Hair loss solutions?

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JudiB
Posts: 71
Joined: Sun Mar 05, 2017 5:30 am

Hair loss solutions?

Postby JudiB » Thu May 11, 2017 9:44 am

Despite believing that I wouldn't lose much hair with Folfox, I find my head becoming increasingly bare!! The Oxyplatin was stopped after 4 treatments, due to severity of neuropathy, and I wondered whether the hair loss would stop without it. 2 treatments on and I reached the point where I felt embarrassed not to cover my head about 2 weeks ago and started wearing a scarf or hat.
I love my scarves but feel as though I now wear a label "I'm having chemo!" I don't always want everyone to know so am thinking of a wig for times when I prefer not to stand out as someone having treatment. Not sure whether to cut or shave my head now as I keep it covered? What will be be most comfortable?
Seeing hairdresser /wig specialist next week but meanwhile wonder what those of you here who have lost your hair.... or most of it, did?
May 2004 Breast cancer lumpectomy followed by radiotherapy, Tamoxifen 5 years, then Femara 2 years.

Jan 2017 resection around colo-rectal junction
T2bN1 M0
March 2017 Chemo Folfox started. Oxaliplatin for 4 treatments, then just 5 FU and Leucovorin for remaining 8 treatments.
June 2017 clear scan
Last chemo August 2017
August 2017 clear scan
February 2018 clear scan

sadysue
Posts: 986
Joined: Tue Aug 02, 2011 6:59 pm
Location: Charleston, TN

Re: Hair loss solutions?

Postby sadysue » Thu May 11, 2017 12:15 pm

I had long thick hair and probably lost 50% of it while on folfox. My hair loss was most noticable on top (like male patterned baldness) but the back stayed quite thick. I used a product called Good Hair Day and bought it from QVC. I think you can buy it from Amazon too. You use the product, which is a powder and applied like any makeup with a brush, on the scalp. It helped me a lot and I never had to wear a cap or scarf to cover my head. It stays on your scalp until you shampoo it out. You just have to rub it in well.
Rectal dx 4/2011 (Stage 3B - T3N1M0)
5FU/Rad - daily/6 wks ending 6/2011
Surgery 8/19/2011
Finished 8 rounds Folfox 2/2012
Ileo reverse and port out 3/2012
NED

teri3
Posts: 405
Joined: Fri Jan 09, 2015 11:03 am

Re: Hair loss solutions?

Postby teri3 » Thu May 11, 2017 1:14 pm

I just wore hats. I felt scarves screamed chemo. Wigs seemed to much of a bother and I heard they are hot.
Good luck,
Teri
58 yrs old female
MSS KRAS mutation G12V
adenocarcinoma sigmoid colon dx 11-14
sigmoidectomy 11-14
Stage 3A
3 out of 20 lymph nodes involved
started FolFox 1-27-15
11 rounds FOLFOX last one 6-30-2015
7-29-2015 PET clear
5-14-2016 CT 2 nodules one in each lung
Confirmed pulmonary metastasis stage 4
FOLFIRi + Avistin started 8-16 11 rounds complete 12-16
CT 12-16 nodules shrunk chemo break wait and see :?
CT growth
VATS l lung 4 10 17
VATS r lung 4 24 17
CT 2 nodules r up and l low :(

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juliej
Posts: 3114
Joined: Thu Aug 05, 2010 12:59 pm

Re: Hair loss solutions?

Postby juliej » Fri May 12, 2017 5:49 pm

One thought might be a hat-with-hair-combo. It's not as hot as a wig, plus a baseball hat looks really cute with summer clothes!

https://www.headcovers.com/headwear/womens-headwear/?type=14294
Stage IVb, liver/lung mets 8/4/2010
Xelox+Avastin 8/18/10 to 10/21/2011
LAR, liver resec, HAI pump 11/2011
Adjuvant Irinotecan + FUDR
Double lung surgery + ileo reversal 2/2012
Adjuvant FUDR + Xeloda
VATS rt. lung 12/2012 - benign granuloma!
VATS left lung 11/2013
NED 11/22/13 to 12/18/2019, CEA<1

Steph20021
Posts: 553
Joined: Sat Dec 27, 2014 4:58 pm
Location: Ontario, Canada

Re: Hair loss solutions?

