Starting Chemo in September?? where are you ladies

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  • nanc512
    nanc512 Member Posts: 98
    edited October 2007

    Hi fellow September chemo buddies:

    My fever finally broke, so I snuck out to the store early today when there were few people around.  I am doing the stomach thing like many of you, rumbling, diarrhea, etc...  My newest problem is all my mucous membranes drying out; eyes, mouth and female area.  My friend brought me some Replens and it is helping, but I need to use it daily.  Someone told me to get KY Liquid Beads, so I might do that later today.  I am just afraid to go out since my wbc was so low and I have been running a fever.

    I don't drink much diet pepsi anymore, just doesn't taste good.  I am have been drinking water and it's tasting good so far.  Some of my favorite foods taste awful.  I do love baked potatoes and mac/cheese, both of those taste good.

    I have continually lost weight, intentionally, and keep dropping a few pounds each week.  I start Emend/Decadron next week, I paid $207 for 3 Emend pills!  I need to ask my doc if he can get samples.  I am wondering when the weight gain will begin........ugh

    Blessings to all of you!

    Nancy

  • Urbie
    Urbie Member Posts: 154
    edited October 2007

    Hi Ladies,  I am so happy to report that I have had a really good day today!  I walked my usual 3 miles this morning (couldn't do that the last couple of days) and took my kids on a picnic lunch and then took them to decorate pumpkins at Michael's.  My kids were SO happy to have mommy back for the day (two girls 5 & 8).  I was getting so depressed yesterday (sounds like that was the way it was for everyone) thinking that I was going to feel crappy for 12 weeks.  Today was six days after tx-1 for me so there is hope that the next two weeks will be good!  I hope that the next treatments give me only six days of yuck too.  Next time though I will take stomach meds before the treatment to avoid this painful tummy.   Hopfully I can stay up late to see the Packers vs. Bears (longtime Packer fan - grew up in Green Bay).  

    And -  I have a recipe to share with you Moose and Venison folks (can use stew meat too).  This is so good.  I will try to put it in a separate post...

  • Urbie
    Urbie Member Posts: 154
    edited October 2007

    (favorite meal as a kid!)  I can remember now..

    Venison & Popperoni  (couldn't say macaroni as a child)

    2 lbs. cut up venison/stew meat

    2 capfuls Kitchen Bouquet

    One 8oz Tomato sauce

    One can Campbell's beef Consume Soup

    One lg. can drained, peeled tomatoes (I use chopped)

    2 tsp lemon juice

    1 Tbs brown sugar

    1 tsp minced garlic

    1 tsp marjoram

    Corn starch & water

    Cut off all fat & gristle on stew meat and brown w/2 capfuls of Kitchen Bouquet.  Put browned meat and juices into crock pot.  Add all ingredients except for the corn starch and water.  Cook all day on low in crock pot or in oven casserole dish at 350 degrees for 2 hours.  Dissolve about 1 Tbs of corn starch in water and add to sauce to thicken.  Serve over spiral noodles tossed in parmesan cheese and parsley.  Serve with Popovers for yummy dinner!

  • paxton
    paxton Member Posts: 577
    edited October 2007

    Thanx for the recipe urbie, I'll have to write that down.  I'm sure I'll be looking for all kinds of recipes with all this meat we have.

    I had a better day today.  Bf came home late from being out with the guys.  He's so cute and talkative when he's had a few.  Laying in bed with him then is my favorite time. 

    He asked me if I was mad at him because I hardly looked at him all afternoon.  (we've never had a fight and I can't really recall being mad at him so I think its funny that he'd say that but I suppose he was clueless).  I told him I just missed him so much that it was hard for me to be around him with all those people because I just wanted to cry.  And it was a little tough seeing the moose and hearing everything when I didn't get to go.  Then he grabbed me and said he just wanted to hold me in his arms all night (he's not a touchy feely sorta person unless we've been apart).  It was just what I needed.  And we spent the day together.  That's how it should be.  We don't talk a lot but its not right if he's not there.  So everything in the world is right again.

