The Cancer Survivors Network (CSN) is a peer support community for cancer patients, survivors, caregivers, families, and friends! CSN is a safe place to connect with others who share your interests and experiences.

Thank you for being a part of the Cancer Survivor Network community. Survivors and caregivers like you have played a unique role in fostering an online environment that encourages connection among those needing support, community, and education. On May 28, the Network will be discontinued. More details are available here . If you have any questions, contact CSNSupportTeam@cancer.org. Thanks again for the support you’ve provided each other over the years. We remain committed to supporting you in other ways throughout your cancer journey.

glioblastoma treatment

Footdoc
Footdoc CSN Member Posts: 13 Member
edited April 2023 in Brain Cancer #1

What was your treatment and what do you know of the side effects , results, experience patient or caregiver. please state patient age as I want to research this for my 75 yo mother.

Comments

  • greatfulGBfighter
    greatfulGBfighter CSN Member Posts: 4 Member

    I was 49 when I got my diagnosis in 2014. Treatment plan was 6 weeks of Chemo (Temodar pill) and radiation. After that went into a "maintenance " phase requiring 400mg of Temodar daily, for a 5-day period every month, with monitoring of my blood platelet count monthly. The negative side effect of Temodar is you become a laxative junkie for a few days as the drug is effective, but also slows up the plumbing in one's body.

    This phase lasted for 5 years (normal period is one, two at a max. But my platelet counts were consistently good, so I told my med team "if it a'int broke don't fix it") Now I have an MRI every 6 months to maintain awareness.

    Negative side effects experienced were: (short- term) brain swelling due to the radiation, which accentuated the effects on me. Was prescribed steroids to mitigate the effects. (Long-term) blood clot developed in my left calve requiring me to take a low dose blood thinner (Eliquis) for the long term. Additionally, I take a low dose of an anti-seizure med (Keppra) twice daily.

    The biggest key to success for me was ATTITUDE. I was determined to not slip into a permanent "pity party" but follow the advice of my med team and take charge of fighting it. Not every day was/is a holiday, but I'm here, I'm up and about, and that's the way I'm living with it.