Subscribe:

Ads 468x60px

Showing posts with label ale. Show all posts
Showing posts with label ale. Show all posts

Monday, June 6, 2011

what the pft?

As most of you know, I have had a terrible year plus. My pft's hit their all time low about 8 weeks ago at an fev1 of 51%. I was sick. It took some time, but the root cause of my systemic infections and inability to fight infections was finally identified and treated.

I went today to blow pft's and THIS is what happened:

That is an FEV1 of 134%.  What???? I was whooping and hollering and happy.. because I've spent, of the last 24 months, at least 18 of them with my port accessed and some cocktail of 2 or 3 antibiotics going into my system.  For the grace of god...
We also drew liver labs and did a sputum.
This topped off a really wonderful weekend.

About 5 miles from our home is a cute little lake and it happens to be ale's favorite summer spot... we spend most weekends there as a family or with friends... this weekend we spent saturday at the lake with some friends:

Ale looking out at the water

Cuddling into his monkey towel

Nitza drinks gatorade

He's the muddy king of the lake!!

... and much to Nitza's dismay.. a tadpole.

**********************************************
On Sunday we went to MA to celebrate my sister's graduation with a picnic.

Erin's Backyard

Erin and her diploma

Erin's card

Mom and Oscar

Kelly and Oscar

Oscar

Tom and Oscar

Brother Mike and his girlfriend and son

Me

Mom, Nitza and Ale

I am truly grateful for the abundance of my life.


Saturday, June 4, 2011

saturday (almost) sunrise

I'm up again. This time, however, it had very little to do with sadness and a racy mind, and much more to do with the great idea I had that we have a family slumber party... we got ale a full sized loft bed to go over his bed for a few reasons... the whole "nook" effect under, having a place for grandma and grandpa to sleep, and keeping his room updated to his age.

SO, i wanted to be sure nitza or i slept in that upper bed for comfort, safety etc before ale slept there alone, so why not call it a slumber party...

and so i am awake. the five year old sundial is skinny with bony elbows and knees, but the bed was fine :)

ale rode his bike for the first time this season yesterday. it was adorable. he is a very very cautious little guy. he has always approached life that way. last year on his bike he peddled, but stayed close to me. this year, i put his helmet on him and did the whole bike safety check thing and helped him on the bike and turned to close the garage door and the boy was gone... like lightening bolt. so he gave me his "taggie" to hold and I ran roadside next to him while he peddled away in flip-flops and crazy looking hair and we were a sight to behold and it was the most beautiful 40 minutes of my day.







Friday, June 3, 2011

rolling along with love in my heart

I never really know which words to capitalize in the title of a blog post.. i'm much more ee cummings-like and would prefer to write in all lowercase letters, but once in a while that auto-correct throws a capital letter and I just don't feel like going back to fix it. additionally, sometimes and i stress sometimes, the catholic school grammar teachers squeal in my head.

and i digress.

(image courtesy of http://favoritethingsforever.tumblr.com/)

on the health front, things are progressing nicely. my lungs are taking in the air, and loving it. the new steroid we've added to my mix has really made a huge difference. unlike some cf patients, i respond incredibly to bronchio-dialators-- this is my asthmatic component. i am grateful for this. my liver enzymes continue to trend downward, and we have identified that it was a toxic reaction to the accumulation of six months of iv antibiotics (with some breaks here and there.) it will take a while to normalize completely, but this whole liver, acute health situation has really opened my eyes... about a lot of things, but at this moment i'm referring to my body.
i'm pretty health conscious. i don't drink. i don't smoke. i don't ingest any product that would harm me, except coffee but that's a whole other post, and even now i'm down to 2 cups a day.  i was taking 16 pills every morning, many every 4-6 hours and then another handful at night. with the help of my doctor, we've cut it down to 4 in the am and 2 in the pm... and i feel good as gold right now. this is my vehicle, my way through life and i really need to push back sometimes and draw the line. some meds are necessary at some points, but heck not always all of them.
i am also back on my every three week ivig infusion cycle that i had gotten off of due to health insurance issues. this is really helping my immune system and energy. i am thankful to god for where i sit right now.

