out! I am going to try to push myself to workout today. I have been having issues with daily diarrhea so I haven't worked out since Wed. but plan on doing something today.

    Luddy - I am sorry Day 4 was tough on you. My worst days were Days 4-6. Hang in there and I hope you feel better soon.

    MaineCoonKitty - So glad to see you have not lost your sense of humor. Laughing You made me giggle with your hair loss post.

    Linda - Hang in there. I hope you are feeling better today.

    Manue - I too tried my hardest to have fun shopping for wigs. It got better with every fitting. Take Care.

    smore - Wishing you regain your energy soon.  I have had the same issues with taste buds and thrush. My first tx was the same as you. I too was able to go to work all week. It was a nice distraction for me.

  • Karen09
    Karen09 Member Posts: 320
    edited August 2009

    Hi all!  I haven't posted here in a couple days.  Lots of new people -welcome to you all!  I hope everyone is doing well. 

    Well I am going to buzz my hair off this afternoon with three of my friends for support.  The time is here!  I am a bit nervous but having a buzzed head has got to be better than picking up hair all over my apartment everyday.  lol!  

    On a lighter note, I was hoping my leg hair/armpit air would hurry up and fall out because I hadn't bothered to buy more razors when I used the last one.  Of course that hair is all taking it's time falling out so I gave in, bought more razors and got rid of it. 

    Take care of yourselves everyone!

  • EngTchr
    EngTchr Member Posts: 184
    edited August 2009

    Hi August Amazons,  I'm visiting from the starting June 09 thread and the TCH thread.  Soon there will be a Sept 09 group and you'll be the old timers.  Stay strong!

    smore, just read your first post.  We are on the same chemo regimen.  I wanted to let you know there's a really good thread that started a couple years ago and is still active--taxotere, carboplatin and herceptin.  It's been very helpful to me.  I had tx 4 last Wed and this weekend is my draggy time.  Weeks two and three between treatments are usually fine.  You'll get through it!

    Also, titch, the woman who started the starting chemo June 09 thread is also from New Zealand.  Just think, if we had all been dealing with this 20 years ago how isolated we all would have been!

    Becky

  • NavyMom
    NavyMom Member Posts: 1,099
    edited August 2009

    Hi everybody.  Day 5 for me and feeling Ok.  Just really tired.  Found out this morning that coffee no longer tastes like coffee.  However, hot tea was still good.  No other SE at this point.  Looking forward to next week. Only one appointment(physical therapy)!.  Ah, the things that make me happy now. 

    Enjoy your weekend Ladies.  Hoping everyone can find a few minutes to feel strong and comfortable.

    Navy

Categories