It sounds very scary.

Stay as strong and resilient as you can. Your strength is key.

I know I'm not the only DUer holding you in mind and heart.

lovingly,
Bright

tell your lawyer to put the hammer down .

if that doesn’t work in 10 minutes , call a TV station

then do a youtube or tiktok video

I like the way you think, Tetrachloride!

Hang in there, murielm99. We’ll keep the vigil with you.

muriel!

Sounds so scary, indeed.

I know Biden is committing to a cancer moonshot. I hope that good strong energy can come your way.

Holding you in light and love.

Hang in there, kiddo.

Do you have a nurse case manager at your hospital?

I cannot imagine how scary this is for you. It seems you deserve answers as to why tests are delayed again. It is difficult to advocate for yourself when you're in a place of anxiety and fear.

Not having information kicks up the anxiety level. I’m sending you good vibes and hugs with hopes the medical staff can get things moving immediately.

We are with you on this journey.

I am sending virtual hugs and keeping you in my prayers.

how terrified you are. Hugs to you.

Pulmonary function tests (sometimes called a PFT or PFT test) help diagnose lung conditions such as asthma,
bronchitis, or COPD. If you have already been diagnosed with a particular lung condition, a pulmonary function
test can also determine how well the medication you’re taking for the condition is working.

This test normally isn't for cancer.
They run a PET scan on me to find cancer from top of head to just above the knees.

keep us posted.

I can’t begin to imagine how frightening this must be. Post 3 has good points. I’d also call my primary care physician and ask for some Xanax.

She is not in today. She has continuing education. I let her CNA have it. A message is being passed along. I threatened to go public with this. I let them know about my condition on July 26. It has been nothing but talk for two months. This could have spread to my spine by now.

I am scared, but also angry. And, dying.

I hope you aren’t dying, but their foot dragging doesn’t help.

here for you.

And I’m very very sorry that you do as I know how stressful that waiting is as it’s horrible on your well-being. That said you still have reason to be optimistic as they found it and now you can focus on treating it which I’m confident you will be able to do!

I would however, as other posters have sensibly suggested, enlist the aid of someone inside or outside of the treatment facility to be your advocate and get them to move with some urgency so you don’t have to endure these horrible delays. I’d start here maybe as they have some good resources to help you find others who will help you through this.

http://cancersupportcommunity.org/

And remember you have all of us who you can vent to any time and who will give you as much support to help you conquer this, which I know you can!

Good outcomes and long life for you

for all your support. I does help.

We all are here for you.

We all are here for you.

Right now I have anger and fear.

I really can't see dying. I see myself alive and doing my activist work for a few more years. I am 74.

and I pray for a resolution and a full recovery Muriel.
I will look for updates, sending best wishes, stay well,