Medical Forum / Diseases and Disorders / Breast Cancer / January 2004
Hair Loss
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darla - 04 Jan 2004 00:16 GMT Hello again,
I find myself really not comfortable with the hair loss due to chemo. I really didn't think it would bother me, but it is. I have a wig that looks natural. My husband is very, very supportive - as is my family. It is me that is having the problem with this. I think it makes the cancer real for me. I don't feel sick, I had a pretty good experience with my first chemo treatment and I don't expect to have trouble with future treatments, but the hair thing has really got me bummed out! I started losing my hair on New Years Day. I pulled as much out as I could and then shaved the rest off since it was pretty patchy looking. Any comments or suggestions? I feel almost ashamed raising this, since I know there are many out there that have such severe side-effects. I guess I need to know I'm not the only one who might have felt like this. Thanks folks.
Darla
allan grossman - 04 Jan 2004 02:15 GMT >I find myself really not comfortable with the hair loss due to chemo. >I really didn't think it would bother me, but it is. I have a wig that [quoted text clipped - 9 lines] >side-effects. I guess I need to know I'm not the only one who might >have felt like this. Thanks folks. Darla, I'm not a woman but what you're feeling is completely normal. Some women have a harder time losing their hair than they do losing a breast. I'm not gonna insult you by telling you it'll grow back - you already know that,
My wife wore a wig exactly twice - once to find out how much she hated wearing a wig, and once to a friend's wedding so the attention could stay on the bride where it belonged.
It's not your fault you have cancer, Darla. In my frequently less than humble opinion, the lack of hair is kind of a badge of honor.
What you're feeling is normal. It'll get better, honest - just hang in there.
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allan
spammers can reach me at abuse@localhost humans can reach me at wizard at pointbeing dot com
alexk - 04 Jan 2004 03:09 GMT Darla, I found the hair loss the worst part of the whole cancer experience. I didn't cry over the loss of my breast but did cry when my hair fell out. I think it is so visible to all - and hard to live a normal life when you are bald. It will grow back though. Alex
Kaye301 - 04 Jan 2004 07:56 GMT Darla wrote << Any comments or suggestions? I feel almost ashamed raising this, since I know there are many out there that have such severe side-effects. I guess I need to know I'm not the only one who might have felt like this. >>
I had similar feelings initially. What helped me, though, was the online support I received before it happened. That helped prepare me and made it easier. I got that support here and later in another group as well. The thought of losing my hair had been the worst part--even more than losing my boobs (I had a bilateral mastectomy). Because I was prepared, after it happened it wasn't quite as difficult than I had anticipated. Then there were the positive aspects that I had never even thought of. I have always had difficult to manage hair. Although it had been at a point where I liked it, it still took at least 20 min to do each morning which was time I could have used to sleep in on those days I worked. Once my hair wasn't there, I had no more 'bad hair' days. Then there was the cost--in terms of saving. It only cost $15.00 to have my wig washed and re-styled. I used to pay ten times that for my real hair--washed, woven, permed, and cut. Then there was the pleasant surprise of learning that my hair dresser had been right all along--that my head was not misshapen as I had thought. It was very nicely shaped and the flat part in the back of my hair was due to what she said--the way my hair grew--in one big cowlick. Another interesting aspect of this whole thing was that I developed a new found empathy for bald-headed men--bald is cold in the winter!
MLEHMAN24 - 04 Jan 2004 15:38 GMT Darla, When I lost my hair I cried and cried then I also knew that the cancer had been real. I bought the wig and hated wearing it. I bought turbons being it was winter. I likes wearing them and when that was to hot I wore baseball hats. My co workers were very supportive. I now sport curly short hair where my old hair was very straight and about chin lenght. Hang in there it is tough but bald women are "Beautiful and Strong." Nancy
darla - 04 Jan 2004 22:56 GMT Thanks so much for all your input. I spent a great deal of time reading the other postings about hair loss. I'm glad to see I'm not alone in this feeling of loss. It is such an obvious sign of our disease. Even though I expected it, it was still a shock. My 12 year old grandson saw me for the first time without hair today and God bless that child, he came over and kissed my bald head. I'm still his nana, with or without hair! He offered to share his baseball caps with me! What a hoot!
