January 2012 chemo
Comments
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A couple of sites for Pre Tied scarves
http://www.coveryourhair.com/pre-tied-bandanas/Page-2.html
http://www.myheadcoverings.com/head-coverings/pc/Pre-tied-Bandanas-c5.htm
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Diane- I found a couple of nice scarves on ebay. In particular. one seller will even make the scarves a litlte bigger to acomadate my big head. She also sells on this site. http://www.cjhats.com/
The American Cancer Society has a catalog of items that might be interesting. I bought a few things from them and was happy with the quality. http://www.tlcdirect.org/
Someone earlier mentioned http://www.etsy.com/ There are some nice things listed there as wll.
I have two that I can't use (big head problem). If you want them I can send. Just pm me an address.
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Peggy - Thanks for posting those sites! They are very reasonably priced. I'll be shopping later today!
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Diane I bought two scarves from http://www.cappelleez.com/. They are soooo soft and just slip over your head and you tie a knot in the back. It is very easy and they were about $14 or $15 a piece. I like those $50 pretied ones also but haven't wanted to spend that much either.
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Kitchenella - Those look so pretty. I will have to order some later.
Gayle
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Thanks for the ideas ladies!! I will do some more online shopping tomorrow morning....working 2 jobs today yikes!! hope my steroid high lasts till 8pm. (:
Janet - Thank for the offer but I afraid I have a big head too!!! Think I may have the same trouble. lol
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I have purchased several Beaubeaus (4women.com) and they are worth every single penny I have paid. They are pre-tied and come with matching scrunchies to do them up in all sorts of fashions. The rayon scarves run about $39 each (but you can get lots of sale scarves for far less). The silk ones can run $59, but some of those are on sale, too. Every morning I slap one on my head and go out.
You can also get a free headscarf through Good Wishes (goodwishesscarves.org). Mine took about 8 weeks to get here, and I've worn it a couple of times. It, too, is pre-tied, but I don't like it nearly as much as my beaubeaus.
My oncology nurse mentioned in passing yesterday that my hair will start growing back once AC has stopped - here I thought I would be bald for the next several months. I may not need these gorgeous scarves as long as I thought! Has anyone else heard that?
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Janet - I'll be thinking about you today and you meet that awesome goal - no more AC!! I can imagine being a little excited (strange as that sounds) to be getting this one last evil treatment done. And then - vaca in Aruba!! Good luck *hug*
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Jane and Gayle As an Orthodox Jewish married woman I've been covering my hair for years in public. If your looking for head cover find a Jew. LOL
Nancy I went the the Beaubeaus site but couldn't see a good picture of what they look like on the head. All the pictures seemed to be small.
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Grateful,
I am sorry for those stupid test but thank them so you can get better treatment . *hugs* and you will be fine during surgery,I will pray for you.Also you are almost done too.. with red devil.
waitress,
I am happy you got to almost end, only one more left. Hopefullly you wont have much problems.
Miniwheat,
Just tell your son you can't make it. you need to take care of your self better.I wish people would understand but...
Any one else who had treatments good luck with SE and feel better
Bela
PS thanks for all the websites for head covers
TY
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Diane - Someone posted this link http://www.goodwishesscarves.org/ on this or another board. They will send a free wrap to cancer patients. I just got an email yesterday that mine was on the way. Took about a month to process, but they look like good scarves. There are a lot of other options - if it wasn't on this board, try looking over the December chemo group as well. I'm not as comfortable with scarves as I've become with the turbans (with the little bunched up material in the front). I can get them for $10 at the wig/prosthesis shop a few towns away (though they've thrown them all in for free when I bought a hat and a wig).
Barb - Congrats on finishing your last AC. I can understand why they'd hold off on the T. I really hope they can figure that out - and that it's not another cancer!
Nancy - I'm sorry you were hit with that tidal wave of emotions. We have so much thrown at us, and while we're able to put up the strong front and meet things head on to make sure everything 'goes right,' sometimes we have to step back and realize just how much effort and emotion it all takes. And yes, even after chemo, we're still stuck with all the concerns for the rest of our lives. Sending you {{hugs}} and wishing you minimal SEs.
