Starting Chemo February 2009?

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  • Jaimieh
    Jaimieh Member Posts: 2,373
    edited March 2009

    I have had only 2 rounds of Chemo but I find that around the second week  is when I have been breaking down.  This past time I was sick and when I was in the doctor's office I just layed on the table crying I can't think of 4 more treatments if this is how I am going to feel every time.  My first treatment I had an allergic reaction which caused my face to turn purple/pink and break out, treatment 2 I got a fever which brought out mouth sores and all over body aches.  Hopefully I am finished my share of side effects and next Monday will bring no SE.

     The good news is my doctor just called and my port is okay :)  There is no bacterial growth in the blood sample they used...

    I am about to start treatment 3 and while I have lost 60% of my hair I still have stubs on my head.   Should I expect them gone after next treatment ??

  • kat4pink
    kat4pink Member Posts: 63
    edited March 2009

    Hello everyone!

    I have been reading trying to get caught up. Love the pics and the stories as usual!

    The family and I are FINALLY over the flu from Hell, and I am scheduled to start my chemo on Thursday. (almost afraid to actually type it again, but I have a good feeling about it.. I have been cleaning my house kinda like when you clean before you go into labor.. you just know)

    Hope everyone is doing good today.. I have missed the interaction with you all lately!!

    XO

  • jancie
    jancie Member Posts: 2,631
    edited March 2009

    I finally feel human today!  That was a crappy 5 days after chemo - I didn't sail through TX #2 like I did TX #1.

    Jaimieh - I couldn't find up at the top what chemo drugs you are on and with chemo fog there is no way in heck I would remember.  If you are on A/C you don't stand a chance of keeping your hair.  On some chemo drugs your hair just thins out about 50% - hopefully you are on one of those drugs.

    Dmoore - please post your thoughts on the Look Good Feel Good class - I am going tomorrow and I am anxious to find out more what it is going to be like.  Right now all I can think of is that it is 2 hours long and I can't keep my focus for more than 30 minutes but I am sure the ladies that put it on are aware of chemo fog.

    Webby - sorry to hear about your eyebrows and eyelashes.  I know my time is coming and I am on dense dose also - funny that my hairs down south are still hanging around.

    KerryMac - when do you start rads?  I was also wondering what type of clothes to wear - I know they should be loose and comfy - very soft but then I also thought about what the heck I am going to do if I get that neuropsy stuff when I do Taxol - how am I going to button my shirts up?

    Had to bolt to the bathroom to see if I still had eyebrows - yep....still there Laughing

    Lisa810 - you still haven't posted about your Look Good Feel Good class!  I have to laugh because that last day before I shaved my head I was pulling hair from the middle of the top of my scalp forward to create bangs under my scarve.  I would comb them to cut them to length and half of them would come out.  My scalp was hurting so bad that I got to the point where I couldn't wait to shave it just to get rid of the pain.  Besides I sort of looked like I had mange.

    Liz - most people avoid spicy food when they are nauseated because we are told to eat toast and crackers and soups and all of that bland stuff.  I remember not wanting to eat when I was sick because nothing tasted decent.  I would say if you have a craving for something spicy - go for it.  Just have some Rolaids on hand if it gets to you Laughing  I have been eating Tortilla soups, chili, indian food, etc.  I get a little bit of heartburn here and there so I pop some Tums and then all is fine but the food sure tastes great!  In fact the church put together a list of who is cooking what meals for us while I am doing chemo, every Wednesday night and every other weekend (the one after chemo - Sat and Sun) - The lady that put it together passed the word that I was craving spicy foods so that is what we get.

    I haven't stopped with the coffee or any other foods.  I figure I am miserable enough that I am not going to worry about totally changing my diet right now.  I did finally buy some raw brown sugar but then again almost on a daily basis I have cinnamon toast with tons of butter and sugar on it - I like it really gooey!  I haven't been as good about drinking water as I was the first round and I think that has a lot to do with me feeling like crap for 5 days after chemo.

    I understand the depression issues - it is normal and I believe that most of us go through it.  I sit back and tell myself that I am being stupid for having a pity party when there are Stage 3 and Stage 4 BC women out here having it really rough and I have no right to feel sorry for myself.  I think about the chances of me getting BC again in 5 years, 10 years, etc.  What will I do if it comes back?  BC has changed my personality - some for the better, some for the worse.   What you are feeling is totally normal and I think it is awesome that we can share our most intimate stories with one another.

