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  • Shirlann
    Shirlann Member Posts: 3,302
    edited November 2007

    Hi Sweet Sue, I agree 100% with Fumi, don't make up your mind about working until you see what happens.  Each of us is so different, but Fumi worked and I worked (no chemo, though) and dozens of other gals have too.  And your boss loves you (as we all do) and seems more than willing to let you pick your days and hours.

    I felt a LOT better working than sitting at home.  For me, it was better to be as near normal as I could.  We are all different.  You may sail through this quite well. I think you need to just see how things go.

    Anyway, I hope you stop that silly worrying about dying.  We are all here, you will be too.

    Hugs, Shirlann

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    Poppy...your boys are BEAUTIFUL...I do hope I haven't missed you before tomorrow...I just wanted you to know I am and will be thinking of you so much while I am at work tomorrow and hoping you will be as OK as can be....You will be in my thoughts and I can't wait to see you back here on the other side....I will have probably had my first lot of chemo by then....I will say a prayer for you ...and send you all my love.... that picture is lovely...I love to look back at my boys ...they grow so quick.... xxxx

    Shirlann...I know ...I am just being silly eh....I think I find it difficult facing up to every bit of this...but I am getting there...and hopeful that I will be around with you all forever xxxxx

  • portiasproudmom
    portiasproudmom Member Posts: 2,125
    edited November 2007

    Poppy, your boys are gorgeous!  They grow so fast, don't they?  My little guy is turing five in 8 days.  It seems like he was born yesterday.  Sigh......

    Hugs,

    Karen

  • Valsul
    Valsul Member Posts: 160
    edited November 2007

    Sue, you are going to be okay.  You will worry about all those things, we all did, and as Shirlann says you will be here in 10 years giving help and advice to other newbies to this awful club.  (Prayers for a breakthrough long before that!)

    I found that two or three days after chemo the tough bits set in.  But by the end of a week after chemo I was okay again.  Water is the secret, I can't stress that enough.  Others drank more than I did and the difference was remarkable - flushing out those toxins must have had a good effect.  Get yourself organised with Immodium and some apple juice - it could go either way and best to be prepared.

    Your taste buds go a bit haywire too, and I found I had urgent desires for a Burger King Whopper ( haven't eaten burgers in years but this was like when you are pregnant and MUST HAVE - NOW!!) and my local Chinese takeaway did a roaring trade in my need for egg-fried rice and shredded chilli chicken.  Of course some days I couldn't even manage two spoonfuls of soup - the food we wasted because I must have it and couldn't swallow it!  I lost and gained a stone (14 pounds) between treatments for all the cycles.

    And the odd thing is, when you are well you can't imagine being so down, and when you are down you don't think you will ever be well again, so it really is a roller coaster.  Like after childbirth when all the pain of it is forgotten.  The body is so resilient.

    You will be given a list of DOs and DON'Ts from your team, and follow them to the letter.  By the time I realised that I needed to drink water I was past the time to take it. 

    If you need any info on the drugs you can check out cancerbackup.org.uk which explains everything in plain language. 

    The main message though Sue is that you are going to be OKAY!  If I can do it so can you.  And I can't see any reason why you can't work in the week or so between treatments - the lady next to me used to go to chemo and then go straight off to work on Morrisons' checkout.  My friend's father-in-law went off to the gym.  I'm not saying that's everyone, but it can be a decent run.  And again, those who did better were those who drank plenty of water.  You take things in your own time, but there will be fatigue.

    Check out the chemo threads on this site, that's where long and close relationships are forged as you go through it all giving each other advice and support.  You can still post here for our love and support, but join with our bc sisters who are sharing your path at the same time.  Just a thought.

    Much love

    Valerie S

  • hockeymomfl
    hockeymomfl Member Posts: 96
    edited November 2007

    What a beautiful picture of the two boys.

    I just stopped in to tell you that I am at my 1 year anniversary of diagnosis and doing fine.

    I know it is often tough to keep positive, we all have our days, but guess what we MUST try to enjoy every day with our family and friends, whether we have been diagnosed with soemthing or not.

    We often rush around doing everything, but enjoying life.

    Stop, smell the roses and cherish every day.

