**NEW** Starting Chemo March 2009

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  • crusader1
    crusader1 Member Posts: 1,222
    edited March 2009

    Hi All,

    Returned from the oncologist and the white blood count was good. So I am ready for treatment two this coming Monday.

    MOB..Jan- How are you feeling? Hope the infusion went well..Any different side affects than last time.

    Donnadio-I think your chemo regimen sounds like 4 TC's. That is once every three weeks for nine weeks. Yes one does loose your hair. It begins on or about 14 days. My head head and each pain a little more sheds.I have cut my hair short in preparation for the big day.

    PattiB and MOB- my makeup class said to definitely buy a kit with stencils for eyebrows. Also she stressed to use a powder not a pencil. She said if one goes to a department store or a Sephora at an off time they would definitely show you how to do it .

    ChrisC--Too bad you are not feeling well.

    Alyad..I like this board and really see no reason to change.I am currently not on FB and really am not interested in joining it. An interesting aside is that the 24 year old founder of Facebook went to the same schools as my son. Zuckerberg lives in a nearby town . Also I do at times check other things on this board ..

    Buddy- No chickens here.The chemo also played havoc on my tastebuds. I ate chicken chow mein for days.

    Ginagina- Loved the up to date chicken joke..You are doing an awesome job on this board. I see no reason to change at all. I am sorry the great picture of your family is on the other board..

    Oh yes we can put nail polish on but not go to a nail salon...

    Hugs to All..

    Francine

  • jdeking
    jdeking Member Posts: 408
    edited March 2009

    I like facebook as an additional way to keep in touch for anyone who might be interested, for pics and etc.

    I second Francine's ques - Jan (MOB) how are you? I hope #2 went well today! Sending good vibes your way!

  • buddy1
    buddy1 Member Posts: 750
    edited March 2009

    I hit 51 post today.  Does that mean I am not restricted to the 5 limit anymore.  I guess I am a blabber mouth and didnt realize it.

    I LOVE THE CHICKEN PIC.  I wish you could have seen us all out there this morning.  Running around in the mud. I was still in my P.J.s.  The hawks and coyotes and racoons and  are just waitng for a chance to get at them. 

    Still now problem from my shot.

    I do have a large hard blood vessle under my left TE. about 2 inches long. Surgeon said to take low dose 81 mg children asprin .and sleep with heating pad.  Kinda scarry 

    I still cant figure out how to post pics.  I guees I have to wait for one of my kids to help me.

  • NanaA
    NanaA Member Posts: 293
    edited March 2009

    For those who were talking about maybe not losing hair with their chemo.  The lower dose of taxol every week instead of more every 3 weeks is one where you may not lose your hair.  Nurses told me some lose it, some have thining and some just keep it all.  No telling which you will be until it happens.  I told the doc today that I would have liked at least one day when I didn't hurt before I started chemo, but it did not happen, I guess we still need to take each day as it comes.  The minute you think you know what will happen, something changes.

  • Alyad
    Alyad Member Posts: 817
    edited March 2009

    I never intended a facebook group to be an alternative  to here- I think we should keep all the discussion here and just have the FB as a way to share pics if we went- totally optional. You can share FB photo albums with people even if they're not on FB- so if you post some pics on FB- you can post the link to the  pics here and people can go look at them if they want. I tried to post a link to a pic on FB here using the add pic tool and it didn't take it- I am going to set up an acct at Picasa to try to post pics here when I have some to post. I'm guessing it works with some websites- and not with others. Those of you who have managed to post piccs- what site are your pics on?

  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    I have used snapfish (test for MichelleinSJ) as well as Flicker and Picasa. The trick (i think) is to right click and select COPY IMAGE LOCATION; that is what you paste into the url line on the little tree icon. I haven't used a PC in such a long time, but it is the right-click equivalent. I will power up the old IBM tonight and post. If you at first you dont suceed, try, try again!

    Smile

  • crusader1
    crusader1 Member Posts: 1,222
    edited March 2009

    Hi Alyad.. Gina and others..

    Here are the directions from this site about posting photos.

    How do I add an image to my message?To add an image to a Topic or a Post, click the image icon in the Post/Topic toolbar. A popup will appear where you can enter the image's URL (see note below), description, and dimensions. Click "Insert" to add the image.

    Note: The image you wish to insert must be saved online somewhere, such as
    http://www.photobucket.com/ or http://www.flickr.com/. Each of these sites explains how to share your images. You should select the HTML code option for the image you want, and paste it into the "Image URL" box.

    Hugs...

    Francine

    Hey all this is fun talking about something beside wigs, constipation etc. Only kidding ..this is a great board with many terrific women who are upbeat..and glad to share their concerns and info in helping all of us get thru this chemo...

  • Alyad
    Alyad Member Posts: 817
    edited December 2009

    Okay, I started a Facebook group for anyone who is interested. I still try to post my shaved head pics here when I get them. I called the group :

    March Warrior Princesses

     it is a closed group so you to be approved to join- search for Dayla Austin to find me. I'd like it there was more than one admin who could approve new members. I posted a few pics just to have something there. I wanted to make the group image a cocktail pic- but FB seems to have some way to tell if a photo is not your originally? so for now its a stained glass suncatcher.

