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Mojo Needed..Fellow HCer is hurting.


Kevman

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Hey Kevman,

So Sorry to hear about your son. I lost a childhood friend to Leukemia in the early 70s. MOJO and best wishes to your son and you and your family. Stay strong and he will follow your example. Good things can come from this; my wife's cancer fight brought me back to playing guitar and singing after many years away.

 

Brent aka gt5litre

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Kevman,

 

I can't say I know how YOU fell right now but I can tell you how I felt when my son was diagnosed with Acute Mylogenous (spelling) Leukemia (AML). I felt like there was no hope. He was 8 years old and he was SO sick. The cancer cells accumulated in something called the mastoid cavity near the ear and caused him extraordinary ear pain. His pediatrician thought it was an ear infection and treated him with several rounds of antibiotics before a different Dr. decided he should see a specialist. That specialist immediately sent him to Childrens Hospital to be assessed and admitted. He went through three months of hell but now he is a 6' 3" college junior preparing for a career in IT. I tell you all of this to let you know that there is a tomorrow and that your son can pull through this. We had a wonderful group of church friends who helped us through the ordeal. One word of advice, when people offer to help . . . let them. We sometimes think we are imposing on others, but they want to help you AND YOU WILL NEED THE HELP. If you would like to talk further with someone who has been where you are I would be glad to do that. You can private message me (I think this forum supports that).

 

God's Blessings! I'll be praying for your family.

 

Dan B

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Thanks again for all the positive vibes mojo and prayer.

 

Dustin started chemo on Tuesday 2 different chemicals (no way I could remember their names now) one into his spinal fluid and the other into the IV port in his chest. He has been on some pretty big doses of steroids (prednosone) since Monday.

 

These are all good things. His white bloodcell count is as of now "normal". He is down to 3mg an hour of morphine from 5mg and he is not using his pain button which supplies and additional 2mg every 10 minutes if needed. His lungs are exchanging oxygen and carbon dioxide much better, to the point that he only needs to be on oxygen when in a deep sleep.

 

He still has some blood clotting in his upper arm and one that has moved into his neck. He was supposed to get the next chemo treatment on Friday which has been put off untill Monday. Apparently he is still in enough risk to be in the ICU under close watch. He is loosing weight, his face is loooking thinner even though the steroids are supposed to increase his appetite he has not been eating much at all (this is a kid who is 6'2" and 225# befoer he got sick).

 

All in all I am encouraged. I have no choice.

Hopefully the blood clotting issues will have worked themselves out by MOnday so that the good doctors can continue with the chemo. The next chemical they need to inject directly into his thigh into deep muscle tissue.

This chemical also has the side effect of causing blood clotting, hence the worry. This is also a stage of treatment that cannot be skipped. INstead of doing 9 seperate doses of this leg shot over the next couple of weeks they are going to give him one super mega dose. I believe that this is also the chemical that tends to cause hair loss.

As I am sure some of you can relate. He is bumming big time about that probability.

 

We are far from out of the woods. We do thank this forum for all of the support though. You guys rule on ice. By the way. There IS a guitar in the ICU now just in case he feels like getting his jam on on.

 

Peace out. I will keep you posted.

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