Updates of the insomnia plagued

It’s 4:30 in the morning and I can’t sleep. My insomnia is not new…it comes and goes like all of my side effects. I’m lying on the couch, listening to classical music, attempting to shut my brain down, but I haven’t much hope.

It occurs to me that I never even posted about my new treatments! How strange!

I’m still on the Z, but on half the dose. I wish it meant 1/2 as many side effects, but instead, it means they’re not as bad. Silver lining?

A standard day lately includes sore soles of my feet (considering learning how to walk on my hands), small cysts on my face and neck that vary in size and pain level, joint pain, fatigue and a rash on my legs. (Let’s not forget the odd big toe numbness!) The funny part is that we don’t know if the side effects are from the Z or from the new treatment (IPI) that I’ve had 2 doses of. Guess it doesn’t matter much!

The infusions have gone well…maybe next time I’ll walk you through it with me. :)

The infusion itself is IV and takes about 90 minutes. I generally read, listen to music or doze off, so it’s not too bad at all.

My biggest and most disheartening issue thus far with my side effects has been my left eye. I had a terrible bout of uveitis and in addition to it being one of the worst cases Dr. K has ever seen, it’s caused a fairly significant change in my vision. While my left eye has always been weaker, I’ve never felt like I needed to wear my glasses all the time. Now, however, the tv is even blurry.

The vision change is probably not going to reverse itself. I think it probably bugs me the most because I know in the back of my mind that the majority of my aches and pains are temporary. This one makes it all seem more real, if that makes sense.

But, things could always be worse, so I am thankful for what I have and more so what I don’t.

Cancer sure is a bitch. I’m certain there is nothing else out there that makes a person thankful for bad things happening to them because (a) it hopefully means treatment is working and (2) knowing things could be worse.

Anyway, treatment 3 of 4 is the day after my birthday and Mike is going with me. I’m supposed to stop the Z that day, too, so it ought to be interesting to see what my body does with that!

Have a lovely Thanksgiving, friends.

Represent! Lego Style

Matt and I made Melanoma Ribbons for the Lego Gallery wall at Lego Kids Fest today. Black isn’t quite the new pink, but we’re putting it out there!

A week of freedom

I’ve been off the Z for almost a full week now, due to the changing of my treatment plan and being so sick last weekend.

As much as I love the Z for SIGNIFICANT SHRINKAGE, I’m so happy for a break from the side effects! It’s funny though, as they seem to be cycling backward. My chicken skin has reduced quite a bit (yay!) but my bones feel so tender, giving a whole new meaning to funny bone not being funny – it’s a searing pain when I hit any part of my body on anything! And my hands/knuckles are totally tender and sore again. The hair loss is still happening, but at least I still have some, right?

I’m not as nauseous, I’m not [TMI] spending too much time in the bathroom, and my brain is almost working full time again!

I’m starting back on the Z on Monday for a week or so – half the dose, just to keep it in my system until we start Ipi on the 24th. The side effects of Ipi are supposed to be similar, but don’t generally kick in until the second + dose. Yay!

That’s all for now! Take care of you and yours, eh?

 

Melanoma Walk

Sunday, I took part in the 7th Annual KDB Melanoma 5K Run/Walk  . It was a chilly but perfect fall morning at Kensington and there was a great turn out! I’d never been involved in the walk before, and I honestly wasn’t sure I’d be able to this year. My mom did a fabulous job not only gathering friends and family to donate but also to walk in my honor.  She was even honored for being a top fundraiser!! She’s been my angel through all of this – we had buttons that say Dawn’s Angels!

 

 

 

Good news!!!!

I had my follow up appointment with MO today for the results of my PET scan.

The words “significant shrinkage” were said.

The phrase “these are the results I was expecting and looking for” was uttered.

We aren’t out of the woods yet, but the light is filtering through the leaves.

I’ll be on the Z for another week likely at full dose and then a reduced dose until I start the next phase of treatment.

Right now I’m just happy to have confirmation of shrinking.

Scan day

Today I had my PET scan to see how the last 3 months of taking Zelboraf has affected my cancer-ridden lymph nodes.

Hopefully they’ve shrunken away to nothing; gone baby gone.

I’ll find out the results on Wednesday morning when we meet with MO.

{all prayers, thoughts, mojo, juju, etc. appreciated!}

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They had a new flavor of contrast to drink today. After the debacle of trying the mocha one once, I tend to stick to berry, but today, I tries new : vanilla.
It wasn’t terrible.
Well, of course it was…it’s contrast. But it wasn’t vomitus so that is a bonus. ;)

I fell asleep during the scan…I think I just have to now.