To everyone else who had tx's yesterday - it was a busy day for us! I hope everything went well.
My #4 was pretty uneventful. I had a different nurse and while she was nice, I wanted my regular one back. I don't think they gave me the usual fluids, but I've been trying to keep up with that on my own. Slept okay and now I'm taking it slow before heading into work. I have just a little bit to finish up and should be okay for a few hours. Then it's the weekend. Hoping to get a walk in as well and metabolize this stuff out of me quickly.
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Kitchenella - I've enjoyed the 'sheitel' look. Had an interesting discussion with my rabbi about whether I still need to 'cover' my wig when I lead services or read, as I did a few weekends ago. He said technically no, but that if I don't want to invite questions from the congregation about why my hair isn't 'covered.' (I go to a conservative synagogue, but our policy is that all women have to cover their head when they're called up for any honors or to lead).
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i ordered a sleep cap and another hat from this place-very quick shipping etc-price wasn't too awful
www.softhats.com--look at the chemoscarves
also goodwishessscarves.prg they will give one scarf but it takes a while-wonderful ppl--i did not buy a scarf so i don't know turn around time
just quick ideas-hth
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I got a scarf from the good wishes program. They are beautiful and are worth about $70 but it did take 2 months to come! It came with a card personally signed by the employees wishing me luck and prayers. I was very touched. Great program!
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Rachel-- that's an interesting dilemma to cover or not cover your wig.... I can see that as a Seinfeld episode!
I did get a few very nice and reasonably priced hats and sleeping caps from a website called headcovers.com -
I'd like to wear scarves... and I did at first ... but get this, from two different people that I see all the time I got the:"Oh dear, you look like a cancer patient...." Ummmm HELLO!!!!
I wear lots of hats now lol
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Kitchenella - as a Jew I should have known where to look for head coverings lol The site with the beaubeaus has a video which shows it a bit more clearly
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Peggy: The Beaubeaus website can be a little hard to see how they really look - I bought scarves based on what the swatches looked like but I can tell you there are *so* much nicer and colorful in real life.
There is a Youtube video that has better pictures of what they look like, and the different styles you can create with them.
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Gayle56 Are the Cappelleez just a tube that you tie? I cant find any decent pictures on their website
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Miniwheat ~ That is not right, although I did Laugh with you...Hellllllo duh..I love it, some people are just not with it. I wear hats too and the most comfortable hat I own are from Snap On, I obviously care less what the say, I'm Comfy!
NancyHB, Janetanned, grateful33, rachelvk, and anyone else I missed thanx for your concern on my Neuropathy. They upped the Lyrica to 1 every 8 hours and it did most of the trick. No more lightening down the arms, hands shut off too, feet are barley noticeable and the fingers tips are all that remain. They are much quieter, I just have some tingling and heightened sensation, but I can open a water bottle now and I no longer have to close them into fists while I shower, to keep them away from the shower head water hitting them. Neurologist is very happy with the immediate turn of events, and once me to continue with this for now and see if the fingers turn off with more time.
Still feel good after the 4th yesterday and had the shot at 5:00+ tonight, I also have new drug Oxtycodone, heres to hoping this one gets me through the bone pain OK. I must say so far day 2 is much better on the 4th AC than day 2 on the 3rd, not nearly has whipped as last time...weird, but happy.
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DonnaDS Yes it really is just a tube open on both ends and you just tie one end. There are no pictures on the site but it was very easy to figure out.
Gayle
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Gayle56 Thanks for info on Cappelleez. I wore my wig "out" for the first time this evening. It is not very comfortable, made my scalp hurt. I think I must be a comfy scarf person. Starting to dread tx#2 on Tuesday. How are you feeling after your second?
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I think I need some perspective, because I'm all about judging myself right now. I'm at Day 11 after my second A/C and feel like I should be kickin' it, able to plan and live normally for at least the few days before #3 next Wednesday. Instead, I'm headachy, incredibly tired, anxious, and overall sick feeling. Why I'm blaming myself for feeling this way instead of the poison that's in my system, I really don't know. Does everyone have those days of grace between A/C treatments and I'm just dogging it?