    Except I have treatment #3 tomorrow.  But one tx closer to done.

    I'm going to ask my onc more about my diarrhea at my appt.  I've had it pretty much the whole time. 

    Well, that's my deal...Take care everybody

  • livinginboji
    livinginboji Member Posts: 85
    edited October 2007

    Good Morning ladies! I have tried to play catch up and read some of the latest messages and then run out of time or get too tired to reply so decided to write first then finish reading. I was on my cruise the week of 9/24 thru 9/29. Had an awesome time! My onc. delayed 2nd tx so I could go and didn't express any concerns regarding the germs on the flight or the cruise. Interesting?!?! I had to shave my head before we left so wasn't thrilled with any of the pics taken on the trip. I won't go bald in public as I think I look like Uncle Fester from the Adam's family. But those of you that have posted your pictures look really beautiful! I applaud you! I had my 2nd tx last Thurs. the 6th, felt great on Fri. took 4mg Zofran Thurs. night and then every 6 hrs. Woke up Sat. AM with nausea and actually threw up a couple times. As I posted earlier I had NO meds after 1st tx (and was really sick with dry heaves). So I was really disappointed that I got sick WITH meds. I called Onc. dept. and spoke to my onc. and he was quite abrupt with me and told me to triple up on the meds! I had taken 1 pill at 6AM and now it was 9AM, so he said to take 2 more. I continued to take 3 every dose and backed down to 2 this Am at 4AM but felt nauseous this AM and just finished taking 3 again at 11:30. Has anyone else heard of doing this? I'm thinking that Zofran is not the drug for me! I don't have any other meds. The premedicate me with zofran, decadron and an ativan push. Then the A/C. I do have some compazine but was told that I should use the zofran first because its stronger. My next tx is 10/25 but I see onc. on the 18th, and would like to have some input on what to ask for meds. I am happy to say that I'm 1/2 way done and will glad to be done! I hate this! For those of you getting great treatment at your cancer center, I am so happy for you! I can't imagine getting a foot massage! How awesome! I've heard that chemo is cumulative so each tx can make you more fatigued, etc. I think I agree! I had a hard time climbing out of bed and getting to work this AM. I just try to stay busy and hope the day goes by fast! Only 3 hrs. to go!

    Take care all of you wonderful women! I look forward to some responses on meds. God bless us all!

    Cheryll

  • livinginboji
    livinginboji Member Posts: 85
    edited October 2007

    Have you tried Aleve instead of tylenol? I have had problems with tendonitis in both elbows in the past and was told to take 2 aleve in the AM and 2 in the PM when it flares up and this has always worked for me. Good luck! If you don't get the neulasta shot then you will have to be very careful not to come in contact with anyone that is sick, which is  almost impossible to do! Especially coming into flu season.

  • livinginboji
    livinginboji Member Posts: 85
    edited October 2007

    Janice & Alylin-I had problems sleeping also and started taking an otc sleeping aid which is actually just generic benadryl and that helps me at night. I take it about 9 PM so it is working for bedtime at 10. Those of you that are taking steriods after treatment will probably have to use something stronger (prescription). Good luck!

    Cheryll

  • livinginboji
    livinginboji Member Posts: 85
    edited October 2007

    I can definitely relate to the chemo brain. I was in the car yesterday and had to seriously stop and think of how to turn the car off!  SCAREY!!

    Back to the nostagia...my lunch box was Barbie, The Partridge Family and The Monkees! lol

    My favorite toys were all my Barbies. Did anyone have the one with plastic hair that came with 3 wigs? blonde, burnette and red head.

    Wigs...now thats appropriate! Smile

    favorite jingles...I can remember all of the ones mentioned but can't be original to come up with any of my own.

