I am starting chemo in July 07. Anyone else?

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  • Gagal
    Gagal Member Posts: 42
    edited July 2007
    Welcome jbw123,

    Sounds like everything really went fast for you from diagnosis to treatment. I still have strange feelings around my port sometimes feels bruised or muscle strain, I really just don't like the way it looks or feels, but I guess it beats the alternative.

    My 2nd treatment was easier than my first less nausea and more energy. I'm facing number 3 this Monday, little nervous don't know what to expect each time hopefully it will go as well as the last. The big thing for me was figuring out all the meds.

    I'm glad you found us, you'll get alot of good info here and it's nice to share with others. Best of Luck with all your treatments.
  • LottaQuilts
    LottaQuilts Member Posts: 212
    edited July 2007
    Hi, JBW123... welcome to our little group.

    Our stats are almost exactly alike! My tumor was 1.4 as well, I'm doing the same treatment plan as you, and my 3rd treatment will be on the same day as your 2nd... we're on a schedule together!

    One of the objections I had to the port was that I said it would drive me crazy. And it does. My bra strap rubs on it, I feel it when I turn on my stomach at night while TRYING to sleep. Quite honestly, I can't wait until I get the darn thing out. But... I'm really happy to not have to do the IV thing 16 times for my treatments. It's like everything else involved in this process.... you just gotta put up with it. And honestly, it does bother me less than it used to.

    Abbi
  • TINAMAE
    TINAMAE Member Posts: 106
    edited July 2007
    Ladies what is taxol, my dr said 4 ac then surgery then maybe 4 more after depending on outcome of surgery, my lump is 4cm no node involvment.

    Thanks Tina
  • 1973vwbus
    1973vwbus Member Posts: 16
    edited July 2007
    I got 2nd treatment yesterday along with the port, not feelig to bad today. However the port tube close to my neck feels like it is tight sort of pulling is this normal. The nurse says the doctor always asks what size breast you have to make sure the tube accomodates the weight of your breasts.
    Anyone experience this feeling with the port?
  • jbw3843
    jbw3843 Member Posts: 46
    edited July 2007
    Thanks for the welcome. It's good to know others on the same timeframe. The port feels better today. Yes, I had slight pulling at first. It's been a week and it is getting better. Honestly, I don't think it will ever be unnoticed by me, it does stick out and I know it's a huge exaggeration but it looks like a saucer stuck up there. LOL I'm still glad to have it as opposed to IV sticks. I mean they have trouble getting blood from me on a "yearly" physical. Which by the way is how often I used to have to go to the doctor before this all happened. So I'll put up with the port and know it's not forever.

    Abbi, I haven't been able to wear a bra since the port was installed. I picked up some $3.00 colored tank undershirts at Walgreens of all places. They've come in very handy. I wear them under either a sleeveless or sleeved shirt. I don't think I could pull it off if I had large breasts, but I don't.

    When did your hair fall out on AC?
  • MLizA
    MLizA Member Posts: 33
    edited July 2007
    Hello ladies, I am so glad to have found this board. I started chemo on 17 Jul. Got my Dx on 9 Jun, surgery for mastectomy 6/20 (7cm), sentinel node biopsy (11 of 13 involved); auxillary node disection, stage IIIC. Treatment is to be 4 AC and 4 T every 2 weeks, 6 wks radiation, 5 yrs hormone therapy.

    First chemo went rather well, anti-nausea meds in IV and three days of Emend at start of chemo - only problem was flu like symptoms 24 hours after Neulasta shot. I drank tons of water.

    I am working from home and now just seem to be waiting for my hair to fall out... I am not sure why that bothers me so much. The hard part for me is just not knowing what to expect - that is why reading these posts are so good for me. I, unfortunately, worry about everything.

    I got my port implanted the week before I started chemo and was so surprised at how uncomfortable it was and still is, while it certainly made chemo easier - I hate it. My surgeon said it would just be the size of bottle cap raising my skin, I thought she meant a beer bottle cap, not a 2-liter bottle cap! So I appreciate reading that others also have the same issues and that it is not just me.

    I am interested to know if chemo gets better or worse with each session, I imagined that it would get worse as your body gets weaker. Also if anyone has any good scarf tying links I would appreciate them.
    Thanks, Linda
  • figsgirls
    figsgirls Member Posts: 253
    edited July 2007
    Welcome JBW123 an Linda. JBW, I'm in education too.

