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celeni (celeni)


June 1, 2008


Alabama


02/01/60


Lung and Bronchus Cancer


adenocarcinoma


April 2008


Stage 4


Taxol (chemical name: paclitaxel)


My boyfriend thought his shoulder pain was due to pulling some muscles. After a couple of months of it getting worse…he thought …oh my Lord…I bet I have a torn rotor-cuff. We only wish it was so…
He went from those thoughts to the doctors finding a tumor on shoulder..(no problem, odds are that it is benign)...to hearing lung cancer with metastisis to shoulder and large bones… and 12-18 months???

I started logging this “journey” from MY perspective. The thoughts, feeling and poetry from someone who loves someone…who has cancer.




celeni's Cancer Blog

June 20, 2008

June 10th through June 21st- getting caught up on journalViews: 965

Well, Wes went to the gall bladder doctoe last Friday and decided not to do surgery since had only one attack. THe doctor said that Wes needed to get back on his chemo and not take the risk of any type of surgery at this time…unless it was life threatening. As he was walking out Freida asked if there was something that he could take…or what kind of foods did he need to stay away from. THe doc said…oh yeah, I can write you a prescription to get rid of the “sludge” in his gall bladder. Thank goodness she asked him about it and got a prescription. SHe said, well he was a surgeon, she guessed that since he wasnt going to cut him open he was just going to walk out and go to the next patient. Sheesh. Thank goodness for the internet. It pays to do a little research yourself since it appears at times it is like pulling teeth to get info from a doctor. I guess in the “good old days” people never questioned their doctor…they just assumed that what they were told was the gospel. So Wes was back on schedule for his chemo that he had done this past Wednesday.

I felt a little guilty because last weekend was my traditional “City Stages weekend with the Girls”. Me and my two best friends have been going for 12 or 13 years now. City Stages is a big music festival in downtown Birmingham. We get there on Friday evening, get a room at the Sheraton and listen to music all weekend long. Anyhow, Friday evening, I took my car in so I could go see Wes for a while and so that I could see him on Sunday on my way out.

When I got there Friday night he was in his room, in the hospital bed, watching tv. I worry that he doesnt get up and about more…or that he doesnt want to go somewhere…that he doesnt want to do anything inparticular. It makes me feel like he is “wasting precious time.” He tells me that he is a simple man…and that he is a rich man. Rich in his family and friends, and simple in the fact that if there was something that he really wanted to do…that he would have already done it…that he is satisfied doing just what he is doing. I think that is as hard for me to accept as the initial diagnosis of cancer.

But how would I handle it if I had a limited amount of time left on this earth? That is hard to say…and I can only imagine. Is he in pain? I ask, and he says he is sore…but I dont know what that means. Is he sore because he is so inactive? Is he sore because the cancer makes him weak? I am just trying to understand…and I guess I have to come to the realization that each individual would handle that situation the way THEY want too..not the way that others expect…or want them to handle it.

So…I went off for the weekend with the girls and came back to see him on Sunday. WHen I came in I was talking about the weekend and showing pictures to his family. I went in his room and I made a comment that must have pissed him off. Right or wrong (probably wrong) he put on his shorts and came into the living room with us and we all had a pleasant afternoon, laughed, talked…he even stayed up with them while they cooked out steaks on the grill after I left. It was a good day…things almost seemed normal again.

Hopefully next weekend he will be feeling good, having survived the aftermath of his chemo, and can come to my house for the weekend. God bless everyone who is battling cancer and an extra God Bless you to the families and friends. Until then!

The aftermath of chemo can be very trying, some days it take all of my energy just to shower and eat, it is hard to understand unless you have lived it. Be patient and just be there for him.

You are wise to see that each person has to deal with this invasion in their own way and time. My wife had a very hard time understanding my response to cancer and my refusal to do some of the things she thought I should. But given time we were able to come to a place that works for us both.

Prayers for you both

Mac

THANK YOU for posting this journal. My husband is a cousin who has lost touch over the years with Wes. Basically we see you all the The Building once a year. We feel like we know a lot more about what is happening. You are a blessing! I am going yo hug my husband a little harder today! Love Kathy




Celeni's Stats

Posts: 39
Photos: 10
Events: 0
My Supporters: 18
I Support: 12
Comments: 115
Views: 33175


My Supporters:

 Brad

 Kathleen

 Gaile

 Gemma

 Patty Morris-Hildebrand

 Heidi

 Jill

 Joyce

 Sherri

 Kellye

 Lisa

 Mac

 staypositive

 Taff

 Louise

 Yuyu

 veronica 

 Sharon Traywick 
Celeni, please send me your email address. I went to HS with Wes and just found out about his battle with cancer. My email is straywick@coosahs.net


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