January 16th, 2016 - Noon-?
Hosted by: Alturas Bar & Night Club
Sponsored by: Mestizos MC
My name is Lennah and I just turned four years old. Last time I wrote a letter I was two years old. (You may read my first letter at www.LennahLovesLife.com). I was trying to help my mommy and daddy reach our goal to raise enough money for me to undergo a procedure as well as a month of Intensive Physical Therapies, which both had the potential to give me a better quality of life.
Let us recap a little, shall we? I was born with Gastroschisis, which means my intestines formed outside of my abdominal wall. After six major surgeries and four months and four days in the Intensive Care Unit, I was sent home to my loving family so we could finally start our life together. Soon after, we found out that I had suffered a stroke during one of those invasive surgeries, which forever changed my life as we all had envisioned it would be. I was diagnosed with Cerebral Palsy at 6 months old.
After hours of research, my parents learned of a potentially life improving, non-invasive blood transfusion using the stem cells from umbilical cord blood. With the generosity of our friends, family, community and complete (yet loved) strangers, we met our goal to raise enough funds for me to have this procedure done. We also were able to spend an entire month at an amazing physical therapy facility call PolFit Wellness in Brea, California that helped to build up my muscles and teach me many things I didn’t know before. In my first letter I said, “I cannot sit, I cannot roll, I cannot walk, I cannot hold things in my hands, I cannot eat, I cannot talk.” Well, after last year’s procedure and therapy I CAN talk! I love to say “hi” to anyone and everyone. I CAN see! I watch my baby sister Truby run around all day and my mommy can’t sneak up on me anymore. I am learning to balance so that soon I will be able to sit on my own and I am learning how to take steps because I WANT to WALK and RUN beside my sister!
Every day when my daddy gets home from work I watch as Truby runs to greet him with open arms and then together they come to greet me. During my weekly therapy sessions I try to keep my goal in mind – I want to run into my daddy’s arms when he gets home from work! I can take reciprocal steps but that is no longer an accomplishment for me. I NEED to WALK! Will you help me?
My parents have put a deposit down of $500 to go back to Polfit Therapy in Brea, California for March 21st-April 15th of 2016. Our insurance doesn't cover it and it costs $8,200 for the four week Intensive Therapy program. I know my parents are trying to figure out how to pay for my therapy but perhaps you could help them out a little? Or, as my parents always say, “Please simply share our story… something good will come out of it!” Please join us on January 16th 2016 at Alturas Bar for a fun raffle, silent auctions, and carnival day.
Lennah Sofia Martinez
WOW!!! One year ago today (November 13), you - our Lennah Believers, helped us to reach our seemingly unobtainable goal of raising enough funds to provide Lennah with a potentially life changing blood transfusion. I will never forget telling her, “Manos arriba!” two days after her procedure and without hesitation she raised both her hands in the air. At that moment I knew that we had made the right decision. I knew that the risk that we took was worth it. I was the proudest papa in the world! We cannot begin to thank you all for believing in our Lennah. Ashleigh says it best, “it takes a village to raise a child.” In our case it took the world…A world who graciously came together to give a child better quality of life.
How is Lennah doing now? Well, if you greet her she will say, "Hi" and wave to you; if you ask her to dance (in Spanish or in English!) she will show you her moves; if you ask her to go, she will take steps; and when you tell her you love her she will blow you a kiss.
Thank you for being our HEROES and changing Lennah's life.
Well, the countdown starts! Lennah's big day is exactly ONE MONTH from today! November 13th, here we come!
Its amazing how quickly this has all happened. To think, it was less than a year ago that we set our goal. At that time it seemed extremely far fetched. How were we going to raise $21,000?! But with the help of friends, family and complete strangers we have been able to book the first day of the rest of Lennah's life!
Making one person smile can change the world – maybe not the whole world, but their world.
We got a special delivery today! The UPSEE arrived! To see the beautiful video of Lennah getting to dance with her daddy and also to follow our blog in the future, please join us at http://www.lennahloveslife.com/
Hi again, It's me Lennah. The world has Hugged and Embraced me with love and support. Words can't express or say how my family feels for giving a child an opportunity to have a better quality of life. Soon I will be able to go down that slide, swing as high as the wind blows or even go to my first dance recital with my little sister...So with out further notice, WE DID IT!!! We have raised enough money to book my procedure!!! YAY!!! With donations outside of this amazing website we have been able to book my procedure. Thank you all from the bottom of my little heart. My mommy and daddy could not have been able to provide this procedure without your help and generosity. Your donations, posts, prayers, thoughts has made this possible. Thank you for turning this chapter of my life and starting a new one with possibilities in witnessing miracles so on October 8th, 2014 mark that calender because you are all welcome to join my family and I in my next adventure in my life.
This is Lennah’s dad, Misael. I would like to personally thank each and every one of you for posting, donating, sharing our story and keeping Lennah in your thoughts and prayers.
You have worked so hard for your earnings and for you to listen to your heart and see the vision I see as a stranger, friend, cousin, sister, brother, mother and father that there is a ray of hope, a miracle, an opportunity to change a human’s life, let alone my Princess Lennah’s life. To hopefully witness her sit, crawl or even walk and take those steps that we see and hear when children are in the playground. For Lennah to feel the wind blow her hair back as she glides down the bright and shiny slide, to swing independently and see how high she can go, trying to reach that enchanting blue sky.
