Can we talk about hair for a second?

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Ok, Ladies.  What did you do and why?

My oncologist says my hair will be gone between my first and second treatment.  Common sense tells me to shave my head, so I don't have to watch it all fall out.  Sensible as it sounds, I know this is going to be harder than I expect.  And what about covering?  I don't really fuss over my hair now, so a wig seems like too much work.  I'm thinking just a scarf or hat.  But I'm also worried about my kids.  I don't want them to be scared because of how mommy looks.

I know this is all a very personal decision.  I'd just like some thoughts on what everyone did and would you do it that way again.  Thanks!

Amy

Comments

  • Zinnia
    Zinnia Member Posts: 8
    edited November 2011

    Hi Amy,

    I lost my hair this summer on the TC regime.  I slowly started shedding around day 14.  I did not shave my head right away as the initial hair loss was from the top of my head so with a baseball cap I still had nice bangs and hair on the sides and back of my head and no one could tell.  I finally had my DH shave it at the end of the fourth week as there were huge clumps falling out everytime I took a shower. I will say that by that time I was ready and it was a relief to have it gone.  There comes a point when there is hair shedding everywhere and that was stressful to see. As for head coverings, I hated the feel of a wig on my head and only wore it a total of 3 times for about an hour each (to church) and switched to either a pretty scarf or a hat for the remainder of my treatment. My son is 11 and he initially wanted me to wear a wig but once he got used to seeing me it did not phase him at all.  At home I usually did not wear anything although if he had friends over I did wear a scarf.  I found beautiful scarves at headcovers.com.  I found that I preferred the square scarves that I could tie myself and it gave better coverage to the back of my neck.  The pre-tied ones are a bit more convenient but I liked the fuller look of the self tied. Big prints seemed to give a younger, trendier look and I got many compliments on them.  I am 13 weeks out from my last chemo and just started going topless last week.  

     Also, didn't lose my eyebrows until 3 weeks after my last treatment.  They thinned and fell out all in about 5 days but regrowth was super fast.  Lost my lower eyelashes at 5 weeks after last treatment but again they came in almost as fast as they went.    Good luck.  Hope it helps.

  • Beebop
    Beebop Member Posts: 206
    edited November 2011

    Hi,

    I shaved my head in June a couple of weeks after my first Taxol when my hair started coming out like crazy. I went out before hand and bought a really nice wig. It's really easy to just throw on with very little maintenance. I also got a free wig from ACS. I also have many scarves, but don't like to wear them out in public because they just scream "here comes cancer lady"! Sometimes I just don't want to be the cancer patient. Although now that it has been 6 months I am so sick of the wig and find myself wearing it less and less. I am 2 weeks out from my last AC and just so ready for the hair to come back. Just wish I knew how long it will take!

    Good luck to you!

  • pejkug3
    pejkug3 Member Posts: 902
    edited November 2011

    I never shaved my head.  I had a friend cut it into a short style about a week before they said it would fall out (Day 17).  My hair hung in there until Day 22.  I had my second infusion and then it let loose.

    My scalp was so uncomfortable that I had my DH cut it down short with scissors.  Yeah, it looked terrible but it was falling out anyhow!

    I was drama, drama, drama about my hair. 

    I was never really fussy about my appearance but wearing a wig allowed me privacy and some normalcy.  I think when I stop wearing them, I'll miss them!  I liked the privacy of not advertising my health status to everyone.  I have several wigs and love that some mornings I have long hair and by afternoon, I have short hair!

    I'm 5 months PFC and I have thick, full coverage over my head.  It's short hair - about 2" - and I can't wait to have some bangs!

    But hair loss was not the worst thing that happened this year.  But it was very, very emotional.

  • Faith316
    Faith316 Member Posts: 2,431
    edited November 2011

    I think hair loss is the thing people most dread when they are about to start chemo.  I know I did.  My hair was long --- half-way down my back.  But, honestly, once it fell out, it was out and a non-issue from that point.  I am too hot natured to wear a wig and mine fell out in the summer.  I wore scarves some, but thought they were also hot.  Mostly, I just wore a ballcap and didn't worry about it.