    There are many stories of wonderful women who are 10, etc years out from diagnosis and are doing fine.

    Keep your chins up ladies and stay postive......

    Cheers,

    Jel

  • livesstrong
    livesstrong Member Posts: 1,799
    edited November 2007

    Hi Ladies,

    Poppy -  the boys are the absolute cutest!!  All the best tomorrow. We'll be here waiting for your return.

    Sue- I think Valsul is right.  Try checking out the chemo board, you might find it helpful. What she said about being down and being well was spot on!!  Did I miss reading when you will be starting? As far as work goes, why not try a wait & see.  I didn't work only because in NJ we have state diasbility and it really doesn't give you the option of choosing what days you can/can't work.  It's all or nothing.  There were days when I felt good enough to work so I would go to lunch with friends and do some shopping, etc. They weren't ALL bad days.  I'm thinking maybe your nurse suggested not working because of where you work.  You'll have too much contact with people and when your immune system is low the least amount of contact the better.  Bottom line, wait and see.

    Hope everyone is having a lovely evening, its cold here in NJ - they are calling for some snow on Saturday!! Drats.

    Take care,

    Valerie

  • honeygirl
    honeygirl Member Posts: 1,718
    edited November 2007
    Hi SueSmile! Sorry I missed you yesterday. But know that you are always in my thoughts and prayers.xx I agree with Timtam , Shirlann and Valsul. No one knows if you will be able to work full time or not. Only you will know that when the time comes. Besides the boilin' bag bootface , you are healthy and young. Thats a big plus for you. Then , your team will make sure you have all the anti-nausea drugs etc... that you will need. And if one doesn't help , call and they will give you something else. My nausea was taken care of by the drugs , but I developed horrible heartburn. I called , they told me what to get and after every treatment I would take it and never had trouble again with it. And Val is right about the water. If you can , drink just before and after your treatment. It really helps flush it out of you. Sue , you can get through this. It sucks. You don't want to do it , but you will get through it. And I don't know why , but the time really does go by fast. I spent most of my time wishing away the summer. And when Aug.1st came ,my last treatment, it really did go quick. Because about a month after the last treatment , your hair starts to grow!! And you get color back in your complexion. And people at work start saying "your looking healthy again and you start feeling healthy again. And yes , its kinda like child birth , you think after , it wasn't that bad.Just remember focus on the light at the end of the tunnel. Remember , you said thats where you see you sons. And in years to come they'll say "remember mummy , that year you were bald" , as they gaze at your lovely locks! Ok , shoulders back , chin , waaaay up. Are you doing it? Don't you feel silly ,lol seriously , keep your head up and remember , the bootface is gone , and if it left any cells , the chemo is gonna take care of that. Ok , its dinner time here. So I gots ta go. Love ya Sue , go get that wig tomorrow. xxxxx Melody
  • honeygirl
    honeygirl Member Posts: 1,718
    edited November 2007

    Hey Poppy , your boys are so adorable!!!! Good luck to you tomorrow. I will be praying for a sucessful surgery and quick healing. Please take care and let us know as soon as you can , how you're doing. Big hugs and prayers to you. xx Melody

  • honeygirl
    honeygirl Member Posts: 1,718
    edited November 2007

    Hi Suneedazee! I went to your blog site. You have such a beautiful family! You are so lovely. Especially in your pink monkey pjs. Doesn't it feel sooo good not to be wearing a scarf or wig. Good for you. I'm sorry you have to do radiation. But it is one more way of getting rid of the beast. I can't believe you are off your pain meds already. You are really doing wellSmile! Well , take care and continue to improve. Hugs and prayers to you. Melody

  • Karyll
    Karyll Member Posts: 235
    edited November 2007

    Just a little wave hello to everyone, I have been trying to keep up. I just had my third treatment today - it is FEC which is a combo chemo cocktail, of 5FU (long chemical name), Epirubicin, and Cyclophosphamide (I think). I have had three of these now, three weeks apart. I took part of the first week off work as vacation (yuck) because I wanted to discover how I would feel and how I could work full time around that. It turns out that I can and have just rearranged my two days off to co incide with my two "low" days. I could even work on them really but it is when my blood count is at its lowest and I am very tired and at higher risk of infection. They give me steroids at the start and for a few days.

