It is finally over
I have been going through the posts because I have not been around for a while. I am really doing pretty good and am very happy and fortunate. For the new people, this is a very tough treatment. Everyone responds differently, you will make it and the treatment will end. To me words cannot describe the ordeal. the best and simple advice is "one day at a time". Try not to project too far into the treatment. Somehow, as humans, we find a way to overcome tremendous obstacles and heal. I mean, 3 weeks ago, I was on the ground and barely cared what my name was, today I feel 500% better. My mouth is dry but getting better, taste is comming back slowly, and I can work without having to take a nap, and I don't have to sleep till noon. Unfortunately, fear and worry are part of the treatment and recovery, to me the worst part. Remember, the tough times will end and your new life begins. Hang in there and be well. Alex.
Comments
-
thanks
thanks for the words of encouragement. just waiting for the big guy to turn the corner for the better.....0 -
Congratulations!
Congrats, Alex! There are still some obstacles to overcome, a number of scans and such over the next few years, for example, (along with the associated worry that you recognize already) but it sounds as though you have weathered the most difficult part of this with flying colors!
Again, congratulations!
Take care,
Joe0 -
Great!Dazey said:Hooray
Glad to hear your news. We started this path at the same time and ended it too! It is sooo good to be done. No matter what comes up, you can do it. Dazey
Keep it up Alex. I am now 7 weeks out form 33 rad and 3 chemos. PEG gone 2 weeks ago. Like you I am amazed that I could go from feeling so bad to feeling so good. The ability to eat real food helped a bunch and back to work and regular activities a key as well. Lots of stretching of the jaw, neck and shoulders everyday as well as walking and ice hockey with my daughter. Trying to return to normal as much as possible. PET scan coming up in couple weeks and looking forward to positive result there as well. Stay positive with your recovery!
Mike0 -
Good for you AlexLandranger25 said:Great!
Keep it up Alex. I am now 7 weeks out form 33 rad and 3 chemos. PEG gone 2 weeks ago. Like you I am amazed that I could go from feeling so bad to feeling so good. The ability to eat real food helped a bunch and back to work and regular activities a key as well. Lots of stretching of the jaw, neck and shoulders everyday as well as walking and ice hockey with my daughter. Trying to return to normal as much as possible. PET scan coming up in couple weeks and looking forward to positive result there as well. Stay positive with your recovery!
Mike
I was doing great post treatment, eating, exercising, generally feeling good but had a neck disection on Monday which has set me back a litttle in the energy department and eating ability although not to bad, I remember when you started and wish you the best from this point on. I've fallen behind you in the race again. I'll catch up soon.0 -
One day at a time
Alex- 8 months after treatment of 34 rads (last 3 were partials) and too much chemo, and doing great- you'll get there, and beyond. congratulations. took me about 6 months to gain back all my weight, but that goes with eating ability, and keeping the calories coming in. sounds like you're doing great. and the "one day at a time" is exactly the right approach, and one that is still with me. very good advice for everyone.
AND FOR EVERYONE GOING THRU TREATMENT- alex, hondo, ratface, delnative, landranger,dazey, stash, Joe,and all of us who are active in this forum- WE ARE PROOF YOU CAN GET THRU IT TO ALL, NO MATTER HOW DIFFICULT IT MAY BECOME, BECAUSE WE HAVE BEEN THERE, TOO, AND WE ARE STILL HERE AND DOING OKAY. A GOOD AND LIVEABLE END TO THE TREATMENTS CAN, AND WILL, BE HAD BY YOU. We are proof of that fact. Believe you can, and thus you can, and will.0 -
Great wordsHondo said:Alex
Glad to hear your good
Alex
Glad to hear your good news
Stay strong
Alex said, " Remember, the tough times will end and your new life begins. Hang in there and be well." Boy is that the truth!!
This site has had great import in my recent recovery!! Thanks all! I wish I would have come to the board sooner.0 -
Thanks Guys! And Girls!Kent Cass said:One day at a time
Alex- 8 months after treatment of 34 rads (last 3 were partials) and too much chemo, and doing great- you'll get there, and beyond. congratulations. took me about 6 months to gain back all my weight, but that goes with eating ability, and keeping the calories coming in. sounds like you're doing great. and the "one day at a time" is exactly the right approach, and one that is still with me. very good advice for everyone.
AND FOR EVERYONE GOING THRU TREATMENT- alex, hondo, ratface, delnative, landranger,dazey, stash, Joe,and all of us who are active in this forum- WE ARE PROOF YOU CAN GET THRU IT TO ALL, NO MATTER HOW DIFFICULT IT MAY BECOME, BECAUSE WE HAVE BEEN THERE, TOO, AND WE ARE STILL HERE AND DOING OKAY. A GOOD AND LIVEABLE END TO THE TREATMENTS CAN, AND WILL, BE HAD BY YOU. We are proof of that fact. Believe you can, and thus you can, and will.