    I have script for nexium...do you think they may help? I don't like taking 3 zofran every dose. Maybe I should take a nexium a day and back off to one zofran. Any thoughts? Today is day 5, last time I started to feel better by now.  Maybe the se are on the way out.

    I'm not taking steriods but its a pretty good bet that those of you that are taking them that is the reason for the weight gain. Be sure to watch your salt intake, including the salt already included in the foods your are eating.

    Paxton, I don't have a man in my life but I hear you regarding the emotions. Oh man! I can (and do) cry at the drop of a hat! Then I get made at myself for crying. I had to call the ER to get more zofran and I started crying while talking to ER nurse. She was very kind but I must have sounded like a babbling idiot!

    Take care everyone!!

    Cheryll

  • Urbie
    Urbie Member Posts: 154
    edited October 2007

    Hi Cheryl, I have taken so many meds for tx one it is hard to keep them straight, but I will try.  

    The day before - 2 decadron am & pm, day of - they gave me benedryl, ativan, decadron then TC.  Day after - decadron am & pm, zofran in am and then compazine if any break thru nausea and then ativan if any more break thru nausea. 

    I should have taken something like Nexium before my tx because I had terrible stomach pain.  I am now taking prilosec otc every 12 hours (plus tums & gas x), but will get a scrip for Nexium for tx 2-4.   I am also taking advil & tylenol for the bone pain caused by the Nuelasta shot. 

     I feel like a f******* pharmacy!  When I walked into my first doctors appointment at diagnosis I didn't have to list ONE medication that I was taking.  Now, when I go to my ps tomorrow I will need two pages to list them all.  

    Ahh, cancer keeps the pharmaceutical companies in business.  Why would they want to see a cure?

  • Urbie
    Urbie Member Posts: 154
    edited October 2007

    Oh, I forgot the big gun that I cannot afford!  The Emend I also took the day of, and two days after.  I do think that it made a big difference and I hope that they approve me for assisatance.  If not, I will have to sell one of my kids Laughing

    And on a good note, I had my white counts checked today and they were 9.2!  Yeah Nuelasta!  I will take the bone pain and smile (with meds) all the way to my ps office tomorrow for a fill in my tissue expanders!!  After tomorrow, I will officially have a bust they may take notice in the right shirt.     Have a great night all...

  • Gillkath
    Gillkath Member Posts: 149
    edited October 2007

    Hi All,

    Urbie, my game plan is almost exactly the same as yours but I don't get Ativan.  I also take Prilosec and I take Senakot tablets for about 1 week after my chemo.  Now, I'm also on a dieuretic because of fluid retention.  It is so hard to remember the names of all of the drugs.

    Also, a tip that I came across here in these boards (and which was confirmed by the Neulasta representative at my oncology office) is to regular Clariton (not Clariton D) for the Neulasta bone pain.  I am going to try that for my next tx which is next Thursday, October 17.

    Good luck with your tissue expansion -- how many have you had?  My PS filled mine partially at the time of my surgery and I have had only two other fillups.  I am staying small chested as I chose not to have an implant placed in my one remaining breast.  (My 16 year old daughter doesn't understand this as she thinks that it is the one time in my life that I can get bigger boobs!) 

    Laurie

  • paxton
    paxton Member Posts: 577
    edited October 2007

    Yea I am so emotional its retarded.  I'm in chemo right now (brought the ole laptop) and I started crying sitting here just thinking about how much I missed my bf while he was away.  I am normally not like this at all.  I do normally miss him when he's away, but he's been home a few days now so what's the deal.  I even cry in the car or wherever when I think how glad I am he's home.  Its so stupid.  I don't want him to see me like this so I'm trying my best to not cry so much.  He's really good about letting me lay on him in his recliner and cry when I need to, but I know women crying makes men uncomfortable so I don't want to do it all the time.  Ahhh!!!!