    Kristine - I am no expert but dose dense is like taking 200 mg of a prescription versus 100 mg.  I read somewhere (chemo fog going here) where there have been studies that dose dense chemo decreases your recurrence rate but then again, those are studies and I have no clue how old that study was.  I am on it because we are trying to shrink this 4 CM tumor small enough to where I can do a lumpectomy so the oncologist is hitting me hard with chemo. 

    Webbie and others - which page listed the instructions to post pictures?  I know it is some probably 4 to 5 pages back but if someone out there with some focus ability can direct me to the page, that would be great!

    Webbie - I understand chocolate week!  In fact whenever my hubby goes to the store for ANYTHING, he always brings me back a LARGE bar of chocolate.  He is a keeper for sure - he knows how to keep my happy when my hormones are raging.  I was so hoping I would go into chemopause and I will be dammed if I didn't start my period 5 days after my first chemo treatment.  Hopefully that is the last one!

    Artemis - I think you are feeling the dread of going to chemo.  I have gotten to the point where I take a valium before chemo each time just to calm myself down.  Even though you are aware of what is happening the fact that you are having to do it is dreadful!  Maybe double up your Xanax - take one before you leave the house and then one when you get there?

    KerryMac - Why is it that we are gaining weight on chemo these days - other than the steroids?  Like you I go in each time weighing 2 lbs more.  I have decided that for the next 2 days I am going to TRY to stick to a liquid diet and see if I can drop off some of those 10 lbs that I gained.  What ticks me off more is that I will weigh myself before chemo and each time I come back I have gained 4 lbs in 2 hours - that is so not right!!!!  I am definately not as active as I used to be so that doesn't help but dangit when you are feeling like crud the last thing I want to do is walk around the block!  And if I am feeling cruddy I sure don't want to think about watching what I eat!

    Ok, I am going to go ahead and submit this and come back in a little bit and get to everyone else.  My focus just went away Yell

  • Anonymous
    Anonymous Member Posts: 1,376
    edited March 2009

    so guess who wound up passing out at the wig salon yesterday? and then had to go to urgent care and get her counts tested, and then deal with a catscan? yeah, that'd be moi.Cry

    some sort of sinus infection or cold, i guess - scary high fever last night before it broke. on levaquin (antibiotic, never heard of). and my WBC are high ... yay. got a call into The Good Onc (thank god he's back!), just want to know what i should be doing besides pushing fluids (which is difficult) and taking my temperature every 15 seconds.

    i'm a little ball of misery./end self pitying post

  • susan13
    susan13 Member Posts: 732
    edited March 2009

    Lisa - Oh my gosh!  Hope you are ok!   What is it with the sinus infections!?!  I'm on Ciproflaxin (sp?) and it's not doing anything for me. Hope you feel better!

  • Artemis
    Artemis Member Posts: 759
    edited March 2009

    KerryMac ~ thanks so much for your encouraging post.  I did manage to sleep some last night, and everything went fine in the Poison Lab.  Aaaaaaaaaaaaaand....

    ...that was the halfway point for me!  Hurrah, hurrah!  *happy dance*  I'm all finished with AC, so bring on the Taxol.

    apple ~ you are an ecouragement with your stories of wearing just a scarf-as-a-bow.  I am working toward getting as brave as you because it would be great not to have to worry:  "GAAHH!!  Is my hat going to blow off?!  Will my wig fall off at the hockey game?!"  (Very funny story, Nancyb!)

    jancie ~ I did take Xanax before I left the house and took the bottle with me just in case I felt like flipping out when I got there!
    Wink

    Lisa ~ oh my gosh!  You poor thing!  Here, have some cookies.  I hope you feel better SOON!

    Hugs to all,
    Artemis

  • jancie
    jancie Member Posts: 2,631
    edited March 2009

    Ok, I am back!!!

    Living4today - So sorry that you have had such a time with illness since starting chemo.  The nurse told me last time that on day 5 is when you have to be so careful as that is when your white blood cell count goes down the most and then the Lunasta shot kicks in and brings them back up.  My hubby is sicker than a dog right now - right on day 5 - just what I need so I have been checking my temperature regularly.  Hope that you don't go through this again!

