Life ain’t always glitter and rainbows... how much you choose to be negative about directly influences how your life will end up. I will always find glitter in old soggy confetti.
Today is the day... I guess I get a new birthday today along with my new immune system. I am so at a loss for words right now. Really I just wanna be with Zoey, Z, mama and sisters. I want to be with my sister while she is going through the process of harvesting the stem cells. I know that isn’t easy. So much going through my head right now... just know that I am eternally grateful to everyone! Ya’ll strength and praying has brought me here. Even if you didn’t pray your well wishes provided momentum. I love you all!
Ask not for a lighter burden but for broader shoulders. - Jewish proverb
Almost there, just have to strap in and push through.
When I'm out of the hospital for a week or 2 weeks I try to document my family as much as I can. They are definitely a huge part of my life.
One of the saddest things about being in a hospital for 3 weeks has nothing to do with me. It is seeing the amount of people being life flighted in everyday. I see this helicopter fly in at least 3-4 times a day... hopefully the people they fly in get to walk out.
Methotrexate is used to treat certain types of cancer or to control severe psoriasis or rheumatoid arthritis that has not responded to other treatments. It may also be used to control juvenile rheumatoid arthritis. Methotrexate belongs to a class of drugs known as antimetabolites. It works by slowing or stopping the growth of cancer cells and suppressing the immune system.
Temporary hair loss may occur. Normal hair growth should return after treatment has ended. Mouth sores, diarrhea, signs of anemia (such as unusual tiredness, pale skin), signs of liver problems (such as dark urine, persistent nausea/vomiting, stomach/abdominal pain, yellowing eyes/skin), easy bruising/bleeding, black stools, enlarged glands/lymph nodes, bone pain, unusual pain and discoloration of the skin, signs of kidneyproblems (such as change in the amount of urine), dry cough, muscle weakness, weakness on one side of the body, neck stiffness, severe headache, vision changes, irregular heartbeat, mental/mood changes, seizures.
This medication may lower your ability to fight infections. This may make you more likely to get a serious (rarely fatal) infection or make any infection you have worse. Tell your doctor right away if you have any signs of infection (such as fever, chills, persistent sore throat, cough).
Reducing the toxic effects of methotrexate and certain other medicines (folic acid antagonists). It may also be used to treat other conditions as determined by your doctor.
Leucovorin is a folic acid derivative. Methotrexate and the folic acid antagonists block the body's production of folate. Leucovorin works by replacing folate in the body.
Though these are very rare, Severe allergic reactions (rash; hives; difficulty breathing; tightness in the chest; swelling of the mouth, face, lips, or tongue); fainting; seizures.
Nausea, vomiting, loss of appetite, diarrhea, headache, dizziness, and pain/swelling/redness at the injection site may occur. Nausea and vomiting can be severe. In some cases, drug therapy may be needed to prevent or relieve nausea and vomiting. Not eating before your treatment may help relieve vomiting. Changes in diet such as eating several small meals or limiting activity may help lessen some of these effects.
Temporary hair loss may occur. Normal hairgrowth should return after treatment has ended. Fever with body aches, muscle/bone pain, chest pain, eyeredness/itching/pain, painful/difficult swallowing, anal sores, signs of kidney problems (such as change in the amount of urine), painful/difficult urination, joint/side/back pain, pain/redness/swelling of the arms/legs/feet, numbness or tingling of hands/feet, freckling, big toe pain, trouble breathing, black/bloody stools, blood in the urine, vomit that looks like coffee grounds, vision problems (including blindness), mental/mood changes (e.g., confusion), unexplained drowsiness, unconsciousness, enlarged abdomen, trouble walking, muscle weakness, loss of coordination, inability to move (paralysis), seizures.
This medication can lower the body's ability to fight an infection. Notify your doctor promptly if you develop any signs of an infection such as fever, chills, unusual cough, or persistent sore throat.
A very serious allergic reaction to this drug is unlikely, but get medical help right away if it occurs. Symptoms of a serious allergic reaction may include: rash, itching/swelling (especially of the face/tongue/throat), severe dizziness, trouble breathing.
I took this image on the day my life changed for ever. My doctor called me and told me to go to the nearest ER because my platelets were extremely low and I was at risk. On the way to 2nd ER (the first was a 24 hr Small ER) my lower back pain was excruciating, my one smidge of comfort came when I folded myself up and put my feet on the dashboard.
After 6 hrs and many, many vials of blood later, I had my diagnosis. Z and I cried for a minute... to be honest, as soon as I heard the words "Leukemia" Zoey popped in my head. I started to think about all the things I wouldn't be able to teach her and all the memories I'd miss. That's why I cried... I didn't give a damn about what was wrong with me. People get diagnosed with cancer everyday, I am no different.
Now this post isn't gonna be all sad and mushy, I'm happy to say I've been in remission since late May. My job is to keep that streak going and that's exactly what I will do. I will be around for a very, very long time friends.
Home sweet home! After 29 days (round one chemo) of being away from Z, Zoey and my home... I just wanted to relax with them. You never truly know how blessed you are until it is taken away. Hold everyone you hold dear tight... very tight, for they could be taken away as soon as they step outside the door.
The title says it all... at the beginning it took me more time to get "in" the restroom than it took to "go" to the restroom. Since this is my 4th round here, I'm a damn pro at maneuvering my IV stand in such a small space. Gotta remember to put that down in my resume.
While I'm at the hospital about to start my 4th round of chemo this image marks the end of my first round of chemo. Going home for a week, the nurses had to remove my pic line. If you don't know what a pic line is, it is basically a direct line to the heart when inserted.Going home for a week, the nurses had to remove my pic line. If you don't know what a pic line is, it is basically a direct line to the heart when inserted.
It is where they gave me the chemo, where they withdrew blood and where they gave me infusions if need be. I thought that since this thing has been inserted in my arm for a better part of a month, that it will hurt like hell coming out. To my surprise, it didn't... it felt like string being dragged over my chest and on to my shoulder. Very weird sensation. All images after this will be from my 2nd and 3rd rounds of chemo.
4 am... I might not look happy but I was elated! The nurse come in at 1am and told me I might be going home in the morning (I did). I'm not a big smiler hence my face but I just couldn't go back to sleep. I was excited to spend time with Zoey and Z, I was excited for fresh air and anything other than level 8 of Methodist Oncology ward.
P.S. This is from my first round of chemotherapy, I'm now about to start round 4.
This series of images are from when I had to have a bone marrow biopsy and a spinal tap. Didn't feel as bad as it sounds, both were painless (well not painless, they knocked me out before the bone biopsy). My protocol calls for a bone biopsy every 3 weeks to check my levels. The spinal tap was just to make sure my Leukemia didn't travel there as well. A quick breakdown of the numbers on the board...
WBC = White blood cell count, normal is 3.5
HGB = Hemoglobin, normal is 15
PLT = Platelets, normal is 100
The day before my platelets were 11 (once you go below 10 you get a transfusion) but was given a transfusion so that my platelets would be high enough so that I wouldn't bleed out after the biopsy. Dropping a little knowledge on ya... the more you know.
Two vials of blood every night between the times of 12:00 - 12:45am. They do this for labs so that they can monitor your blood levels everyday to see if you might need a blood infusion or platelet infusion. Waking up at 12am or so isn't as irritating as you'd think it would be when your life depends on it. I just learned not to go to bed until after labs are drawn.