  • reesefoggy
    reesefoggy Member Posts: 65
    edited November 2011

    I am ten days out from round 2. I still have a lot of hair. However, day 14 after my first treatment it started coming out and I said screw it and got a mohawk that night at the hat party I had. Everyone had to bring me a hat and a scarf, I had vendors come that sold jeans, jewelry, candles, naughty girl, makeup etc. About 30 women came and it was great.

    A week later the mohawk started coming out a lot so I had my husband shave my head (after we went to a Halloween party and I was an 80's punkrocker :) I have areas that are gone but coming back and areas that have never come out. I am seeing a bit more stubble coming out.  My brows are thining and I don't have to shave my legs, pits, bikini anymore.  I got professional eyelashes done and will continue to get fills throughout this torture. I HIGHLY recommend doing this. They look amazing. I can handle everything but the lashes, to me it screams I am sick.

     I wear scarves/bandanas under hats. I have fancy hats, ballcaps, beanies etc. I have always been a hat person so that helped.   I have tried to make it as fun as possible and also wear winter neck scarves to match my outfits and hats and that helps my look. I have a thin face and longish neck and my face has gotten thinner losing weight due to chemo so I need it. 

     You just have to make the best out of this and have fun with it as much as you can. 

  • Faith316
    Faith316 Member Posts: 2,431
    edited November 2011

    A lint roller or better yet, a piece of duct tape pull that stubble out!  It is not attached, but just hanging out in the hair follicle so it doesn't hurt.

  • reesefoggy
    reesefoggy Member Posts: 65
    edited November 2011

    YIKES! I find a nice warm wet cloth to work.

  • otter
    otter Member Posts: 6,099
    edited November 2011

    The lint roller doesn't hurt.  It's basically really wide masking tape wound around a cylinder.  It's good for lifting out those short hairs, but it's also good for picking up the personal "litter" you leave around the house -- like, on your pillow or the back of the recliner.  If the hair is still attached, the lint roller doesn't tug on it (it doesn't hurt).

    It does look really weird, though, to be rolling your nearly-bald head with a lint roller!  :)

    BTW, Amy, there are lots of threads about dealing with chemo-associated hair loss over on the "Chemotherapy" forum.  Some of them are "pinned" to the top of the thread list, I think, so you should be able to find them easily.

    otter

  • Faith316
    Faith316 Member Posts: 2,431
    edited November 2011

    The duct tape doesn't hurt at all.  Those little hairs/stubble are not attached to anything so they just slide right out.  After my hair fell out, I had a lot of stubble that was just there.  It wasn't coming out on its own but wasn't attached.  I didn't want stubble and that's why we used the lint roller and the duct tape.  We called them prickles and they were only about 1/8 of an inch long.

  • momand2kids
    momand2kids Member Posts: 1,508
    edited November 2011

    Hi

    I knew I would lose my hair- so right after my first treatment, I had the hairdresser buzz my head and I left there with a human hair wig--- very close to my own hair (which was shoulder length and very thick).  human hair wiggs are expensive, but I worked all through treatment and had not shared widely about my diagnosis- and I wanted to control that, not have it controlled by my hair.  My kids were 12 and 7 and I figured it would be easier for them too.. but really, it was about me.

    I actually found the wig easy--I am lazy about my hair and I cannot tie a scarf.... so the hair was simple.  I loved never having to style it and not having to blow dry my hair in the am--- but I can tell you, the hair was the hardest part of all for me. I had small cotton caps from the hospital store to wear at night, but I never left the house without the wig on--- I eventually bought 2 and would have one styled every other week--- I really had a hard time with the hair, so decided to really treat myself to good wigs and good care of them.  On the last day of chemo, I had my husband shave my head completely bald (I had actually kept some hair) so that it would grow back evenly. 

    I started wearing the wig in January and by June had about 1/4 inch of hair- so stopped wearing it and spent the next year with fabulous short curly hair that I loved.   

    Today, my hair looks and feels exactly like it did before I started---- it really does all go back to normal....

