I spent the last week up at Snowbird Resort with some of my closest friends. It was a great get away, even if it is only 30 minutes away. Snowbird has a lot of fun activities to do and is just beautiful. We spent our days relaxing and hanging out - being lazy mostly. We went to the pool. Cooked some good food. Went to dinner. Went up the tram to the top of the mountain, 11,000 feet. Had some fun visitors. It is always fun to spend time with the Alston clan, happy they include me on their family fun! Here are some pictures from the week.
I'm a 34 year old Utah girl who is fighting stage IV melanoma for a second time. Former caramel queen and coffee slinger. Finding out whats next, one day at a time.
Sunday, August 16, 2015
Monday, August 10, 2015
The car accident that saved my life
A year ago today I was leaving Vegas after a very fun weekend. We had gone to the Justin Timberlake concert (my favorite past time... #1 fan over here) and enjoyed some good girl time with my good friend Brooke. We hit the road to head home and when we were about half way home I dozed off (Brooke was driving). Shortly after that I was awaken by a large bang and then Brooke trying to stay in control of the car. We had been side swiped by the car next to us changing lanes. The speed limit at that point was 80mph. Both cars gained control and pulled off. I immediately was concerned for my back since I had had back surgery a short 5 months before. Nothing immediately hurt except my neck was a little tender. We were SO lucky we didn't lose control and flip or hit the median, it is amazing we didn't have more damage to us or the car. We exchanged information with the other driving and the car was alright to drive and we headed off. It took about 45 min of driving for me to fully lose it and freak out. I was so upset at the thought of a car accident so soon after my surgery and that something so quick could derail all the progress I had made in my rehabilitation. But I was so grateful for Brooke handling it so well and that we weren't hurt fully. As the days went by I started to feel a bit of nerve pain down my arm so I decided to get it checked out. The doctor ordered an MRI of my neck to see if there was any disc damage - and there was. About a month later I had a steroid injection into one of my discs and I thought that was that. It was two months later that the neck doctor called me and said that they reopened my MRI and there was a very large lymph node that needed to be checked out. I called my general doctor and was seen the next day. Thankfully my doctor is very thorough and ordered a CT scan to confirm the findings - just to make sure it wasn't that I was sick the week of the MRI as that can make your lymph nodes swell as well. The CT scan confirmed it and that it was a bit larger. My doctor then ordered a needle biopsy to see what was happening. That biopsy was THE WORST thing. It was traumatic even. The lymph node was so hard/firm that it bent the numbing needle! The biopsy was hard for the doctor to do and required a ton of pressure so it was intense. And you need three samples, What was supposed to take 15min (I googled it before going in to know what to expect) ended up taking over an hour. Definitely a rough day. After that I waited for the results and after two and a half long weeks it came back that it was in fact metastatic melanoma. My cancer had returned. That was January 14, 2015.
And so here we are. I say that the car accident saved my life because I wouldn't have had another scan for who knows how long. After you have 5 years of clear scans they stop scanning you and just do skin checks. My last scan before the accident was December 2013. It is only because I was hurt just enough to see a doctor that I was able to find the cancer before it spread past the lymph nodes in my neck. If not caught then it would have spread fast and most likely be terminal.
It is crazy how something that seemed so terrible at the time could be such a blessing in the end. Something I am truly thankful for. Whether it was my Gram pushing that car into us or some other force, who knows (that's about as spiritual as I will get... but something or someone was looking out for me that day)
Although it has been a crazy year it would have been even crazier if the car accident didn't happen. Everything does happen for a reason, as annoying as that sounds.
And so here we are. I say that the car accident saved my life because I wouldn't have had another scan for who knows how long. After you have 5 years of clear scans they stop scanning you and just do skin checks. My last scan before the accident was December 2013. It is only because I was hurt just enough to see a doctor that I was able to find the cancer before it spread past the lymph nodes in my neck. If not caught then it would have spread fast and most likely be terminal.
It is crazy how something that seemed so terrible at the time could be such a blessing in the end. Something I am truly thankful for. Whether it was my Gram pushing that car into us or some other force, who knows (that's about as spiritual as I will get... but something or someone was looking out for me that day)
Although it has been a crazy year it would have been even crazier if the car accident didn't happen. Everything does happen for a reason, as annoying as that sounds.