    My port also shows a lot more than I thought it would. My friend told me her mother's didn't show at all. Then she looked at mine and said "WOW! Yours is really noticeable!!" Fortunately she is my good friend so I didn't smack her. You can see the port sticking straight out, exactly like a 2 liter bottle cap, and the tube running up to my neck. And the steri strip is still hanging on, nearly 3 weeks later.

    Well, my AC #2 is Monday 7/30 so I am one cycle behind GaGal. This is my off week and I have felt so great! I went running- boy was I slow!- and cycling, and the darn headache finally went away. It's a relief but at the same time it's making me dread Monday even more.

    Ladies with ports, do you care if your port shows, or do you try to dress to cover it? Just wondering. Although I don't care about the tube that runs up to my neck, I've been pretty uncomfortable with that bump from the port itself showing.

    Donna

    P.S. GaGal, are you in Georgia? I used to live in Marietta.
    Oh, and Linda P., I got some stuff from the ACS website and I think their scarves come with tying instructions so maybe they are right on the site as well.
  • liven42day
    liven42day Member Posts: 76
    edited July 2007
    Hi Ladies,
    I am starting AC chemo July 30, I am 2 txs behind one of you (Donna)and 3 txs behind (Calgal). Maybe I am just overly worried, but did you have your port checked to see if it works b4 AC? Does the chemo nurse run anything through it b4 AC to make sure it works? I have not been told anything other than to eat breakfast and take my Emend 1 hour b4 chemo Monday morning. My port was put in July 23, it has a tight feeling still but the tube going into my throat is the most annoying part of it. I feel that the tube sticks out more than the port in my chest. Thank you for any comments, just venting a bit I guess, Charlene
  • LottaQuilts
    LottaQuilts Member Posts: 212
    edited July 2007
    Welcome Linda and Liven42day

    My port is in a place that it really doesn't show when I'm dressed. Before they give me my A/C, they attach the tubing and check to see if they get a good blood draw from it. I've never had a problem. Then they wash it out, if you will with a little saline injection, hook up my saline bag, steroid, anti-nausea. It takes a good hour or so before she comes in and actually starts the drugs. First up is the "red devil" (the A) which she controls with a syringe (takes 30-45 minutes). After that, she hooks on a bag of Cytoxin (sp?). That usually takes about 30 minutes, but I got a headache last time so they're going to increase that to 45 minutes.

    The first time, when my port was only 2 days old, they put a numbing cream on the skin before they "stuck me" as well... that was nice.

    BTW - where IS everybody from. I'm from Pittsburgh, Pennsylvania
  • LottaQuilts
    LottaQuilts Member Posts: 212
    edited July 2007

    Oh, I almost forgot. Someone asked about timing for hair loss. Mine started coming out on day 14 after my first treatment. On day 16 I had DH shave my head!

  • Gagal
    Gagal Member Posts: 42
    edited July 2007
    Figsgirls, I'm from Kennesaw, Georgia, in west Cobb County one street over is Marietta. I see you're in New York that must be a big change from Marietta and the Big Chicken?

    My port sticks out like a bottle cap also, I try to hide it in public it just looks gross to me.

    Linda P16, I'm interested to find out if chemo is going to be worse each time also, this will be the 3rd for some of us on Monday, so stay tuned I'm sure we will have updates for you, so far it seems everybody is a little different.

    Good luck to everyone next week.

    Pat
  • Gagal
    Gagal Member Posts: 42
    edited July 2007
    Asia, we haven't heard from you hope all went well with your first treatment and you'll be joining in soon.

    Pat
  • bonny1963
    bonny1963 Member Posts: 450
    edited July 2007

    Congratulations! You are doing great and you will get through this. I was dx 09/06 and had 4DD A/C and then 4 DD Taxotere and I made it through it all. I had 33 radiation and came through with flying colors. Chemo is very hard (I think more mentally than physically-even though it was hard physically) but each day brings you closer to the end of it. I finished on2/19/07 and I have hair. It does come back! I actually had a trim on my very short hair the other day to shape it up. I didn't post in a regular chemo group but I posted all the time in the Tennessee Thread. The friends we make here understand everything we are going through. Stick together and you will make it. We are all in this together. Good luck! Bonny

  • figsgirls
    figsgirls Member Posts: 253
    edited July 2007
    Well this morning I was running my fingers through my hair and ended up with several strands in my hand. Every time I take a little pull, a few more come out so I guess it's begun. Hubby will shave it tomorrow or Monday I guess.