Now, this is why God must of directed me to this website! I'm not a Bible thumper, but Now I know there is a God!! lol! Every time I come on this froum and read everyone's story, it uplifts me! Thank you!
P.S. I go for my 1st follow up, with my Oncologist this Monday. I hear it'll be the scope down the nose? Can anyone tell me what else he will do on the 1st appt.?
Cindy0 -
Mondayfishingirl said:Thanks Guys! And Girls!
Now, this is why God must of directed me to this website! I'm not a Bible thumper, but Now I know there is a God!! lol! Every time I come on this froum and read everyone's story, it uplifts me! Thank you!
P.S. I go for my 1st follow up, with my Oncologist this Monday. I hear it'll be the scope down the nose? Can anyone tell me what else he will do on the 1st appt.?
Cindy
Yes, Cindy, about God, and that of the Spiritual realm. I am not a Bible thumper, either; but, rather, of the unorthodox in regards to Jesus, and God, as I have sought, rather than be complacent with what I am told is true, and do believe in. There may be something to what one of ancient times taught in regards to every Soul's connection to God, and Jesus, without all the red tape and trappings of religion for the masses. Imagine a plane with only two upon it- your Soul, and the presence of God. Believe...
The first visit was nothing more than routine, for me. Should not be a cause for anxiety. They will assume everything is as was expected, and it will be. What you must go with is what you know of from what you are experiencing with your body. If there is cause for concern, in your mind, then tell them about it. But realize, only you know what's really what with you, and your body has been dealt a bigtime right hook with the treatment; and, thus, your body is still trying to get a grip on the aftermath of that punch. Were I you, if my Oto were to give me cause for concern, then I would put my Oto under analysis in the name of motivation for his/her opinion. My first post-treatment PS showed something under my tongue, but my Oto is not concerned about it- where it showed is a place for typical false-positives, according to him, and that opinion gained him foundational place. And he is directly linked to the University of Iowa, which claims to be the 2nd-best in America, when it comes to head and neck.
kcass0 -
PEG and eating real foodcwcad said:Great words
Alex said, " Remember, the tough times will end and your new life begins. Hang in there and be well." Boy is that the truth!!
This site has had great import in my recent recovery!! Thanks all! I wish I would have come to the board sooner.
Hi everyone! I'm new here and it's great to see all the useful info you guys have contributed.
I finished treatments of radiation and Erbitux on Sep 25th 2009(not sure how many of each but approx 7 weeks (erbitux once a week and radiation 5 x week).
Dry mouth is really bad and wakes me up several times at night so I end up sleeping a lot the next day to compensate.
My taste buds got fried and food tastes terrible and all food smells really awful as well. So I still am relying 100% on the PEG tube since eating tastes and smells so bad. If this continues I would have to force myself to eat food that tastes really bad in order to get rid of the PEG> My daughetr keeps trying to get me to try different foods but they all taste and smell terrible.
I cannot imagine having this not get better but the possibility really scares me not to be able to eat or smell normally and to have an ongoing dry mouth problem.
Jeff0 -
Alex
Yeah for you!!!! You finished and are going forward. It's a frustrating process - this recovery thing. My husband is about 9 weeks out and is doing very well. Eats and does just a little supplementing with Boost to keep the calories and weight up. He has alot more energy and does not nap anymore. He even went pheasant hunting in SD last week for days. This is sooooooo encouraging!!! Life is going on. Yahoo!!!! PK0 -
The scope of thingsfishingirl said:Thanks Guys! And Girls!
Now, this is why God must of directed me to this website! I'm not a Bible thumper, but Now I know there is a God!! lol! Every time I come on this froum and read everyone's story, it uplifts me! Thank you!
P.S. I go for my 1st follow up, with my Oncologist this Monday. I hear it'll be the scope down the nose? Can anyone tell me what else he will do on the 1st appt.?
Cindy
My first post-treatment visit consisted of the radiation doc scoping my throat (through the nose, of course) and my ENT looking down my throat, holding my tongue and asking me to say "EEEE" (which you can't do when someone's holding your tongue) and feeling my lymph nodes.
As for there being a God, I'm not generally too outgoing about my faith -- I have too much of the reticent Scotsman in my DNA for that.
However, the coolest thing happened last week when I went back to Johns Hopkins for my PET scan. I was running late, and when I arrived on the campus I wasn't sure where the PET scan building was located.
I said a silent prayer, asking God for help in finding the right place. I then spotted a security guard sitting in a little outdoor booth. I gave him the address, and just as he was trying to point me in the right direction, a lady came up behind me and said, "I'll take you there." Turns out she's an employee, and she took me in through an employee entrance, down through tunnels and passageways and other places that the public never sees. And I got to the registration desk with one minute to spare.
