Hi All. Anyone else out there with a triple negative BC diagnosis? I have started a group for anyone interested in joining and sharing their stories? Hope to hear from you soon, xo Christie.

I am here, will post this link in a blog post to get more members xo

Thanks Liz. Im traveling well. Round 2 next week :( Yesterday was a big day for me. My hair had started to come out in BIG clumps! So out came the clippers. Very confronting and emotional! But it is done now, im shaved no.4 and my 3 boys laugh at me every time they look at me! The innocence of youth hey! My husband keeps telling me it looks good but Im not convinced! xo Christie

Christie, I understand how you feel about the hair falling out. I thought I was all prepared by shaving it down to a number 1 a week before it was due to fall out. I felt I was in control by doing that. Then when it completely fell out, it was a different story. I didn't think that it would bother me so much, but it did. Especially since my second chemo session and hair falling out happened during a miserable week of constant rain and terrrible weather. I felt even more miserable. I think I'm now a bit more used to it, but I can't wait for the chemo to finish so that it can grow back. I've been told my wig looks pretty good too, but I can't say I'm a big fan of it. It's probably because I know that it's a wig and just think that others will notice, even if they don't. It's true that there are more important things than our hair, of course, our health. However, I can understand the need to just feel and look like everyone else is also important. It's good that your boys are laughing about it at least. It might help if it rubs off on you too. I guess it's good to be able to laugh at something. :) Liz xox

Hi ladies, I hope your all feeling as positive as possible even though it's an up hill battle to do so at times.....I am day 6 after chemo & I must say I am thankful that i've basically sailed though number 1...i've had a few joint pains in mainly my feet and ankles and ulcerated mouth which panadol rapid soluble is marvelous for it :-) I've just had to take all my jewelery off as my ear rings and neckless even though gold is causing a very itchy welt of a rash :-s Oh & the scap....hahaha...I have to laugh to myself about it otherwise I may crash & burn at the thought that my hair folicules dying...the itching is unbelievable I now know how a flee ridden dog feels :-D I'm not actually sure when the hair starts to fall out but I too will be doing the number 1 or 4 with the clippers when it's time, I think the chemo nurse said at around day 10 it all starts to happen & then I'll cross that bridge when I come to it though! The test results are back from the familial genetic group it only took 2 weeks but I don't find out the results until September 1st a great way to start spring off isn't it. I could have found out last thursday but I had my 1st round of chemo so that was that. I'm not too sure how I feel about finding out the results but I think it's best considering I have 4 daughters and 2 sons for their sakes to find out for sure, but once again I'll cross that bridge when it arrives! I'm insistant that I stay as positive as can be as I don't intend to let this major hiccup bring me down it's just another learning curve in the road of life and I do intend to learn from the experience as much as I can! I hope you girls are the same! Brightest Blessings, Susan xx

Good to hear you are feeling good after round one. I too felt pretty good by day 6! No major issues other than the tiredness. My hair by day 2 felt dead. It was dry and yuck. By day 12 it started coming out and yesterday was day 14 and Im bald. It just all came out in the shower! Very confronting and I did have a cry in the shower. I knew it was gonna happen but I was not prepared for how quickly it occured! Hope the genetic testing goes well. I will be doing this after treatment. I have no family history so my oncologist wants to make sure Im not the first in the chain. I have a sister, niece and 2 boys of my own. I would rather they know the possibilities. Im heading into round 2 on Tuesday, and hoping it goes as smoothly as the first. What chemo are you on Susan? Im scheduled for 6 rounds FEC x3 Tx3. With neulatsa injections. Enjoy your week xo Christie.

Triple Negative BC | BCNA Online Network

83 Replies

pacwood
Member
14 years ago
Hello girls. Sheree You are such a nice person to include anyone in need who fits our face book group age range! To Liz and Deeay I hope you girls are feeling well in your selves. I send you hugs and positive thoughts.

Is anyone heaing to Sydney for the BCNA conference? Im hoping and wishing to get there and meet up with many of the friends I have made onlne!

xo Christie.
shereejoy
Member
14 years ago
unfortunately it is secret group... as we don't want randoms... and what we say we feel safe that other's can't find our group or read or see what we say or do... happy to add you though...

Add me as a friend on facebook here:

https://www.facebook.com/#!/sheree.mcleod

And then I will make sure you are added to the group/s

Sheree

xxx
shereejoy
Member
14 years ago
Also if you want to be added to our facebook group.. let me know.. there are ladies there that are suffering 2nd time reoccurances that maybe able to offer you some support.

If you add me as a friend her:

https://www.facebook.com/#!/sheree.mcleod

I will make sure I add you to our group/s.

Sheree

xx
shereejoy
Member
14 years ago
the biggest of hugs to you lizzy :( xxxxxx
shereejoy
Member
14 years ago
Hi Tina... I am having trouble locating you on facebook... here is a link to my personal page.. if you add me as a friend I will ensure you are added to the breast cancer group... it is a very active group for young women :) xx
shereejoy
Member
14 years ago
Hi Catherine... I had trouble finding you on facebook... the link to my page is here :

https://www.facebook.com/#!/sheree.mcleod

So if you add me as a friend, I will ensure you are added to our breast cancer group :) xx
Deeay
Member
14 years ago
Twice for me in 2 years! I'm about to hit anniversary of 2nd diagnosis last year. Can't help but worry. I'm having a full double reconstruction in August so feel like I need a PET scan or something before that to see if I'm still cancer free. I'd like to join the Facebook group too. What's it called?
Deeay
Member
14 years ago
Twice for me in 2 years! I'm about to hit anniversary of 2nd diagnosis last year. Can't help but worry. I'm having a full double reconstruction in August so feel like I need a PET scan or something before that to see if I'm still cancer free. I'd like to join the Facebook group too. What's it called?
Tina_P
Member
14 years ago
Hi Shereejoy

i would appreciate you adding me to your group. My surname is Piggott.

I'm feeling well, enjoying work and having another round of chemo on 11th April, scans on 10th.

Tina
shereejoy
Member
14 years ago
If you tell me your surname Tina I can search for you and add you to our group... Pacwood is also in our group

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