    I'm in the Buffalo, NY area. Except for my year in Marietta GA, I've lived around Buffalo all my life. It's not nearly as bad as its reputation. The summers are gorgeous.
    Pat, Kennesaw Mountain was our very favorite place! It has beautiful trails for running. We lived just a couple of miles down the road so we went there a lot. I loved the area but alas my husband did not, so we came back in 2003. But we still talk about running at Kennesaw Mountain!

    Donna
  • MLizA
    MLizA Member Posts: 33
    edited July 2007
    Donna,

    I dress to cover my port as best I can, it still sticks out of most tops, I am still quite black and blue around it but the tube up to the neck does not show on mine. I had to go out and buy some cheap bras to get some where the straps would not rub it. All of of the mastectomy bras I got rub it.

    Has anyone had problems with blood counts being high enough for the subsequent chemo sessions? I am trying to figure out what the right balance is with exercise and boosting my immune system versus depleting it. I try to walk on the treadmill each day but haven't done any jogging. Maybe I am being overly cautious.

    My second tx is on the 31st ... first one went better than I expected but am already getting anxious...

    Oh and by the way, I am from Colorado.

    Linda

  • Gagal
    Gagal Member Posts: 42
    edited July 2007
    Figsgirls, I guess it is a small world, my son loves to run the trails at Kennesaw Mountain also.

    Good luck with your hair cut in a few days, I'm still shocked everytime I look in the mirror.

    Pat
  • rspayne
    rspayne Member Posts: 49
    edited July 2007
    Hi Linda, and jbw123,

    IHad Lumpectomy and sentinel node biopsy on6/1/07. Three of seven nodes had cancer cells. Went back on 6/15/07 to have margins redone and port inserted.

    My port has been uncomfortable from the start, but I must admit that it iis quite small and is nicely hidden right below my collar bone. Unfortunately they are unable to do blood draws from it. I had a dye test to have it checked and they tell me that the tip of the catheter is against the wall of the vein. They tried putting some TPA(used to bust clots) but it did nothing, so it's only good for infusions. Fortunately most of my bloodwork is finger sticks. They only need blood from arm every three weeks, right before my tx.

    I have found that the softer sports bras (I like the under armor ones) are just right as they do not push or press on the port. It is best to look around and find the most comfortable one for you.

    Diet wise, I have found that several mini meals is best to avoid nausea. First tx was good. My center insists that I drink 96oz. of liquid the day of tx and two days to follow. It's hard, but I think that it is very vital for quickly flushing the no absorbed dose.

    I think that the decadron given the day before and after (pills) and the day of tx.(via iv) is the worst. I didn't sleep till 3:30 am the morning after my tx. I felt like I was on speed, although I must say that I got my kitchen spotless before I finally slept. The next morning I felt weird.

    Oh yeah, I started tx TAC every three weeks for six txs on July 9th. I could have started sooner but I had two big family weddings, June30th and July 7th, both out of town. I had a very nice time at both despite the looming threat of chemo.

    My next tx is Monday 7/30. I will be glad to have another one to mark off my calendar!!

    My best to you all, Rose
  • jbw3843
    jbw3843 Member Posts: 46
    edited July 2007
    Hi girls. I'm from a northwest suburb of Chicago.

    Welcome Linda. Sounds like you fared pretty well with chemo #1.

    Rose: Good luck on Monday. I had 3 family weddings in July. One I'll have to miss because it's out of state.

    Donna: good luck with AC #2 Yes, I like to cover the port. I agree, it's a definite bottle cap protrusion.

    Abbi: We do have a lot of similarities with treatment. I went for a blood draw last week and they sprayed some numbing spray on the port. The draw went like a breeze.

    Gagal: good luck with chemo #3

    I continue to gain energy, slept 8 hrs. total, gardened for 3 hrs. with my daughter. Very therapeutic. I was careful with the sun and wear heavy rubber gloves, hat, and long sleeves to avoid any cuts. I know they warn about the sun, but is that for all the time you are on chemo or just the week after treatment?