Darla
Kaye301 - 05 Jan 2004 07:14 GMT Darla wrote: << saw me for the first time without hair today and God bless that child, he came over and kissed my bald head. I'm still his nana, with or without hair! He offered to share his baseball caps with me! What a hoot! >>
How special! My husband offered to shave his head so that I would not go through this alone. I told him: "don't you dare." That's the last thing I wanted--was to be reminded of what I was dealing with whenever I saw him. Some, however, do find that act comforting. I also had some interesting moments. We had out-of-town guests along with my two oldest daughters home from college the summer I was bald and going through radiation. We had a total of 12 or 13 guests for several days. That included another family with 3 girls with their youngest who was 3 years of age. I can't recall the circumstances exactly but her aunt had come upstairs to get directions off the computer one morning. She was being interviewed for a TV newscast and needed directions to the studio. I hadn't gotten dressed yet nor put on my wig. She (the 3 year old) had never seen me without it. She came upstairs with her aunt and when she saw me her mouth dropped open in what was both a surprised and horrified expression. I then quickly went and got my wig and gave her an age-appropriate explanation and hopefully allayed any fears that resulted. However, I am sure that visual impression may last a lifetime. Another time my wig/baldness resulted in shocking and scaring one of my doctors. It was during the time I had developed a positional vertigo/dizziness. The treatment involved taking me by the hair, throwing me down rapidly and quickly turning me over (Epley maneuver which repositions calcium deposits in the inner ear which had broken loose). Well, when my neurologist grabbed me by my hair he pulled my wig off. I thought it quite amusing, but he was so startled, he didn't know how to react--it was quite a shock for him.
Barb - 05 Jan 2004 13:53 GMT Hi Kaye,
I know I've related this story in this group before, but your story made me think of it again. Apologies to group members who have read it before.
I so disliked picking hair off of my pillow each morning that I wore men's large handkerchiefs to bed at night. I was also very sensitive to how my husband and children would feel about looking at my patchy/balding head. After about a week of settling into bed each night, clad in that handkerchief, my husband said, "Would you take that *&#$%^ thing off. It's like sleeping with Willy Nelson!" He made me laugh at the thought and off came the hanky. I was a lot more comfortable without it, and apparently, so was he!
Barb
> Another time my wig/baldness resulted in shocking and scaring one of my > doctors. It was during the time I had developed a positional [quoted text clipped - 4 lines] > amusing, but he was so startled, he didn't know how to react--it was quite a > shock for him. Kaye301 - 05 Jan 2004 18:25 GMT << I know I've related this story in this group before, but your story made me think of it again. Apologies to group members who have read it before.
Hi Barb, I hadn't heard your story (must have missed it or it was before I got here). There is no need to apologize. I am sure there are many people who are new here since you first reported it and enjoy hearing it for the first time. If someone has already read it, it is easy enough to delete or move on to the next post. It is almost a type of 'mind-blindness' to think we know who is reading this group at any one time. I am sure there are many who occasionally surf or read and a great many others who read without posting. Your story made me recall another humerous moment I had when going through my initial hair loss. I was close to tears if not already crying, when my husband made me laugh. He said--what do you think it was like for him going to bed with me and waking up next to Telly Savalas. I was hysterical with laughter (not tears) after he said that. It was what I needed. I am sure I mentioned this here at least once before. However, I am sure that many others never heard it and hopefully will appreciate and benefit from the humor ;-)
Tim Jackson - 05 Jan 2004 19:21 GMT > << I know I've related this story in this group before, but your story made me > think of it again. Apologies to group members who have read it before. [quoted text clipped - 3 lines] > here). There is no need to apologize. I am sure there are many people who are > new here since you first reported it and enjoy hearing it for the first time. Look, we get to answer the same question sixteen times or so every time a new reader comes along with it, so why on earth shouldn't we get to re-tell our stories now and again.
If you want, send me the stories and I'll put them on the FAQ. I could even make a humorous stories section.
Tim
Xiugiami - 06 Jan 2004 17:12 GMT What is the FAQ? Does this list have a website?
> > << I know I've related this story in this group before, but your story > made me [quoted text clipped - 16 lines] > > Tim Tim Jackson - 06 Jan 2004 23:33 GMT > What is the FAQ? > Does this list have a website? www.cancersupporters.com See separate post.
