Anyone starting chemo in Aug. 08?

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  • mommy3abm
    mommy3abm Member Posts: 221
    edited September 2008

    Hey girls!  Just wanted to wish everyone an se free week.  I won't be back on until next week as I am leaving for NYC and then have Tx #3 on Monday next week - the day after we return!  What a welcome home gift!

    Hood - Thanks for the nice head comment.  I don't go anywhere but home sporting the bald look, but I am actually quite comfortable with it!

    BetteLou - Congrats on the wonderful man in your life and on the shrinking IBC!!  You go girl!

    Tonya and MamaShift- Good Luck on #4

    Misty - How's it going girl?  Smooth sailing on #4 I hope!

    Jeannine - So glad you like the scarves!  I just ordered 3 more and that is all I wear anymore!

    To everyone else I didn't mention personally - You are all in my thoughts and prayers.  I am soo tired and need to tuck in for the night!  I will catch up when I get back!  HUGS to all!!

    Stacy

  • Corinne6
    Corinne6 Member Posts: 311
    edited September 2008

    hi everyone, Had my second round of chemo and am doing really great. Went to that Look good feel good program last night and got lots of makeup and a free wig. Ordered some hats and bangs to go under them today. I am waiting to for symptoms to catch up to me. my hair is almost gone but my wig looks great. I will try to download a picture today. 4x more to go. I end in Dec. anyone here going to be that long?  To the ones having chemo today I am praying for you. God Bless, Corinne

  • DFOnt
    DFOnt Member Posts: 145
    edited September 2008

    Corinne, if all goes as planned my last chemo will be Dec. 5.  I'm going to the Look Good Feel better seminar this afternoon.  I'm pretty sure we don't get wigs here but it should be fun.  My sister is coming with me.  Have a great day everybody!

  • Anonymous
    Anonymous Member Posts: 1,376
    edited September 2008

    I am getting a buzz cut after work today. The hair is making a mess in my apartment, and it is just too traumatic watching it come out in handfuls in the shower. Better to make a clean break with it. The wig continues to get compliments at work. I have been told that I look like a new woman. I have been transformed from a cancer "victim" into someone who is taking charge of the situation. My IBC breast continues to shrink. "Go chemo go"

    Bette

  • Tonya36
    Tonya36 Member Posts: 66
    edited September 2008

    Hey Corinne.  If all goes well and I have figured right I won't end chemo until the week of Christmas.  I start 12 weekly taxol txs on 10/1.  I will be right there with you girl.

    Bettelou...I found once I decided to shave it that it was much easier to do than I had thought.  The week up to it was horrible but once it was done I was happy I didn't have to worry about it anymore.  I hope you have an easy time and feel better once you are done with it also.

    Stacy...I hope you have a wonderful time in NY.  Enjoy your husband and celebrate that tumor shrinking.  You deserve a good time!!! 

    God Bless,

    Tonya

  • Corinne6
    Corinne6 Member Posts: 311
    edited September 2008

    Okay if I did this right my picture will come up with my wig on. What do you all think? I had a Neulasta shot today and feel really good. My counts are all fine except platlets. Does anyone know what I should be watching for with these?

    BetteLou68: loved your Bible verse. God has been so good to me and His Word has been of such comfort. How is your buzz cut. I just could not bring myself to do it yet.

    Tonya36 and DFOnt: I am with you to the end on our dates. It will be of great joy when our last one is complete for ALL of us!!

    Tonya and Mammashift how was #4

    Praying for you all on this whole entire thread, Corinne

  • Anonymous
    Anonymous Member Posts: 1,376
    edited September 2008

    Well the hair is GONE, and although it was traumatic the first time I saw my head, I am used to it already and relieved that the mess is over with.

    I went to my therapy session tonight wearing a fuchsia turban with a coordinating scarf coiled around it. My therapist said it looked good, and that I had the face to pull it off. the dangly earrings helped the effect.

    I came home and treated myself to a bubble bath. Trying to be gentle with myself today. It was a milestone. I'm glad it's over.

    What will Tom say when he sees my stubbly head?  He left me a message on my phone to have a good hair day. Wait til he finds out what kind of hair day it actually was.

    Tonya and Corinne, I will be ending up December, too. That will put my surgery around Christmas or New Years. Happy holidays to us all!