  • nicole0714
    nicole0714 Member Posts: 48
    edited March 2009

    Hi, I have been reading and posting on other forums before this, but finally started chemo on March 12th. I am getting TCH x 6 cycles. First one went fine, no nausea. Got neulasta and fluids the next day and no bone aches either. I was pleasantly surprised. A cousin who went through chemo for ovarian CA told me to take Glutamine powder mixed in a drink for three days following chemo. She said it made a huge difference with the bone pain and the neuropathy sometimes associated with the taxols. I did catch a cold from one of my sons, and spiked a fever. Had to go back in for antibiotics and more fluids Other than the headache from the URI, I just felt run down. I know they say subsequent treatments usually get worse, but I am just hoping I am tolerating chemo OK! I also used those "cold caps" to prevent hair loss so we will see...

    I hope the rest of you are doing well. I will pray for each and every one of you tonight!

  • Alyad
    Alyad Member Posts: 817
    edited March 2009

    HI Nicole0714, welcome to the group! Gina will add you to the list soon. I'm glad you are handling your first treatment fairly well. I had my first 6 days before you and I am back to feeling almost normal. I had TAC. I want to try the glutamine next treatment. I didn't have any feeling of neuropathy but I think that can get worse the more treatments you have.

     Keep us posted on whether the cold cap has an effect or not. Maybe it might delay it at least?

  • nicole0714
    nicole0714 Member Posts: 48
    edited March 2009

    how do you post your diagnosis info?

  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    Hi Nicole - if you go to the top of this page, you will see several tabs, the 3rd is MY HOME. Click that and it will take you to your home page, which includes a link that says + Edit Diagnosis. Let me know if you get stuck

  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    Alyad - i just went to FB. Did you get my group request.

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009

    Dayla....I just sent a request for the FB group....I can admin if you need one.  Thanks, Diane.
    FYI the new FB format stinks.....UGH I can't find my own groups....maybe it's the chemo...ERG.

  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    Nope, it's not you. It took me 10 min to find it too.

  • crusader1
    crusader1 Member Posts: 1,222
    edited March 2009

    Alyad...I had menitoned glutamine to my oncologist and he said definitely not to use anything natural where one does not know how it affects the treatment. The only natural viatamin one should take is Calcium with Vitamin D.

    Please no one should take any supplements without first speaking with your oncologist..

    Hugs,

    Francine.

  • Alyad
    Alyad Member Posts: 817
    edited March 2009

    This is the first FB group I've started- it does take a bit to find where they've hidden everything. you'd think requests to join the group would be on the group page - but no. There are two ways to join- you can friend request me and then I can send you an invite- or you request to join the group and then one of the admins (I made the two people who have requested to join already admins too) accepts it.

    If anyones knows any more about this - if I need to do something else- let me know. I'm not sure how many admins a group is allowed to have. I think it'd be good to have as many as possible so someone requesting to join can get accepted sooner.

    for all of you who want nothing to do with this- bear with us while we get it set up- then discussion of it will fade.

  • MichelleinSJ
    MichelleinSJ Member Posts: 133
    edited March 2009

    Dayla, I had to friend request you on fb, was that the right way to join the group?

    I love fb.  Totally addicted.

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009
    You can have as many admins as you want....I created a group for my HS class and a few others....The nice thing about the group is that you can message all members.
    As for finding the group, go to the search field and type the name of the group.  It should come up with "all results" then just click group.

    I have first post chemo oncologist appointment tomorrow for bloodwork and followup.....bringing my 16 month old and 2 1/2 year old with me.  Think I will be in and out? :)  After they meet my kids I hope so.
  • Alyad
    Alyad Member Posts: 817
    edited March 2009

    Didle20-   I   suppose every office is a little different. I had my post chemo follow up yesterday and I had lab appt at 1230 - they drew blood and I was back out to wait until my appt at 130- gives them time to process the blood work? I remember going to an onc appt a long time ago with my g-ma and I think they processed it right there as we waited- so your process may vary.

  • didle20Diane
    didle20Diane Member Posts: 404
    edited March 2009
    My onc's office has a machine and it took not time at all when they did my pre chemo bloodwork.  I told them in advance that my peeps would be coming to my follow ups....too much of a hassle to drop them off...blah blah blah....They should be good. 

    I hope the counts are OK>....I didn't get the nuelasta shot.  Feeling good though so hopefully the next 3 treatments will be kind to me, too.
  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    LindaNY - hope you got through today WARRIOR GAL! Needing some more color, we offer you a....

    I really hope that purple is not your all time least favorite color. If it is, let me know I will fix it!!

    If anyone is interested, I think this is a Blueberry Pomegranate Martini. Oh.

    MOB - here's hoping you are well and resting!

  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    Up Next:

    Tomorrow Premier Day for DebbyB and Rusty123!!! We know you gals have been getting ready, but also possibly worrying and stressing out. Remember that the anticipation is worse than anything. Sending you good vibes for a restful night and successful day!