--Jim in Delaware0 -
check upfishingirl said:Thanks Guys! And Girls!
Now, this is why God must of directed me to this website! I'm not a Bible thumper, but Now I know there is a God!! lol! Every time I come on this froum and read everyone's story, it uplifts me! Thank you!
P.S. I go for my 1st follow up, with my Oncologist this Monday. I hear it'll be the scope down the nose? Can anyone tell me what else he will do on the 1st appt.?
Cindy
I had my first check up two weeks ago. Prior to the visit I had a cat scan. The radiation doctor said I was too swollen and inflamed for him to do a scope and I had mucositis. I was happy to actually hear him say that, it validated my pain and my issues with mucous. However, he also said "your cat scan is perfectly normal, you have to have patience to heal - it will take a long time." His parting words were to have a happy holiday and he will see me in three months. We have all heard from many on this site that we are all different. So true; this was my experience with the first check - up. The doctor was reassuring and I keep reminding myself of his words - especially as I still struggle with the mucous and pain with swallowing. It WILL get better! Dazey0 -
Peg and down the roadjdeh@comcast.net said:PEG and eating real food
Hi everyone! I'm new here and it's great to see all the useful info you guys have contributed.
I finished treatments of radiation and Erbitux on Sep 25th 2009(not sure how many of each but approx 7 weeks (erbitux once a week and radiation 5 x week).
Dry mouth is really bad and wakes me up several times at night so I end up sleeping a lot the next day to compensate.
My taste buds got fried and food tastes terrible and all food smells really awful as well. So I still am relying 100% on the PEG tube since eating tastes and smells so bad. If this continues I would have to force myself to eat food that tastes really bad in order to get rid of the PEG> My daughetr keeps trying to get me to try different foods but they all taste and smell terrible.
I cannot imagine having this not get better but the possibility really scares me not to be able to eat or smell normally and to have an ongoing dry mouth problem.
Jeff
It'll all come back. Just takes time. I've have my PEG since January, and know I will have it at least until next March. I have gained all my weight back, and still drink at least one Ensure/day. Trial and error with the real food. Salads with different dressings might be a good place to start. I am addicted to chef-types w/French dressing. 8 months after the last rad, dry mouth and foam saliva are still with me, but Biotene does help. Just keep the calories coming in. The taste will come back. Believe, and it will. As for the dry mouth- all that really matters, Jeff, is that you are still alive, and that ain't gonna change for quite some time. We have all been where you are, and we still are alive.
kcass0 -
Congratulations! There is hope!! It has been one week since I completed Radiation treatments (6 weeks) and I have to say that I do feel better every day!! I do have the tube because I still do not have my taste buds back completely, but I am hopeful they will come back soon because there are a few foods I can taste just a little of....so that is encouraging for me. I will definitely try salads with different dressings to see if I can tolerate any of them. I am going back to work next week and I couldn't be happier. Thanks for your posting, you have no idea how much it has meant to me.
God Bless.0 -
Congratulations! There is hope!! It has been one week since I completed Radiation treatments (6 weeks) and I have to say that I do feel better every day!! I do have the tube because I still do not have my taste buds back completely, but I am hopeful they will come back soon because there are a few foods I can taste just a little of....so that is encouraging for me. I will definitely try salads with different dressings to see if I can tolerate any of them. I am going back to work next week and I couldn't be happier. Thanks for your posting, you have no idea how much it has meant to me.
God Bless.0
Discussion Boards
- All Discussion Boards
- 6 CSN Information
- 6 Welcome to CSN
- 121.9K Cancer specific
- 2.8K Anal Cancer
- 446 Bladder Cancer
- 309 Bone Cancers
- 1.6K Brain Cancer
- 28.5K Breast Cancer
- 398 Childhood Cancers
- 27.9K Colorectal Cancer
- 4.6K Esophageal Cancer
- 1.2K Gynecological Cancers (other than ovarian and uterine)
- 13K Head and Neck Cancer
- 6.4K Kidney Cancer
- 671 Leukemia
- 794 Liver Cancer
- 4.1K Lung Cancer
- 5.1K Lymphoma (Hodgkin and Non-Hodgkin)
- 237 Multiple Myeloma
- 7.1K Ovarian Cancer
- 63 Pancreatic Cancer
- 487 Peritoneal Cancer
- 5.5K Prostate Cancer
- 1.2K Rare and Other Cancers
- 540 Sarcoma
- 734 Skin Cancer
- 653 Stomach Cancer
- 191 Testicular Cancer
- 1.5K Thyroid Cancer
- 5.9K Uterine/Endometrial Cancer
- 6.3K Lifestyle Discussion Boards