     Like today, I worked very early till noon. I went for my chemo where they gave me steroids first and an anti nauseant and then the "cocktail". Right now I feel absolutely fine (well okay, maybe a little bit buzzed from the steroid) I will feel fine until Monday afternoon afternoon, when I have taken the last steroid dose and I can work through the weekend. Then I get very tired Monday night and I have to admit a little edgy and nervy.(not good to have a nervy, slightly irritable manager so I take Tuesday and Wednesday off work  because I kind of feel like I have a bad hangover. ( I haven't drank alcohol for 12 years, but I remember that feeling). I have not thrown up once - I have had a little tiny bit of nausea, but more of a gaunt feeling....and easily remedied. I take all my meds whether I think I need them or not. I drink a ton of water two days before, during and after (like 4 liters a day). I started shedding hair on the 14th day after my first chemo. I had a buzz cut on the 16th day. On the 17th day, there was more pubic hair in the toilet than on my whole body. I still have leg hair.... lol...and eyebrows. I have had so far, all my treatments by IV injection - and they don't foresee the need for a port in fact, discouraged it. I can't say I am symptom free - but you know? I feel better even in my "down" week - than I did waiting for test results, and maybe even better than I did last year at this time, because this thing was growing without my knowledge.

    So it depends so much - I was more tired before diagnosis than I am even on the low days! Remember that Sue - just like the mastectomy, the anxiety about it is worse than the actual effects... And they will give you something for that anxiety pre-chemo as well. That helped, even if I did feel like a zombie... lol. It's all about knowing what to expect.

    Oh yeah, I will lose my taste buds on Sunday but they will be back by Friday. I use biotene mouthwash and paste and have had tender gums but no sores. I think the best thing in the world to help this is drink water, drink water, drink water - even if it tastes funny - get the fluids in. I worked on the cancer unit where people had chemo years ago, and that was the key... they loaded them up with fluids, flush flush flush... and you should be doing that too... pee pee pee... lol...

    I was close to chest wall too - and will have to have radiation following the chemo. And then that too is it for me, being triple neg.

    Although, who knows by then they might have another tx, or even dare I say it... A CURE.

    Blessings everyone - Here is to putting one foot in front of the other, one day at a time, and enjoying every moment for what it is!

    Love and Hugs to all

    Karyll

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    Hello Everyone xxx

    Karyll from the bottom of my heart thankyou for posting about your experience...it has meant so much to me tonight...and every glass of water... I will have an image of you in my head .... thankyou ! xxx  and Valerie and Melody and everyone ...big hugs xxx

    Well thanks to everyone for the strength you give me...I have been physically and mentally low since I went to see oncology on Weds...I can't get my head around the nightmare and feel bit rundown...well very...but I think its stressssssssssssssssssssssssss  lo...l  I am cursing so much in my head big time...

    So I have been to work today ...not my usual perky energetic self to say the least. The hospital phoned me to arrange Tuesdays' treatment...and told me there was no way that I would be able to work...and if it was a question of money they would sort a grant out......and sickness benefit etc....but it won't be enough and I so need to work...I will see how I go ...its only for 6 months...

    So I go on Tuesday at 1230pm and wont leave until 9pm Surprised .....maybe as its my first appointment.Treatment is always on a Tuesday...and she said the hospital is as busy as Heathrow Airport...

    Well they will send me away with mouthwash and all the medication etc and give me a helpline number...She told me I wouldnt be able to work and also said I would need radiation after chemo. I had a glimmer of hope that Mr Welsh was retesting the triple neg bit...but she said I scored 0 out of 8 for all the receptors which is a sure sign I wouldnt be having any hormones....

    Dragged myself off to the wig shop and placed an order for 2 wigs...which were very nice.. prob pick them up next week... it is the same wigshop my mum used 20 years ago ...

    Sorry there has been no life in my posts lately ...I am consumed with stress...lol

    I posted on chemo board so thats good.... get the ball rolling....need to find out more about this menopause for life business....hot flashes an all that....

    (Thinking of Poppy and sending lots of wishes xx)

    Much Love xxx

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    Oh btw....my third treatment falls on christmas day...boo hoo....boo hoo ...(surely they dont do christmas day)  but the whole of my chemo finishes on May 29th woo hoo...

