dmhboyds

Activity

  • Jimstoneback
    hi donna ,
    had surgury , the doctor was worried about my scalp since i had 33 doses of radioation in 2012, now i have to hav e 33 more, he said hes gonna consult a plastic surgeoun
    i have 2 little tumors he coulnt get to,
    this one grew tothe size of a plum in two months time
    behind my left eye .
    so these other two tumors scare the crap out of me ,the radiologist is gonna hit the front one , but she doesnt thinkshe can hit the back one since she hit it already and she doesnt want to over radiate my brain
    July 2014
  • Jimstoneback
    it was a stage 2mengioma ,i have trouble with words lately


    June 2014
  • Jimstoneback
    i had my cranionoty may 22, now i have to go to the neurosugeoun and get the other half the stitchches and staples taking out this wed and fri go to the radiologist and see what she has planned out for me
    it never ends it ended up being a stage 2 crainometry
    it was a supriseto hear when the surgeon said it has to come out asap
    June 2014
  • Jimstoneback
    I too am having another craniotomy, may 22, its behind my left eye , they are gonna take the top of my head off again .I may have to go throu speech thearapy.
    April 2014
  • Jimstoneback
    Hi donna , whats going on ?
    February 2014
  • Jimstoneback
    hi donna ,im going for blood work this thurs, have another MRI to schedule in march or april then going to my neurosurgeoun after i get the results,how are you doing ?Was just reading what you wrote , hang in there , its all any of us can do
    January 2014
  • Jimstoneback
    hi donna, just thinking about you .
    December 2013
  • Jimstoneback
    im hanging in there!!
    November 2013
  • Jimstoneback
    donna,
    ill be thinking about you on mon.Be brave ,
    jim
    November 2013
  • Jimstoneback
    hi donna , i went to my nuerosurgion last wednesday , no change so far, he gave me a referral for another mri ,
    on the written mri report it says the superior sagittal sinus my be occluded , i asked him about this, he had to remove it , the way it works other radiologists look at the MRI and then they give it their impression , so the written MRIs my vary a little bit .
    of the 4 since my resection 4 different radiologist s gave their impression.
    remember to ask for a written report and the MRI CD.
    I'm so sorry you have to go thru surgery , hang in there .I'm here for you if you have any questions about my surgery , i dont remember too much about it , i had a seizure on fri . and had surgery on thu..All remember is wanting that thing out of my head
    October 2013
  • Jimstoneback
    hi donna , i didnt go to see my nuerosurgeon , im going to see him oct 2. his office called the day before my appt . and said he had to be in surgery .I also have fatigue, but its due to the keppra i have to take , i'm getting used to not being able to do the things i used to do , but i hope to one day.
    Good luck with your appt on thursday , let me know what he or she says .Hang in there!
    September 2013
  • Jimstoneback
    did you see a neurosurgeon about your small meningioma . ?
    if so what was his comments ,
    i had another MRI last wednesday , the results were depressing .
    September 2013
  • Jimstoneback
    I watched a webinar about meningiomas yesterday , the only way they can tell what grade it is is to remove it or do a biopsy and put it under a microscope and go by W.H.O .grading system .if its small and doesnt grow they can monitor it
    August 2013
  • Jimstoneback
    hi donna ,
    sorry to hear that your dealing with health problems
    it all depends on how big it is ,and where is , how they treat it and what stage it is ,and your age , i had a seizure while driving to work and crashed my truck ,i was given a cat scan at lehigh valley hosp.and from there they found it
    it was the biggest mengioma my neurologist ever seen , they can tell more from an MRI with dye i go for one about every 3 months they can be very agressive or they can chose monitor it , if its small and in a region that it'nt important and you dont have any symptioms, memory loss , weakness in arms or legs they may chose to do nothing ,i had surgery to remove it but they coulnt get it all, then 33 doses of radiation treatments and i had a second seizure 3 weeks after rad . it causes swelling , scar tissue causes seizures , now i have epilepsy and can't do my job as a pilot .
    i suggest you google mengioma ,and go on the brain tumor web site and some reshearch , it was a major life changing event for me ,
    they are more common than you think , Cheryl Crow the singer has one and from what i hear last theyare just monitoring hers .
    August 2013
  • Jimstoneback
    dmboyds just checked my email and see you also have a mengioma ,i can do my best to answer any questions you may have
    August 2013
  • carm
    Hello,
    I am an oncology/end of life nurse. Welcome to the “What Next” family. If you should have any questions or concerns that you feel that I might be able to help you with, please do not hesitate to ask. There are many excellent people here always willing to help in any way with the latest information or experiences to share. You are among friends….there are no strangers here. I hope you find all the information and support you seek, Carm RN.
    August 2013
  • stillerfan
    Have you made a decision as to where you are getting your treatments? Find a doctor that matches your outlook on your condition and treatment. I worked in Conshohocken for 10 years and I am familiar with hospitals in your area.I am not an expert.
    August 2013
  • emsavard
    Hi there. What type of thyroid cancer have you been diagnosed with? Is there a treatment plan? You are not alone in this journey. I have been through it all. Join me on my blog www.papillarythyroidcancerguide.com for my story and lots of helpful info. Please do not hesitate to message me if you have any questions.
    Elaine
    June 2013
  • GregP_WN
    Hello and welcome, we are glad you found us. Please feel free to join in the conversations. Here is a link to our cancer dx page for your type of cancer. Take a look at it to get you started on some information. You will notice at the bottom of that page 4 of our active users who have had that journey already, you may wish to contact them for their experience and wisdom. Also, I encourage you to go to the questions page now by clicking on the questions tab at the top of the page and post what is the most pressing issue you have right now. This will introduce you to the community and get you started on the help you need right now.

    https://www.whatnext.com/conditions/cancer/thyroid-cancer

    There are also subtypes listed on this page to narrow down the type of cancer to match your dx.

    You may also find our "Beginner's Guide To Cancer" page helpful Click Here for that=> http://bit.ly/10BQKCi

    Also, if you can take a few minutes and fill in some details of your journey so far, it will help others as they try to answer questions for you, it also helps others as they search through the data base to find someone like themselves. Confirming your email will allow you to receive updates and notices from the site when someone answers your questions or writes on your wall.

    Thanks for being with us and let me know if I can help you find any information on the site. After you have an opportunity to look the site over and see what great things there are here, we encourage you to invite your friends, family or anyone you know that may be helped by the connections on WhatNext to join the site also. Just click this link to invite them to join. http://www.whatnext.com/recruit-a-friend

    Follow Us on Twitter Click Here =>http://bit.ly/XExkce
    Find Us on Facebook Click Here =>http://on.fb.me/zjBAPl

    GregP
    3X Survivor
    Team WhatNext Community Mgr.
    June 2013
  • DeanaBeana
    Welcome to the site! We're happy you found us. If you find any conversations that interest you, feel free to jump right in and join them. There are some wonderful people on here just waiting to connect with you. You'll have a great support system on this site. I hope today is a good day for you.
    June 2013
  • BuckeyeShelby
    Hi DMH. Welcome to What Next. There are lots of great people here. I'm glad you found us but sorry for the circumstances that led you here. Wishing you the best.
    June 2013
  • DaveWaz

    Welcome to the WhatNext family! The WhatNext family is made up of people like you who are looking for help or looking to help others. To help you along your journey the WhatNext family has put together a Beginner's Guide to Cancer that I highly recommend you check-out here: http://bit.ly/10BQKCi. Also, please do not hesitate to reach out to others or ask for help.

    Wishing you the best.

    David
    Founder, WhatNexter
    June 2013