Tim Jackson
Tony Lima - 04 Jan 2004 20:20 GMT >Hello again, > [quoted text clipped - 11 lines] >side-effects. I guess I need to know I'm not the only one who might >have felt like this. Thanks folks. Darla, my wife went through pretty much the same thing. Here are a couple of strategies she used. First, when your hair is getting down to pretty much nothing, ask your hairdresser to shave the rest off. Getting rid of it all at once seems to lessen the shock (or at least cuts down the time). Second, go out and get a couple of wild-colored party wigs. If you're gonna be hairless try to have fun with it.
HTH. - Tony
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Kaye301 - 05 Jan 2004 06:58 GMT Tony wrote: << First, when your hair is getting down to pretty much nothing, ask your hairdresser to shave the rest off. >>
I forgot about that part. I had a very understanding hairdresser. In fact she gave me her home phone # and asked me to call her when it was 'time.' I didn't need to the 'time' was on a day when she was in the shop. However, interestingly, although she knew why I was coming in, she didn't realize that I walked in with my wig on. It looked so natural and so much like my 'real' hair in terms of both style and color weave. She was so surprised that I had found a wig that looked so much like my hair. I did ask her to shave my head but she wouldn't and said that what she had learned that would increase my risk of infection if she went that close to my scalp with the razor. Instead, she first cut it really short and then gave me a butch which was about one-half inch in length. It did fall out but didn't result in the mess that would have occurred had it been longer.
Glenfiddich - 05 Jan 2004 13:39 GMT >Tony wrote: << First, when your >hair is getting down to pretty much nothing, ask your [quoted text clipped - 12 lines] >one-half inch in length. It did fall out but didn't result in the mess that >would have occurred had it been longer. As a guy who does his own hair, I can assure everyone that you can get much closer than half an inch if you use electric clippers. For the first few days, it (almost) looks like bare skin - and with zero risk of cutting anything except hair.
Kaye301 - 05 Jan 2004 18:29 GMT Glenfiddich wrote: << As a guy who does his own hair, I can assure everyone that you can get much closer than half an inch if you use electric clippers. For the first few days, it (almost) looks like bare skin - and with zero risk of cutting anything except hair.>>
Although my hairdresser said she left 'half an inch,' in retrospect I am guessing it was more like between that and a quarter of an inch if not the latter or even less. And I am sure she did that to be on the cautious side because of the potential risk at a time when your immune system is generally compromised.
madiba - 04 Jan 2004 23:02 GMT > Hello again, > [quoted text clipped - 10 lines] > that have such severe side-effects. I guess I need to know I'm not the > only one who might have felt like this. Thanks folks. The responses to your post were interesting, I never realized that some women have a harder time accepting losing their hair than losing a breast.. Apart from knowing that your hair will grow again (it often comes back thicker and sometimes greyer than before) you should consider a 'cold cap' if its really a problem. Obviously you've lost your hair so its too late to use this time, but should you need chemo again in the future (hopefully not) this may help. These cold caps are commercially produced (check Google under 'cold cap chemo', I don't favor any particular brand) the idea is it keeps the hair roots cool during chemo and slows the blood flow to the scalp through vasoconstriction, together this prevents hair loss. FYI, CMF for breast cancer and 5FU for colon cancer (normally) cause very little hair loss. Hair thinning varies between patients, very occasionally it can be severe. However, the drugs: Etoposide, Ifosfamide, Taxol and Taxotere are associated with severe hair loss.
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Tim Jackson - 05 Jan 2004 01:08 GMT > you should consider > a 'cold cap' if its really a problem. I had heard suggestions that cold caps might increase the risk of skull mets. What is your feeling on this Madiba?
Tim Jackson
madiba - 05 Jan 2004 17:28 GMT > > you should consider > > a 'cold cap' if its really a problem. > > > I had heard suggestions that cold caps might increase the risk of skull > mets. What is your feeling on this Madiba? This has been mentioned as a possible risk, AFAIK no such case has ever been proven. Scalp mets (the skull is somewhat deeper and stays warmer) are rare, much more so than mets to the eye for eg. The strong desire to keep one's hair if at all possible is also not that common. Together this makes it highly unlikely that cold caps lead to more scalp (or skull) mets.
