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Inoperable Brain Tumor

Brain Tumor | Last Active: Feb 21, 2017 | Replies (10)

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Hi @spammy, welcome to Connect.
I'm sorry to hear about your sister, but glad that you found us here on Mayo Clinic Connect. I'd like to introduce you to other Connect members who have been in your shoes, either caring for a family who has an anaplastic astrocytoma or they themselves do. They can help you learn from their experiences what you might expect. You can read more about each of them in this discussion:

- Anaplastic astrocytoma: Can anyone recommend a great neurosurgeon? http://mayocl.in/2e0InOQ

Spammy, do you live with or near your sister? How old is she if I may ask?

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Replies to "Hi @spammy, welcome to Connect. I'm sorry to hear about your sister, but glad that you..."

Hi Colleen. Thank you for responding. My 4 other siblings and I all live in the same city. My sister, Pati just turned 65 a month ago.

Hello @spammy - I am also sorry to hear about your sister. My daughter was also diagnosed was AA about 6 months ago. We live in Denver and can recommend a very good neurosurgeon at University of Colorado Anschutz Medical Center but I am not sure where you are living? I also noticed that you stated the tumor was inoperable? Have you got a second opinion on the original diagnosis?

Hello @parker80138. Thank you for writing. I live in Illinois. She did not get a second opinion which I believe was a mistake. Siteman Cancer Center, which is associated with Barnes Hospital in St. Louis and about 90 minutes from our hometown, was mentioned for a second opinion, but was not pursued.
Did your daughter have surgery? I hope she is doing well. Is she going through radiation and/or chemo treatments? My sister had her 4th treatment yesterday. I guess this tumor has feelers (?) which is why operating is not an option. Without any treatments the DR said she could live weeks to months, with could be months to year(s). I'm discovering that so many important facts are not discussed with the patient or family. The handling of the chemo drug was mentioned by a visiting nurse. This same nurse told us certain fruits and veggies were a no no. I was hoping to receive some tips from this group. People who have already been down the road we are just beginning.
Have a beautiful day!!

I think a second opinion is the smart and safe way to proceed. Depending on the location and the size of the mass there may be no safe way to resect the tumor but finding a good neurosurgeon and arranging to send him/her the MRI would provide you peace of mind that two specialists concur on the diagnosis.

My daughter is 34 years old and has had two surgeries to remove a 5.5cm mass from the left frontal lobe region. She had the initial chemo and radiation regimen and is about to start her 3rd monthly chemo treatment at 3x the dose she had during the post surgical treatments. This will last for 12-18 months. I hope your sister agrees to that second opinion soon but she will ultimately need to make that decision and everyone will need to accept her wishes and move forward. Best of luck!

@spammy Should your sister wish to consider a second opinion from experts at Mayo Clinic, please call any of our 3 campuses, http://mayocl.in/1mtmR63. She will be offered an appointment within 48 hours. Be sure to tell her to mention the Brain Tumor 48-access program. They can help her navigate her healthcare journey and answer your family's questions about treatment options.

I'm not aware of particular do's and don'ts with regards to certain vegetables and fruits. Anyone else heard of this?