CSN Login
Members Online: 16

Checking in

Roar's picture
Roar
Posts: 252
Joined: Mar 2013

Just checking in- I have been lurking in the shadows popping in and out just reading posts and just wanted to say hi to everyone. I am coming up on 15 months post treatment and have learned to live with the side effects. I am back to my normal weight. Back in the rat race fully. Biggest side effects remain dry mouth especially at night, taste is still not right yet' hearing is really bad and the tingling In My feet. But I refuse to give up- working 70- 80 hours a week - hitting gym- and even manage to help teach at a non for profit martial art dojo. My co worker who was diagnosed with prostate cancer that spread had his operation and is doing fantastic. He will not need chemo or radiation- or at least that is what they are saying now- I guess in a few months after the pet scan we will know for sure. Thanks for the prayers for him. Keep strong all my fellow survivors/ warriors, and keep battling. It's good to be alive - even if life is different than it use to be.

Skiffin16's picture
Skiffin16
Posts: 8125
Joined: Sep 2009

Do't give up yet as for improvements...

It took all of two years for all of me taste to come back.. Even at five years I tend to dry out a little at night. But not too bad, something that I live with. I have to say, that is about the only thing that I have as a lasting side effect..., other than a thinner beard.

Best,

John

debbiejeanne's picture
debbiejeanne
Posts: 2769
Joined: Jan 2010

roar, glad you checked in to let us know you're doing ok.  very happy to hear your friend is doing well also.  we always love to hear good news.  thanks for sharing.

God bless,

dj

CivilMatt's picture
CivilMatt
Posts: 3172
Joined: May 2012

Roar,

You are a glass half full kind of guy, I commend you for that.

I can tell you, for me, the Tampa 2 year plan wasn’t long enough, so I got an (open ended) extension for as long as it takes.  For dry mouth I still use Xylimelts with good luck.

Question, where do you find “80 Hour Energy”?

Matt

Roar's picture
Roar
Posts: 252
Joined: Mar 2013

i work 6 days a week - i have learned to listen to my body - when i feel my battery running low i back off a little - maybe take a full weekend off and only work to about 4pm on a friday. i have also learned not to stress so much. i use to do a lot of yelling at work. radiation cured that and i had to learn how to get what i want without yelling. and in doing so i found i dont stress as much. my wife finnally got the soft spoken man she always wanted. so everything happens for a reason. i will definatley try the Xylimelts - over the counter? your humor and wisdom is always a pleasure to read. I hope your doing well.

jim and i's picture
jim and i
Posts: 1707
Joined: May 2011

Good to hear all is well with you and your friend. I pray all continues to improve.

Debbie

Grandmax4's picture
Grandmax4
Posts: 600
Joined: Dec 2011

to be alive, happy to hear you're doing well, your friend also, keep kickin'

 

patricke's picture
patricke
Posts: 491
Joined: Aug 2006

Congratulations on getting back into the race of the proverbial rats, that's great news!  Hopefully the side effects that you are still experiencing, will diminish and possibly disappear in time.  For us, time truely is the great healer, and the resiliency of the body never ceases to amaze me.   I do hope that in the process of working the 70 - 80 hour work weeks, that you incorporate the time to sniff a rose or daisy, and check out a moonrise or two.  Your awesome positive attitude will continue pave the way for your continued tremendous recovery!  Keep it movin forward!  I hope that your friend keeps getting good news for the outcome of his treatment and recovery.

PATRICK 

Roar's picture
Roar
Posts: 252
Joined: Mar 2013

SKiffin - i know what you mean about the hair - havent had to shave under my chin in 15 months - Matt- i am truly blessed for a multitude of reasons - i love what i do, i work for a company that stood behind me and my familly in my darkest hours and treats me very well and truly appreciates my efforts - i choose to work the extended hours, as i am in construction and have an A type personality. i can not go home until i clear my desk and email box every night. i like to begin fresh every day. in between projects my company forces me now to take a week or two off and smell the roses. going to florida to see my mom after this one in april,maybe i will stop in and see skiffin.  when i was sick, i found out who my friends were. and i must say some people that i thought were my friends were really only aquantences . i am just happy that all the fatigue after treatment has finally subsided - diet has changed substantially. i juice dailly and eat healthy. i choose to keep my weight down  to 175-180 - was 190 before treatment but do not want the extra weight. i could easilly put it on if i want. thank you to everyone for the prayers and well wishes for my friend and myself. i too , wish and pray for all of you. This place keeps it real for me. i am not as smart as a lot of you in here when it comes to terminology of our disease and associated treatment so a lot of the time i just listen. there is definately a lot to learn in this room and just wanted to say thank you - keep up the fight my friends - and for those of you not in such a great place right now, keep the faith - i will say a prayer for you right now, and i hope you begin to feel better soon - be well everyone- ralph

Hondo's picture
Hondo
Posts: 6056
Joined: Apr 2009

I was doing that for a while too but just had to stop flying and come in for a landing. Thanks so much on keeping up on how you are doing.

 

God Bless

Tim Hondo

Subscribe with RSS
About Cancer Society

The content on this site is for informational purposes only. It is not a substitute for professional medical advice. Do not use this information to diagnose or treat a health problem or disease without consulting with a qualified healthcare provider. Please consult your healthcare provider with any questions or concerns you may have regarding your condition. Use of this online service is subject to the disclaimer and the terms and conditions.

Copyright 2000-2015 © Cancer Survivors Network