Cat_mioux's new home

:^O
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Cat_mioux's new home

(((HUGS))) Catty. I'm glad the service went well. It would be strange if you weren't feeling a bit flat now it's all over.
The important thing to remember is: be kind to yourself. Don't deny your feelings and don't scold yourself when you fail to put on the brave face you might feel is expected of you. Grief is not a flat path, it is a roller coaster and the downs are every bit as necessary as the ups. Roll with them, learn from them, and dont feel you need to fight them. :-x
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she-ele :-x

I have taken your advice and called in sick today. I'm going to bed to sleep and/or cry .. what ever I feel the need to do today.
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tende thanks for the kitty hugs :-x


braf - the funeral is at 12. I know I'll feel all the OK'er's sending me strength.

I wrote something for my sisters to keep with them on the day, I'll post some of it here ..


22 March 2011

We stand together on this day, united as four strong courageous daughters, to say goodbye to our dad.

Our grief and sorrow contain varied emotions, similar and unique, according to our individuality and our shared experiences as ******'s daughters.

I appreciate our differences and similarities but especially our differences because without this contrast we would not have the potential to see the โ€˜bigger pictureโ€™ nor would we be a force to be reckoned with when we come together as a united front against the storms we have had to endure as a family.

It is no accident we were born into this family. It is said we choose our parents and our siblings to help us become the person we aspire to be.
We have the free will to reach our full potential - to develop and grow from our experiences to become women of greater wisdom, compassion and integrity. The connection we have as sisters offers us the shared mission of overcoming the karma of our family into a triumph of the spirit, not only for ourselves but for our children.

It is with gratitude I sit with you here today. Gratitude for being able to share part of my lifeโ€™s journey, with you, my sisters. Gratitude for being able to spend time with dad, getting to know him and watching and learning as he fought his battle with illness. Above all gratitude for being *******'s daughter and being given the gift of this precious life.





That is so nice to read Cat!


Freddie, your brother is way too young. I too can get how you are not getting much sense out of you SIL at the moment. How totally devastating.

I have spent 4 yrs in the world of childhood cancer. Thought it was all over but have to go back every month for check ups and blood tests for another 4.5 yrs. Was not expecting that.

Every single time we go in we see a new face. Kiddies from all over QLD have to come to our hospital for cancer treatment. Each time I see a new kid I feel my heart plummet, just knowing what that child and there parents will be going thru, and they have ni idea about it yet.

I think in some ways mentally it is easier for kids to cope as when they are the age my boy was when diagnosed, (6), they don't understand what the possible outcome is, and really, there is no need to tell them. But with adults, they know, and I imagine that is all they can think of.

My Mum got breast cancer 6 yrs ago. She rang me at work to tell me. my brother and I headed over. I stopped at bottle shop for some Scotch, unknown to me brother stopped at Target for a fairy floss maker. Between us mum got her favourite junk food made fresh, plus got her drunk enough she fell asleep on the couch so could at least stop thinking about it till the next day.

She had a mastectomy and has passed her 5 yr mark.

My aunt has also survived breat cancer, discovered 2 weeks before my Mum.

My grandfather died of Leukemia.

Mitchells grandfather ( his fathers side) died of a brain tumour 3 months after Mitch started his stay in hospital. He only lived for 2 months from being given diagnosis.

Mitchell's grandmother, again, fathers side, died of breast cancer just prior to Mitch's birth. She belonged to some fanatical church who refused to let her have treatment. ๐Ÿ˜ฎ ( Potters Wheel or some such rot). mitch's Dad took 3 months off with long service leave to nurse her at home. At least the church "allowed her" to have morphine for the pain at the end.

Both Mitch's dad, his brother and sister all found out they have pre cancer bowel cells and have all had lazer surgery in the last year. His sister has also been diagnosed with MS a few yrs back.

When I look at the family history on both sides, I think maybe Mitch hardly stood a chance of not getting some form of cancer. Who knows.

All I can suggest is if you are able to have regular phone contact then do it. I don't mean ringing every day to ask about treatment, just to say "hi" sort of thing. Just letting him bring it up if he wants. I say this solely so he knows you are always thinking of him, as it can be very lonely. It may sound selfish and self serving, but knowing others are thinking about you does help.



I did not get much support from the person I thought would give it naturally, having been thru similar themselves, and only working 10 mins from the hosp. All I had wanted was a "hi", to remind me there is life outside of hosp. We spent the first 5 months living in the hosp, me in fold up beside his bed, then another 4 months in a unit within the grounds, so quite an isolating experience.

I am assuming from your posts that the outcome for your brother is not great Freddie?
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That is so nice to read Cat!


Freddie, your brother is way too young. I too can get how you are not getting much sense out of you SIL at the moment. How totally devastating.

I have spent 4 yrs in the world of childhood cancer. Thought it was all over but have to go back every month for check ups and blood tests for another 4.5 yrs. Was not expecting that.

Every single time we go in we see a new face. Kiddies from all over QLD have to come to our hospital for cancer treatment. Each time I see a new kid I feel my heart plummet, just knowing what that child and there parents will be going thru, and they have ni idea about it yet.

I think in some ways mentally it is easier for kids to cope as when they are the age my boy was when diagnosed, (6), they don't understand what the possible outcome is, and really, there is no need to tell them. But with adults, they know, and I imagine that is all they can think of.

My Mum got breast cancer 6 yrs ago. She rang me at work to tell me. my brother and I headed over. I stopped at bottle shop for some Scotch, unknown to me brother stopped at Target for a fairy floss maker. Between us mum got her favourite junk food made fresh, plus got her drunk enough she fell asleep on the couch so could at least stop thinking about it till the next day.