    What is wrong with me ...I am so fed up ...I think I have a slight flu going on....and I feel so lonely inside....like cut off from everything...I am still taking anti Ds ....xxx

    xxxxxxx

  • geebung
    geebung Member Posts: 1,851
    edited November 2007

    Dear Sue,

    I haven't posted for a couple of days - had visitors - one of whom has been hogging my computer! However, that doesn't mean you haven't been in my thoughts. You are in another waiting phase and it must be extremely stressful. Wish I could do something to make you feel better but can only send you...

    Lots of love and hugs,

    gb 

  • Valsul
    Valsul Member Posts: 160
    edited November 2007

    Hi, Sue sorry you are so down, but glad you have posted on the chemo thread and hopefully buddy-up with the sisters there.

    They won't give you chemo on Christmas Day, as mine was due on that date and they deferred it to the first available day after the holiday.  That was good as it meant I was okay for Christmas and New Year (glug, glug)

    Karyll, glad your doing well - I did FEC, too and it's no picnic.

    Sue, we love you - and while you are down I wish I could just put my arms around you and give you a big hug to make you smile again.  You are going to come through this - with all the other sisters who are doing this right now.  Chin up, sweetheart.

    Much love

    Valerie S

  • Valsul
    Valsul Member Posts: 160
    edited November 2007

    btw, Sue, I go for my Herceptin infusion on Tuesday and I usually finish around 12.30 so as I am making my way out of Clatterbridge Hospital I shall think of you at Christie's on your way in.  Good vibes, hey?

    V

  • portiasproudmom
    portiasproudmom Member Posts: 2,125
    edited November 2007

    Hi Sue.  I'm sorry you're feeling so low.  Chemo is definitely not fun, but knowing you the way I've come to know you from your posts, you're going to be just fine!  I HATE feeling ill.  I hate it with a passion!  There really are so many more good days than bad though.  You honestly won't have to take that many days off from work.  I felt really well yesteray (day after chemo) and today I'm a bit tired, but still feeling ok.  I'm doing my shots to bring the white blood cell counts back up by myself at home now.  injecting myself was a piece of cake.  I thought I'd be nervous, but it wasn't bad at all.  I'm hoping that the small injections will work better than the big one.  The docs are always willing to work with you if you're having major side effects.  They honestly don't want you to suffer. 

    Hang in there sweetheart.  You're going to be fine.  I have to do this for my kids.  They need me just as your boys need you.  Just keep that in mind.  It will get you through this unpleasant experience.  Just keep your mind on the ultimate goal--your health, so you can raise those boys, see them get married, and enjoy your grandkids one day!!

    Rest well tonight. 

    Much love and double the hugs,

    Karen

  • Shirlann
    Shirlann Member Posts: 3,302
    edited November 2007

    Hi Sweet Sue, as Valerie said, they won't do anything on Christmas Day, so don't worry about that.

    I am leaving Sunday, so I need to get all my prayers and best wishes to you, dear girl.  See, all these lovely ladies, been there, done that, and you can just see how the work goes.  Some, it works, some, it doesn't.  So just don't get down too far.

    Just know all you have to do is make it to the computer to talk to us.

    You are loved, Sweet Sue, hugs and kisses, Shirlann

  • portiasproudmom
    portiasproudmom Member Posts: 2,125
    edited November 2007

    Valerie and Shirlann are absolutely right, Sue.  They will get you in the first available day AFTER Christmas.  Don't worry about spending the holiday having poison injected into your body!  I go in six days before Christmas and day six is usually bad.  I'm keeping my fingers crossed though.  You should be feeling GREAT on Christmas, you lucky girl!

    Love and hugs,

    Karen

  • livesstrong
    livesstrong Member Posts: 1,799
    edited November 2007

    Sue, I'm sure by now you are sound asleep and having sweet dreams.  Just wanted you to know I'm thinking of you. There isn't one lady on this thread you hasn't had the same reactions as you are having.  We all know EXACTLY what you are going thru physically & emotionally.  We are here to help in any way we can.

    Stay strong, you can do this!!