    No big revelations on the diarrhea from onc.  She thought maybe those days I feel like complete shit are from the neulasta (muscle aches etc) so I might try that Clariton when that sets in and see what happens.  I personally think its just from being poisoned by the damn chemo.  It happens after the days where I'm nauseated so about 5 days after tx I get sick.

    well, gotta go.  chemo's almost over....thank god

  • Urbie
    Urbie Member Posts: 154
    edited October 2007

    Hi Laurie - I have had three fills at 100cc each.  It is funny because I am bigger now than I was before my bilateral, but 200cc more to go to get me to a full B or small C.  I was an A before...

  • Karyll
    Karyll Member Posts: 235
    edited October 2007

    My tx is different than you guys but the nurses load me up with zofran pre chemo and lots of pre hydration. Drink water water water she told me, two days before so I slosh when I get there and then keep drinking for two more days close to a gallon a day. She felt that minimizes the dehydrating effect of the chemo, helps flush it all out and stops nausea. The meds they give me make me so thirsty that it's not at all hard to do. Then she hangs a mini bag of dexamethasone prior to the IV push of 5FU, and Epirubicin. Lastly with another bag of Saline, she hangs the Cyclophosphamide. They send me home with oral dexamethasone and zofran to take twice a day whether I think I need it or not. And breakthrough, metoclopramide and gravol (your dramamine?) for nausea. Also a very good supply of ativan. With the back pain I am also taking pain medication - so hard on the guts- I had to buy one of those little weekly pill boxes because I was getting everything mixed up with everything... lol Then I just carry the little compartment around with me all day. I have also been taking some Vitamin C and a good multi mineral in between treatmets. I don't take them the 4 days I am on the steroids - don't ask me why, just seems like too much I guess *rolls eyes*

    What I will do differently is take the stool softener the day of and not wait two days, and will request something for the massive heartburn and acid reflux and have something very bland on my stomach so as not to let that stuff start churning acid up.

    Have a great day/week everyone.

    Karyll

    PS - been thinking about the emotions - could be "chemo pause" as well. Don't beat yourself up, your hormones have a mind of their own right now and they don't what the hell they are doing either.

  • Gillkath
    Gillkath Member Posts: 149
    edited October 2007

    Hi Paxton,

    Just wondering how you were doing today.  You are in my thoughts.

    Laurie

  • paxton
    paxton Member Posts: 577
    edited October 2007

    I'm doing pretty good.  The night went well.  I took the kyrtril, decadron, and ativan when I got home.  And I took compazine and more ativan at when I woke up in the night. 

    I dropped my car off at the body shop this morning.  I did alittle house work (one nice thing about decadron; gives u some energy, although it makes me real jittery if I sit and do nothing).

    I'm going to bake 1/2 a cake this afternoon and work on finishing the dvd I'm making of the moosehunting trip.  Then I suppose I should relax and watch tv.

    I have a cold, too, but I don't feel massively sick yet.  So, wondering if it will be like last time where at the end of the week when the nausea part gets better, the fatigue and just feeling crappy sets in.  I almost liked getting it over all the first week so I had the second full week to feel good.  I only felt good about 3-4 days last tx.  But I only have one more of the AC tx left, then onto taxol which is not suppose to make you so sick.  Yay...I'm hoping.

    How is everyone else doing?

    MJ: I've wanted to learn clogging.  I took a little workshop at the bluegrass festival 3 summers ago.  The next year they didn't have the cloggers so I filled out the survey and they were there this year.  I really like watching them.  Often between the drinking and playing guitar at our site with all the cool folks in our area, we forget half the time to go up to the stages and watch the shows.  But I almost always set my drink down and head up solo to watch the cloggers. 

    Well, hope everybody's hanging in there. 

  • paxton
    paxton Member Posts: 577
    edited October 2007

    I enjoyed rolling down memory lane to take my mind of bc so I thought I'd share another funny childhood story.