    Jane
  • gshoemate
    gshoemate Member Posts: 190
    edited July 2007
    Hello all, hope everyone is having a good weekend. I go for AC #3 Monday and am trying so hard not to think about it. I get so worked up about the needles.

    Yes, my port sticks way up. Between US and surgery, things happened so fast it was hard to keep up with it all. I forgot all about talking about the port with my surgeon so when I woke up from surgery and there was this big lump under my collarbone, I freaked. It does stick way up. Mine was put in during my mast. on May 9th and has always had some pain. I used to dress so it couldn't be seen but I just don't care anymore. I mostley wear tank tops and it shows a bit but I think my wearing scarfs on my head gets all the attention now.

    Well, I made it to the gym 4 days last week. I still feel like everyone is staring at me but I somehow just need to get over it. I was talking with one of the trainers and was telling her how I feel like everyone is staring and I don't want people to think of me as "sick". She said she doesn't see it as sick at all but as me being a very brave person because she is not sure if she could go through something like this. So that made me feel a bit better. I just march in, do my workout and then do my best to hide my bald head and mast. scars in the locker room.

    My energy last week was terrible. I was fine until about 2:00 pm then I would get so tired. I would get home from work and go straight to bed and be asleep by 9:30. I did start my period last week so I think that contributed to my low energy. My onco. said that my period may or may not stop....whats everyone' experience with it? If it stopping would mean more energy, then I hope it stops.

    We went out and about today. I'm in Orlando Florida......right by the one and only Mickey Mouse!!! The kids have been so wonderful through all this. Their summer has completely stunk so we went to one of the Disney water parks today. I was nervous, I wore one of my baseball caps from headcovers.com and didn't go underwater but we had a great time until we got rained out. I didn't feel like anyone was looking at me at all.

    Hope everyone enjoys the rest of their weekend. And welcome to all the newbies......this is a great place to be. I live 1500 miles from family so this has been my support group and everyone here is wonderful.

    Best of luck to everyone going for treatment this week. Hang in there, we'll all get through this.

    Ginger

    P.S. I have lost so many long post that I have typed that my new habit is to hightlight all of my text and copy it before I hit continue....just in case:)
  • roh50773
    roh50773 Member Posts: 52
    edited July 2007
    Hi everyone and thank you Pat for asking about me. It prompted me to post when you're right, I haven't done for a while. There are 2 reasons - firstly our rickety rural broadband has been playing up but the main reason is that my stay in the bristol Cancer Centre has changed my life quite profoundly. i have still been following the thread through getting the emails but I used to post a lot early in teh morning like now (4.45 in Ireland). My stay in Bristol gave me a lot of helping tools, including meditations and T'ai Chi type exercises and keeping a journal of my feelings. So most of the time this is what I now do in the early mornings. I find that really helpful and I just can't do everything. I have just had my 2nd chemo and finding it more manageable than the first. I just wanted to die i felt so awful and I know someone else posted saying that they were telling their husband that they couldn't go back - well I was just the same. I did of course but they changed the anti nausea meds and although I still feel pretty sick I'm not so bad that I can't sleep through some of it. the first weekend I felt so sick I never fell asleep for more than 5 minutes and the nights were like long nightmares. My hair is just starting to loosen.
    I have my chemo on a Friday and have now booked leave every Monday afterwards with an acupuncture session on the Monday. That will hopefully minimise my time off work.
    I find I'm pretty tired all the time but have managed to streamline my life so that i am keeping up with my two main aims which are work and my veggie garden. I have got a cleaner in (yippee) and most nights I get home from work, eat and go to bed. Luckily my kids are 18 and this summer are in and out and pretty much living their own lives so don't need me so much. I am also following a pretty strict diet, prescribed by the cancer centre and that takes a bit of time - although my husband is happy to eat what I do when the kids are home they want their normal food. I also have to make up my lunch in the mornings to take to work. I do break it occasionally when I eat out at work and find that oriental food is the closest I can get to eating what I should. Interestingly the incidence of breast cancer in Oriental women is tiny compared to Western women. If anyone is interested in the diet they put me on please let me know and I will be more detailed. the biggest no-no is dairy food - and I did love my butter and cheese! But part of the course in Bristol was about cooking and so I came home with some nice recipes.
    Like others I have found my surgery spots re-activated and more painful again. I am managing to do a bit of walking and the meditation is definitely helping me to live through the day with less stress and more enjoyment of life in general. I feel that I am learning a lot about what was wrong with my life and that this cancer is an opportunity for me to stop in my tracks and re-evaluate a lot of things. I'm still a bit of a workaholic but calmer about it! Oh yes, one of the things that they said at Bristol was that the research these days suggests that being always positve is not helpful in beating cancer. It's important to have a free flow of feelings and acknowledge the fear and down bits but to move on back to a positve state. That's why they suggest keeping a journal - to keep in touch with feelings and to discharge them onto the page. I do find it helpful.
    Well this is quite a long post - I do hope everyone continues to manage their treatment.
    Have a good day,
    Asia
  • mmcp
    mmcp Member Posts: 69
    edited July 2007
    Hi everyone!

