How to cope with the loss of hair ?
My moms 14th day after her 1st Chemo is tomorrow which w all know is the enfamous day for your hair to fall out. It started coming out by the strands yesterday but today it is coming out alot more (handfuls). I dont know how this is going to affect her but I am scared for her. How will it be easier for her and I to deal with, she has always had such beautiful hair.
Please help! Thanks so much,
mandy
Comments
-
Mandy,
I lost my hair in April and it is now coming back so the experience is very fresh for me. everyone reacts differently to the hair loss. i was not too bothered by it because I just thought of it as something that would have to happen in order to get better. Somethings that might help:
1) Shave it when it starts to look really bad. For me, that was about 10 days after the loss started.
2) Leave some of the hair around the hair line as this makes it look better with a hat and with a wig
3) Learn how to tie scarves and use them
4) Buy great hats and lots of them so it is fun to wear
5) Many people find a wig a neccesity. I did not and never wore mine
6) make sure she has a hat to sleep in as it gets really cold without hair
7) Remember it is temporary
8) Go to a Look Good Feel Better session. It is fabulous
9) Tell her she looks beautiful daily
10) Make her feel proud of the strength it takes to go through this and to wear her baldness with pride.
I hope this helps. How is she feeling about it?
-
For me losing my hair was traumatic and I am not the typical vain person. However, during chemo I felt so bad I could have cared less that I was bald. Once chemo was over I became obsessed about it growing back.
I do agree - a nice soft sleep cap is a necessity for when your head gets cold.
I went overboard on the wigs and ended up buying 7 of them - 3 different colors - all different styles and I loved wearing my wigs until it got HOT! It took me a long time to just go out in public with a hat on instead of a wig.
I shaved my head with doggie clippers when it first started to fall out. I didn't want to walk around with bald patches and I in a way wanted to take back control of what was happening with my body.
Your mom might experience a whole range of emotions - just be there for her. Let her know that you love her no matter what. I was too embarrassed to even let my husband see my bald head and the only time he would see it was late at night when we went to bed and I was going through hot flashes - I would have to take my sleep cap off.
-
Hello, I never considered myself to be vain either..but of course when it happened I cried. But something a DR said during one of my support group sessions changed my point of view ..he said that we should celebrate that our hair falls out..it is a sign that the chemo is getting to every part of our body..isn't that we want? We want to heal and if that is what it takes, I will take bald any day. Maria
-
Very good way of looking at it Garciamx. I totally agree, but still am not able to leave the house with nothing on my head 95% of the time it's a wig, the rest it's a scarf. 1 time I wore a hat. I just can't do it! I know about 14 days into my treatment my shoulder length hair was coming out a few strands at a time. That started driving me nuts, so 4 generations of women in my family all shaved my head. It is a hard process to go through, but like Garcia said it's totally worth it for what it's doing!!
-
Don't get me wrong..I always wore a wig!! But thankfully you sort of get used to being bald and thankfully deep down you know that it is only temporary..I think you end up embracing the "new" you..thinking back ..Wow, I have come a long way!! Maria
-
Mandy
Remember this is only temporay and she'll have new hair one day. My hair started falling out right before christmas, my family made a party out of shaving my head. After it was done, I felt alot better. I felt I had taken control of this and it WASN'T controlling me!
I did purchase two wigs, but found out I really didn't like wearing them, they were too hot. I did buy a bunch of different scarves and just matched them to my outfits. I probably have around 20 different designs (little pigs, camo, skull & crossbones, zebra stripes, puppy paws, clovers, stars & stripes, etc) I decided if I have to lose my hair I might as well have fun with it. In June I was able to stop wearing my scarves and just go with my 1 inch hair.
Wishing you and your mom the best with this journey.
Categories
- All Categories
- 679 Advocacy and Fund-Raising
- 289 Advocacy
- 68 I've Donated to Breastcancer.org in honor of....