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Tony Lima - 05 Jan 2004 01:25 GMT [snip]
>FYI, CMF for breast cancer and 5FU for colon cancer (normally) cause >very little hair loss. Hair thinning varies between patients, very >occasionally it can be severe. However, the drugs: Etoposide, >Ifosfamide, Taxol and Taxotere are associated with severe hair loss. YMMV. My wife is currently on low-dose weekly Taxol and still has most of the hair on her head after several months. Different people respond very differently to each of these drugs. - Tony
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madiba - 05 Jan 2004 17:29 GMT > [snip] > >FYI, CMF for breast cancer and 5FU for colon cancer (normally) cause [quoted text clipped - 6 lines] > Different people respond very differently to each of these > drugs. - Tony Precisely, YMMV. Same story with WBI (whole brain RT). 30Gy (3Gy/day) is a dose which causes baldness in some, hair thinning in others, some are not affected at all. In some centers in the UK one-shot RT is done with brain mets, not sure what this does to hair but I imagine complete baldness is common.
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Kaye301 - 05 Jan 2004 07:02 GMT Madiba wrote: << you should consider a 'cold cap' if its really a problem. >>
I have read mixed information about the effectiveness of cold caps. However, in addition I was told by the nurses while getting chemo that they don't recommend it because it might interfere with the effectiveness of the chemo in that area if there were any type of metastatic cells there.
Barb - 05 Jan 2004 14:00 GMT Hi Madiba,
I had CMF (as well as Vincristine) twenty years ago and the chemo nurses used a cold cap then, to no avail. I did lose most of my hair on that regimen---enough so that I needed head coverings. Back then, there was no special concern that the use of the cap could allow for cancer cells to grow in the head. I did ask them to discontinue when it became apparent that it wasn't really working. Doesn't mean it wouldn't work for some women on certain chemo agents now!
Barb
Apart from knowing that your hair will grow again (it often
> comes back thicker and sometimes greyer than before) you should consider > a 'cold cap' if its really a problem. Obviously you've lost your hair so [quoted text clipped - 11 lines] > -- > madiba madiba - 05 Jan 2004 17:29 GMT > Hi Madiba, > [quoted text clipped - 5 lines] > that it wasn't really working. Doesn't mean it wouldn't work for some > women on certain chemo agents now! The method is not new but the caps may have improved somewhat since then, so now it may be worthwhile. Theoretically (rare) scalp mets could be protected by the cold, skull mets are kept warm by the brain, so its wise to do the crosswords during chemo.. :-/
 Signature madiba
A. P. Thorsen - 05 Jan 2004 15:02 GMT > I find myself really not comfortable with the hair loss due to chemo. > I really didn't think it would bother me, but it is. Hi, Darla,
Under the "when life hands you lemons, make lemonade" theory: I always recommend to women who lose their hair during chemo that they treat themselves to a visit to a massage therapist for a cranial massage. It feels soooooo good, you deserve the treat, and it is *much* nicer when bald than when hair is in the way!
Take care, now --
Ann T. Remove 'dontsendspam' from address to reply by email
*Annie* - 07 Jan 2004 06:43 GMT Darla... Although this suggestion won't help with the emotional aspect of this...I hope it helps you get through this. This is a very hard thing to deal with indeed. You can cover a multitude of sins with clothing, but once you're hair is gone..it screams "cancer patient coming through" A brief history...I have been through chemo twice for breast cancer. I was dx in 1999, and went through a lumpectomy, rads , and then chemo. I had CMF the first time and my hair thinned considerably. This last time I was dx in Nov of 2002 and had mastectomy with recon and then chemo treatments. I had 4 rounds of AC and 4 rounds of Taxotere...completing all treatments 6/6/03. I seemed to do much better this time, and the hair loss wasn't as traumatic as I thought it would be, once it actually happened. I actually surprised myself at how calm I was about the whole thing. I was very fortunate to have found a wig I really liked, and looked alot like my own hair, except for the bangs, which I never wore. I went and got it prior to my treatments starting so they could get a good match to my own hair. {the color swatch disappeared into my hair yes!!} I really detested all the phrases I was hearing initially.."it'll grow back", it's only temporary", and my all time personal favorite "it's only hair" {grrr!} But saw them in a different light once it happened. I lost all my hair this last time. The first time {99-00} I spent money on Nioxin products, as I was told this was a good idea for treatment of my hair while going through chemo. Lots of money, and not all that impressed with the results. This time I heard about, and purchased a shampoo called "Formula 1" The company that makes it is located in Kansas. This product is specifically made for chemo and radiation patients. It's a bit pricey at $12.95 + shipping for an 8oz bottle. But this contains no fillers of any kind. {substances that can clog hair folicles during growth} I spoke to the woman that formulated this directly the first couple times I called to order. She'sa very nice woman. I like the idea that she has a hands on role as far as products that are sold through this company. She's a cancer survivor of 12 years herself, and worked with doctors and chemists to formulate this after being dx. She had been working on something like this prior to her dx, and was able to implement those plans shortly after her own dx.