    I'm new here. My name is Margie, I'm a 32 year old wife & mom to two young boys age 3 & 1. I was diagnosed with breast cancer July 4. Was supposed to have surgery July 17, went to the hospital that day and was told they couldn't proceed due to unfavorable results on my cat scan. The nodes behind my chest muscle were enlarged, to try to operate would have risked nerve damage. I'm having chemo first then surgery. I started July 27. The first day was rough, I was very nauseated & vomited a bunch but yesterday and today I feel pretty good. I'm trying to drink a lot and eat small meals, make sure to take my anti nauseant pills on time. My chemo is called FEC - D, 3 treatments FEC & 3 treatments of D after. Is anyone else on this? Also, any other runners out there? I'm a runner and would like to try to keep at it if I can.
  • diag061307
    diag061307 Member Posts: 14
    edited July 2007

    Hi--this is my first post. I just had my first chemo treatment on 7/26/07. I'm expecting to have 6 sessions, each 3 weeks apart. This is only day 3 after my first treatment, and so far there's been a little nausea and extreme exhaustion, but I've only thrown up once or twice. I'll be back at work tomorrow, so we'll see what that brings!

  • Gagal
    Gagal Member Posts: 42
    edited July 2007
    Asia, I'm so glad to hear things are going well for you. I find it so interesting to read your posts and see how things are done in Ireland. I like the way your cancer center does things, treats the whole body our state of mind sometimes gets overlooked. I've not had anyone mention diet or exercise or anything other chemo and radation. Continued good luck with your treatments and I hope you have much success with your garden.

    Margie glad you found our little group, I don't know anything about the chemo you are having but someone else may. I really admire anyone going through this and rasing two small children it must really keep you focused. I have heard others mention running while on chemo, I'm just to lazy. Best of luck with your treatments.

    diag061307, hope things go well for you at work. Just keep up with the nausea meds, I had more exhaustion on the first treatment than on the 2nd. Welcome to our group.

    Pat
  • diag061307
    diag061307 Member Posts: 14
    edited July 2007

    Thanks for the nice reply. My next hurdle will be when the hair goes(I'm getting Cytoxan and Adriamycin).As much as I'm dreading it, I also think I won't be able to relax until I get it over with and get used to not having any hair! So as soon as it starts coming out, I'll be making that emergency call to the hair dresser! Have a good weekend, everyone!

  • lthigpen143
    lthigpen143 Member Posts: 45
    edited July 2007
    Happy Sunday, Ladies,
    (As a reminder, I am 44, divorced, an 11 and a 20 year old daughters, 2.0 cm tumor, lumpectomy then another to "improve margins", no node involvement, and have had my first of 4 chemo treatments. Next 3 are Aug 8, Aug 29, and Sept 19. Then 6 weeks radiation. Then 5 years of hormone therapy.)

    Asia - I am VERY interested in the diet. As Gagal mentioned, we do not get much integrative medicine here. Is there a website? I am thinking that a massage right after chemo might help things move on out of my body. Some people recommend acupuncture, as well. I just started yoga, too.

    Are any of you suffering from headaches? I am and it is in my shoulders, neck and head. Like a tension headache. Ideas? Stretching helps and walking but they keep coming back.

    Also, I still struggle to sleep. I seem to have a lot of energy some days and be, as someone said, almost like on speed. Then I crash and feel tired. No middle ground.
    I am taking Lunesta for sleep but still struggle. Plus I don't like taking a sleeping pill every night. Suggestions?

