[64 y/o husband has SCLC and I'm fearful]

Hi,

I've been reading this forum for days now and finally decided to participate. We live in Hot Springs, AR and he's been through all his Rx (chemo, chest radiation, & PCI).

He had only two lesions. one in the right upper lung and one in the lymph of the mediastinum and he is now NED. I know I should be happy, grateful, etc., but I still keep looking over my shoulder, waiting for the other shoe to drop. I am so fearful and realized I need to talk with others that have had the same experience.

I need to hear from other SCLC, especially those in my place who are married to someone with the illness. How do you get past this?

Thanx so much

[64 y/o Husband Dx SCLC, need buddy]

Hi,

I've been reading this forum for days now and finally decided to participate. We live in Hot Springs, AR and he's been through all his Rx (chemo, chest radiation, & PCI).

He had only two lesions. one in the right upper lung and one in the lymph of the mediastinum and he is now NED. I know I should be happy, grateful, etc., but I still keep looking over my shoulder, waiting for the other shoe to drop. I am so fearful and realized I need to talk with others that have had the same experience.

I need to hear from other SCLC, especially those in my place who are married to someone with the illness. How do you get past this?

Thanx so much

[PCI , fatigue, confusion]

Can anyone tell me, from your experience, how long the fatigue and confusion continues after receiving PCI.

It's been 4 weeks post PCI and my husband still walks around in a fog and feels as if he has the life sucked out of him.