First, the good news: Chuck is doing very well with his liver transplant. April 29 will mark the one year anniversary of his transplant at the Mayo Clinic. He's showing no signs of rejection, is off 80% of his medications, and his follow up tests and visits show him to be a super star. He's back to photographing birds every morning with my son, even in minus 5 degree weather, so that pretty much says it all. My avatar pics are of his birds.
Now for the bad news: I've mentioned before having a surface melanoma on my arm removed in October of 2021. An "in situ" mole of no consequence where all the melanoma 'was removed successfully'. This was a result of having a dozen beauty marks on both arms blow up like balloons after the 2nd Covid shot, grow scabs on them, and when the scab fell off, the beauty mark disappeared entirely. Except for the one. And all of it was not successfully removed after all, as a few cells must've escaped into my body and caused metastatic stage 4 cancer in my lymph nodes, liver, and bones. I went to the ER 3 weeks ago for excruciating pain in my left side where a CT scan with contrast was ordered. The cancer was discovered at that time, and I've spent the last 2 weeks in testing. The cancer is not in my brain, thank God.
The Oncologist told me there is immunotherapy available now for malignant melanoma. 2 types at once, administered via IV (no port) every 3 weeks x4. That's the goal. To turn on my immune system to kill off this cancer. 50% of immunotherapy patients are alive 2 years later. Idk what the percentage is at the 5 year mark. I've avoided doing research bc I'm overwhelmed enough already.
I'm having tremendous pain in my spine, ribs and liver, where the cancer is the worst. The Oncologist gave me some heavy duty pain meds and told me to wait it out until the IV starts kicking in to relieve my pain. He said I would live less than 2 months without treatment so my first treatment is tomorrow morning. The side effects can be gnarly and these infusions WILL kick my butt, he said. I'm ready, I think. Ain't no beauty mark gonna take ME down at 65! 😑
I'm useless at home, so Chuck is doing everything. Laundry, cooking, grocery shopping, driving to appointments. I have a housekeeper coming in to do the heavy cleaning and my stepson and his wife are cooking 7 dinners for us and bringing them by on Saturday. I have to make sure HE'S not overworked during this treatment process to where he gets sick. He's already overcome with worry and shock over all this as it is. I'll ask my stepson to repeat that meal making plan, too...they want to help & we need help.
We've had a lot to deal with the past year, and now my issues, which were there all along, just not apparent until recently. We wouldn't have been able to handle TWO of us sick at once anyway, so this is how it had to play out, I suppose.
The one bright spot I hold onto here is the dime I found on the floor of the ER room I'd been in ALL DAY where there was no dime on the floor. And when the gal was wheeling me back into the room from the CT scan, there it was. I kicked it across the floor to Chuck and he said, "what's that?" I said, "it's a dime from dad, telling me everything will be alright." He was speechless. Dad used to send me dimes all the time after he died in 2015, but stopped the past few years. I have a whole piggy bank full of them.
We can use all the prayers we can get right now, friends. I believe in prayers, in miracles and in signs from our deceased loved ones that they are with us in tough times. If you do too, please send up some prayers for Chuck and I right now.
Many thanks.
"Leave a little sparkle wherever you go and watch the world light up around you".
This is you!
Thank you all for the support and kind words XOXOXO
That you still come here despite your vision challenges and are helping others is a wonder!
So thankful for you and how you’ve talked so many of us off of a ledge when we were so desperate.
May God grant you a successful surgery on your cataract!
Glad to hear Chuck is doing okay. 3 years post transplant is impressive.
Said a prayer for both of you.
Good luck with your eye surgery.
You are a marvel!
I often think of you when I'm feeling sorry for myself for
something/anything. I think if Lea can still be there for others
why can't I?
I don't know that I could maintain any kind of positivity
given your circumstances. I know you probably have your
moments but I would most likely be curled up in a fetal
position.
Stay strong. Both you and everyone on here.
I started PT for vestibular therapy in Sept I think it was. It's not helped me much, I can't get past a certain point w/o the vertigo symptoms getting SO BAD they incapacitate me. But I still do the head exercises which are for balance. I've come a long way from where I WAS 2 yrs ago, thank God.
Still No Evidence of Disease *NED* on the PET scans 😁
DD married in November and it was a fantastic wedding. We all looked beautiful, especially the bride.
Chuck is coming up on his 3 yr liver transplant anniversary, believe it or not, and down to monthly blood draws now!
We've both been quite sick the past month with what's being called the "para flu"......extreme cough, wheezing, stuffy nose, extreme fatigue and I've had a low grade fever for 3 weeks now. Recovery is a witch with a capital B 😑
Thats about it. I hope you are doing well after losing dh unexpectedly, I've thought of you often GG. And everyone else on this thread who's been so kind to me. Love to all.
You do very pretty work. It’s such an exciting time for your family. Thanks for sharing with us.
So happy for you, and thanking the Lord for you!
Bring on the bling!!!! ❇❇❇
I'm so thrilled and thankful to God that you'll be there.
Exquisite! Yes! That's the word for the bouquet!
Saw the bouquet and it is exquisite!
http://bit.ly/BouquetbyLea
Thanks to Colleen and thanks to God I was able to make this and that I'm still here to attend her wedding!! Hope you like it.
😊