• We are a multilingual website again. Read the notice about this.
  • Understand AI use at MyPTSD: all AI use is explained in our AI help page. AI use is by choice here. It exists if you want it, but does nothing unless you choose to use it.

Stem Cell Transplant ( Sct )

Status
Not open for further replies.
Hugs from me too.

I'm glad that you started this thread. I think that many of us suffer in silence. We don't want to bother others or to upset others. Of course, I can't speak first hand as one with PTSD but I think the environment of secrecy associated with PTSD contributes to this.

But, we all need support. We all deserve support. YOU deserve support.

Not only are you getting supportive feedback, I hope that others will perhaps see that it's OK to ask for support and to share their story. Especially here!

(((((HUGS)))))

ISH
 
Hepburn quote.webp

:hug:
 
Feeling much better mentally tonight than I have in weeks. Probably a good time to reflect a bit since I started this thread for dealing with cancer and PTSD.

Having PTSD seems to amplify the effects of the drugs used to treat cancer. Many of us here have experienced cognitive problems. inability to focus. forgetfulness, short term memory issues etc. Chemo drugs also have this effect called "chemo" fog. It makes it difficult for a person to distinguish between what may be drug related, PTSD related, or a combination of both.

Then there are the steroids. For "normal" people, steroids an cause sleeplessness, increase anxiety, irritability, depression, personality changes, hallucinations, etc. For my particular cancer treatment the steroid dexamethasone is an integral part of the treatment. However, it created exacerbated my PTSD symptoms so badly that I had to reduce the dosage and counteract the side effects with other drugs.

This last round of chemo was particularly difficult since it was "double" chemo. Twice the frequency so four rounds were covered in a period covered normally by two rounds. So the chemo fog was worse, the fatigue was worse, and the of course it was double the steroids so all the fun symptoms that exacerbate the PTSD were even worse. Add in all these drugs, the stress of dealing with cancer and it is was a PTSD roller coaster.

One thing I cannot stress enough is how much the tools that I have learned in therapy have helped. Mindfulness has been a lifeline, and the tools I learned in CBT to identify negative thinking patterns and cognitive distortions and how to redirect my thoughts. DBT has helped me process some of the extreme emotional swings, and regulate emotion.

But there have been times between the chemo, the stress, and probably some very normal reactions to having cancer the PTSD has gotten the best of me. My "can do" attitude has its place, but it also makes me want to "handle things" on my own and that has gotten me into some trouble.

My oncologist and psychiatrist have been very good about prescribing medication to help offset the side effects of the drugs and to help me manage the mood swings. It is me that has trouble taking it. Funny I don't have trouble taking my chemo drugs, but give me a psycho pharmaceutical and my compliance drops. I am being compliant now after banging my head on the wall a few times, as I have to accept this is not a personal "failure" but a body full of drugs that are wrecking havoc physically, psychologically and emotionally.

There is a lot of information about how cancer can be a cause of PTS and PTSD, but very little information about people who have PTSD and cancer. I joined a support group for the type of cancer I have, but I find that I have a really hard time relating. First I feel extreme guilt that my chemo didn't make me as "sick" as a lot of people. I also hate to admit that I find the cancer less difficult to deal with than I do the PTSD.

One thing a cancer diagnosis has done is make me want to get this disorder under the best control that I can as fast as I can. If I have limited time, then I want that time to be the best that it can be. Having PTSD wrecking havoc in the present is not acceptable so I am fighting it as hard as I am the cancer.

The type of cancer I have is considered "incurable", but I elected a treatment plan that is about as aggressive as they come. Monday I have my bone marrow biopsy to see if this last round of chemo finished off the last of the cancer so I can be ready for the transplant. The chemo will put me in remission, but the stem cell transplant is the best option I have of staying there for the longest period of time possible.

To bad there is a transplant to replace that part of my brain where everything is all scrambled. But there isn't a quick fix for the PTSD and there isn't a quick fix for this cancer. But they are both connected as some level and I need to put both into remission to live and enjoy the time that I have.

So the battle is on!
 
The type of cancer I have is considered "incurable", but I elected a treatment plan that is about as aggressive as they come.
You are a warrior, Deb, and though I know you have mentioned before that you don't know how to NOT fight, what you have been dealing with is enough to take down even the most determine of us. You have been wise in keeping with your team, sharing here, taking good and thoughtful care of your body. Your decision to get Luke is one that feels like one of the most important. Animals have such gentle healing spirits.

I LOVE that you have opted to go with this aggressive treatment, it's only fitting for the woman you are. I have no doubt the challenges it presents. My heart is with you. I am not a religious person either but I do believe in powers greater than myself so prayers are always with you.

((((((((((((Hugs))))))))))))))))))
Rain

le_courage.webp
 
Status
Not open for further replies.

Donation drives

2026 Donation Goal

Goal
$1,800.00
Earned
$910.00
This donation drive ends in
0 hours, 0 minutes, 0 seconds
  50.6%

Trending content

Featured content

Back
Top Bottom