Friday, August 7, 2015
Baby Hairs
It has been over a week since my last treatment (injection/infusion) and I am feeling so good! I haven't had any side effects besides some fatigue but I don't really count that. I am hopeful that I will continue to not have any and things just keep going as good as they have been. It is really a great feeling to have energy to do things and not be sick. I feel like I am starting to have a handle on my life again, which is a great feeling after 8+ months of dealing with my cancer returning.
My hair has really started to grow - I didn't realize how much until I took a picture of it and compared it to one I took on 7/22. (2 1/2 weeks ago) Here are the pics..
It's amazing how much I lost but I am still thankful to have some of it left. My doctor said that I lost more than most people who go through biochemo. It's not a ton, but they are baby hairs and they are there!
Here is a picture of the tumor(s) and the size they are today. .
All in all things are going good and I couldn't be happier. I have two more weeks off before the next treatment and have some fun things planned.
xoxox
My hair has really started to grow - I didn't realize how much until I took a picture of it and compared it to one I took on 7/22. (2 1/2 weeks ago) Here are the pics..
7/22/15
8/7/15
It's amazing how much I lost but I am still thankful to have some of it left. My doctor said that I lost more than most people who go through biochemo. It's not a ton, but they are baby hairs and they are there!
Here is a picture of the tumor(s) and the size they are today. .
All in all things are going good and I couldn't be happier. I have two more weeks off before the next treatment and have some fun things planned.
xoxox
Thursday, July 30, 2015
Some good news on treatment day 4
I have now completed 4 days of injections and 2 infusions - two more combo days left! Half way there! Yesterday was a long day. I got to the hospital at 11:30 and didn't leave until about 6:15.. That's a long day at the hospital for anyone. They had a hard time starting my IV (nothing new) so that took much longer than needed and then they were behind in clinic - lots of people with cancer sadly. I had to see both my clinical oncologist and my surgical oncologist (which is also my clinical trial physician) as well as my clinical trial nurse for the injection. As I was being examined they said that the tumors feel softer and my main one that we are injecting all 5ml of drug into has shrunk 1cm. The newest spots, #3 and #4, are almost gone or untraceable. So we are only measuring the first two. Finally some good news! My oncologists are both optimistic about the treatment and pleased with my reaction thus far. After clinic I headed down to infusion and got my second infusion of Ipi while watching Cops and playing solitaire until my good friend Courtney came up and visited.
Huntsman Cancer Institute is so great. They know how to take care of their patients and spoil them. During infusion I get asked multiple times if I need anything and volunteers are so nice. I hope that when I feel better and have the time that I can volunteer up there. Their main volunteer is a charming older gentleman and when he asked if it was my first time there and I responded with it being my second, he asked if I had received my goodie bag. Nope - I got some great snacks but no goodie bag on the first one so he hurried off and got me an adorable chemo care kit. The kit included a book, a magazine, a neck pillow, an eye mask, hard candies for during treatment and soft socks. Such a small gesture that means more than people know.
I feel good today, no side effects except a bit of fatigue. I am told that I will probably feel some stomach issues come on in the next few days but for now I feel good. I tried to go to California this past weekend but I was flying on a buddy pass and the flights were too full to risk not getting back. I was pretty bummed cause I was looking forward to seeing my best friend and her extended family. I am hopefully able to get out to Cali sooner rather than later and that the side effects aren't too bad and allow me to do so. I will say that one of the hardest things about dealing with cancer is the inability to make set plans for the future because you just don't know how you will feel and if you will have the energy to do some things. I am doing soooo much better since chemo but I'm still not 100% and it could be months until then. I miss working and having things to do but have enjoyed meeting up with people for lunches and dinners and just enjoying my free time. I truly have some great friends and family.
I have three weeks off of treatment and am hoping I feel good throughout it and have some fun times ahead. I have a week long staycation planned with some good friends up at Snowbird, Utah so I'm looking forward to that. It has become a tradition and should be a lot of fun.
Until next time, taking everything one day at a time. . .