    Nancy - what an attitude!!  I would have been mortified!  I am just now allowing my hubby to see my bald head and actually let him touch it last night for the first time.  I hope that jerk sitting behind you had a huge guilt trip!

    Apple - I bow down to you!  I do love your avatar picture that shows a scarf just around the front of your head.  I hope one day I can get to the place you are at with being bald.

    Susan13 - Bad enough we have to poison our bodies but the weight gain on top of that?  Can't we somehow get a break?

    Terri42 - I need to take up your suggestion and get out of the house.  I am having one of those days where I don't want to go anywhere at all.  Tomorrow I have to leave for an appointment.  Once I get out of the house I am fine but it is finding that motivation to leave to begin with.

    Kat4pink - was wondering where you were at!  Glad you are feeling better and finally got your chemo appointment scheduled!

  • Gramof3
    Gramof3 Member Posts: 301
    edited March 2009

    I had AC #2 Friday and the steroids have kicked in this time.  Saturday I could look down and see the puffy cheeks coming up to meet my lower eye lids.  By Sunday, without my cap, my face looks like a jelly bean.  My friend said, "Better a jelly bean than a choclolate bunny!"  oh well...Have a good week, everyone.  Helen

  • Jaimieh
    Jaimieh Member Posts: 2,373
    edited March 2009

    Jancie~ I am on TCH (I don't think webbie every put me up top) which all says hair loss.  I don't care if it stays it just a very interesting pattern and I was wondering if anyone experienced it. 

  • KerryMac
    KerryMac Member Posts: 3,529
    edited March 2009

    Oh, mine has come out in interesting patterns. It will be interesting to see how it grows back - lots of people say it comes in like baby fuzz.

    I have to say though, my eyelashes are really starting to think out noticably.....

  • kmn0701
    kmn0701 Member Posts: 117
    edited March 2009

    buddy1, yes they are still sick but on the mend I think. We kept our older daughter home from school today but she seems to be bouncing back. Little one still has a cough but that's about it, her activity level is pretty normal. I'm just hoping I bounce back too. Still no fever though I was chilled last night for a bit, just general aches & chemo fog...which I THINK is normal??

    webbie, I PM'd you....tell me if you can see it that way?? I don't know why you can't see it but it's weird because sometimes I can see it & other times I can't. Computers!

    Kerry, I have checked out that stage 3 thread, not in the past couple days though. You're right, it's encouraging & heavens knows I need that right about now. Heck, we all do!  It just sucks because before I came "here" to this board I had no idea that my ginormous tumor was, well ginormous! I literally felt that sucker growing. I cannot believe it grew so fast. I just wish someone could figure out HOW you get cancer. I mean, genetics aside, what the heck caused it? Did I stand too close to the microwave too many times? Not rinse off pesticides from fruits/veggies well enough? You know?? I wish we knew how to prevent it.It's so frustrating to me.

    Lisa810, glad you're doing better! Hang in there!!

    Does Ativan have a sedative in it?? I was thinking of taking one but don't wan't to get spacey while DH is still at work. 

    My hair stubble is driving me NUTS!! It's pokes & itches & scratches. I'm dying for it to all just fall out. And yeah, weight gain?? I thought chemo was going to kill my appetite. Dammit! Yell We don't get no breaks, do we?

  • kmn0701
    kmn0701 Member Posts: 117
    edited March 2009

    Ok, I want a buff! I found these....has anyone seen any others??

    http://www.cancersurvivorstuff.com/survivor_buffs.html 

  • webwriter
    webwriter Member Posts: 535
    edited March 2009
    Someone here, in this thread, recommended PlanetBuff.com and I'm STILL slobbering all over the screen. Those things are the SHITZNIT! (And I would LOVE to thank the original poster!)
  • webwriter
    webwriter Member Posts: 535
    edited March 2009

    Oops! Yup! I DID finally get to see your lovely family! Thanx for taking the time to send it! I'll quit gritching about it now. (Wouldn't want you to have to go all phere-moaning about it! ;)

