Hi!
So much has happened since I last updated
this blog! I have to admit, the last time I wrote, I was not in the best of
places. I was really run down, feeling sad and just wanted everything to be
over. Over the past 30 or so days things have really started changing for the
better.
I'm home- as in my home, the place where my
stuff is, for the foreseeable future! I don't have to worry about going in for
more chemo, leaving my daughter or have any more scheduled hospital stays! Of
course if I got sick that all changes, but its nice to know I don't have any
more scheduled treatments and its mostly just recovery from here on out. I
still have to travel into the city for my doctor appointments once a week which
can be a long commute, but its so worth it.
At my doctor appointments, I get my blood
taken every week where they check for various things such as hemoglobin,
platelets, white blood cells, electrolytes, my medication levels, and so many
other things. There's probably about 8 tubes each time! My doctor also checks
for any signs of graft vs. host disease, which I have been mildly experiencing.
Since I left the hospital, I had a pretty bad rash all over my face and neck.
It is most likely graft vs. host disease, where the donor cells attack your
own, but just a mild form. It's been going on for a little over two months now,
but its getting better. I have to be very diligent about wearing sunblock as
these graft vs. host rashes are light sensitive.
Now that I am approaching 100 days, many of
the restrictions I had are slowly starting to be lifted. The first place I went
to was the mall to take Emma to see Santa. I had to wear a mask and gloves,
which is weird but I didn’t care. I was just so excited to be out in the
community again! This week my doctor said I don’t have to wear the mask and
gloves anymore, but I cannot be in any large crowds or near sick people. I just
try to time my shopping trips when I know the stores won’t be crowded. I am
also allowed to go to restaurants now, but have to still be very careful with
cleanliness and choose trusted places. I still have to avoid raw vegetables and
salads unless I make them myself to ensure everything is washed properly. My
next countdown is the next time I can have a drink! I have to wait until I’m
off certain medications, probably about three more months.
I still have a PICC line in my arm and have
to give myself IV magnesium, probably for a few more months. It’s getting
easier, kind of just a way of life now. The last few days I’ve been getting it
over with in the morning and it kind of frees up my whole day (it takes 4
hours). Its definitely a challenge because I have to take care of Emma and
wheel around a pole that’s connected to my arm, but I’m getting the hang of it.
Last week was Thanksgiving. We had a small
but great Thanksgiving with my parents. Thanksgiving has always been my
favorite holiday- its about family, being appreciative for what you have and
food. I like that there’s no stress of gifts and people can just be happy
together. I’m always thankful, but in
particular this year I am thankful to be alive. I would say there were probably
three solid instances where I came pretty close to dying throughout this
process so far; but instead, I’m here and got to celebrate with my wonderful
family. I’m so thankful to have the best doctors taking care of me- who have
showed such skill, but also compassion for treating our delicate situation. I
am thankful for my husband who has never left my side, literally sleeping in a
chair for months in the hospital. I am thankful for my daughter, who lights up
my life and keeps me going. I am thankful for my brother for donating his stem
cells, without them there’s a chance I wouldn’t be here. I am thankful for my
mom for putting her life on hold to take care of Emma and I. I’m thankful for
family that traveled thousands of miles to come see us. I am thankful for the
continued love and support I receive daily from friends, family, and loved ones,
it truly makes such a difference. There’s definitely more I’m thankful for, but
I’d be here all day.
On that note, I’m definitely looking forward
to the holiday season and being together with my family. My life has changed
and all for the better. Obviously I wish this never happened, but I have such a
deeper appreciation for life and for the love that surrounds me.
As always, thank you for the continued love
and support! Have a wonderful holiday season!
Kristin
What a beautiful message of gratitude. Thank you for continuing to share your story. I hope you continue to be stable in your recovery and wish you the best always. Enjoy your first Christmas with your beautiful daughter. Much love to you all.
ReplyDeleteAs always kristen you are always in our prayers .you are truly amazing .a beautiful soul. We love you and will continue to pray for you and your beautiful family xo
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