Hello Melissa and welcome to the forum.

Due to the pandemic there are still backlogs and delays to results so how long you've waited could be fairly normal in your part of the country at the moment. Having said that, if you were told you would receive your results slightly sooner then there's no harm in getting in touch with your GP to see if they can chase this up for you. 

Waiting for results is always a challenging time as so many of our members here have found out, so you are not alone and hopefully you will receive some support and advice from the community soon.

We're thinking of you Melissa and will have our fingers crossed for good news when your results come through.

Kind regards,

Steph, Cancer Chat Moderator

Hi Steph, thanks for getting in touch. 
 

I have just heard back from my consultants secretary today that they are having a MDT meeting to discuss my treatment. Please could you tell me what this means if you know, I am slightly anxious and not sure what to expect next 

thank you 

Melissa x

Hi cath , 

thanks for your reply. She said they were having a MDT meeting this morning, she did mention they was suppose to of done it last week but has been delayed due to pressure on the departments / NHS at the moment. It's the first time I've heard of a MDT meeting, it's been 4 weeks since my op and they sent the tumor of the lab along with a lymth node biopsy. She said on the phone that they will be discussing my treatment plans. I thought my last treatment would be a follow up appointment post op. Thanks again x

Melissa x 

Hi Melisa,

I think it's a pretty new thing the MDT. It really means that not just one person can make a decision on your treatment or the way forward. The team will have multi disciplines on it and will come to an agreement on your treatment plan. I think that's how it works. I had bowel cancer 10 years ago had the tumor removed a right hemi colectomy and a adjuvant chemo treatment. I don't think there were MDT then. Unfortunately it has returned although my original surgeon thought it might be a sarcoma because it's in my pelvis. You will be well looked after and it may be the case you won't need treatment they will be discussing that. Don't worry you've got this. 

Hi Melissa, 

You can find out more about MDT meetings just here but if you'd like to discuss this further with one of our cancer nurses, they're available on 0808 800 4040, Monday - Friday between 9a.m - 5p.m.

They're very knowledgeable, and supportive, and will do all they can to answer your questions and put your mind at ease.

Kind regards,

Steph, Cancer Chat Moderator

Hi,

After radiation treatment is it normal to have a 7  week gap before oncology appointment. ?

Hi Cath, 

Unfortunately I can't answer this question but if you give one of our cancer nurses a call on the number I've just given to Melissa in my previous post, you should be able to get some more clarity on this. Plus they'll be able to answer any other questions you may have about your treatment at this time.

I'm sorry I can't be of more help but I hope you're able to find out more soon.

All the best,

Steph, Cancer Chat Moderator

Hi,

No problem. I will just wait the 7 weeks until my oncology appointment. 
 

Thank You. 

Hi Melissa

just reaching out to see what was the histology report said and to connect, currently finding myself in a waiting situation and very likely to be sarcoma.