Postby Steph20021 » Fri May 12, 2017 6:57 pm

Ive been steadily losing hair on folfiri and I'm just wearing scarves I don't have to tie, but have an elastic band that hold them in place. I don't care if people see me and think I'm sick, but I'm more self conscious without them. Tried a loaner wig but is scratchy and hot and heavy and irritates me so I can't be bothered. Sometimes I'll just go out without anything on my head, and I care less and less about others. Eff it. Early onset cancer bit*ches, bit*ches be aware.
DX 1/31/14 @ 33- SPS-T4a(invades visceral peri), N2a(6/106 LN), M1a(ovary) (Stage 4a) MSS; BRAF V600E
2/1/14-subtotal col, lost R ovary, temp ileo
3/14-9/14- folfox; sepsis
11/14-CT/PET: L ovary met, pelvic met, (?)ghost liver met(?)
12/14-folfiri -13 rds kept me stable from 3/15-6/15
8/15-HIPEC, NED
09/15- cea 0.9
05/16- recurrence in abdo wall and lymph nodes
01/17- pulmonary embolism
02/17- 1 wk radiation to abdo wall
08/16- on folfiri
01/18-folfox
11/18- Beacon trial-encorafenib & cetuximab

JudiB
Posts: 71
Joined: Sun Mar 05, 2017 5:30 am

Re: Hair loss solutions?

Postby JudiB » Sat May 13, 2017 1:31 am

Thank you for your suggestions. I'm not usually that concerned about my hair but, at the moment, it just feels like the chemo is stealing a little more of me with each treatment. Being able to look "normal" (whatever that is.... I've forgotten!), would just give me back a littke of what I was.
My hair is aweful now so I plan to get it cut really short this week. I find my scalp is very sensitive and more comfortable when covered.
I know I'll find wigs hot because I find a cap and scarves hot..... Summer will be uncomfortable!
I know it may seem vain to care about how I look but it would just be good not to stand out as a chemo patient and there's still a way to go yet as I'm only half way through treatment. Saw
May 2004 Breast cancer lumpectomy followed by radiotherapy, Tamoxifen 5 years, then Femara 2 years.

Jan 2017 resection around colo-rectal junction
T2bN1 M0
March 2017 Chemo Folfox started. Oxaliplatin for 4 treatments, then just 5 FU and Leucovorin for remaining 8 treatments.
June 2017 clear scan
Last chemo August 2017
August 2017 clear scan
February 2018 clear scan

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Sophy
Posts: 261
Joined: Fri May 27, 2011 2:46 am
Location: New Zealand

Re: Hair loss solutions?

Postby Sophy » Sat May 13, 2017 5:24 am

My solution is a bit ick - i stopped putting any chemicals on my head. No shampoo no conditioner. Allowed my hair to grow long and brushed it with boar hair brush many times each day.
dx T3N1M0 Feb 2011 when children age 11, 7 and 2
Xeloda/rad March 11, LAR June 11 temp ileo
Xelox 6 rounds, NED
Lung mets Oct 13
Laser surgery Germany Jan 14. 3 mets left lung.
Laser surgery UK Jun and Aug 14 one met each lung, NED
Aug 14 Started Xeloda and Celebrex (ADAPT)
June 20 CT shows nodule, bronchoscopy confirms is scar tissue, still NED
Dec 20 stopping Xeloda continue celebrex, cimetedine
Aug 21,March 23 scans show still NED
March 2023 CURED - discharged from Oncology, no more scans or follow up

Stewsbetty
Posts: 170
Joined: Thu Jul 14, 2016 7:08 am

Re: Hair loss solutions?