    I think I was about 5 years old. I was just learning to write.  We were at grandma's house and I was big into singing to commercial jingles.  I, of course, love the "plop, plop, fizz, fizz, oh whatta relief it is." But I also loved singing along to "R-O-L-A-I-D-S, spells 100% Relief.  Funny how they're both for indigestion.  Anyway, grandma had this old lipstick that was bright pink.  I took it and wrote on the inside of her armour door, "R-O-L-O-I-D-S, spells 100% Relief.  Then I went and wrote my brother's name on the wall behind the vanity where it was still visible.  I kind of remember my brother getting in trouble; suppose because they didn't know I could write.  I really don't remember much after that, if I got in trouble.  I can about imagine what they must have thought when they saw that.  And I swear the lipstick in the armour was always there after that. 

  • nanc512
    nanc512 Member Posts: 98
    edited October 2007

    Paxton:  Glad to see you are feeling better. 

    I have AC #2 on Thursday.  I have my Emend and Decadron, so I am ready.  I just started feeling better today, I am hoping and praying this one doesn't knock me down like the last one.  The not knowing part is scary and not being able to plan.

    I am finding myself more emotional now.  I feel like a castoff from my friends.  They just expect me to be sick all the time, since I have had so many problems from the beginning.  I know how tired I am of this, so I don't bring anything up to them, until they ask. 

    I really don't think anyone can even come close to understanding until they have gone through it.

    Prayers being said for all my September 07 chemo buddies!

    Nancy

  • trigeek
    trigeek Member Posts: 916
    edited October 2007

    Hey twin!

    I have my #2 on thursday too, will be thinking about you. I  am hoping that I will not need to page my doc at 2 AM this time( the sole thought of that night is making me nauseaus !)

    Starting  hydrating/drinking lots of water 1- 2 days before tx it is supposed to help flush the toxins out so tomorrow I will load up on liquids.

    What is your hair state ? My scalp is itching.  

    I understand you Nancy, one of my 'so-called' friends who has been incessently calling me since my diagnosis and 'acting' as a caring friend is hosting a party that is similar to 'Pampered Chef' or 'Beauty Control' parties .. where products will be introduced and sold. But heres the catch .. (umhh I hope this does not offend anyone ) the products are ' adultWink . hint hint .. products' . SHE INVITED EVERYONE WE KNEW BUT ME !!!! That certainly would have been an extremely interesting/distracting event and I think I got discriminated because of my current state. ( she did not want the 'atmosphere' of her party spoiled by a chemo girl ).

    Guess we just have to learn to live with this type of thing.. anyone watch the Desperate Housewives and how Gaby reacted to Lynette who wanted her to be her chemo-buddy ?

    Aylin( possibly pcs*'ing )

    Armed with Emend this time!

    *pcs: pre-chemo syndrome

  • janiceb00
    janiceb00 Member Posts: 30
    edited October 2007

    Hi All :)

    Just checkin in. I had a pretty good thanksgiving weekend. Went to wedding on Saturday...didn't get home til 2:30. Hubby was a little ticked, he thought I over did it, but knew I was having a good time. Good to see extended family that you haven't seen in a while.

    Needless to say I didn't cook turkey dinner or anything major on Sunday..had to have dinner on Monday which is fine since I'm off work anyway.

    Just finished my 2 tx yesterday and I have been up most of the night with extreme heart burn / acid reflex. I drank a bottle of water took my pill and propped my pillows up so I wasn't lying down flat seemed to help a little, I kinda dozed here n there. I'm going to try gravel  tonight  for  a sleep aid. hopefully it works.

    Finally shaved my head last night too! Hey did you guys find your head tender where you shaved it? It's okay where the hair came out on its own but where the clippers cut my hair it is tender.:( I will take a pic later and post. 

    I also gained 10 pounds since this all started. I'm kinda worried and hoping alot is water but it still is scary.

     Take care and hugs to all

    Janice 

  • nanc512
    nanc512 Member Posts: 98
    edited October 2007

    Hey twin:

    My hair is very thick, but I am shedding more.  My scalp is kind of tingling, so I expect chunks to start falling.  I got really down about this last night, so I am thinking of it as the hair being associated with my cancer, so it has to go!  I am losing hair on other parts of my body.