on the family front, life is beautiful... and beautiful doesn't seem to cut it, you know? i adore my family. i am in love with them... and it's not the big things... i can do without the big things... it's the little things. two nights ago i was cleaning up the kitchen and preparing dinner for nitza and myself (ale had already eaten) and he had his 475 thomas and friends engines out. he has been a die hard thomas lover since he received his first engine from a family friend at the age of one. he is five and a half and those engines, though they get put away sometimes, are a dear confidant of this young boy... so, in the middle of moving around the kitchen at seven pm (when bath time should be commencing), he wanted to draw faces on tiny squares of paper and tape them to the front of the engines so that every face would look like the troublesome trucks

(image courtesy of http://www.thomasandfriends.com)

(why the troublesome trucks and not my personal favorite Percy i'll never know), and i looked down at his serious little face, scrutinizing the line of engines and i stopped what i was doing, went to the craft bin and got white paper, a gray marker scissors and tape. (dinner was starting to burn). I cut teeny tiny squares (scissor anxiety) while he drew the faces and then upon request i taped them... (and dinner turned out terrible) and these were the most rewarding, happy moments of my day because i am alive and have this beautiful boy and have the time to cut tiny squares... a thousand times over i would cut tiny squares because Sarah Jones cannot cut tiny squares with Conner and so while I was cutting tiny squares with ale, i was also cutting tiny squares for sarah... for conner... and later on, after ale was many moments into sleep, i cried... in sadness for those who have lost and for true gratitude for what i have.

(image courtesy of http://www.zedge.net)

i have always been a feeler. it has worked against me at times. it is hard to be in this world when sometimes you don't feel like you have skin. as kids we went to a public swimming pool just over the bridge from home. they had 45 minutes for child swim and 15 minutes for adult swim every hour. one day during adult swim there was a young girl in the water splashing around with her mother. i asked my mother (out of curiosity, not envy) why this little girl was in the water (i was always afraid of breaking rules), and my mother told me it was because she was blind and needed to be in the water when it was safest for her.  i was quiet. i sat back and watched. the fifteen minutes of adult swim passed and the girl got out of the water, but i couldn't go on laughing and playing like i did before i understood what i perceived to be this girl missing out (whatever that really means in hindsight). the rest of my day i just wanted to play with the girl and i was sick about this for a few days. i have pain when others have pain. i don't love it and i have learned to deal with it, but at times its really really hard. and that's why i am awake. something wakes me in the evening and my mind starts on a movie reel of what ive taken in from the day... just life and sometimes there is just enough sadness that i cannot go back to sleep, but you know that's ok. i like the person i am and if it means some sleepless nights, so be it. i am able to truly connect with people and i believe that its a part of me (and so many others) that god has put in my heart... and there is a whole lot of strawberry eating beauty in this world for me to take in


and did you know my favorite color is orange... i love everything orange and i mean everything, and it makes my heart so happy to see this orange gerbera daisy blooming in our garden after nitza replanted it from when my mom brought it to me in the hospital.


wow this is getting long and babbling.  today is friday and i am looking forward to today and the upcoming weekend.  we are making the trip to see my family for my sister's graduation party...
DID I MENTION THAT ERIN IS A NURSE?? (i love you my dear baby sister). hopefully there will be pictures to follow.
Beautiful Erin the the processional to the stage.

Erin.

let the madness ensue with a endless face squeezing hugs from my blondie nephew to my gorgeous grandmother, his great-grandmother.


ive been having trouble uploading pics, hence the last number of posts with a whole lot of words, but ill get it figured out.


for today, this is how i am going to take on life.

 thanks for reading my very long windy monologue about troublesome trucks and a whole lot of feeling.

