My update
Brooks
Comments
-
Update
Thanks for the update and it sounds like you are doing relatively well. I'm also having problems with neuropathy and probably always will according to my oncologist. My pooping schedule is another story, one that is rewritten new everyday. I'm never ever sure what to expect. Glad to see your post.
Kim0 -
KimAnnabelle41415 said:Update
Thanks for the update and it sounds like you are doing relatively well. I'm also having problems with neuropathy and probably always will according to my oncologist. My pooping schedule is another story, one that is rewritten new everyday. I'm never ever sure what to expect. Glad to see your post.
Kim
My pooping schedule is somewhat like your's. Some day's I go 10 times then somedays I cant get off of the toilet. Thank gosh we have 2 bathrooms!!0 -
Hey Hey
You know it's funny...this is a true story...I can't remember how many times I'll think about someone and say they have not checked in for a long time...wonder what has happened or if they just left the building.
That day or the next day, I'll see a post from them. Too weird....
I remember you were in Timbuktoo last time you updated....I was just down the road from you in the quaint village of Fukmetoo:)
It's a small world, isn't it?
LOL! Brooks:)
Good seeing you - sorry you're still having so much trouble, but the disabled plan sounds like the plan for you now. Great!
-Craig0 -
Happy things going good
I'm really happy that things are going good for you. I know the pooping problems, I try to go to stores where I know where the bathrooms are for you never know when the quick need will arise!! I'm praying everything goes well with you and your family.
Jeff0 -
Congrats!!
Brooks,
We finished up about the same time - and I also just "checked" in this week - I am all thumbs up too -
Just wanted to find out how you got thru disability....I have the neuropathy in the feet, hand are bothered by the cold - and my hips/back are stiff after a long day....I would love to find out more - and who to begin this process with - any info would be appreciated!
Glad you are A-OKAY!!!!
Happy Holidays and Happy 2012~
Michelle0 -
Update
Great news regarding your update. It is an inspiration. This site provides so much information. I thought that I was the only one going through neuropathy. The feelings in my hands returned somewhat, however, my grandchildren now button for me. I can button but it takes a lot longer. As for my feet, I still have the numbness and tingling. I make sure that I wear shoes with good soles (just in case I walk on something and not feel it right away.)I am also glad that you got your disability, the first time trying. The real reason many people are turned down for Social Security Disability, is not because they aren't disabled, all of the necessary medical information is not sent in from the medical sources, that we need. I say "we" because I have been a disability examiner for the last 31 years. When I received my diagnosis it was kind of hard because I knew exactly what the doctors were saying to me. The good news is I have been cancer free for a year and two months. I pray to stay that way. By the way, you can call your local Social Security field office and they can make sure that you receive a copy of your award letter for it is kept in your file. As for the poop situation, my son is helping me to change my diet and eat more natural foods. He's a vegetarian. I am hoping that it helps. Have a blessed, healthy and wonderful new year.
Peace and Blessings,
Karen0 -
Brookstootsie1 said:Good!
I love it when things go well for you, Brooks!
*hugs*
Gail
I am also experincing alot of pain from the OXI. Mine is feet, hip and shoulders and neck. Is there anything you are doing to help it. I cant seem to get under control. Especially in my neck and shoulders. Feet are bad too, but I can't seem to get my GP to acknowlegde anything about the OXI. Any suggestions?0 -
Glad to hear
Glad to hear from you and that disability went through w/out a problem! And ofc no cancer is great too!
As for the pooping. I had problems too. Now me and my ileostomy are living happily very after. I was so miserable. I have a life now. Here is to hoping you get more of your life back and giving less to the ceramic throne.0 -
Neuropathy and OxaliplatinRickMurtagh said:Glad to hear
Glad to hear from you and that disability went through w/out a problem! And ofc no cancer is great too!
As for the pooping. I had problems too. Now me and my ileostomy are living happily very after. I was so miserable. I have a life now. Here is to hoping you get more of your life back and giving less to the ceramic throne.
Hi Brooks: There have been lots of discussions about neuropathy caused by oxaliplatin on this board. I had 12 treatments of oxaliplatin and never really had any problems. I think because I daily took the following: alpha lipoic acid tablets (good quality) 3 times a day, 5 grams L-Glutamine Fermented in juice once per day, Vit B6 once a day, and calcium/magnesium once a day. These are things recommended for fibromyelgia, another "nerve" disease.
Cheryl0 -
Tinageotina said:Brooks:
About time you checked in, been wondering about you. Don't say away so long, our newer members need your wisdom and knowledge.
Good job getting the disability. If you can get the kids covered that should ease up the finances a bit.
Take care - Tina
LOL@ my wisdom and knowledge0 -
MichelleMchapp said:Congrats!!
Brooks,
We finished up about the same time - and I also just "checked" in this week - I am all thumbs up too -
Just wanted to find out how you got thru disability....I have the neuropathy in the feet, hand are bothered by the cold - and my hips/back are stiff after a long day....I would love to find out more - and who to begin this process with - any info would be appreciated!
Glad you are A-OKAY!!!!
Happy Holidays and Happy 2012~
Michelle
I was waiting to get better so I can go back to work but it never came. My neuropathy and pain is really bad and I have the pooping thing going. I just went on line and filled it out with the my wife. I also kept records of all my surg's, hospital stays and doctor visits sence my dx in 2009 so having all the dates was a big help.0 -
iluvmmsiluvmms said:Brooks
I am also experincing alot of pain from the OXI. Mine is feet, hip and shoulders and neck. Is there anything you are doing to help it. I cant seem to get under control. Especially in my neck and shoulders. Feet are bad too, but I can't seem to get my GP to acknowlegde anything about the OXI. Any suggestions?
I'm on a pain patch and pain meds. The patch seems to keep the pain under a 5 or 6 then I take the oxy's when it really gets bad. Sometimes I hurt so bad I could just jump out a window!!
Copy information from on line and bring it to him and tell him it's not right for you to live in 24 hr pain and it that doesnt work get a new doc and go see a pain doctor too.0
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