  • Kaara
    Kaara Member Posts: 3,647
    edited November 2011

    The wigs they make today are so easy and cute!  You can match you own color very well.  My DD and I went shopping the other day and we both bought one.  She wanted to cut her beautiful long hair and I said try a short wig instead.  I have the worst hair in the world, so the wig for me was a blessing...don't know why I waited so long.  I'm still waiting on my dx, but getting used to the wig..just in case.

  • triple-positive-attitude
    triple-positive-attitude Member Posts: 5
    edited November 2011

    Hi, 

    I too have three kids and got a wig.  A good one and wore it three times.  I wish I had gotten two more cheap / fun ones from the catalogues since when I started to get my hair back the wig I had needed tape to stay on and then I really did not want to wear it - I was keeping any hair that came in.  I got it cut short and had friends send me scarves and hats.  My favorite and most practical was the 1$ bandana's since they tied just right (not too long), I could buy them to match outifts and they could be sorta fun for my kids.  We made some with tie dye together and sometimes they wore them with me in support.  Great kids!  Blessings to you.  You can do it.  I found most people thought I was glowing - little did they know it was the hot flashes!  

  • ruthbru
    ruthbru Member Posts: 57,235
    edited November 2011

    Other people have totally different takes and none is right or wrong, but here is my story: I was teaching middle school kids and had a kid still at home when I was doing chemo. I wore a wig because I wanted to keep things as 'normal' as possible. It was also psychologically better for me because people reacted to me more naturally because I didn't look 'sick'. The one time I answered the door with just a cap on, my friend's eyes filled with tears and I just couldn't deal with that (plus without hair I looked like an escaped convict!). My wig was really, really cute, easy and natural looking. In fact, I ran into an acquaintance who I hadn't seen but knew I was doing treatment, and her comment was, "Well, at least you didn't lose your hair."

  • Deep81
    Deep81 Member Posts: 51
    edited November 2011

    i started losing my hair around 2 weeks post chemo 1. I was shedding like crazy so i had it cut short to shoulder length. 2 weeks later, my work colleagues shaved it off for me at work, took awhile as i had a lot of hair but my scalp was super sore, it was itchy and i had enough so i said lets get rid of it! I bought 2 wigs, they were awesome in the winter! kept my head super warm. I didnt buy real hair wigs as they tend to be super itchy. So i bought synthetic ones. I wore bandanas too-mainly to the gym and yes they did scream out "cancer lady" but then im the sort of person who doesnt really care about what others think. Great thing about wigs is that you just throw them on and thats it. It is unfortunate that we lose our hair but when it grows back in its so soft and beautiful. My hair started to grow back in about a month after chemo ended so now i have around 2 inches of thick curly hair BUT im now losing it again as i have to have rads to the brain-its all good though! thank goodness i kept the wigs!

  • bella76
    bella76 Member Posts: 113
    edited November 2011

    If I could do it again I wouldn't shave it because amazingly I've still got hair after 4 FEC treatments. I would just get it cut into a short hairstyle.

  • Patriotic
    Patriotic Member Posts: 281
    edited November 2011

    Depending on your chemo regimen, you may not lose all of your hair. I did 12 weekly Taxol and then 4 bi-weekly AC. My hair thinned a little but I kept it through Taxol and the 1st 2 AC's. Even then, I still had some around the temple and the nape of my neck. So, wearing hats was still doable. Then, AFTER treatment ended, it all fell out. I also kept eyebrows and eyelashes almost to the end. I have a very nice wig and no one can tell. But, it's itchy an annoying. So, I only wear it to work.

  • Rockym
    Rockym Member Posts: 1,261
    edited November 2011

    My hair was always my pride.  It was thick and long and I knew (or at least thought) I was going to miss it more than anything.  Guess what??  I gave my hair to Locks of Love, sported a short do for a week and then buzzed off what was left.  I think I lost maybe 75% with treatment since about 25% keeps growing, but I was happy to have the rest off by that point.

    I bought two wigs.  One is long, brown/red with beautiful streaks and a great cut.  The hair looks very natural, has a monofiliment scalp that I can part anywhere and NEVER itched or bothered me.  I also bought a blonde halo wig that is also very pretty and I wear it with hats and do rags.  The wigs were $300 and $100, but insurance paid for them.  I never tried to hide my BC because I have a wealth of info. for those who are interested.  Also, I like the different hair styles and both are so easy.  No styling, no trouble.  Just flip it on and go.