Thursday, May 19, 2011

the "e" key & and a thankful thursday

It started yesterday. my the's were th's and e was conspicuously absent from every word I typed... and you've probably gotten by now that I am a talker so that's a whole lot of e's. As a matter of fact,

The following information has been retrieved from wisegeek.com:

The most commonly used letter in the English language is the letter “e”. This is the case in the general language, in fiction and non-fiction writings, journalism, religious works like the Bible, and even in Morse code.

With “e” being so common in the English language, one would think that it would start the most words. Actually “t” begins the most words, followed by “o.” “E” is the letter which most commonly occurs third in a word, and is the third most common second letter in a word. The most common second letter in a word in the English language is h.

Actually, “e” is far down the list of English language word beginners, and comes in at the 15th place. The five most common letters beginning words are “t,” “o,” “a,” “w,” and “b.”



I miss my macbook. We are very attached. This whole macbook in the shop thing got me to think about how much I value routine and things that belong to me. I am on nitza's macbook air and all the favorites are hers, naturally because its her laptop, and I miss my favorites... all those kind of odd things.


At any rate, I'm thankful for my Macbook and that the apple store was happy I was forthright a about the incident of Ale and the Gatorade that they will try to fix my keyboard for free. No liquid got inside because I flipped it pretty darn quick.  I'm grateful for Nitza who knows me... like really really knows me  which includes the great things, the annoying things and the downright secret things I don't share... she is amazing to me and since we've been together I've never gone a day without feeling loved... or a moment for that matter... she may have put it on hold a few times when I have come home with Ale and great ideas that are really really noisy and she has a headache, but those are fewer and further between.
I'm so grateful and proud of my sister Erin who completed her last nursing school exam and she needs to be pinned and pass the boards and RN world you will welcome another wonderful loving giving nurse. I'm grateful that nitza's parents Dona Lydia and Don Carlos will be coming to visit us the second week of June... YEAH!!! I am grateful for my mom.. who I call a lot of times each day, and she answers a lot of times each day, and she talks to me a lot of times each day.--- I am grateful for S.Tom. If I were every destined for a dad, he is it. He got 4 kids when he married my mom a lot of years ago and we each have a ton of baggage and he loves us for who we are and I'm not sure he even knows we're not his blood children (shhh don't want to upset him!!)


I guess what I am getting at "e" key and all, is that I am incredibly blessed with new friends (DMM) and Old friends (KJ and HJ)... and I have an amazing family and an amazing community and the most precious nuclear family and 2 fluffy doggies. What's better?
Pause
Pause
Pause
Not going to oral surgery today.. that's not better, but I have insurance and hell if they already went into the bone twice and need to again today, what's a third time right?


Pics will commence when I get my laptop back :(


Happy Thankful Thursday All... 

Monday, May 9, 2011

Potassium, Steroids, and Numb Faces

I have had to stop and be still so that I could remind myself that there are truly things in my life that are beautiful and that I am grateful for... these are the reasons I experience such gratitude:


and I am so very fortunate to have a great friend give me a bracelet that says "positivity". I have been looking at it A LOT today..



This hospital stay has been hard. Nitza hasn't been able to be here as often and for as long as she has in the past and I miss her to badly. But its been great in the sense that we've addressed my stomach issues with meds. My mind crushing headaches were referred pain from the horrendous mouth abscess. We found the abscess.  My lungs are rocking.. I will start running when I get out...

It's the mouth healing that is difficult and my Potassium is VERY high right now, which is dangerous for my kidneys. They are doing another draw to determine it the first draw was accurate. My kidney function had been off for most of the 2 weeks so far, but has normalized so I don't know. I am back on IV S O L U M E D R O L... i have 845 personalities on that stuff... and none of them are very nice.

Oral surgery is coming today to reassess. I am numb in my face and the swelling is going back up a little and my fever hovers near 101... but I'm no dentist so they'll have to figure it out. I do have osteomylitis  and I also have a severely compromised immune system so those two don't make for a great date.

So that is the end of my whining session. I know God is watching me. I have family and friends thinking about me and praying for me, but I'm just kind a scared.

