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Randi's journey with melanoma

Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Friday, December 30, 2011. We will all miss her dearly and hope that her posts gave you the encouragement and support she welcomed from others coping with this relentless disease. Always have hope, always stay strong and never give up! Links to this post. Friday, December 16, 2011. NURSE CAME OUT A COUPLE OF TIMES TO DRAW BLOOD AND CHANGE PICK LINE DRESSING. HAD TO BE TAKEN TO DR OBARAS OFF...

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Randi's journey with melanoma | randisohnomelanoma.blogspot.com Reviews
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Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Friday, December 30, 2011. We will all miss her dearly and hope that her posts gave you the encouragement and support she welcomed from others coping with this relentless disease. Always have hope, always stay strong and never give up! Links to this post. Friday, December 16, 2011. NURSE CAME OUT A COUPLE OF TIMES TO DRAW BLOOD AND CHANGE PICK LINE DRESSING. HAD TO BE TAKEN TO DR OBARAS OFF...
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Randi's journey with melanoma | randisohnomelanoma.blogspot.com Reviews

https://randisohnomelanoma.blogspot.com

Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Friday, December 30, 2011. We will all miss her dearly and hope that her posts gave you the encouragement and support she welcomed from others coping with this relentless disease. Always have hope, always stay strong and never give up! Links to this post. Friday, December 16, 2011. NURSE CAME OUT A COUPLE OF TIMES TO DRAW BLOOD AND CHANGE PICK LINE DRESSING. HAD TO BE TAKEN TO DR OBARAS OFF...

INTERNAL PAGES

randisohnomelanoma.blogspot.com randisohnomelanoma.blogspot.com
1

Randi's journey with melanoma: PRETTY FEET AND TOES

http://randisohnomelanoma.blogspot.com/2011/08/pretty-feet-and-toes.html

Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Sunday, August 7, 2011. PRETTY FEET AND TOES. LOOK AT MY PRETTY FEET AND TOES! SKINNY TOES AND PAINTED NAILS. NO SWOLLEN FEET OR ANKLES! LITTLE SAUSAGE TOES ARE GONE. 2 WEEKS ALMOST WITH SAUSAGE FEET IS ENOUGH TO DRIVE ANYONE INSANE. OKAY SO NEW CAMERA AND MUCH EASIER SOFTWARE TO USE-GEEZ. DONT BUY SAMSUNG ANYTHING! CAN'T WAIT TO GET OUTTA THE HEAT HERE. CALIFORNIA WEATHER SHOULD BE NIC...

2

Randi's journey with melanoma: BACK TO LA

http://randisohnomelanoma.blogspot.com/2011/11/back-to-la.html

Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Thursday, November 17, 2011. BACK TO LA NEXT WEEK. YES, I KNOW ITS THANKSGIVING BUT I NEED TO FOLLOW UP WITH DR HAMID AND HE HAS AN OPENING AT THE BEGINNING OF WEEK. SCANS WILL BE RIGHT AFTER THANKSGIVING AND I AM NOT LOOKING FORWARD TO IT AT ALL. HOPEFULLY I CAN EAT-SINCE MY SALIVA IS LIMITED BUT SEEMS TO BE JUST A LITTLE BETTER NOW. NOTHING IS EASY ANYMORE. WHO HAS THE LIFE? May 1, 2016.

3

Randi's journey with melanoma: Fridays

http://randisohnomelanoma.blogspot.com/2011/12/fridays.html

Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Friday, December 16, 2011. WELL-SPENT THE WEEK LEARNING HOW TO CHANGE LINES AND NUTRITION BAGS BUT WE HAVE IT ALL PRETTY MUCH FIGURED OUT NOW. DON'T HAVE TO CARRY ALL THIS STUFF TO BATHROOM NOW-WE HAVE ALL THAT FIGURED OUT TOO. NURSE CAME OUT A COUPLE OF TIMES TO DRAW BLOOD AND CHANGE PICK LINE DRESSING. NOTHING TO EXCITING- MOSTLY ABOUT ALL THIS STUFF. 65279;. NOODLE IN THE TREE-HAH.