She had a mastectomy and has passed her 5 yr mark.

My aunt has also survived breat cancer, discovered 2 weeks before my Mum.

My grandfather died of Leukemia.

Mitchells grandfather ( his fathers side) died of a brain tumour 3 months after Mitch started his stay in hospital. He only lived for 2 months from being given diagnosis.

Mitchell's grandmother, again, fathers side, died of breast cancer just prior to Mitch's birth. She belonged to some fanatical church who refused to let her have treatment. ๐Ÿ˜ฎ ( Potters Wheel or some such rot). mitch's Dad took 3 months off with long service leave to nurse her at home. At least the church "allowed her" to have morphine for the pain at the end.

Both Mitch's dad, his brother and sister all found out they have pre cancer bowel cells and have all had lazer surgery in the last year. His sister has also been diagnosed with MS a few yrs back.

When I look at the family history on both sides, I think maybe Mitch hardly stood a chance of not getting some form of cancer. Who knows.

All I can suggest is if you are able to have regular phone contact then do it. I don't mean ringing every day to ask about treatment, just to say "hi" sort of thing. Just letting him bring it up if he wants. I say this solely so he knows you are always thinking of him, as it can be very lonely. It may sound selfish and self serving, but knowing others are thinking about you does help.



I did not get much support from the person I thought would give it naturally, having been thru similar themselves, and only working 10 mins from the hosp. All I had wanted was a "hi", to remind me there is life outside of hosp. We spent the first 5 months living in the hosp, me in fold up beside his bed, then another 4 months in a unit within the grounds, so quite an isolating experience.

I am assuming from your posts that the outcome for your brother is not great Freddie?


(((((((((((((hugs)))))))))))))
Photobucket
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Oh wicks :-x

To have a child battling cancer must be the biggest heartbreaking experience. I can kind of understand when you said you were in the 'world of childhood cancer' because that would be your whole world, everything would have revolved around cancer, hospitals, doctors, tests, medication, fold up beds, other children with cancer, parents lost and bewildered ... for such along time.

And then when you think it's over, it's not because then you have to wait .. wait for the test results that have to be done on a regular basis to make sure the cancer hasn't returned.

I agree with you when you say just a 5 min call to say "hi" would be a wonderful way to keep in contact. Texting is also another way to stay connected. One of my good friends and my daughter are the two people who have texted me almost every single day since the 'break up'. They just text "remember we love you" or "hope you are having a good day, thinking of you". I often re-read their messages at night when I go to bed.

It's the consistency that I appreciate and knowing they are thinking of me every day. All it takes is a minute to text but it means so much. My friend and my daughter are also the ones that will often pop over with a Care Package. Food and meals are another great way to support someone. I also really appreciated the gifts and cards sent by the OK'ers. The same CS people who post almost every day in this thread is also a HUGE comfort as well as those who can only post every now and then but I can feel their love and support.

Sending cards with inspiring words or funny ones, if appropriate, are also such as sweet gesture.

My best friend supports me by always making time to talk for literally hours to me, with total honesty.

I guess what I'm trying to say is when faced with trying to comfort or support a loved one who is suffering, these little gestures help in so many ways.

And consistency is also really important. In fact I think it is the most important.

I have friends that might have phoned once or twice during these last few months. And that hurts. I can't be bothered phoning them now. They will probably say "oh I thought you would phone me if you needed me". BULL SHIRT.

Sorry for the rambling but I guess these months have really taught me the value of other peoples actions and behaviour when it comes to supporting and comforting another person.

I have finally learned what is important and how to comfort a loved one or friend is suffering through my own suffering.
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Hi Cat.

Yes, you understand what I was getting at. It takes no time to send a text, like your example, yet it means so much to the person on the other side.

I am not much good at words, sorry. ... and for other people like me who never seem to know the right thing to say, a quick text is perfect.

Too, as you say it is the fact that they keep contacting you that reaffirms they are genuine and do care.
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Hi Cat.

Yes, you understand what I was getting at. It takes no time to send a text, like your example, yet it means so much to the person on the other side.

I am not much good at words, sorry. ... and for other people like me who never seem to know the right thing to say, a quick text is perfect.

Too, as you say it is the fact that they keep contacting you that reaffirms they are genuine and do care.


Absolutely spot on wicks. BTW You expressed what I tried to say in a rambling post in one concise sentence:

Too, as you say it is the fact that they keep contacting you that reaffirms they are genuine and do care.Too, as you say it is the fact that they keep contacting you that reaffirms they are genuine and do care.


:-x
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I just wanted to also say that one night, last week, I got a text from a work friend at 3am. They just texted "You are loved xxx". It was perfect timing and perfect words. The person just thought of me at 3am and acted on their intuition.
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dtrh3
Community Member
Goodness,I think wicks and Ms Cat are psychic-I was just thinking along the same lines and posting and then the screen flipped out and my post disappeared into the ether.:O spooky
Ms Cat,I was posting that I hope Im not being a pest posting so regularly...Im writing this v fast so it doesnt disappear & can post it :^O

weird
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dtrh3
Community Member
I hope you dont mind me naming you wicks,but I really feel for you-what a journey you are on :-x

If you dont mind me asking,what do you do for yourself to keep your chin up?
I hope you are able to do something just for you.

I am thinking of you and your family,and send calm and positive,life affirming energy :-x

keep the faith
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