    I have my wig and decided I would buy more hats and scarves, I have a few, but I don't want to wear my wig all the time.  I am going to order a fall to wear under some hats.

    Hopefully, I will feel like posting my update tomorrow.  I am really apprehensive about doing this again, but I have to.

    Nancy

  • paxton
    paxton Member Posts: 577
    edited October 2007

    I shaved my head 2 1/2 weeks ago with a clipper and my scalp was really tender.  I was leary of using a razor but marietta said she did it cuz her scalp hurt, too, and it felt so much better.  I highly recommend doing that.  I don't know why it makes a difference. 

    Nancy: hope you get used to all the new hair accesories.  I've only worn my wig out about 3 times.  I wear a cotton turban with a bandana over it a lot.  And I bought a "fall" as well and that works great under hats.  I'm wearing that right now actually.  I think its a good time of the year for this...cant imagine the summer heat.  At least no we can sleep in a winter hat if we want. 

    Janice: glad u enjoyed your thanksgiving.  Every little event helps to get out and feel normal.

    Good luck to everyone having tx coming up.  Just had mine monday and feel good.  I seem to hit a fatigue/sick time about a week into it though so I'm not home free yet. 

    Hi to both MJ's and methusala who we haven't heard from in forever.  Hope you're hanging in there.  Things sounded rough. 

    Other than that I had stitches coming up from my port incision that needed to be cut out.  They're suppoe to dissolve but doc said prob chemo is causing them not to.  He cut little holes above the other ones you could see under the skin.  He didn't us any numbing stuff either when he cut.  I was sort of proud in a weird way.  Isn't that dumb?

    Well, take care everybody! 

  • trigeek
    trigeek Member Posts: 916
    edited October 2007

    Started shedding today, hubby wanted to shave but am holding on. 2nd tx is tomorrow, chemo sickness + being bald.. seems a bit too much to stomach for one day.


    Urgghh.. I am not looking forward to this part at all.

    I am sick and tired of 'being an inspiration for handling bc so well' I want to be just a normal coward person who does not have to face challenges.

    Hate to be a whiner but thanks for letting me vent gals ( as if you were given a choice hehe ) but sometimes I just need to let my guard down and I know that you gals have been there and will understand.

    Aylin.. who is seriously PCS'ing. Sealed

  • Methusala
    Methusala Member Posts: 285
    edited October 2007

    wow I can't believe I just spent half an hour catching up on this thread!

    Back to Roswell tomorrow.  Was thinking I was going to go ahead and try Dr. Levine's 'new' drug, but after reading this, I think I can't do it again !  I want to skip right to radiation.  seriously, I do not want to be sick all over again.

    You gals are so positive.  I am such a party pooper.  And a bald one at that lolme and son

  • Methusala
    Methusala Member Posts: 285
    edited October 2007

    ps, my stubble hurts and is falling out.. but in this I DO find humour LOL

  • paxton
    paxton Member Posts: 577
    edited October 2007

    Glad to hear from you Methusala.  What new drug were consider trying? 

    I'm a little shaken by the news report on taxol.  It said that it lowers risk by 40% for those with her+, but is not as effective as thought for those that are ER+. 

    Well, I'm triple negative so where the hell does that leave me??  I have one more AC tx and then am on to 4x Taxol, so this is a bit unnerving for me to hear.  Especially with the side effects and if it doesn't really help lower my risk.  Why does it always seem to get more complicated? ACKK! Yell