    Bette 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited September 2008

    HI ladies.. i go in for chemo number 3 tomorrow.. well today its 1:41 am wednesday morning..for some reason i am scared... its like when i start to feel good i have to go get chemo.. it seems like knowone understands how i feel.. i try to talk to my husband about it and he just says the same thing..it will be alright.. things will be okay.. the only thing that keeps me going is me wanting to still be here.. i get so depressed everytime i have to go get chemo everytime she brings those bags its like i have to fight not to cry about it.. all my friends and family say how strong i am having to deal with this.. my cousin in law in japan told me that i was taking it better than she would of.. but its like i have the bigget smile on the outside but inside sometime i just want to give up and run away from it all.. but i know how much it will hurt my family if i did so i countine to go to chemo and get the treatment..i hate the way i feel after it.. granted the second session went well but i here it gets better then i hear each session is different.. and its hard cause everytime i am at chemo someone always ask me my age and say OMG you are so young to have breast cancer and i am thinking to myself.. i am not up for the age thing today...

    all i can say i have 3 more sessions to go.. november is look to wonderful to me right about now.. i think will have a ladies night out once i am done with chemo and go see my godson cause i will be in chemo for his birthday and he is just turning 1.. i feel so robbed.. i just feel so robbed..

    thanks for reading ladies.. i guess i just need to get my cry out and vent..

    best wishes to all having there chemo wednesday and other days this week

  • Corinne6
    Corinne6 Member Posts: 311
    edited September 2008

    Hey Lashon2008: I am wide awake too. It could be the steroids?? Anyhow, I know how you feel. when I went for my second one I had all those same feelings again BUT you are going to be half way through. oh, how wonderful is that!! My scripture verse for this is Joshua1:9. I keep reciting it over and over. Also if you can look up Psalms139:10 I take that with me whatever test or chemo I have. I hope that it helps.

    BetteLou68: My heart is with you. My last day of chemo if everything goes right is on Dec.8th. I then face more surgery because margins showed precancerous cells. Then I have 6 weeks of radiation. My husband saw my balding head yesterday and he is just so kind. I am so greatful for his love and support through all this. He won't even let me look at the bills when they come in to protect me from worry. Isn't that cute!

    Does anyone here live near Connecticut? That is where I am.

    I want you ALL to know YOU ARE IN MY PRAYERS!!!

    Corinne

  • Corinne6
    Corinne6 Member Posts: 311
    edited September 2008

    BettyLou68: You make me laugh. Tom will love you no matter what...you will see. I bought a wig yesterday that stays on at night. I found it in American Cancer Society booklet "tlc" It has a short curly top with a type of headband that goes around you ears and has detachable bangs. My husband commented on how adventurous I was- "in a positive way!!" Well,  it will be a new style for night time but I cannot bring myself to being too humble and going natural because I must be vain!!

    Corinne

  • Tonya36
    Tonya36 Member Posts: 66
    edited September 2008

    Corinne your pic is beautiful.  Love the wig.  I need to figure out how to do that.  Maybe I will work on that this week once I get my school stuff done (YUCK).

     Bettelou...Tom sounds wonderful.  You are a very lucky lady to have someone that loves you so much.  He will love you hair or no hair he has already shown that.  Just enjoy that beautiful relationship you have and let it give you strength through this horrible process you are going through.

     Lashon...I am so sorry you are having a rough time.  I hope today goes well for you and you have as few se's as possible.  My second tx on EC was my easiest actually so I hope the same for you.  I too get very anxious the day before chemo.  Its like I know what it will start out like but its always an adventure because I do get more and more tired after each one but God has been very good to me and has made this very doable.  I still get tired, constipated, thrush, mouth sores, uti infection, stomach cramps, nausea, hair is gone but again everything has been doable.  We just learn how to deal with each thing as it happens.  The worst for me is the exhaustion.  I feel so like I am being lazy and weak but sometimes I just can't do.  For about 3 days each session I just have to lay around and then it takes me a few more days to almost normal and its time again.  I was so tired yesterday at tx I just wanted to sleep but as I looked around the room to the 8 other people getting tx I couldn't do it.  Everyone in there was in their 50s to 70s and they looked so frail, pitiful and they were all asleep.  It was so sad.  I realized that yes as unfortunate as it is for me to be 36 years old and have cancer there are some that don't have as much fight in them as I do.  I pulled out my ipod and watched tv. No sleep for me.  I have to fight with all I have. and you do to Lashon.  We are young.  We do have more energy and health than some of those that are much older than us.  These people come in there and give it all they have so why shouldn't we.  We MUST BE STRONG.  There will be times its hard for all of us and when it is we are here for each other.  If I can be of any help at all to you please let me know.  Pm me if you like and we can talk.  I don't know how everyone feels but I wouldn't mind having addresses to send some cards to each one of you.  If anyone is interested you can pm me with that info.  If you are not interested I understand that also.  This is the internet afterall. LOL

    I hope you all have a wonderful day.  I think I am going to try to look at my online classes for a few and then a nap is in store for me today.  Talk to you all soon.