Postby Stewsbetty » Sat May 13, 2017 7:08 pm

I lost quite a bit of my hair on folfox. It was coming out in clumps so I decided to shave what was left. I used hats, scarves and wigs. My hair loss was in the fall and we have cold winters so I never ended up too hot. I have been off chemo since February and thankfully my hair is coming back in thickly. No one would know now that i was sick. Just look like someone rocking the pixie cut. :)

Beth
42yo At diagnosis. Female in BC, Canada
Dx: CC ascending
Right Hemi colectomy 06/16 clear margins
Adenocarcinoma 6cm High Grade
pT3 pN2a Stage 3
10 out of 16 lymph involved
MSI-h, Kras mut, Braf wild
Finished chemo Feb. 2017
PET scan showing active area April 2017
July 2017 CT showing LN mass and spread to other LN
Stage 4
Aug 2017 failed Fofiri
Sept 2017 keytruda scans every 3 months showing shrinkage and stability
November 2018 CT shows only 1 small tumour left
September 2019 clear CT finally NED!!!

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waw4
Posts: 847
Joined: Sun Sep 12, 2010 8:44 am
Location: Durham, NC

Re: Hair loss solutions?

Postby waw4 » Sun May 14, 2017 7:48 am

I switched to silk pillowcases while undergoing chemo and in fact still use them years later.

Less friction = less drag on hair when turning your head while asleep.
Bill's Colonoscopy 6/29/10; Dx Stage I or II
Surgery 7/15/10; Dx Stage III,15/32 lymph nodes
FOLFOX4 start 9/14/10; end 1/20/11 (9 tx)
2021 dx MSH6 Lynch Syndrome positive
(as are my brother, sister & son, but not daughter)
Grateful for 2nd Chance NED time!

Cathie
Posts: 78
Joined: Fri Mar 28, 2014 12:09 pm

Re: Hair loss solutions?

Postby Cathie » Tue May 16, 2017 3:48 pm

I wore a cute straw hat I bought at target. $7.00 and I bought some ribbon from the craft store in a couple of colors to go with my outfits and I made my own hatbands I still have that hat a still wear it.

I was lucky that my hair lose was mostly on the top. my neckline had more hair so I let it grow, I did not cut it. when I felt like looking nice I'd use a curling iron and felt like I looked completely normal. sometimes I wore it and sometimes I didn't. it depended on how I was feeling that day. it's been 15 years and I still wear hats, I now have 7 hats and I get compliments every time I wear one.

another reason to cover our heads is summer is almost here and I remember feeling my skin burn, and I mean burn, if I was in the direct sun for only a few minutes.

blessings

cathie
Dx'd colo rectal cancer Oct 2002
radiation chemo November December 2002
Surgery Mar 2003 which was a temp ileo
Summer of 2003 more chemo
Ileo reversed Mar 2004
Cancer free since then

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BeansMama
Posts: 959
Joined: Thu Jan 28, 2016 1:38 am
Location: North Carolina

Re: Hair loss solutions?

Postby BeansMama » Tue May 16, 2017 4:03 pm

I lost quite a bit on Folfox and folfiri so I shaved it and wore hats or bandanas. It all fell out on folfirinox. I have 2 wigs, I didn't wear them for a while but did start wearing them eventually. It was nice to go out without people staring, they didn't when I had a wig on.
41 yrs old
Tumor found 9/2015
Surgery 1 - 11/2015 LAR and colostomy
Surgery 2 - 11/2015 wound vac
Surgery 3 - 12/2015 revise resection, move colostomy
Mets to liver - tumor inoperable - one add'l met destroyed
Stage IVa (T3 N2a M1a)
Primary tumor 9 cm x 7.5 cm x 2 cm
Beginning Folfox 1/2016 - Failed
Beginning Folfiri and vectibix 8/2016 — Failed
Beginning Folfirinox + Avastin 11/2016 - Failed
Beginning Keytruda 1/2017
CEA drop from 345 to 7.3 after starting immunotherapy
Lynch positive 3/2016


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