Huntsman Cancer Institute is so great. They know how to take care of their patients and spoil them. During infusion I get asked multiple times if I need anything and volunteers are so nice. I hope that when I feel better and have the time that I can volunteer up there. Their main volunteer is a charming older gentleman and when he asked if it was my first time there and I responded with it being my second, he asked if I had received my goodie bag. Nope - I got some great snacks but no goodie bag on the first one so he hurried off and got me an adorable chemo care kit. The kit included a book, a magazine, a neck pillow, an eye mask, hard candies for during treatment and soft socks. Such a small gesture that means more than people know.
I feel good today, no side effects except a bit of fatigue. I am told that I will probably feel some stomach issues come on in the next few days but for now I feel good. I tried to go to California this past weekend but I was flying on a buddy pass and the flights were too full to risk not getting back. I was pretty bummed cause I was looking forward to seeing my best friend and her extended family. I am hopefully able to get out to Cali sooner rather than later and that the side effects aren't too bad and allow me to do so. I will say that one of the hardest things about dealing with cancer is the inability to make set plans for the future because you just don't know how you will feel and if you will have the energy to do some things. I am doing soooo much better since chemo but I'm still not 100% and it could be months until then. I miss working and having things to do but have enjoyed meeting up with people for lunches and dinners and just enjoying my free time. I truly have some great friends and family.
I have three weeks off of treatment and am hoping I feel good throughout it and have some fun times ahead. I have a week long staycation planned with some good friends up at Snowbird, Utah so I'm looking forward to that. It has become a tradition and should be a lot of fun.
Connect the dots...
Happy my energy is coming back (and my baby fuzz hairs)
In the infusion room
Still swollen but it actually has gone down if you can believe it
Until next time, taking everything one day at a time. . .
Friday, July 24, 2015
Treatment #3 Done and New Hair!
Wednesday I had my third treatment and all went well. Last weeks injection made me super swollen and huge, this one not so much which is nice. Hopefully that doesn't mean it isn't working as good.. but we shall see. The injections haven't hurt really thanks to me not having any feeling on that part of my neck due to surgery. It has been a bit tight from the swelling and I can feel it inside my throat it was that swollen. This round isn't that bad. Next week I have my next infusion of Ipi and I am supposed to start feeling more of the side effects after that.
One fun thing that started on Monday is my hair is starting to grow back from chemo! My friend pointed it out and I told her that was a mean joke to play on me, but when I looked it really did start that day! It will be a slow process but I can see a dark hair in each follicle, it's a start! I'm excited to see what it is going to grow back in as... curly? a different color? We shall see!
I went to Bear Lake this last Monday for a night. It was a good getaway. I went with Maryann and Marty and their two boys, Ben and Jack. We camped and went to the beach. Had some food and just relaxed in a beautiful setting. I was pretty tired when I got home but it was worth it.
Today is Pioneer Day in Utah and I'm looking forward to my dads insane firework show tonight. He is a nut and has some of the biggest and scariest fireworks - it's great! I love big fireworks and it is always good to have the whole family together.
Tomorrow I am hopefully going to California to see my best friend until Tuesday. I am flying on a buddy pass so here's hoping I get on the flights! Her cousin, aunt and mom are visiting too so it will be a fun group of people. I need to go to Cali every 6 months or so for my sanity.. I am overdue. It will be good to get out before more side effects kick in.
I may have cancer but cancer doesn't have me. I will have as much fun as possible as I feel better. On to the next adventure!
One fun thing that started on Monday is my hair is starting to grow back from chemo! My friend pointed it out and I told her that was a mean joke to play on me, but when I looked it really did start that day! It will be a slow process but I can see a dark hair in each follicle, it's a start! I'm excited to see what it is going to grow back in as... curly? a different color? We shall see!
I went to Bear Lake this last Monday for a night. It was a good getaway. I went with Maryann and Marty and their two boys, Ben and Jack. We camped and went to the beach. Had some food and just relaxed in a beautiful setting. I was pretty tired when I got home but it was worth it.
Today is Pioneer Day in Utah and I'm looking forward to my dads insane firework show tonight. He is a nut and has some of the biggest and scariest fireworks - it's great! I love big fireworks and it is always good to have the whole family together.
Tomorrow I am hopefully going to California to see my best friend until Tuesday. I am flying on a buddy pass so here's hoping I get on the flights! Her cousin, aunt and mom are visiting too so it will be a fun group of people. I need to go to Cali every 6 months or so for my sanity.. I am overdue. It will be good to get out before more side effects kick in.