I started using this shampoo right before the last of my hair fell out. She told me you really should start using this prior to your hair falling out. It just so happens I didn't hear about this till almost after the fact. I've been using this since Feb of 2003, and have had great success with it. The fact it has no fillers in it, it does not restrict the growth of new hair.{doesn't clog hair folicles like other shampoos} The result is an overall regrowth, as opposed to a patchy type of regrowth. I continued to use this everyday, even though I was bald. This is great for keeping the scalp moisturized while going through treatments.
Now that I blinded you with all the reading here...This is the information you'd need to locate the products if you think this would help you. http://www.brianjosephs.com Brian Joseph's 8012 Stateline Road Suite 201 Leewood, Kansas 66208 1-800-889-8960 Fax: 1-816-943-8857 $12.95 + shipping. It was $4 for shipping to my area. I live in Northwest Ohio. HTH's Take care there dear/God bless you annie p/s if you need anything else, please don't hesitate to ask..we're all here to make this a little easier for you and others.
Ultimately.....we know deeply that the other side of every fear is a freedom.
"Courage"...is *fear* that has said it's prayers.
darla - 07 Jan 2004 18:34 GMT Although this suggestion won't help with the emotional aspect of
> this...I hope it helps you get through this. Annie, you are a dear. I am so glad I've found this support network since there aren't any where I live (a small town in the middle of Iowa). As I mentioned in my previous post I expected my hair to fall out, I'd been told by my onc and the nurse who administered the chemo. I talked about it freely with my friends and family UNTIL it fell out! Like you said it screams "Cancer victim coming through" I'm not particularly vain but my hair has always been something I took a great deal of pride in - it was thick and a beautiful auburn color. Many people commented about it over the years and to have it suddenly gone was quite a shock. I also had spent some time beforehand and have a wig that matches my own hair so well that it fooled my husband, daughter and grandson! I wore the wig out yesterday and found it to be quite cold and scratchy. I'll look around for a solution to that little problem. It is cold in Iowa right now and I am wearing stocking hats indoors and out.
I have come to grips with the hair loss knowing all the little things people say, it is temporary, it will grow back etc. But the most important thing I'm finding out is that I'm not alone and almost everything I feel - someone else has already felt. It is a comfort to be able to come here and offer and receive support. I have a wonderful family that has been with me every step of the way but they can't really know how I feel about some of this. Thank you again Annie, for your lovely post. It was a great help.
Darla
A. P. Thorsen - 07 Jan 2004 22:12 GMT . . . .
> I also had spent some time beforehand and have a > wig that matches my own hair so well that it fooled my husband, > daughter and grandson! I wore the wig out yesterday and found it to be > quite cold and scratchy. I'll look around for a solution to that > little problem. Hope you won't mind me butting in here!
I had the same problem, going through chemo here in Michigan at this same time of year. A friend of mine bought me a couple of hats that were perfect -- they covered enough of my head that I could wear them out for errands & such and feel semi-inconspicuous without my wig.
Both are sort of cloche-type with a turn-up brim. One was a red (!) fleece, and the other a dark-brown faux fur. I'm still happily wearing the red one (the fur is a little tight with hair back on my head).
You probably know it, but in case not: You can get a sort of fringe of bangs that you can wear with a hat or scarf, if you feel the headcovering still leaves you with a bit much of a "cancer look".
With the wig on, I usually just took a long rectangular winter muffler-type scarf, put it over my head, and wound the ends around my neck. My wig was a short style, and less easily disarranged than my own (ultra fine) hair, so this worked OK. Hoods, of course, are another option.
Like you, I wore head coverings at night, too, in order to stay warm enough. I was *amazed* how much hair contributes to keeping one's head warm!
Take care (and stay warm!) --
Ann T. Remove 'dontsendspam' from address to reply by email
Tim Jackson - 08 Jan 2004 09:09 GMT There was a thread a while ago extolling the virtues of the headscarves that bikers wear (doo-rags) as a comfortable chemo-time head covering. They got them on Ebay or from motorcycle stores.
