Menigoma grade 3

Hi bee1956

a warm welcome to the group. Sorry to hear about all that's been going on. 

There's a diverse group within this community so I am confident that someone in a similar situation will reach out soon with their words of wisdom. My personal experience lies in supporting my late husband through a stage 4 glioblastoma journey so a different journey to the one you are on. G did have radiotherapy and to be honest coped really well with it. HIs biggest complaint throughout the six weeks was that the nurse squashed his nose every day when the mask went on. The only side effect he suffered from was fatigue which started after about 4 weeks and lasted for about a month after the treatment finished.

This is a safe and supportive space so please reach out here anytime.There's always someone about to listen who gets it, someone to hold your hand and to offer a virtual huge when its needed. You're not alone. We've got you.

It’s always good to talk so please remember that you can also call the Macmillan Support Services on 0808 808 00 00 - most services are open 8am to 8pm, 7 days a week Clicking here to see what is available. This service provides lots of cancer information, emotional support, benefit and financial guidance or just a listening ear.

For now though I'm sending you a huge virtual hug and lots of positive energy.

love n hugs

Wee Me xx

Thank you very much for your kind words!

And I'm sorry to hear your story. 

Hugging you back :-)

Hi, my husband is going through exactly the same thing. He had his operation 6 weeks ago and starts his radiotherapy tomorrow (30 treatments in total). He's feeling really well at the moment and very positive. He seems to be dealing with it better than me. Hope you get your treatment plan soon.