     God Bless,

    Tonya

  • Monique
    Monique Member Posts: 121
    edited September 2008

    Hi ladies -

    I haven't been on for awhile, but I have been reading and catching up on everyone.  I had my second tx last Tuesday and after the Neulasta shot I was in bed for a few days.  That bone pain really gets me :(

    Lashon - I understand completely how you feel - I am already dreading #3 in two weeks :(.  But I agree with the girls that we can do it!  Try to have faith - prayer - and take one thing at a time :).  I hope that your treatment goes well today and you are back on the board soon (because that would mean your SE's were not too bad). 

    I am getting ready to leave for a Look good feel better seminar in a few.  Seems like quite a few of us have attended one of those.  Did everyone like them?

    I would love to have people's addresses to be able to send out cards too!  What a great idea.  If anyone is willing, you can pm them to me also please.

    Hope everyone has a good day today!  The weather here in Virginia is beautiful!

    Monique

  • Corinne6
    Corinne6 Member Posts: 311
    edited September 2008

    Monique, I really did enjoy the class but I got kind of depressed when I found out that one lady there in her early 30's had three inopperable brain tumors and a set of 5 year old twins. I have not gotten over that. Nor have I forgotten a lady that was in her early 30's that is in stage 3B of breast cancer that is doing chemo first then bilateral masectomies followed by raidation. Another lady is fighting a second round of chemo - this time she has the rarest form. Inflamatory breast cancer. My heart just aches for these people and each on on this site. I am praying for all of us. The class was great in learning some new makeup techniques and I did get a new funky wig. The biggest part of it all was how very much I love these people and wish that there was something I could do.Got any ideas? I did take all of their addresses and I am going to send notes and cards. I am praying for each one on my list but I feel so inadequate. Perhaps in the future I will become a nurse of some sort to help out. I am at such a loss.  Ifelt so alone when I first got cancer thinking I was going to die. I feel so fortunate to have the stage I am at and the opportunity to reach out to others. Who knows what the future holds for any of us BUT God is the one that holds the future.

    Lashon, I am with you all the way today and you are not alone. May you have a day that is filled with blessigs from above  You go girl!!!

    Hugs,

    Corinne

  • Roya
    Roya Member Posts: 346
    edited September 2008

    Hi Ladies,

    Corinne,  I luv your photo with the new wig!  Looks gorgeous!

    So many of you are completing your chemo in December.....Now I am starting to wonder if I am getting enough chemo since I am finishing up the first week of November.   I'm getting 4 rounds each of A/C & Taxol.

    Mamashift, I totally understand your feelings of going thru this alone even though you are not.  My DH has to travel a lot and is gone most of the time leaving me alone.  It's very lonely in a different kind of way.  I'm so glad that we have this thread and our BC sisters to help us through.

    Lashon, you are not alone!  As Tonya wrote,  'we have to fight with all we have'.  Life is a precious gift.  I am sorry that we are going through such a rough life's challenge but it is only for right now.   Someday this will all be behind us.......look forward to that!

    Bette, that fuscia turban sounds so cute! Wink

    Stacy, have a wonderful, funfilled, romantic trip to NYC!

    As for me, I will go for my last A/C this Friday.  After that I start Taxol.  Nearly halfway  thru with chemo!  Just can't wait!!

    Wishing everyone a great day!

    Roya

  • DFOnt
    DFOnt Member Posts: 145
    edited September 2008

    Roya, you're getting more treatments than I am - I get 3 each of FEC and Taxotere, every 3 weeks.  I guess it depends when you started, and probably on your individual treatment.  I was told they input all of the info from the tumour, pathology etc into a computer program and that determines what drugs, dosage, how often etc for each person.  Wow, halfway - that's fantastic!!!