Tim Jackson
> Although this suggestion won't help with the emotional aspect of > > this...I hope it helps you get through this. [quoted text clipped - 25 lines] > > Darla *Annie* - 08 Jan 2004 09:40 GMT Darla.... Another idea. The first time I went through this {99/00}..I ordered some stuff from the American Cancer Society's TLC catalog. You can also look at stuff on their website. The stuff they offer is not really all that expensive...I've ordered some caps for night time and some scarves, but hardly wore those. I was never really all that impressed with the "doo rag" look or how hats looked on me. Nothing against Tim's suggestion about the "doo rag" but that's another thing that screams "cancer patient" to me. You see alot of women with scarves and hatsand I judt didn't have the head for those...{jmho} Sorry I was rambling..here's the url for the TLC site. http://www.tlccatalog.org
Also..There are things you can do to make the wig warmer to wear, or make it fit better. They have little cotton caps you can wear under the wig. I have one, tried it once, and it made the wig fit funny, so never used it again. It just seemed too bulky to me. I've worn another type, similair to a panty hose and that works better. Most times didn't wear anything under the wig, but the mesh on my wig wasn't scratchy on my scalp. If that's you're only problem with the wig then maybe the little panty hose type cap would solve the problem for you. Actually, there the same things they put on you when you go in to try on a wig. I baught 4 of them and they worked well, when I needed them. Alot of women who wear wigs on a regular basis {who aren't bald} use these to hold their hair in place while wearing a wig. I'm in Northwest Ohio, just outside Toledo and it's VERY cold here right now. I've always worn my hair short, so it really wasn't much difference for me when I went out. I'm finally to a point where I don't need the wig anymore. My hairs still abit thinner then I'd like it, but I can go without the wig. Take care there dear. HTH's God bless annie
Ultimately.....we know deeply that the other side of every fear is a freedom.
"Courage"...is *fear* that has said it's prayers.
Kaye301 - 08 Jan 2004 16:41 GMT Darla wrote: << I wore the wig out yesterday and found it to be quite cold and scratchy. I'll look around for a solution to that little problem. It is cold in Iowa right now and I am wearing stocking hats indoors and out. >>
I can't relate to the degree of 'cold' you are experiencing, but it was definately alot colder being hairless, even in the 'warm' house. I usually wore a terry cloth cap to bed (100% cotton I think) that I was able to get in a beauty supply store. As far as the wig being scratchy, I learned that may be a property of the wig. I was fortunate not to have that problem with the wig I first purchased. I tried on different ones after I lost my hair and found some brands to be scratchier than others. The brand that I liked best was Rene' of Paris, and I wound up getting a second wig by them--same kind--one I straightened, and the other I kept curly and 'professional-looking.' After I had selected it, the gal who owned the wig shop said that she had been getting more positive feedback in terms of comfort re. that manufacturer from her customers (most who wore wigs regularly). If you are planning on getting a second wig you might look into trying them on by feel now that your hair is gone. You might check and see if any stores carry that brand or check with your local wig store. The degree of scratchiness is hard to test for before you lose your hair. It is a very important factor, though.
Kathleen Langwell - 13 Jan 2004 03:46 GMT Darla,
I hope you become more used to the hair loss situation so that you won't be thinking about it so much. I never had great hair so I actually looked better in the wig and it was so darned easy to just put a wig on in the morning. No messing around with the curling iron or bad hair days.
On thing I did for fit and comfort was to buy one of those soft, stretchy cotton headbands sold in the haircare sections of lots of stores and wear that under the wig. I think I ended up using a thinner one about 1-1/2" wide.My 2 wigs were very short (like my own style) and I ended up wearing them all the time because I looked dorky in scarves or hats. At night I wore a bandana type covering cut from an old soft T-shirt.
My head wasn't cold in the winter -- and it can get VERY cold in Chicago in the winter, but it was hot in the summer. I think you'll soon find your own style that's comfortable for you.
Kathie
A man - 08 Jan 2004 20:52 GMT This is a big, but temporary change in your life (losing your hair). But remember, it is only temporary and is part of the treatment and likely cure for you. Don't be ashamed.
My wife made a big party out of shaving her hair. Friends came from all over and brought food (yum) and they all shaved part of her hair off. She had lots of fun meeting this challenge head on (so to speak). Then we all commented on what a great shaped head she has (she really does).
I think she should show her bald head as a badge of honor, so people will be extra nice to her in the stores, etc. But she doesn't want to. We also threaten our kid that if he doesn't behave, mom is going to take off her wig "in public". Heavens!
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