  • suzmarks
    suzmarks Member Posts: 83
    edited March 2009

    Hi all, been quiet for awhile but of course keeping up with my nightly reading. So much info out there. Last night I ordered a PlanetBuff head thing. They do look awesome and I hope it will be a functional piece of headwear I can enjoy in all seasons. I wear my wig at work (I teach) but love not having anything on my baldness. I sometimes forget about it and recently found myself out in my backyard, letting the dog out with nothing on my head. My neighbors can see into my yard so I quickly covered my head with my hands.and ran back in. Last week I almost walked out of the house on my way to work bald. Luckily one of my daughters noticed it and stopped me before I got too far. If you've ever had dreams about being naked at work, this is almost like that. I'm wondering if my chemo is working (I'm on TC). Not that I want to jinx myself but I feel great. I've had 2 TX so far. I did feel some symptoms after TX 1 but aside from some minor stuff this second time around I have nothing to complain about. I didn't use my nasal spray or anything this second time. I had the Neulasta shot and was also fine. I have TX 3 next week. I have an offer to go to Florida a couple of days after TX 3 and I'm tempted especially since I'm feeling good now. I read that some people say it's TX 3 where things really kick in. Not sure what to expect or if travel is a good idea. I actually have no choice about travel as I'm going to my dad's 80th birthday party and have to catch a flight to the Twin Cities.at the end of March,, that will be 9 days post treatment. Well I feel like I'm writing too much about me and should just erase this whole thing. But I do want people to know that sometimes you do feel ok. My best to all and hope you're comfortable.

  • dmoore2009
    dmoore2009 Member Posts: 8
    edited March 2009

    Janice..  As for the Look Good Feel Better Class it was great.  There were about 9 women there.  We first were given our bags that contained over $200.00 worth of makeup.  They showed us how to apply your makeup and also how to make eyebrows in case you have lost them ( I lost the hair or started and shaved it but I still have my eyebrows and lashes)  Then they had a huge selection of wigs for us to choose from.  I was a brunette but after today I am a red head.  We also got a hat and scarf that people made and donated.  I really enjoyed  it and had a very good time.

    Well only two more days until my next A/C treatment wish me luck!  Is it true that you feel worse after it than the first? 

     Hope everyone is doing well and have a blessed day!!

  • jancie
    jancie Member Posts: 2,631
    edited March 2009

    Dmoore - thanks so much for giving details on the class!  We are having a pretty good snow storm tonight so I expect there will be 6 to 8" of snow in the morning minimum.  But that won't stop me from going.

    I felt so much worse my 2nd treatment of A/C.  First time I had 8 hours of nausea but also an allergic reaction to compazine.  The 2nd time I had 4 days of nausea, major constipation issues and felt much worse.  I am also having another allergic reaction tonight.  My right hand is swelling up really bad to where my skin is starting to feel tight.  I took 2 benedryl and am going to get some ice on it right away.  I guess I will be up most of the night popping benedryl and checking for further complications.  I don't want to wake up my hubby as he has been so sick the last 2 days and he is sound asleep right now.  I just hope I have some energy to get through the class tomorrow but thinking that I will since the benedryl will definately put me to sleep.

    The weird thing is that I haven't taken any meds today at all but am having a swollen hand - yep.....I am wired ass backwards (that one was for you Apple!) Laughing

  • KerryMac
    KerryMac Member Posts: 3,529
    edited March 2009

    Love those buffs! It is a nice website actually, they have some cool stuff.

    jancie - hope your hand is better - is it a reaction to the chemo?? I am having my drugs through IV, and the veins on the arm where I get it are all black and hard. Lovely. Anyhow, hope you really enjoy your class today, hope getting there isn't too treacherous. I am not sure either what to wear during rads. I am thinking I will be sore, like sunburn sore, so something loose will be good. I had a Mast. so I am imagining I won't be able to wear a bra with my falsie, so I will just have to look a little lopsided. So again, loose is good! I'm due for treatment in June, so I am hoping it won't be too hot then. I don't think you are allowed to swim or anything during treatment.

    suzmarks -  glad to hear you are fairly SE free! Enjoy it!! My 3rd round was no harder on me than my 2nd, it just lasted a little longer, and I felt a little more tired. But I am 12 days out and feel totally normal again.

    Kristine - glad your kids are feeling better. Hope you manage to avoid getting more sick too. I have had a bit of a sore throat (thanks to my son) but it hasn't turned into anything. I am so worried about picking something up from the kids.

    kat4pink - yah for a start date!! 

    Hoping everyone has a great day today! It is going to pour with rain here all day, we have a huge puddle in our back yard already, the extra rain won't help. It is so dark now in the mornings now the clocks have gone forward, but I am loving the lighter evenings. Makes me think Spring is not too far away.