Annie -
PCBarbie, I've been following your posts about your neuropathy and am so glad you found relief from Lyrica. I have experienced neuropathy since my 3rd T/C infusion almost 3 weeks ago. Mine hasn't been as severe as yours, but I have the pins-and-needles feeling (more like knives sometimes!) in my feet and hands, very sensitive fingertips, and some loss of sensation in several toes and fingers. My MO knows about it, and we'll talk before my 4th and final infusion on Tuesday.
Of all the SE, the neuropathy and fatigue are the only ones that have lingered every day through the chemo cycle.
Hope you continue to feel relief!
Ladies, on head coverings, I have been quite happy with the wigs and hats I bought from the American Cancer Society's TLC catalogue. My favorite is the fringe of hair that I wear underneath the caps and hats to make it appear that I am not bald. It's like short hair attached to a headband; it gives me bangs and a halo of hair, without the heat and heaviness of a full wig.
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Annie ~ They tell us to write it all down, but that hasn't worked for me at all...every session was a little different some new suprizes, a lot of repeats. I find a good cry in the shower works for me, when I can finally take one. and yes I do feel sometime it's me not able to get back to myself again, ecpecially days 8,9,10, and I keep reminding myself it's the poison not me, but I'm not listening. I have to say with all my SE's this has been the hardest thing I have every done. I read about people going out to eat, working, even working from home and I wish that was me, but the best I can muster up is a guest for coffe on day 8...that's the start of me actually wanting any interaction. Day 9 I was finally able to leave the house....That getting out makes it better for me, give me some drive and I start mentally turning around.
I hope you find that inner streghnth, something you want to do...go outside...once you start seeing other things beside pill bottles, TV, couches and your bed..you may feel better, it works for me. ((HUGS))
Barb
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I so feel for you ladies, I've got two days to 2nd treatment and trying to talk myself into it. Trying to keep faith that if God brought me to it, he will bring me through it... And also hoping for a miracle that this one won't be as bad.
Giant hugs to all of you!!
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I find that week 2 is only a little bit better than week 1 after tx. The only respite time I get is week 3 when I feel 80% of normal (which I use to clean the house and shop for everything I won't have the energy to do in the following weeks 1 & 2). I am finally going back to work (50% schedule) next Saturday and am not sure how I will get through it, but I'm going crazy at home -- and I really need the money.
Tx #3 went OK yesterday, although the chemo nurse had a bit of trouble getting the needle inserted. I was really tired the rest of the day, but similar to the first two times. Today is much the same.
Hope everyone is hanging in there with their own SEs.
Joyce
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PCBarbie,
I cannot imagine having neuropathy on top of all these other side effects. I too am envious of those that can work, go out to dinner etc.... I am also only looking at my bed, pill bottles, couch, and TV. When I can, I walk to the mailbox, but that is definitely something I can't do until the end of the second week. I try to read to my 4 year old every night but even that is sometimes too much. You are not alone in your feelings and I hope it gets better for all of us soon...
{{{HUGS}}}}
Brooke
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annie3310: i think that what you are experiencing must be normal for us-if there IS sucha thing! i am so exasperated with myself, my body, my emotions, my attitudes becuz i cannot plan anything; i have no motivation to DO anything yet i see so much taht i want to do-even just lil teensy things- i have a phone interview for a job this ocming week- i need the income desperately yet i dunno if my body will allow me to work or if the company really will gamble on hiring me right now. i have basically had few SE's after this first tx and i am grateful however i am also waiting for the other shoe to fall after the next few tx...
when we are of a nature to want to be in control of our lives and situations it becomes very hard to face this...
i know that i have not said anything extremely brilliant- i just want you to know that you are not alone nor are you crazy for what you are feeling. people keep telling me that i am allowed to have these feelings so i am rolling with that!
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Just a note www.cancercare.org and get the toll free # .They will reimburse your copays for anti nausea meds and will also send a stipend (150 to 175) dollars for transportation or for paying someone to take you to treatment. At this time everything helps. They are there 24/7.
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