Puffball

My partner started radiation on her brain and spine one day after diagnosis of SCLC. She had lost all feeling in her legs up to her belly buttom from a spinal tumor. The last radiation was Jan. 5 (10 treatments in all). While most of her feeling has come back, she is resigned to the fact that some of it will probably not come back due to nerve damage. Is there a certain time period that radiation lasts? i.e. will she need to have treatments again after a certain lenght of time? Thanks Laurie

Thanks for the replies. I'm hoping to upload a photo of us soon - its on the other PC of course . I haven't been able to find much info. on small cell (SCLC) specifically since it appears that most lung cancers are of the other types and SCLC only affects approx. 15 % of lung cancers from what I can determine. I would like to connect with some SCLC folks or obtain more info. on SCLC. As I said before, Kris doesn't do research and doesn't want to know to much. I started reading about clinical trials (tho' none seem to be for SCLC) and she said "I don't want to hear about it now". I'm on 'overload' right now so thought I'd reach out to folks. Thanks as always. Laurie

3rd try @ intro. The first two times I got an error message . My name is Laurie and my partner of 26+ yrs. is Kris. I took Kris to the ER on 12/18/14 as her legs and tummy were numb; this happened quite suddenly/3 days. Following a spinal MRI, we were told that Kris had cancer, specifically tumors to the lung, spine & cerebellum. She was admitted to the oncology unit that day and radiation to her spine and brain began the next day. It was quite a shock needless to say – we had no idea! Kris is 57 yrs. old and a brain MRI and lung biopsy while she was hospitalized revealed that the lung cancer was small cell (Stage IV) with metastasis to the spine and brain. No symptoms to the lung or brain. The tumors on the brain are called lesions and are very small. The thoraxtic spinal tumor was the big tumor and caused the lack of feeling. Kris was in the hospital until Christmas afternoon and continued with the spinal and brain radiation; the last one on 1/5/15. Gradually most of the feeling has come back to her legs and tummy – not all but most. Following a 2 wk. break, chemo began on 1/18/15. She finished round 2 of 3 scheduled rounds on 2/20/15. Round 3 will probably begin on March 11. I am really happy to have found this site! Looking for support and education. Kris can use a PC but rarely gets ‘on’ it so I am her voice. She also doesn’t want to know to much. From the old school, hadn’t been to a doctor for at least a dozen yrs. before her ER visit. I do the worrying for both of us J. We live in the boonies – no cell phone coverage and I sometimes don’t get on the PC every day. I will always get back to folks; just ask your patience. Thank you! Laurie