I may have cancer but cancer doesn't have me. I will have as much fun as possible as I feel better. On to the next adventure!
Tumor borders
Extremely thin hair but with lots of little guys coming in - especially in the front!
(scar on my scalp is from my first round of Melanoma in February 2009)
Right after the injection - not too bad!
Beautiful Bear Lake, Utah
Thursday, July 16, 2015
Day Two Of Treatment Done
Yesterday was my second day of my new treatment and it went well. This past week has been good and I haven't had many side effects besides being tired and swollen at the injection sites. Inflammation at the site is a good sign as it means that white cells are swarming the area and hopefully fighting the cancer cells. When I went in yesterday there was 4 swollen areas, possible tumors but we aren't sure (two are for sure tumors). It just means that if the medicine is working that the areas are swollen because they are being destroyed! That's the hope. The main tumor almost doubled in size which is scary but like I said I'm hopeful that it is the drug working and not the tumor growing out of control. My doctors feel it is the medicine which is nice to hear.
My surgeon saw my healed scar for the first time yesterday and wasn't too happy with how it looked. As you can see in the pictures, it isn't a happy scar and he wasn't happy about it. He said once we kick this cancer to the curb that he will go in an fix it. I'm not excited for another surgery but happy to have a better scar as it is pretty crazy. We shall see how it all works out.
I truly am so lucky to have such a great medical team at Huntsman Cancer Institute. They are invested in my fight and talk to me as a person and not a walking melanoma case. While waiting for my drug to be ready yesterday a nurse and I talked about local restaurants to try. It's the little things that mean a lot to me.
One of my best friends has made the comment that I'm not a walking melanoma, I'm still Alexis. I just happen to be fighting melanoma. This hit me hard because for the past 7+ months that's what I have felt like - like all my worth is tied to my fight right now. I need to still focus my energy on being me and not just my fight. It is a hard thing to change focus on but it will be needed so I can start my new life after cancer. Whatever that life will be.. That part I'm still trying to figure out.
Wednesday, July 8, 2015
First day of new treatment
I have officially finished my first day of the new treatment. It was a semi long day but not too bad. To explain the treatment I am doing again I am receiving injections of HF10 (a modified herpes simplex virus) directly into the two, yes two, tumors in my neck. The injections are supposed to alert your immune system to a problem in the tumor and in turn it will attack the melanoma. Then in turn it should act as a vaccine so if there are other melanoma cells in the body it will kill them as well. I will receive 7 injections. I am also receiving 4 infusions of Ipilimumab (Ipi) which is an immunotherapy drug approved for the treatment of melanoma.
Today I was told there is a second tumor in my neck, right next to the other one. Also, the larger tumor of the two is growing fast so I am hoping this treatment starts working soon. The injections were virtually painless and quick once the drug was ready which was a pleasant surprise. The infusion was done in a very nice setting and a good friend came and helped me pass the 1 1/2 hours it took to infuse which was great. I haven't felt any side effects besides being tired, soreness of the injection site and a slight headache. The Ipi has the potential for more severe side effects - mostly bowel issues. I'm hoping they aren't too severe and pass quickly.
I am happy to have this treatment underway and have good feelings about it. Hoping things all go as planned and this is my final treatment. Period. Here's hoping the next few months are beneficial!
Today I was told there is a second tumor in my neck, right next to the other one. Also, the larger tumor of the two is growing fast so I am hoping this treatment starts working soon. The injections were virtually painless and quick once the drug was ready which was a pleasant surprise. The infusion was done in a very nice setting and a good friend came and helped me pass the 1 1/2 hours it took to infuse which was great. I haven't felt any side effects besides being tired, soreness of the injection site and a slight headache. The Ipi has the potential for more severe side effects - mostly bowel issues. I'm hoping they aren't too severe and pass quickly.
I am happy to have this treatment underway and have good feelings about it. Hoping things all go as planned and this is my final treatment. Period. Here's hoping the next few months are beneficial!
Subscribe to:
Posts (Atom)
