    Tomorrow round two for KathyAlex1960! Fingers and toes crossed.

  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    MichelleinSJ - you are posting, so you've not been rushed into ER for an IV. That's good thing. How are you feeling? I was thinking about your daughters bday (mine dd is next weekend...not the one coming up) and the dissapointment not being able to celebrate with her.

    i was thinking about you and the appointment with the hair guy. This guy is going to make you a custom wig with your own locks? Just wondering because you mentioned that you were going to cut it yourself first.... SurprisedSeriously? I want to hear more!!

    Jdeking - how is the hair thing going for you? I am glad I am level 0 buzz, however I have been taking multiple showers every day because the these little guys are falling down the back of my shirt continuously (like I have just gotten my hair cut AGAIN) and the prickly sensation is driving me nuts. Someone on the Feb 2009 thread recommended a lint roller and I am totally addicted to it. So is my daughter. We are running that thing all over my noggin just to see how much we can stick. And it's a lot.

    Morbid fascination with hair today. Sorry!

  • laurie41
    laurie41 Member Posts: 61
    edited March 2009

    jdeking..i work nights so this is the first time I have worn a scarf. I'm not use to it yet. At home I wear a winter stocking cap because my head gets cold.Brrrr!!



    michele54....where did you order your buffs from? I have such a hard time tying a scarf, I'm all thumbs. Fashion and me are not so good of friends. i need lots of help at times.



    ginagina...thanks for the pep talk. day two of my lost hair is better but my head still hurts. how do i get that to stop?



    Laurie

  • sakura73
    sakura73 Member Posts: 467
    edited March 2009

    Hi Laurie,

     I too am crap at tying scarves so I have gone for loads of these - http://www.headwraps.com.au/index.htm - I have 10 of them in different colours. you just loop them over your head and then twist. They are stretchy cotton and very comfy. The lady who makes them is, like me, in Australia and does send overseas but maybe something similar is made in your neck of the woods.

  • ginagina
    ginagina Member Posts: 327
    edited March 2009

    Laurie - did you get any relief from the buzz? I did (probably about 12 hrs) but it is back to hurting again. And like you...it just continues to fall out!   I think the only solution is to shave off what remains.  I still have a brown halo, but it is very, very splotchy.  I am going to try and wait until the weekend (I have a girl scout meeting tomorrow afternoon and chemo on Friday) so I'd rather not do anything drastic until I can get through those.

    I ordered some buffs from PlanetBuff.com (coupon alert! if you put HAYLEY at checkout, you get free shipping). I am hoping to get them soon. I have attempted to use my scarves (the ones I have had for neck wearing back in my financial-district-job in the 90s but I can't figure out how to wear correctly either). I am signed up for a Look Good Feel Better class on Monday night and I hope to take whatever I have a learn some new tricks. Otherwise, its going to be Bald Gina All the Time. Which isn't the absolute worst thing that could happen. It just sometimes (in my limited 3 day experience) attracts more attention than i want.

  • ginagina
    ginagina Member Posts: 327
    edited March 2009
    sakura - hey, I like the look of these.
  • gymmom8
    gymmom8 Member Posts: 86
    edited March 2009

    The sleep fairy missed my house again tonight.  I am getting so frustrated with being awake at night.  I have tried three different sleep aids and nothing will keep me asleep.  I try so hard to keep quiet when I wake up so I don't wake anyone else.  A sleepy (and cranky) 7 yr old is horrible when it comes to getting up for school!!  I was going to try another pill but then I remembered I have a dentist appt this morning and don't want to end up sleeping thru it.  My mouth is getting worse.  The cheeks feel like I can scrape the insides out and the sores have begun.  I am using "magic mouthwash" that was prescribed and it does seem to help. It is not very pleasant tasting however. 

    I will try again today to post pics of my new 'doo.  I will also see about joining the FB group.  I am new to FB and am not on it very often. I do like this board but who says we can't have more than one place to meet?

    I ordered some hats and scarves from tlccatalog but have not received them yet.  I am hoping they will come soon as I don't think I have too much longer until the hair starts to come out.  Today is day ten so I know I do have a little more time.  I am not really a hat person and I'm not sure I'll be able to tie the scarves but we will see. 

    Here's to a great day to everyone.  I think I'll clean out my youngest daughter's room/closet today.  Maybe if I work extra hard today, I'll sleep better tonight. 

    See what happens when you are up at 4am?  You start rambling on and on. 

    Thanks for letting me go on and on....

    Cyndi

  • laurie41
    laurie41 Member Posts: 61
    edited March 2009

    ginagina...I'm signed up for a Look Good Feel Better class on March 25. I hope they can show me how to wear the scarves I have and help with my eyebrows. I noticed that they are starting to shed also. I have such a hard time with my scarf because my ears get hot and if I put the scarf behind my ears I look to much like a pirate. If my head wouldn't get so cold and me feeling so unsure about how I look with almost no hair, I would just wear nothing, but I'm not ready for that. What's a girl to do!

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