Saturday, May 7, 2011

a little of this & a little of that

Yesterday I got the very relieving and wonderful news that my bone marrow biopsy was  N O R M A L. That might be the only thing about me that is normal (joke -sort of). I was so relieved. It narrows down the immune system issues, which I think they have gotten to the root cause of.

I am here with no discharge date on the horizon... but that's okay... I'd rather be here with immediate access to doctors than at home with none.

I had a second oral surgery 3 days ago, and I am still struggling with my mouth and the pain and infection. More to come on that. Nitza brought Ale on Thursday night and it was so great.. I miss them so much-- Last night my dearest friends Kim and Hugh came to visit and I love them... they always make me laugh. Today Mom is coming which I am so excited for as well as nitza and Ale...


Alejandro playing engines on my bed..


Alejandro and Nitza.

School Picture are back!!!!


This one is my favorite!!

Happy Saturday everyone and have great strides walks to all my friends that are doing them today!!

Thursday, March 31, 2011

My Shower-- Thankful Thursday

I love my home shower. It is large, walk in.. has a few seats in it. Tonight I took the longest most wonderful shower. I am anxious. I am having some difficulty breathing...I did my treatments...it is a horribly scary feeling to feel short of breath.

My heart is racing less now that I lay in my warm bed beside the love of my life with the little fluffies running around and the cutest boy asleep down the hall.

I live a life with a heart full of gratitude. I am not all better.. Dr P says my baseline will take 6 months to come back (and that's without complications.)-- I can get there.. Ask my mom, I'm stubborn as hell and incredibly impatient.

I was struck by a number of things today.. this afternoon... Ale told me that he was afraid his best buddy wasn't going to come home... he is so resilient and expressive that I never realized how much these last 2 hospital stays affected him...We're open to suggestions. He wants to visit and loves being there and flirts with Miss A and Miss M with his cute long eyelashes.. but he's still 5 and one of his parents is still ill.

I talked to my mom on the phone tonight and I was short of breath and with the most loving tone full of pause she asked me to please sit down... I thank god for my mother-- every moment.. every day.. she is my dearest friend... my trusted confidant.  I talk to her at least 6 times a day.. and sometimes that is not enough... She has been my strength..

Nitzita and I were able to openly talk about her fear.. her fright of me being sicker.. and I've been sicker and I pause and know that I spend every day and night with the love of my life...my best friend.. we laugh.. we shake our heads.. we were two fledgling souls that landed right beside one another and happened to look up at the same time... I have a life partner that I truly truly enjoy and am every day grateful for....

and so tonight, we unloaded a week's worth of Hartford Hospital bags into our freshly smelling clean home and got the boy ready for bed and read together like we do each night and as I stepped into my shower I had a moment of pause and really understood that the gift of stepping into that shower is truly what life is about.

Friday, March 25, 2011

Family Friday

I'm very fortunate. As I sit here at 4:20pm Eastern Time I am as excited as I possibly be to see my family. A and N will make their appearance in the next 1.5 hours or so...They light up my life.

She has worked a long day after a long night alone at home with a 5 year old boy and 2 dog, but she comes and she doesn't complain and she really wants to be here near me

and this boy will bombard his way into this room with such joy to look out the windows at the city that looks just like "Christmas"when it is lit up in early evening.

He'll most probably tell me about a magnificent lego creation and who brought what for show and tell at school today.. the letter was "Q"

I love them with my entire being. This weekend we are going to watch Misty Island Rescue (a Thomas movie)-- and my mom is coming to see me tomorrow and I am so lucky to have a mom that is my closest friend...

*********
I have a PFT of 51%. I have never had a PFT that low. It scares me, but what scares me more is that I am doing all the right things.  Today I started solumedrol. We'll see where that brings the PFT's... 

I am also dedicated to using this time to assessing my own happiness... am I where I want to be (not family and personal life wise) in all aspects of my life. What can I do differently... what do i want to do differently... where do I go from here... 

