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Stem Cell Transplant ( Sct )

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You made the best decision you could with all the info/facts in front of you. That is all ANYONE can do! You knew it was not the easiest road, but so far it has worked out. So trust that this last step will do what it needs to as well!

(((your concerns)))
 
Been tweaking on my thinking this morning. I have been doing a countdown in my head to the day I enter the hospital. Only this countdown has been something like checking off days before I go to prison, or in some cases to my execution. WRONG! Definitely "stikin thinkin".

So time to look at it from a new perspective and a much healthier perspective. See, next Wednesday, December 19th, I will receive my new stem cells. Not that the transplant is a big deal, it is basically an IV bag and the new cells go in. But from a medical standpoint this is called day zero, as it is a total new beginning for your immune system. A new birth of sorts.

So today is day 9 and I am counting down to day 0, when I get my cells back and start to build cancer free bone marrow and a healthy immune system. Instead of dreading the procedure and the chemo and steroids that proceed it, I am going to focus on day zero and what that means. It means life for me, bottom line.

Instead of feeling sorry for myself for having to go through this, I need to count myself as blessed. First of all because I am able to do this procedure and secondly, because this is a second chance that not many get. I need to not only look at this as a second chance for health reasons, but it is also a second chance at life. Now how I approach it and what I do with it is entirely up to me.

As I go through this, I will journal as it benefits me and I hope that it benefits those that read it, whether it is battling PTSD, cancer or any other chronic illness. Yes, there will be ups and downs, but I am bookmarking this page for myself to remind myself why I am doing this and what it really means.

I really appreciate the support, encouragement, positive thoughts and prayers. I am going to need them as I do this and for all that contribute, I want you to know that you make a positive difference. I only hope to return it when you need it or pay it forward.
 
Deb you can do this. I believe in you. You are so strong, even if you do not feel strong right now. you have made all of the preparations and gotten yourself ready. Good for you for catching your thoughts. You will get this over with and begin your recovery. Mabe a book will come out of this. You are a talented and gifted writer. Something to think about. Hugs and prayers that your thoughts will be positive and prayers for inner strength to go on.:hug:
 
The Christmas tree is up and still need to have the ornaments put on it. I will have various children coming by here throughout the day. It is tough thinking that will be my last day at home for so many weeks. There really is no way to prepare for this, no matter how hard you try.

Been feeling scared today, but to be away from home during the holidays and know what a battle lies in front of me would scare anyone. I know I made the best decision based upon all of the recommendations by my doctors and all of the information I have been given and that I have found on my own.

Funny thing is, I am not afraid of the chemo, and I am not afraid of having my immune system destroyed. I am afraid of what happens to me when I take the steroids. I cannot put into words what it feels like, nor can I put into words how it effects me. All I know is those that have seen it happen say that I am "not me". The problem is, there is still a "me" inside that gets drowned out by the constant adrenaline. I remember the hallucinations and it is after I know they are not real. But in the midst of it it feels so real, even when I am trying to talk myself down from them.

It is the shock and the pain that I see in the faces of those around me that cuts the deepest. If I could stop it I would and I am glad this time I will be for all practical purposes locked in a room. I am also glad the medical staff is on notice and can keep me under control. I have also done my best to time things so there will be no one with me and no visitors when those drugs are administered and until they have me sedated enough the crazy train isn't a run away.

It is amazing how much worse mental pain is over physical pain. It is so hard to know you are losing control over your mind and there isn't anything you can do about it. People without PTSD also experience steroid psychosis, it is just a lot faster and harder with PTSD.

I am so hoping the test they are going to run indicates the medical problem I suspect. Because it is does confirm the underlying physical issue, it can be treated. There are no guarantees that it will eliminate the extreme reaction to the steroids, but anything that can help is welcome at this point.

This is the beginning of the road to recovery. I just want to leave the hospital with mind, body and spirit intact.
 
(((((((Dearest Deb)))))))), Big Big Prayers, LOVE, and support for you. You've done and are doing everything you can to prepare, and you've informed those who need to know what to expect- they WILL help you. Let go and let them do their specialty.

We love you and it will be ok, try to rest, be gentle with yourself, you are in Good hands.

Xoxoxoxoxoxoxoxoxoxoxoxoxoxoxoxoxox, (((((((((Deb)))))))).

(We can fight over who gets to eat the fruitcake when you get out. ;) :inlove: (((((((Love and strength to you))))))))) :hug:.
 
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