    It has been 11 days since my first tx so I expect my hair to fall out this week. Take care everyone.
    -Laura
  • klwinsa
    klwinsa Member Posts: 34
    edited July 2007
    Well, I made it through the first treatment on Thursday 7/26 with minimal se's. For some reason today seems to be the hardest, very emotional, headache is worse, and very very tired.

    I'm scheduled for 4 TC tx's followed by 5 years tamxifan.

    For those that are just joining our group. I was dx'd in April april with bilaterial masctomy on 5/23 with immediate DIEP reconstruction. Had trouble with abdominal would healing and second surgery on 7/5. Stage II, no node involvement, ER & PR + ; HER2-;

    I'm really glad to get this firt hurdle behind me, not ready to loose my hair yet, but I think I will cut it all off this week. I've been off work since May and hope to go back to work on 8/9 - don't want the emotional baggage with the hair loss right after I go back to work.

    Good luck to all, we will get through this, I know that just reading the boards helps me get through most days.

    Kim
  • Marie853
    Marie853 Member Posts: 45
    edited July 2007
    Hi Everyone!
    Just dealing with my first weekend without any hair. It's tough emotionally, but, yes, we will get through it!
    2nd AC TX is this Wednesday....then, just 2 more AC and 4 taxotere to go! Oh, ya, and herceptin for a year!
    I'm in tears right now. This is all just so hard. I want to be normal again! I feel sooooo NOT sick. In fact I feel better physically then I have in a very long time. This is such a horrendous disease!
    Thanks for listening...
    PS How many of us are Her2 +?
    ~Barb
  • diag061307
    diag061307 Member Posts: 14
    edited July 2007

    Hi, Barb--As I mentioned, my first chemo was Thursday, 7/26. I'm so sorry about your hair loss. I'm dreading mine as well. I think that's going to be worse than the chemo or surgeries. I was diagnosed mid-June via an excisionary biopsy, followed by additional surgery to get "clear margins", aspirate a cyst, remove 9 lymph nodes (all negative) and implant a port. And still, the thought of losing my hair is worse than if I had to go through those surgeries ten times over again! I'm expecting mine will start to come out in about 10 or 12 days, and then I'll have it shaved. It's gonna be a nightmare alright, but one thing you can see from this website is how many women there are going through it all at the same time. I hope you're feeling better soon.

  • gshoemate
    gshoemate Member Posts: 190
    edited July 2007
    Hi Barb and diag061307, the hair loss was very hard for me as well. I was able to get over losing a breast faster then I am the hair. I have my good days and bad. My good days when I march into the gym with my scarf on as if saying "yep, i'm fighting cancer and i'm here so that means I'm kicking it's butt". Then I have those days where I feel like people are staring at me thinking i'm a 'sick' person. I keep try to stay positive and my husband is always there to 'ground' me by telling me maybe someone will see me and think "hey, i missed my mamm. or i'm late for my mamm. I better make that appointment". Or maybe someone will see me and think "wow, she's so young, maybe I need to take this more seriously". You never know when you will make a differance in someones life. And your not alone sisters, there are alot of us 'bald' folks out there. It took being at a stop light one day, late for work because of traffic and this was the 3rd detour that I took. I looked in my rearview mirror and there sat a women behind the wheel, bald as a baby. And that made me think to myself 'i'm not alone in this' and a big weight was just lifted off my shoulders.

    I choose not to do a wig because it just didn't fit into my life. I can't wear it to the gym because it would slip off my head in the middle of spinning class. Work is like my extended family, they were there after surgery when I was vomiting so my bald head wasn't a big deal for them. And yesterday we went to a waterpark with the kids, a wig just would not have done it so I choose to stick with hats and scargs from headcovers.com they seem to be doing the job.

    But remember, your not alone and the hair will grow back, maybe better then it was before.:)

    Hugs
    Ginger
  • Marie853
    Marie853 Member Posts: 45
    edited July 2007
    Thanks Ginger & Diag0601307. I took and nap and feel better now. I know I do better on days when I am well rested. I just over did it this past week. Today, I'm taking care of me. My kids just left for the night with their dad.
    Unfortunately, I have to do the "wig thing". My job is such that I have to be around so many people. When I wear it, the wig is driving me crazy. My head is so ichy. My girlfriend shaved my head and couldn't get it as close as I had hoped. I have stubble that will be falling out for awhile.
    I know it will get better. It just has to.
    It feels good to have so many people to share all this with.
    ~Barb

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