Until the next update folks... Thank you for reading. 

Monday, March 21, 2011

I Outrun CF- My Story.

Today is my 36th birthday.
Today I decided to check on the median age of survival of a person with CF.

The info below is directly from the cff.org



I was diagnosed with CF on 9/1/2009.  I was 34.  My brother was diagnosed with CF on 9/19/1980 at the age of 14 weeks. 

What does this have to do with anything you ask?   It has everything to do with everything..  I was an elite runner. I ran 3:15 marathons. Won Olympic distance triathlon's, sprints and placed really well in 1/2 Ironman Distance triathlons... I played soccer from the age of 5 or 6 and played sports all year round. I became a runner 15 years ago or so and fell in love with it. I had chronic lung infections, upward of 5 a year. I had chronic sinusitis and a few surgeries to clear out the sinuses. 

I kept running.

In 2005, while training for Ironman Wisconsin I was clipped by a car on a training bike ride. My front brake punctured the structure of my right kidney.  I had 18 surgical procedures and eventually lost the kidney. You ask, what does this have to do with CF... I tell you-- Everything. For the first time in my life I was inactive. Between surgeries I'd get up to run again, only  to be sidelined from another surgery. After each procedure I got a lung infection. I had my kidney removed in November of 2008. I had 11 bacterial lung infections in the 9 months that followed. My nephrologist's partner sent me to a pulmonologist.

I saw Dr.C.  He asked me a lot of routine questions.. Do you smoke? NO.. Drink. Occasionally... etc etc. He went on to ask if anyone in my family had CF.. I thought it an out of the blue kind of odd question and old him my brother did, but I was CERTAIN I did not have it. He nodded his head and ordered a sweat test and labs. 

I went to UCONN for a sweat test and wrote it off as another routine test I'd have to go through after all this time and really-- I was so sick of doctors with the kidney charades... I walked out of UCONN, talked to N and my mom and said wondered what they'd do next when the CF test came back negative.

On 9/1/2009 Dr C called me and asked me to come to his office for a quick visit. I thought nothing of it. (DENIAL) I mentioned to N that Dr C called and she asked if I wanted her to come with me... I said no, she had meetings and I was sure it would be a quick visit to discuss my sputum or something.

I walked in and they were a lot nicer to me than they had been.. maybe nicer is not the right term.. they are and were always nice.. but perhaps more attentive.. did I want water or coffee... Dr C came in with 2 nurses and a pile of results. 

"I'm very sorry to tell you Tara that your Sweat Test was positive for CF, confirmed by your Ambry Genetics blood work." 

Stomach drops.. WHAT??? 

I can't have CF. Michael has CF. I do not have CF... but I do have CF.

Dr C brought Dr P (my current CF doc and ultra amazing best ever pulmonologist) in to meet me. They would start following me in the clinic and he would be my primary doc.

He went on to tell me that his theory on my specific late diagnosis is that I had spent 29 years doing my own CPT. At my peak (of at least  years) I was running 60+ miles a week. He told me that I was clearing my own lungs and that when I got in the accident all the mucus settled and I became more symptomatic.

Here we are, the 4 of us. I am the tall one with the white hat. I have CF.


I kept myself alive and healthy by outrunning cf every day. I keep myself alive and struggling to stay healthy by outrunning cf.

Every day I step on my treadmill. Yesterday was no different.

Yesterday I outran CF. N and I outran CF. We did our three miles (mine walk/run)... but it wasn't that moment (though I specifically logged my CF mileage yesterday morning for I Outrun CF)  that I realized what outrunning CF was truly about.

It was this one:
My beautiful sister and beautiful boy outrunning CF with laughter on my mother's front lawn.

It was this one:
Because I outrun CF, I can sit and enjoy my family.

And because I outrun CF, I can blow out birthday candles

with the help of this guy:


and I wake every morning to them:
and these folks


and I am blessed...and I have CF... and I outrun cf each day... which gives me another.