4

Randi's journey with melanoma: At Peace

http://randisohnomelanoma.blogspot.com/2011/12/at-peace.html

Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Friday, December 30, 2011. We will all miss her dearly and hope that her posts gave you the encouragement and support she welcomed from others coping with this relentless disease. Always have hope, always stay strong and never give up! December 30, 2011 at 8:04 PM. December 30, 2011 at 8:47 PM. December 30, 2011 at 8:52 PM. My thoughts with Randis family for whom she had conveyed her love s...

5

Randi's journey with melanoma: NEW DEVELOPMENTS

http://randisohnomelanoma.blogspot.com/2011/12/new-developments.html

Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Saturday, December 10, 2011. WELL HAD TO HAVE A PICK LINE INSERTED AT SUNRISE YESTERDAY. NEED FLUIDS AND NUTRITION-SO HOME HEALTH CARE CAME OUT AND GAVE ME AND TIM OUR FIRST LESSON. I WILL HAVE FLUIDS WITH VITAMINS THEN EASE INTO SOME NUTRITION. THE DRS WANT ME TO BE STRONG ENOUGH TO TAKE MY NEXT DOSE OF YERVOY WHEN THE TIME COMES AND THIS IS THE WAY TO DO IT-. December 10, 2011 at 1:04 PM.

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thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: Update

http://thewilemansjourney.blogspot.com/2011/09/well-if-you-live-around-here-and-dont.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Sunday, September 18, 2011. Well if you live around here and don't love this weather something is wrong with you. Of course the three days of the coolest weather we had here I had to spend in Houston where it was still 100 degrees! Remember everyday to put one foot in front of the other, drink a lot of water, and don't forget to breath. September 19, 2011 at 10:05 AM.

thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: Too Long

http://thewilemansjourney.blogspot.com/2011/11/too-long.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Friday, November 25, 2011. Remember everyday to put one foot in front of the other, drink a lot of water and don't forget to breath. November 25, 2011 at 10:51 AM. Praying for you and your family. Bobby and Laura Smith. November 26, 2011 at 10:24 AM. November 29, 2011 at 3:21 AM. November 30, 2011 at 12:42 PM. December 2, 2011 at 5:16 PM. December 3, 2011 at 10:10 PM.

thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: November 2011

http://thewilemansjourney.blogspot.com/2011_11_01_archive.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Friday, November 25, 2011. Remember everyday to put one foot in front of the other, drink a lot of water and don't forget to breath. Subscribe to: Posts (Atom). You can now donate to benefit account via paypal using the button below. View my complete profile. Kicking off 2015 with a bang! Randi's journey with melanoma. Em and Michael's Blog. September 18, 1999.

thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: May 2011

http://thewilemansjourney.blogspot.com/2011_05_01_archive.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Monday, May 30, 2011. The visit consisted of a CT Scan, MRI, Dermatologist visit, and Oncologist visit. Along with meeting with the research nurse to pick up the new chemo. (The MRI was much better on me this time! Well that is all for now. Don't have much to say, but wanted to give an update. Saturday, May 21, 2011. Dear Heavenly Father,. Thank you for my wife and the ...

thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: August 2011

http://thewilemansjourney.blogspot.com/2011_08_01_archive.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Friday, August 19, 2011. And it will be that way for months until soccer is over! Thank you again for all your thoughts and prayers. We need them now more than ever. I will try and do a better job of blogging and keeping everyone updated. Remember everyday to put one foot in front of the other, drink a lot of water, and don't forget to breath. Subscribe to: Posts (Atom).

thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: July 2011

http://thewilemansjourney.blogspot.com/2011_07_01_archive.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Saturday, July 30, 2011. Well that is about it for now. We are getting ready for school to start. I think the kids are ready, which is amazing. Everything else is well, except for this heat and lack of rain. Hopefully we will get started on the new drug sooner, rather than later. As soon as we know something we will let everyone know. Tuesday, July 19, 2011. Remember ev...

thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: October 2011

http://thewilemansjourney.blogspot.com/2011_10_01_archive.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Thursday, October 13, 2011. Remember every day to put one foot in front of the other, drink a lot of water and don't forget to breath. Wednesday, October 5, 2011. It was a great day. The kids are doing good, staying busy as always. Lots of sports and school work. Rebecca is good with another crazy work week and taking care of me. Subscribe to: Posts (Atom).

thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: April 2011

http://thewilemansjourney.blogspot.com/2011_04_01_archive.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Tuesday, April 26, 2011. When it rains it pours. But, as I have said many times, we cannot do this without each of you and the thoughts and prayers you have continued to offer up for us. We pray simply for peace, guidance, and comfort. Thank you again to each of you. Remember everyday to put one foot in front of the other, drink a lot of water, and don't forget to breath.

itsonlymelanoma.blogspot.com itsonlymelanoma.blogspot.com

It's Only Melanoma: December 2011

http://itsonlymelanoma.blogspot.com/2011_12_01_archive.html

Saturday, December 31, 2011. How do you say goodbye to a year that has both blessed and cursed you? How do you welcome in a New Year with all the promise it brings while you live in fear of more health problems, and while you watch while people with your kind of cancer drop away? I am conflicted this New Year's Eve. I'm stronger than I thought I was. When I wonder if it will come back, and when.where in my body.how long will I fight. Welcome to Cancer-Land, it's a whole other country. Cry for the people ...

thewilemansjourney.blogspot.com thewilemansjourney.blogspot.com

Our family's journey with Melanoma: February 2011

http://thewilemansjourney.blogspot.com/2011_02_01_archive.html

Our family's journey with Melanoma. Andy's diagnosis of Aggressive Melanoma, the surgery, treatment and our family's journey throughout. Thursday, February 24, 2011. I was asked by someone this week to share my thoughts on living and dying. The request was based on the question, if you were told you had a year to live, what would you do? One of the other things I hear is, I would quit my job. So far, the cancer has taken care of that for me! Do I have a few things I would like to do before I die? But I w...

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Randi's journey with melanoma

Randi's journey with melanoma. My Personal daily fight to kick this cancers BUTT! My peeps in San Fran last summer. Friday, December 30, 2011. We will all miss her dearly and hope that her posts gave you the encouragement and support she welcomed from others coping with this relentless disease. Always have hope, always stay strong and never give up! Links to this post. Friday, December 16, 2011. NURSE CAME OUT A COUPLE OF TIMES TO DRAW BLOOD AND CHANGE PICK LINE DRESSING. HAD TO BE TAKEN TO DR OBARAS OFF...

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Visit my on line store. Saturday, July 25, 2015. July Pop By Gift Ice Cream Scoops. For all Realtors whom want to stay in close contact with their clients . These are cute Pop-By work great to achieve to stay in close contact with your clients. The Tag reads; Giving you all and all your referrals the Real Estate news! The Ice Cream Scoop Tag will hold your standard size business card. Links to this post. Make it special make it handmade. Subscribe to: Posts (Atom). Follow us on Instagram. You Blow Me Away.

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A Day in the Life of Randi Sparks

A Day in the Life of Randi Sparks. Wednesday, October 29, 2008. Visit from the Letniaks. Tuesday Moring after Angie and kevin did their routine visit to the docotrs, they where told that they would be reffered to Edmonton to the burn unit at the University Hospital of Edmonton and that they would have to report there on Wednesday morning. I was devistated as I thought that our visit was cut short and was overwhelmed with concern that they would get bad news from the specialist in Edmonton! With all of th...

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Georgia on my Mind

Georgia on my Mind. Monday, November 2, 2015. I'm sure this photo was taken when a great song was on, like yeah by usher. I put a little bit of effort into this get up. I am not good at this game, also we didn't have doughnuts. These are much harder to eat. Not the mouse in my pocket, but the other PCVs living in Poti. This was really just me in a red dress and make up. Monday, October 19, 2015. Saturday, October 10, 2015. The Black Sea receives more fresh water then it evaporates. Poti for the win.