    I thought the Look Good Feel Better workshop was great!!  It was a little different because I've been going to a support group for breast cancer and had already met most of the women there so we didn't really discuss our stories, just had fun and got to be kind of silly without having to worry what we looked like.  My sister came and she said she couldn't believe how great everyone looked great with their bald heads,  when they took off their hats / wigs.  I left my hat on because I've still got the thin on top longer on the sides hair.  I feel like I'm conducting a biology experiment on how long it will take for all of it to fall out!  Anyway, we got a great box of cosmetics and some good info and tips on wigs etc.  No free wig though, that must be a difference between the American and Canadian programs. I also recommend going to an in person support group if you can.  I'm not normally big on that kind of thing, prefer the internet, but it is nice to actually see and get to know some local women that are going through something similar, and exchange tips, complain etc. 

    I've notice the reflux / heartburn is worse this time, especially when I first eat in the morning.I'm going to refill the reglan rx and have been taking pepcid ac. other than that I've had very little SE's this time. 

     Corinne, love the blonde wig!!

    Tonya, I've also seen a few of the much older (usually men) sleeping with their mouths wide open at the chemo sessions and I feel bad for those that do not have the energy and strength and wish them all the best.  Cancer is just evil, they shouldn't have to go through that at that stage of life. I was able to joke with the nurse and discuss silly magazine articles and help my sister play video games.  Maybe it makes them feel a little better to see some young(er) people going through it, laughing etc, maybe it gives them a little energy to fight.  I also find it kind of entertaining listening to some of the older men talking, telling each other stories...

    Well, back to tidying up the house.  Had a nice day, we took our daughter down to the beach here and just relaxed, went for a walk and had ice cream, watched the squirrels and dogs in the park.  It was a beautiful warm sunny day. 

  • MamaShift
    MamaShift Member Posts: 70
    edited September 2008

    Had tx 4 out of 6 yesterday.  And today I fired my oncologist.  I have seen her twice before tx and both times she's been an hour late AND thought BOTH times that I have four rounds and not six.  So yesterday she's practically congratulating me on being done! She is a very popular oncologist here, but I need to be SEEN as an individual!  Undecided

    So far not much in terms of SE.  It seems to get better each time.  We'll see tomorrow if I crash all day as usual.

    Has anyone lost her eyebrows yet?

    Roya -- thanks for the commiseration!  We should meet up when all this over.  I usually get to Paris a couple times each year, though I've been considering not going anymore because of a toxic situation with my MIL.

    Agnes -- my mom had/has the neuropathy.  I'll tell her about the B6.

    Best wishes to everyone.

  • Hood1980
    Hood1980 Member Posts: 537
    edited September 2008

    I had my 3rd treatment today and so far it has been much better than the 2nd. I have been guzzling water since Sunday and it has seemed to help. The fog is lighter and no headache! I 'm actually getting sleepy too! I took a frozen italian ice with me in my cooler and ate it during my taxotere drip and my mouth is only warm tonight ...no burning. I hope it keeps going positive, but as you all know tomorrow may be entirely different.

    Good luck to all having treatments tomorrow!

  • Monique
    Monique Member Posts: 121
    edited September 2008

    Well the Look Good Feel Better class was canceled today so I didn't get to go.  Maybe I'll make the next one. 

     Corinne - I don't think that you should feel inadequate at all, your prayer's for all those women that you met at the class and sending them cards, etc. are those things that make a big difference in people's lives. 

    Roya - My onc told me the same thing that Deirdre was told about treatments.  He talked about putting all the information in a program that would suggest what treatment should be.  He said treatment for bc is becoming very specific to each person, unlike years ago when everyone generally took the same treatment.  I have had two of my six total treatments of TAC.  My last should be the beginning of December.

    Mamashift - Sorry about your onc. - I hope you get a more personal one this time :)  I  was wondering about the eyebrows and eyelashes too?  For some reason I am more upset about that happening than I was about shaving my head?

    Hood1980 - What does your treatment consist of beside Taxotere?  No one told me about eating ice during Taxotere?  What exactly does that do? 

