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....Not sure but looks like a hamburger.... |
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....whatever it is, she's enjoying it... |
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Meanwhile our church Young Women's leader had decorated our door! |
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....and left a Graduation giv |
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Lena's dog Leo was SO SERIOUS ... it had been WAY too long since he'd seen her! |
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....her cap and gown and cords we |
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Theatre medal...from the banquet she missed... |
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The Theatre Officers, "leaving a space for Milena" at the banquet.... |

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Home AT LAST |
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Its really YOU!! |
14th Day Post Op - 22 May 2019 - HOMECOMING!!
- Erick and Lena drive from the Ronald McDonald House in New Haven, CT to Laguardia Airport in New York....and obviously got hamburgers on the way.
- Lena's dog Leo waits impatiently.
- Mom attends Theatre Banquet - and cries alot.
- Mom gets EVERYTHING READY.
- Door decorations
- Happy reunions
Jen's wordy version of the day's events (and more of course)....
Erick and Lena drive from the Ronald McDonald House in New Haven, CT to Laguardia Airport in New York....and obviously got hamburgers on the way.-
Erick and Lena had about an hour and a half drive from the RMH to the airport in NYC. Origionally I was super worried about this...but Lena had been doing so well in the car (this was NOT the case prior to her surgery)... that I was less concerned about her discomfort during the car ride. They made the trip without a hitch...and I see they had some adequate sustenance along the way.
Lena's dog Leo waits impatiently. Lena (we) have an "emotional support" dog (although we have absolutely failed at training and socializing him enough to go the doctor with her or really anywhere in public at this point). Leo is about 40 lbs, and he is classic MUTT (St. Bernard/Chow/Rottweiler/American South Stratfordshire Terrier/ Pitt Bull/Shih Tzu mix) But he's about 18 months old now and getting out of the "puppy" stage. He's a lover and he was VERY confused at the events of the last few weeks. Why isn't "mom" here? Why can I HEAR her in the phone but I can't SMELL her in the phone. Ok. I'll just abuse the cat in her absence.....
Mom attends Theatre Banquet - and cries alot. Lena's Theatre Banquet actually happened over the previous week end, but I forgot to mention it. I went in her place...she has been very active in the Celina Theatre department for the last 3 years that we have lived here. She's worked hard to earn parts in productions, she has served as an officer for two of those years, she's managed parts in plays in spite of her growing list of diagnosed conditions and issues/declining health. Mrs.Cindy Baker, the Theatre teacher has been an amazing mentor and support for Milena; the other Theatre students have been best friends and her family during her challenges.
Lena missed EVERY one of her SENIOR YEAR ACTIVITIES due to her health issues and the timing of her surgery in Connecticut. Don't get me wrong...the timing of her surgery was a MIRACLE and in the grand scheme of things it has all worked out for the best...but that doesn't mean that it was ANY easier for Milena to miss these events. And as she was in CT healing, she was seeing posts and watching all her peers go to: the Scholarship night; the Senior trip to Six Flags; the Baccalaureate; the Senior class walk through the elementary school (where Hurley would've seen her and said, "THATS my sister!"); and this Theatre Banquet. The reality of missing those events due to things that she really had no control over was hard and sad for Milena.
In addition, it would be good to point out how precarious the last 4 1/2 months had been for Lena...not only healthwise, with her ability to eat and drink diminishing, losing roughly 12% of her body weight in a short period of time, and the constant pain she was dealing with. The pain that MALS patients deal with has been compared to the pain that end of life patients with Pancreatic Cancer. In addition, the genetic condition that Milena and her older sister Annika have been diagnosed with, and have suffered with since birth (although we only figured out the diagnoses within the last 2 years....) has been compared to the pain that terminal cancer patients suffer with. The difference is, that may daughter's "look" normal and have always had pain. They have ALWAYS had pain, and so they are masters at functioning in spite of the pain. The story of their journey is for another blog...but when you have known pain all of your life, that is your normal. It seems much of the time, that my daughters are penalized medically (and at times overlooked, judged or questioned socially) because they are able to "deal with" their pain in a quiet way.
In any case, basically from February of this year on, we had no idea whether or not Lena would have the energy to finish her classes (her metabolic function has been recorded at 70% of a healthy female her age... and this is WITH medication and therapies), or if we would be able to work it out with the school for her to graduate. It was so awful that she had been somehow managing all of her illnesses (EDS, Dysautonomia, POTS, MALS, Gastroparesis, Nutcracker Syndrome, Mays Thurner Syndrome, Scoliosis, and a variety of comorbidities that go along with these chronic conditions...) and she was SO close, just so close. Even the scheduling of the surgery left only roughly 40 hours from the time she would fly into the Dallas, TX area to actually participate in the graduation ceremony.
Mom gets EVERYTHING READY. I washed her sheets. I did my best to dewrinkle her graduation gown. I hung her gown, cords, cap, and medal in the closet so she could "find" it all ready (and to keep it safe from Leo). I laid out her yearbook, that her other "school" family - the SWAT (Students Who Advocate Technology and her amazing mentor/teacher Mrs. Tisha Poncio) had lovingly signed since she missed any opportunities to have her classmates sign her yearbook. She had a few graduation cards waiting for her too. I worried some about her walking through the airport (I had arranged a wheelchair but many times if "mom" isn't there....well she IS an adult....)
Door decorations Lena has some amazing church support. Her Young Women's Leader's have been checking in on her regularly...as have her Seminary teacher (who has cheered her on for the last 2 years as Lena has managed online seminary.) Sis Smith showed up and decorated the front door and dropped off a cutie grad gift. I was SO thankful.
Door decorations Lena has some amazing church support. Her Young Women's Leader's have been checking in on her regularly...as have her Seminary teacher (who has cheered her on for the last 2 years as Lena has managed online seminary.) Sis Smith showed up and decorated the front door and dropped off a cutie grad gift. I was SO thankful.
Happy reunions! Got Lena coming in the front door...and BOY WAS LEO HAPPY TO SEE HER!!! The feelings were absolutely mutual and as she wandered into her bedroom to take in all the comforts of home and sights of her gifts and graduation paraphernalia...I ahem, left for 20 minutes because mom needed a Sonic Blast to take out her stress via a sweet treat. When I got back...I think the long day (read: WEEKS) caught up with her. Although she was worn out physically and sore, she had taken her meds and was preparing for bed (it was almost 9:30pm by now)... But she also got very tearful as the power of all her graduation items and what she felt "robbed off" due to the surgery set in. Lena, Annika, and myself (and I'm sure the boys in our family, although I am not as good as understanding their "feelings") have had to switch alot of "plans" these last few years. While we always seem to "make it there" and have amazing successes along the way...What many do not see are the quiet moments that the loss of the idea of "how it was going to be" or "supposed to be" sets in. We have alot of that around here. I am pretty sure everyone can identify with this in some way. But my daughters seem to have to deal with this concept daily or even hourly as their bodies just can not perform or function. The future for Lena or Annika feels pretty much like a crapshoot at this point...they have plans...but as we learned this year - any one of the 8+ conditions each daughter has can dip into "symptomatic" at any time...really. It's like standing in the center of a wobbly teeter totter. I try not to spend too much time in worry mode...but more often than not in the last 3 years, we've had constant, extreme and complex medical crisis to piece to together....without much break to catch our breath...
So it was a tearful end of the night. I'm certain I didn't help with my tight lipped concern regarding the choice she made NOT to use the wheelchair. But really, that is my problem. Milena has made so many amazing decisions and choices along this road and I have committed to support her. But moms have feelings and grieve too. Off to bed and GRADUATION PREPARATIONS THE NEXT DAY....