    Valerie

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    Hello Everyone xxx

    Thankyou for all your posts....Karen I take heart from your posts I know you are having an up and down time physically but it really is a comfort to know you are 'ok' ...thankyou xxx ...thankyou to everyone I would be lost without you all....and I am sorry to whinge lately...

    I went to work today but came home at 4pm...there is a flu type virus going around and I have definitely got it...it is the only time I get really down when I am ill...I feel so rough! and a mess....I do hope it goes before next Tuesday...its not a cold or anything..just sore mouth and weak as anything etc...

    Well I am still very miserable....I have only just started to really really think of the consequences of this illness and I feel like I have let everyone down terribly. I am also today very sad about the way I look now and that it is for life...my arm aches so much at times and my scar feels raw....so I am not too well at all...I know it has something to do with this virus...I am always the same .... if I didn't feel ill I would have the energy and happiness to fight... at the moment I am flaked out and thanking God so much that I have a day off tomorrow .....which is so out of character!  grrrrrrr

    I hope you are all 'ok'.....and I so need to keep posting on this board and being with you......I should be back from Manchester on Tuesday evening...I am so frightened... I will be drinking like a fish to get it out of me....

    Sorry sorry sorry for this post...I am really trying hard...I am just rundown...

    Shirlann ... have a wonderful cruise....I will be thinking of you .... and hoping that you have a truly great time....you are in my heart...

    Much Love xxx

    Can anyone tell me if they went through the menopause permanently on chemo...I did ask on the chemo board  ...

    I love you all  xxxx

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    .....so today I feel like it has been such a rush since I was diagnosed on Sept 11th.....so much stress and sadness piled inside my heart...I am on the verge of breaking into tears...I don't think I have cried more than three times since I found out....I am not sure I can fully comprehend nor had the time to gather my feelings....as time goes on I am getting further away from the person I once was....and realising my breast won't ever 'appear' again...... I am very cut up...I know I have to go through all this or the anger will eat me up......

    Sorry for rambling..I just need 'let it out' ....

    Hopefully I will feel better....soon.....my mum had cancer at the same age as me  (38)...I was fourteen and I remember feeling very sad....maybe going to the same wig shop has disturbed the unresolved grief I carry....I was so angry walking to the shop...and found it very painful inside...and then stomped back to my car angry in a lost stormy sea.....I feel for all of you and what you go through...xxxxxxxx YOU ARE ALL SO MUCH BRAVER THAN ME XXXX

    OMG sorry xxxx

    Everything for us all is very cruel ....I will pick up....Am I normal ..... I don't know anymore xxx

  • portiasproudmom
    portiasproudmom Member Posts: 2,125
    edited November 2007

    Oh my goodness, Sue.  Of course you're normal!  We've all been (or still are to a degree) exactly where you are.  I'm sorry that I can't relate to the loss of your breast.  Although, the breast I'm left with after the lumpectomy certainly isn't the same breast I had prior to my diagnosis.  The scar is quite long and ugly and the nipple points upward rather than straight ahead.  It looks pretty weird compared to the other.  You know, I don't even think my husband has seen it yet.  I'm pretty self-conscious about it.  So you see, we all have our hang-ups.  None of us will ever be the same again.  This disease changes you forever, but I'm not convinced it's always for the worse.  I appreciate the little things so much more now.  I really wasn't living life to the fullest before.  That's going to change once I'm finished with my treatments. 

    As for the menopause caused by chemo, I started my period right on schedule this month.  I was sort of hoping it wouldn't---oh well.

    You are one of the bravest and most inspiring women I know, Sue!  Don't you think for a moment that you aren't! 

    Enjoy your day off tomorrow.  You need to get rid of that nasty flu bug before Tuesday.  The sooner you start the chemo, the sooner it will be OVER!!

    Love and hugs,

    Karen

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    Am I really brave and inspiring...lol... but I feel a wimp at times...

    Yes Karen I need to get rid of flu....then I can begin treatment...I will be halfway through the epibrucirin before xmas...

    I am not looking forward to the CMF after until May.

    Yes you're right it does change us...for better and worst...I am only tipped to the worst at the moment...maybe cos I am coming to terms...and about to start treatment......so I am cross...and nothing in life feels good at the moment lol...save for this board...but I know I will turn the corner... my rollercoaster journey is a bumpy one at mo...lol....and my bum hurts from being thrown back into my seat frequently...