    Monique

  • Hood1980
    Hood1980 Member Posts: 537
    edited September 2008

    Monique-I've read on some of these discussions boards that eating ice (or something cold - slushie, italian ice) during the Taxotere lessens mouth sores.  I had thrush the first time around and my mouth was hot and sore for days after each treatment, plus the tastebuds would we out of whack.  This time, mind you it hasn't even been 24 hours yet, but I have not noticed any mouth changes.  All this water I'm guzzling even tates normal!  It may all change in the morning, but right now I'm celebrating with another drink...of water!  Wink

  • alibug05
    alibug05 Member Posts: 182
    edited September 2008

    Hi ladies!!!! Corrine - LOVE, LOVE, LOVE the blonde wig!!!! It looks great!!  Hood1980 glad you aren't having very many se's so far - hopefully that continues!!!! Mamashift - sorry about the doc - I have to go over an hour to get to ALL of my stuff, doctor, chemo, and radiation when it starts because the QUACKS I have here in my hometown aren't worth anything.  I hope you find one that suits you better and who actually knows what is going on with you!!!!!  Roya - I too am only getting 4 treatments and I finish up October 10th!!! YAHOOO!!! Well ladies I hope EVERYONE is going good and having the least side-effects as possible this time.  I go tomorrow for #3 and then I only have 1 more left - time is flying by and we are ALL making it through this - one more thing - I want ALL of you ladies to know I couldn't have done this without you!!!!!!!!!!!! So THANK YOU ALL!!!!!  Loves!!!

  • Corinne6
    Corinne6 Member Posts: 311
    edited September 2008

    Good morning everyone, Got some needed rest after having those steriods. I certainly feel less gloomy. I did call all the people that I met last evening from the Look good feel good program and feel much better about contacting them.

    Monique/ I never read that either about the ice thing. makes sense though and I will try it on my next one.

    Mama Shift/ So how many do you really have left? Wow, that must be so hard for you to go through all of this and try to keep your sanity at the same time. I am so glad you made out well yesterday.  hope you continue in that path.

    Lashon/ still waiting to hear how you made out. Hope your getting needed rest.

    Still have my eyelashes and eyebrow after 2x. I was told that not everyone looses them and I may not.

    Does anyone here use Agave Nectar instead of sugar. I just started it and really like it. My naturopathic doctor told me to use stevia but it has an after taste. Agave is all natural and even diabetics can eat it.

    Gotta run but I am with you all in prayers and will check back tonight. My thyroid is a mess so I am going to see my endocrinologist today. The chemo may have had something to do with that so they adjusted my meds.

    Wishing you all a beautiful day and for those of you getting treatment- You are in my prayers.

    Corinne

  • Anonymous
    Anonymous Member Posts: 1,376
    edited September 2008

    I am having a sleepy day at work. Everybody says I look tired, even though I got 10 hours of sleep last night. I am NOT getting much accomplished. Tomorrow I have off, and will spend time with Tom, which is something to rest up for tonight.

    Does anyone have a really runny nose? I am using tons of tissue, and my nose aches. Could the hairs inside be falling out?

    Every day the wig feel a little bit better. It still comes off when I get home. I am wearing a wig cap under it to cushion my bare bristly head.

    This weekend my daughter and I will shop for cute hats, scarves, and dangly earrings to set off my new look.

    Bette

  • dlb823
    dlb823 Member Posts: 9,430
    edited September 2008

    Hi, all...  Glad to see everyone seems to be doing well, and congrats to all who have or are completing tx's  this week!  It's wonderful to see that we all are getting through this together!  I had tx #3 yesterday, and so far so good -- except for being up at 5:00 a.m., after a totally wasted night trying to sleep - and also hiccups earlier today (???).

    Mamashift... Let us know what you do about a new onc.  Do you have someone in mind?  I can't believe that an onc (of all docs) would keep patients waiting an hour -- seems incredibly inconsiderate + a poorly run office; and be uncertain of your tx schedule to boot!  Who needs that kind of  "care?"

    Diedre & Joyce ... Hats and wigs (that's my ACS freebee in the photo) both feel totally weird to me.  Baseball cap visors annoy me, especially when driving.  And I am constantly aware of the wig, not to mention an occasional itch.  The wig also makes my head feel constrained, like I can't think clearly. 

    Agnes... I read a comment somewhere else on these boards that neuropathy is a sign of Taxotere toxicity.  I'm going to ask my onc about it today, as I've also had just a touch of neuropathy in my little toes.  I doubt if they'll change anything, but I still want to know if he perceives it as a common SE or toxicity.

    Corinne...  Thanks for the tip about Agave Nectar.  I'm going to try it.