  • apple
    apple Member Posts: 7,799
    edited March 2009

    KerryMac

    rads are accumulative.. most people don't experience discomfort at first and often even near the end the discomfort is minimal because the nerves are dead anyway.. i certainly wouldn't buy anything special.. just wear 'loose'.

    I am still hoping to see a picture of a human in a buff.

    it's raining/foggy in Kansas.. grey and moist.. dreary, but things are beginning to grow.

  • KerryMac
    KerryMac Member Posts: 3,529
    edited March 2009

    Do you think I will still be able to wear a bra?? It's not really a big deal, I am just thinking I will not only be bald, but obviously lopsided.

  • apple
    apple Member Posts: 7,799
    edited March 2009

    i avoid bras whenever possible - always have.   you'll be fine for the first couple or several weeks.. then it might become uncomfortable.  everyone of course if different,  i am VERY fair, yet hardly got 'burned'.. my Peruvian girlfriend was VERY uncomfortable the whole time.

  • MicheleS
    MicheleS Member Posts: 937
    edited March 2009

    Hi,

    Just checking in... this round was pretty bad; the nausea/vomiting was terrible.  (Plus, I still have the nausea and dry heaves...)  I had to get IV fluids the Friday after treatment.  Saturday, I was *lost* and couldn't even manage basic self-care.  After that, things got a bit better each day. (tho' I wish the nausea would go away...)  I had to go to work for an hr or so yesterday and am here today (for only a few hours)...

    That's it really.  I'm glad (and jealous!) that so many of you are tolerating things so much better than I am.  I'm praying that taxol is better for me.

    Michele

  • susan13
    susan13 Member Posts: 732
    edited March 2009

    Kerry-I'll be doing rads too probably starting end April, I was told to wear something loose, and no bra, maybe a soft camisole would work.

    Ok, this weight gain thing has me nuts.. I'm trying to not harp on it but how the heck can someone gain 4 lbs. in one week??? Cripes.

    So here's some humor on the subject for ya'll.....

    This is a specially formulated  diet designed to help WOMEN cope with the stress that builds during  the day

    BREAKFAST

    1 Grapefruit

    1 slice wholemeal  toast

    1 cup skimmed milk

    LUNCH

    1 small portion lean,  steamed chicken with a cup of spinach

    1 cup herbal tea  

    1 biscuit

    AFTERNOON TEA

    The rest of the  biscuits from the packet

    1 tub of Gino Ginelli ice cream with  chocolate topping

    DINNER

    4 bottles of wine (red or  white)

    2 loaves garlic bread

    1 family size Supreme pizza

    3  chocolate bars

    LATE NIGHT SNACK

    1 whole cheesecake (eaten  directly from the freezer)

    REMEMBER :

    'stressed' spelled  backwards is 'desserts'

    Send this to four women and you will  lose two kilograms

    Send this to all the women you know (or  ever knew) and you will lose 10 kgs

    IF you delete this  message you will gain 10 kgs

    Finally, here's some advice for  you:

    Dr. Neil proclaimed the way to achieve inner peace is to  finish all the things you have started.......

    So I looked  around my house to see things I'd started and hadn't finished; and,  before

    leaving the house this morning, I finished off a bottle of  Merlot, a bottle of Chardonay , a bole of Baileys, a butle of  Kehuha, a pockage of biscuits , the mainder of bot Prozic and Valum  scriptins, the res of the Chesescke, some saltins an a bax a  cholates..

    Yu haf no idr who gud I fel.

      

  • KerryMac
    KerryMac Member Posts: 3,529
    edited March 2009

    OMG, that is soooo funny! I keep telling everyone I am having a little Chemo baby! I am gettimng a nice round tummy....It must be the steroids, why anyone would take them voluntarily is beyond me!!

    Michele, I am soooo sorry you are sooooo sick. Rest, and take it easy. The nurse told me last round that the taxatore is much easier, sure the same applies for taxol. 

    Thanks for the advice guys regarding rads, I had a friend who was totally fried by them. I usually tolerate the sun well, hope the same applies....

  • susan13
    susan13 Member Posts: 732
    edited March 2009

    Kerry, there's also creams that can help with keeping the burn away from rads.  Try to look on the radiation forum. Something called "Jeans Cream" sounds pretty good. I'm getting it myself.