- Test
- 322 Walks, Runs and Fundraising Events for Breastcancer.org
- 5.6K Community Connections
- 282 Middle Age 40-60(ish) Years Old With Breast Cancer
- 53 Australians and New Zealanders Affected by Breast Cancer
- 208 Black Women or Men With Breast Cancer
- 684 Canadians Affected by Breast Cancer
- 1.5K Caring for Someone with Breast cancer
- 455 Caring for Someone with Stage IV or Mets
- 260 High Risk of Recurrence or Second Breast Cancer
- 22 International, Non-English Speakers With Breast Cancer
- 16 Latinas/Hispanics With Breast Cancer
- 189 LGBTQA+ With Breast Cancer
- 152 May Their Memory Live On
- 85 Member Matchup & Virtual Support Meetups
- 375 Members by Location
- 291 Older Than 60 Years Old With Breast Cancer
- 177 Singles With Breast Cancer
- 869 Young With Breast Cancer
- 50.4K Connecting With Others Who Have a Similar Diagnosis
- 204 Breast Cancer with Another Diagnosis or Comorbidity
- 4K DCIS (Ductal Carcinoma In Situ)
- 79 DCIS plus HER2-positive Microinvasion
- 529 Genetic Testing
- 2.2K HER2+ (Positive) Breast Cancer
- 1.5K IBC (Inflammatory Breast Cancer)
- 3.4K IDC (Invasive Ductal Carcinoma)
- 1.5K ILC (Invasive Lobular Carcinoma)
- 999 Just Diagnosed With a Recurrence or Metastasis
- 652 LCIS (Lobular Carcinoma In Situ)
- 193 Less Common Types of Breast Cancer
- 252 Male Breast Cancer
- 86 Mixed Type Breast Cancer
- 3.1K Not Diagnosed With a Recurrence or Metastases but Concerned
- 189 Palliative Therapy/Hospice Care
- 488 Second or Third Breast Cancer
- 1.2K Stage I Breast Cancer
- 313 Stage II Breast Cancer
- 3.8K Stage III Breast Cancer
- 2.5K Triple-Negative Breast Cancer
- 13.1K Day-to-Day Matters
- 132 All things COVID-19 or coronavirus
- 87 BCO Free-Cycle: Give or Trade Items Related to Breast Cancer
- 5.9K Clinical Trials, Research News, Podcasts, and Study Results
- 86 Coping with Holidays, Special Days and Anniversaries
- 828 Employment, Insurance, and Other Financial Issues
- 101 Family and Family Planning Matters
- Family Issues for Those Who Have Breast Cancer
- 26 Furry friends
- 1.8K Humor and Games
- 1.6K Mental Health: Because Cancer Doesn't Just Affect Your Breasts
- 706 Recipe Swap for Healthy Living
- 704 Recommend Your Resources
- 171 Sex & Relationship Matters
- 9 The Political Corner
- 874 Working on Your Fitness
- 4.5K Moving On & Finding Inspiration After Breast Cancer
- 394 Bonded by Breast Cancer
- 3.1K Life After Breast Cancer
- 806 Prayers and Spiritual Support
- 285 Who or What Inspires You?
- 28.7K Not Diagnosed But Concerned
- 1K Benign Breast Conditions
- 2.3K High Risk for Breast Cancer
- 18K Not Diagnosed But Worried
- 7.4K Waiting for Test Results
- 603 Site News and Announcements
- 560 Comments, Suggestions, Feature Requests
- 39 Mod Announcements, Breastcancer.org News, Blog Entries, Podcasts
- 4 Survey, Interview and Participant Requests: Need your Help!
- 61.9K Tests, Treatments & Side Effects
- 586 Alternative Medicine
- 255 Bone Health and Bone Loss
- 11.4K Breast Reconstruction
- 7.9K Chemotherapy - Before, During, and After
- 2.7K Complementary and Holistic Medicine and Treatment
- 775 Diagnosed and Waiting for Test Results
- 7.8K Hormonal Therapy - Before, During, and After
- 50 Immunotherapy - Before, During, and After
- 7.4K Just Diagnosed
- 1.4K Living Without Reconstruction After a Mastectomy
- 5.2K Lymphedema
- 3.6K Managing Side Effects of Breast Cancer and Its Treatment
- 591 Pain
- 3.9K Radiation Therapy - Before, During, and After
- 8.4K Surgery - Before, During, and After
- 109 Welcome to Breastcancer.org
- 98 Acknowledging and honoring our Community
- 11 Info & Resources for New Patients & Members From the Team