    Thinking of you all ~   Deanna

  • Misty1
    Misty1 Member Posts: 272
    edited September 2008

    Hey Girls,

    Just checking in on everyone.  Sounds like some of us got over #3 this week!! Woo-hoo!!  I am on day 8 of TX#3 and feel pretty good.  Went today for the WBC count, and I was a whopping 40!  That Neulasta has really done its job the past two times.  My DH says maybe I should go without it for the last TX, but I want to recover quickly from the last one.  So, I count down until 9/30.  I know some girls are right behind me.  I will have to keep going for the Herceptin every three weeks, but I don't count that as giving any SEs like chemo.

    It's nice to see that Sept. is going by quickly for all of us.  Remember when we all started this up at the end of July/early Aug?!

    Hope everyone is having as nice of weather as what we are having here in MD.  It actually is starting to feel like fall.  After a horrible summer(DX in June), I can't wait for it to end!!!!

    Have a good night everyone!

    ~Misty

  • DesertRider
    DesertRider Member Posts: 178
    edited September 2008

    Hi Team,

    Just got back from TX # 2. Made a couple of pre-drug changes to try & avoid the bad headaches that lasted for days the first time. We eliminated the Aloxi and just did an IV of Kytril with Kytril pills to take if needed. We'll see what this does.

    And , yikes, I'm putting on weight which has never happened. Oh, well, halfway through the 4 TX's. YES!

    Also, only few wisps of hair on top but the back still looks kinda short & cute, can't seem to let go of it! SOMEBODY PUSH ME OVER THE EDGE TO GET THIS BUZZED! 

     Am pretty wired so will probably be reading this site most of the night.

    Love to all, 

    ~gail 

  • DFOnt
    DFOnt Member Posts: 145
    edited September 2008

    Gail, congrats on halfway!  Here's to no headaches.  I'm also still hanging on to my hair.  Had the wig on yesterday trying to get used to it, that's it in my pic, but I don't know.....I think I just want to see how long it would take to lose it all "naturally", it's looking pretty sad though on top.  I wonder if the rest of it would come out 14 days after the 2nd treatment.

  • dlb823
    dlb823 Member Posts: 9,430
    edited September 2008

    Gail...  I won't push you over the edge to get your hair buzzed.  I think it's a toss up.  The falling strands or clumps are annoying, but, like you, I sort of liked the wisps that hung on and think that looked better than buzzed if you're wearing a baseball cap or other hat.  Glad you got your pre-meds tweeked.  Let us know if that helps this time.

    Deidre...  Your wig looks really nice.  Very natural.  Is that your actual color?  I would love to go red for now if I could find the right shade.

    Joyce... How're you doing?  I'm hoping your SE's are much less this time.  There's a post on the TC board about wheat germ oil as a possible help for SE's. 

    Hope everyone is up to enjoying the weekend.  My DH went to a family wedding in TX, so I'm riding out the SE's without him this time, which is okay.  Still concerned about Peaches and miss hearing from Stacy, but hope she's having a wonderful time in NYC...      Deanna

  • Hood1980
    Hood1980 Member Posts: 537
    edited September 2008

    Hi Deanna & all,  I'm here checking in.  Immediatedly after getting my neulasta injection yesterday the pain started.  Just the arm I got the injection in, but the two times before it wasn't bad until later.  Took the day off work today (day 3 after 3rd tx) and slept all morning, crashing from the steroids!  dd came over in the afternoon and took care of me.  She's so good to me. Hoping to have enough energy to go to the Look Good Feel Better program tomorrow.

    Hope everyone is feeling well & up and about.  It's gorgeous here in MD with low 70s, wish I could go on a bike ride....maybe next weekend.... 

  • Anonymous
    Anonymous Member Posts: 1,376
    edited September 2008

    HI ladies.. doing okay.. just very tired.. everything taste like dirt.. dont know why.. i so cant wait till this is over..thanks for the words ladies.. will write back when i can..

     Peace and Love

    Lashon

  • DFOnt
    DFOnt Member Posts: 145
    edited September 2008

    Deanna, the "natural" colour of my hair depends on what colour I dyed it last!  Usually pretty close to the wig, there always seems to be some red in it.  My husband came home and said he liked my "hair", but today we were going out and I asked him if I should wear a hat or hair and he said hat.  The wig is pretty itchy though, even with a wig cap under it.

     Good to hear from everybody, take care of yourselves! It's my daughter's 11th birthday tomorrow so we're going to try to have a fun weekend.

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