    I am so happy I can talk with you Karen...xxxxxx I wish I was in October group..I am sad about that xx

     .

    Thankyou Karen from the bottom of my heart for listening to this rambling  xxxx

    Stay Safe   xx

    Much Love xxx

  • portiasproudmom
    portiasproudmom Member Posts: 2,125
    edited November 2007

    You're very welcome, Sue.  And you do NOT ramble!  I just hate to see you so down.  I was scared before starting the chemo too.  It certainly doesn't help that you're not feeling well. 

    I wish you were part of my October group too.  They are a wonderful group.  So funny, encouraging, and informative.  I'm sure you'll love your November group, as well.  Give them a chance, but remember, you had US first!  We LOVE you, Sue!

    Double the hugs and love to you!

    Karen

    PS  Round two of chemo has been so much easier for me!  I'm just a bit tired.  If you have any bad side effects after your first tx, call your doc or chemo nurse immediately.  They will make adjustments to keep you more comfortable.

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    I will ...thankyou Karen ..you have helped me so much tonight...I think I am having a meltdown as these 2 months sink in...truly thankyou....I have been willing my breast to grow back today...thats how deluded I am..or unaccepting ....

    I also had a five year financial plan ...thats all gone out the window...everything is a mess financially now...another stress of the bootface....lets get throught this ...I need to be stronger...

    I will keep you posted on Tuesday evening ..yikes....xxx

    have a lovely day xxxx

  • honeygirl
    honeygirl Member Posts: 1,718
    edited November 2007

    Hi SueSmile! Please don't be sorry for sharing your feelings with us. We really don't expect you not to be down or angry or any of the feelings you are having. Bootface definately sucks the big one! And where you are right now , is where we have been feeling just like you. And on top of all this , you are having memories of your mum and all she went through , and I would be feeling pretty angry too. Aw Sue , I wish I could give you a really big hug right now (((((((sue)))))) , and I would make you some chicken soup to help you through your flu. But I can't  , so please know I would if I could!xxxx

    I never went into chemopause. I had my period all the way through tx. But when I started the tamoxifen , I have not had a period since. But the nurses thought I would stop my period after my second tx. So I guess thats more the norm. But , as we all know , I am not normalTongue out!lol

    Try to stay home tomorrow and drink plenty of fluids and get plenty of rest. You can't start chemo if you are sick. And like Karen said , the sooner you start , the sooner its over. Hugs my dear Sue , xx Melly

  • TenderIsOurMight
    TenderIsOurMight Member Posts: 4,493
    edited March 2008



    YOU ARE AN AWESOME, INSPIRING, HARD CHARGING, TRUE WARRIER, FUNNY, DEEP, SHAKESPEAREAN SUE!



    Never a let down, always an appropriate question, a down the road wonderer who mirrors our experiences in words from afar.



    So do keep up your posts, as they are by far some of the most, insightful openings of windows to one's brain, challenging us to re-think again, the what why where how and when of all we've been through and then....



    Tender

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    Melody ...thankyou...I am crying right now..I wish you were right here in my home...and that Karen was...I just need to cry cry cry...I am so full of sadness...and exhausted waking up day after day to the same nightmare...and putting a face on...

    I will rest up tomorrow big time and drink plenty of fluids.....I want to get through this...everything is such a mess in my life...a true botch up.......

    I am going to get focused somehow...and rest /water is the key...

    I wish I was normal...but I feel like I have been afflicted forever..and have let everyone down xxx

    Much Love......xxxxx  I WILL BE OK...XX Think I am a bit traumatised xxx

  • sueps
    sueps Member Posts: 2,266
    edited November 2007

    Thankyou Tender  xxx.....I am truly grateful for every word you give me...... I know it is good to be honest and raw about my journey..its the only way I can travel through it...moving from storm to storm...with the sun coming out in between....

    Much Love to you always xxx

  • Lucy1234
    Lucy1234 Member Posts: 289
    edited November 2007

    im mailing  from my hospital bed!

    now thats dedication lol

    ouch is all i can say.... it looks great but i am apparrently loosing alot of blood?

    thought id get in touch as u guys cheer me up loads

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