  • mariettaj
    mariettaj Member Posts: 179
    edited October 2007

    Hi all,

    • I'm still here Paxton, thanks for the shout out! I have been feeling really well and have been cramming in as much as I can before my next treatment. Time is passing really quickly, I can't believe I have tx 3 next week. That will be my half way mark.
    • My little boy confided in me that he is worried that I am going to die. Talk about breaking your heart. He has been walking around thinking about this....everytime I have chemo he thinks it's another surgery...I think I've got him set straight now, but can't help but worry.  He's only 7 1/2, Methusala, how old is your little boy? He's so cute. How is he handling all this?
    • To all of you with tender scalps, it will get better. I have to say though, my head itches a lot. I've made peace with my wig pretty much...but it still drives me a little crazy, it creeps in the back and sometimes it feels like it could go flying off! :)
    • I've been having issues with the steroids causing water weight...on Saturday I was 6 lbs heavier than I am today..My doctor prescribed me some pills to help and they made a huge difference....
    • How was your last tx Paxton? I hope your diarhea is gone...that is miserable. I had it for 3 days last week and thought, my gosh, how is Paxton doing this for weeks at a time?
    • Have a great day everyone.
    • Marietta
  • paxton
    paxton Member Posts: 577
    edited October 2007

    Marietta:  It is strange how the time does seem to be passing.  My next tx will be my 4th and that is my halfway point for chemo.  This last tx has been going well so far.  I was a little worried because I have a cold with coughing, but I don't feel totalled.  And, I have not had diahrrea in 6 days Cool.  But about this time is when it strikes up so I'm hoping it doesn't come back or at least isn't so bad as it was. 

    I'm slow cooking bbq moose ribs for supper.  I'm excited to see how that goes. 

    Does anyone else's skin turn red and get really blotchy once in awhile?   What do you do for it?  I've been using Proactive cuz someone suggested it in a thread on advice.  It usually seems to help.

    How u doing MJ?  I'm thinking about you and miss you.  I'm not working and have no children so I'm home on the farm more.  I've been slowly working through the supplies and clothing, etc, from the hunting trip.  And I got the house ready for the wood stove. 

    Well, have a good day EB!!!   

  • Urbie
    Urbie Member Posts: 154
    edited October 2007

    Marietta, I really feel your pain with your son.  My 8 year old daughter literally went off the deep end when I was diagnosed.  Her Grandma (my step mother) died two years ago from breast cancer and in her mind, that meant that Mommy was going to die too.  IT WAS AWFUL, AWFUL, AWFUL.   I was trying to deal with the whole thing myself and she went into obsessive, compulsive mode and was washing her hands constantly and not eating because the food touched the plate...  She lost 6 pounds and she started out at only 52 pounds to begin with.  She would cry for an hour at a time, uncontrolably, several times a day.  I took her to a therapist, which didn't really help and then two days before my surgery I took her to see our family doctor and requested that he put her on an anti-depressent.  He put her on a low dose of Prozac and I will tell you that it saved our lives.  She stopped crying, washing and freaking out and she was able to accept the fact that mommy had to have an operation, chemo and then she would be fine.  She has always been a "high anxiety" child so it shouldn't have come as such a big surprise that maybe her brain wasn't producing something that it needed to be happy.  It has made her a happy, more confident, more outgoing, delightful child.  All of our family, who has known her to be quiet, reserved and hardly every smiling, can see a huge difference.  This BC thing just was too much for her to take in.  I have never been an advocate of medicating children, unless it is really necessary for their quality of life.  Prozac saved her.    This is big stuff for kids to handle.  Just thought I would share my story.

  • trigeek
    trigeek Member Posts: 916
    edited October 2007

    Oh Urbie, Methusala, Marrietta.. my heart goes out to you gals.

    My kids are 15 and 18. 18 year old is in college and is worried sick about me I can tell since she is calling constantly and coming home everyweekend. And she is scared that she might also get this crap.

    The 15 year old seems to be in a denial phase, living in her own teenage world.

    The Cancer Hospital has a monthly workshop for kids with parents having cancer. I am planning to take my 15 year old.  Do you think your oncologist could suggest such a group ? They group the kids up in one room and the parents in the other, thought it was a good idea.

    Big Hugs !!!

    Aylin

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