  • KerryMac
    KerryMac Member Posts: 3,529
    edited March 2009

    My Rad Onc said he will give me a prescription for something that they make it up specially in the pharmacy of the Cancer centre. 

    It is silly, as I am starting to stress about it all already, and it is still so far away. Not happy unless I have something to worry about!! If all goes as scheduled, I finish Chemo May 1st, then get a month off and should start June 1st. And we are still only in March!! Guess I am in a hurry for the treatment to be behind me a bit. Well, in all honesty I would like the next five years to be safely behind me...!

  • susan13
    susan13 Member Posts: 732
    edited March 2009

    Let me know what that script is, I'm on the paranoid side myself about the rad burn!

    I am done with chemo this Friday!  8 treatments down, thought the day would never come.  I also want the rads to come and go quickly. And I agree on the 5 years being behind us!

  • Terri42
    Terri42 Member Posts: 56
    edited March 2009

    MicheleS and Jancie - I have had three rounds of AC and am doing OK - I'm not sure what you guys are taking but I added the steroid on days 2 and 3 and cut back on the anti-nausea pills - I personally think they make you feel WORSE.  I got headaches from Zofran so I only take Compazine sparingly - I know you can't take that one Jancie but they also recommended another - I can go find it if you need a suggestion.  I do have the downer from the steroids and yes I'm tired but overall functional.  I hope this helps - I have also met a lady in my "group" who confirmed the Taxol portion is much easier - she's motivating me like a mom reminding me how much older she is and she's doing this so can I!

    Susan13 - love the diet - I miss my wine...

    Furies - I am losing my taste - is anyone experiencing this? I can't remember if we talked about this already - but I could eat a bottle of hot sauce and barely taste it now.  My onc actually gave me a perscription in case my tongue was coated with something but I don't know it looks the same to me - not that I looked at it much before???  Plus I don't want to take anything else - enough's enough!  I'll take my hot sauce straight up....

  • susan13
    susan13 Member Posts: 732
    edited March 2009

    Terri - I have zero tastebuds ... this is why I have no idea why I am eatting like a cow... I can't taste anything!  Almost 2 weeks out from last tx and still no taste.  I sure hope it comes back.

  • elizzim
    elizzim Member Posts: 146
    edited March 2009

    Ohh, so much new to read and respond to, but I'm leaving in a few minutes to have my HEAD SHAVED! Trying to stay calm...

    Just a few random notes:

    Kristine - Yeah, these boards are such a blessing, as we all know, but at times a double edged sword, as well.  So much support and so many wonderful women and friends, so many uplifting stories, but I, too, have gotten pieces of info, or statistics, that have kept me up in a panic the entire night.  Just remember - there are PLENTY of people with large tumors that ultimately never hear from their cancer again, and plenty of people with small tumors that have recurrences despite throwing all kinds of treatment at the cancer. As far what gave rise to this in the beginning, I have at times felt like I was losing my mind trying to answer that one. I, for one, exercise, eat healthfully/organically (except for the occasional mountain of ice cream!), breastfed both my girls for an absurdly long time---in short, did so much "right", and still developed breast cancer as a relatively young person.  My neighbor, the same age as I am (both of us in rural, natural Connecticut) developed lung cancer last year. No family history. It's such an enigma, and it can drive you crazy if you let it.  

    I'm feeling now that once we've done everything we can from the medical/health perspective, the challenge becomes one of learning to adopt a mental/spiritual/emotional outlook that somehow allows you to feel hopeful and open, even in the face of this.  I think for me, in my life, this will become the primary challenge.  I just lived so long with the "well, it may be a big problem, but at least it's not CANCER" attitude. What has actually happened to me (to all of us) now had become my worst case scenario.  It's going to take a lot of hard work from deep inside for me to change that. 

    Lisa810 - Hope you're feeling better!

    Susan13 - Just so you know, I, too, am eating like a pig on chemo! No idea why.

    Michele - I'm so sorry you're feeling so sick. The nausea is the worst; I had it to some extent, even with the meds. Ativan, which, yes, Kristine, is anti-nausea, anti-anxiety and a muscle relaxant, was a wonder drug for me, really did curb my nausea. 

    OK, off to become bald. I'm trying to be a big girl, but I am dreading this. I feel like a wimp next to all of you! 

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