    One more thing...  as my hair grows back, I will finally see how much grey I have and I will have many new hairstyles during the next few years..... should be fun!

  • AmyIsStrong
    AmyIsStrong Member Posts: 1,755
    edited November 2011

    I cut my hair very short once  knew chemo was imminent. Then I had it cut even SHORTER right after the first treatment.  Then when it started to shed, my husband buzzed it with a trimmer with no guard (shortest setting).  I did TCH and it never completely fell out. It was actually UGLIER than being completely bald - this salt/pepper stubble all over my head. BUT when it was time to grow back, it came back a lot faster because I had a 'head start' (get it?).  I was also told that shaving with a razor is not recommended b/c you can get folliculiits (infection of the follicles).

    I used a trusty baseball cap, some scarves and a wig for business meetings (occasional). I hated the wig - it was itchy. People ALWAYS complimented me on my hair when I wore it though - it was pretty funny - made me think that my 'real' hair had looked pretty bad before! (I didn't tell business associates about the bc so they didnt' know it was a wig.)

    SINCE my hair grew back, I have gotten really into hiking. I bought a 'buff' at the hiking store. It is AWESOME and super easy to use and I wish I had it when I was bald. You can get them online (google: buff - and a few sites will come up)., in all kinds of patterns.  It is FAR easier than scarves and fits nice and tight. I wore it on a hike yesterday and pulled it up over my head b/c it was raining, and I thought AGAIN, "I wish I had had this during chemo."  They are around $20, not cheap, but if someone wants to buy you a present, ask for one.

    Be sure to get something soft and tight fitting (like a baby's skull cap - cotton) to wear while sleeping. Your head WILL get cold.

    Being bald was not such a big deal (to me, anyway). I found it sort of interesting. And SUPER FAST - you will see first hand why men are always ready to go places before we are - they just hop out of the shower and GO!

    One more thing - the Amer Cancer Soc has a program called "Look Good Feel Better" which helps with wig/makeup/nail tips for women going through cancer treatment.  You can find their site online and search for a place near you. They give it once/month or so. Once you are into treatment, DEFINITELY go. Hard to believe, but it really IS a fun evening and you will learn a lot.

    Re the kids - if you put on some earrings,a pretty scarf and a bit of makeup (so you don't look scary-pale),  I think the kids will be ok.  They really pick up on our signals more than anything. I have read about moms letting their kids buzz their hair and doing mohawks and all kinds of crazy styles as they cut it shorter and shorter. I don't know if yours are old enough, but that could be fun.

  • kennylynne
    kennylynne Member Posts: 152
    edited November 2011
    Deep 81 Great attitude that you have, way to stay postitve throughout this. Good  luck with your rads will be thinking of you. IN STRENGTH AND HOPE
  • boxcars072000
    boxcars072000 Member Posts: 43
    edited November 2011

    AmyLb,

    Well you couldnt have had better timing, I am 19 days in and today my buzzed off hair is starting to fall out. It is a little unneving. A little sad, but I have been so emotional lately its not even funny. I buzzed it before my first treatment, and usually wear a bandana, but I got a really nice sythtic wig that if you dont know me, you dont know its a wig- and it does make getting ready alot easier and faster. I had someone else give me the same advice about a lint roller. My main problem with the wig is I tend to get headaches. I am kinda excited about it growing back in and never never having to dye it again. Best of luck to you!

    Connie

  • AmyLB
    AmyLB Member Posts: 24
    edited November 2011

    Thank you all for your thoughts and suggestions!  I've found a local shop that sells great wigs and everything else cancer patients might need...beauty wise, that is.  Making an appointment with them next week!

    I have long hair and I think I'm going to take some tips from here and get it cut short first.  When it is time, my husband has asked to buzz it for me.  I'll already have my wig by then, so hopefully it will not be too noticable.  I am sure it is going to be more painful than I think right now, but I know it is just temporary.

    Trying to have a more positive attitude...

    Amy

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