You have made an impact in someone’s life. We have all united for this cause because we believe that a child deserves a better life. I am on my knees weeping with tears of gratitude for what you have done and the life you have chosen to touch. I will personally thank you in this life or the next for your generosity and I leave you with an Unknown quote my brother and sister-in-law wore on their backs on their most recent race, “I run because I can. When I get tired, I remember those who can’t run, what they’d give to have this simple gift I take for granted, and I run harder for them. I know they would do the same for me.”
Lennah's therapists have been using phrases like, "noticeable difference" and, "this is different" when they have been working with her during the recent weeks. Lennah has been 'talking' a lot more than ever before and she is obviously able to see more clearly. Her hands have been more open and relaxed, her fingers are separating and becoming individuals. Oh yeah - and she ROLLED!
What is making the difference? What is waking her up? At the end of March we began taking Lennah for Hyperbaric Oxygen Therapy (HBOT). Our expectations were set very low, we didn't want to get our hopes up. But to our pleasant surprise, we have seen amazing results after just a dozen 'dives!' This form of therapy is not covered by insurance (of course!), which is why we are only able to provide this opportunity to our princess with YOUR help!
We THANK YOU all so very much for your generous support! Lennah would not be where she is now without all of you.
Go Lennah, go!
We are SO close to our goal! But we aren't there yet!
A huge THANK YOU to Bully's Sports Bar & Grill on Vista ... They will be hosting a fundraiser evening for our Lennah girl! (And thank you to Emory for helping to facilitate this!)
When: Tuesday, May 13
Where: Bully's #5, 2898 Vista Blvd., Sparks
Details: Print the attached coupon out & BRING IT WITH YOU. 15% of your tab will go towards Lennah's goal!
If all works out well we will be booking Lennah's treatment for THIS OCTOBER! Please, please - come enjoy a meal & beer for a great cause! (We are in a race against time --- the younger the patient, the better the results!)
PS - You can share this coupon with anyone and everyone! Print it out and bring it to work! Post it on lamp posts! Stick one in your neighbor's mailbox! (We just can't hand them out that night at Bully's.)
The 4th annual Dodge, Duck, Dip & Dive Dodgeball Tournament is almost upon us! (This Saturday, 4/26).
This also happens to be Lennah's 2 year anniversary for when she was brought home to us from her 4 month & 4 day stay in the hospital!
April 26th is a good day.
The tournament is going to be a blast - we are so honored and excited to be a part of it this year!
Thank you to everyone who has signed up to play, donated raffle & silent auction items & agreed to volunteer to help with the potluck, registration & kids craft table. You are all amazing people! I love this community!
If you are not able to come out and enjoy the festivities but you would still like to support our cause (raising funds for two little ladies with Cerebral Palsy & a friend who is battling cancer) you can buy raffle tickets NOW!
The prizes simply are amazing. (House cleaning, carpet cleaning, art work, hair cuts, colors & styles, Scentsy goodies, Tupperware, gift certificates to Outback, Campo, Juicy's, Texas Roadhouse, PJ's Restaurant & Saloon, Olive Garden, Peg's Glorified Ham & Eggs, Squeeze In, Sardina's Fine Italian Bistro, Scoopers and SO MUCH MORE!)
You can either meet up with Misael or I to buy the tickets tonight or tomorrow (we can come to you! Call/Text me at 775-772-7332) or you can make a donation online at http://www.mommyyouknowwhat.blogspot.com/ . Just send me a photo of your confirmation page and I'll set aside your raffle tickets and deliver your prizes WHEN you win!
Get your tickets now!!!
1 for $3
3 for $5
5 for $10
10 for $15
20 for $20
Thank you to all the Galleria Home Depot associates, AKA - our Home Depot FAMILY! The Homer Fund is an amazingly generous opportunity that Home Depot offers to its employees. We are SO grateful for it!
Because of this we were able to order the UPSEE for our Lennah girl! We simply cannot wait to see that smile... The smile that makes it all worth while.
Hello! My name is Lennah Sofia. Every day of life has been a battle. I was born on December 22, 2011 with Gastroschisis; all my intestines were outside of my abdominal wall. Doctors don't know what causes this, but 1 in 10,000 babies are born with this defect. I spent the first four months and four days of my life in the hospital in the Intensive Care Unit. My parents and I were delighted when I was stable enough to go home! At last they didn't have to leave me hooked up to machines with strangers taking care of me. We could finally begin our lives together! It wasn't long after I got home though, that I was put through a barrage of tests and eventually diagnosed with Cerebral Palsy. Apparently, during one of my six major surgeries I had suffered a stroke.
Have you ever wished that your energetic children would just be calm and sit still for a few minutes? My family will never wish that. My family wishes for the exact opposite. I cannot sit, I cannot roll, I cannot walk, I cannot hold things in my hands, I cannot eat, and I cannot talk. I just lay where and how I am placed or when I am held by a loved one's arms. I am two years old and I am unable to do things a "˜typical' child my age can do. When I am at my grandparents' house with my cousins, they all run around in circles and play while I can only listen from a distance: or as I like to call it, "hang with the adults." However - I CAN smile, I CAN laugh, I CAN give you a high five and I DO love life!
My daddy, Misael, works two jobs while my mommy, Ashleigh, stays home with me and my little sister. Mommy isn't able to go back to work because of my medical needs. I have a great team of specialists and therapists that I see frequently. My sister, Truby, is six months old and is already sitting and rolling all over the place. I watch and wonder at how she does it all. I am so very grateful that she doesn't have to endure the therapies that I go through.
My parents have done research on ways to improve the quality of my life. They have found a promising procedure that will be fairly painless for me! However, it is currently not covered by insurance. I have met a local friend who has gone through this simple blood transfusion and now at age 7 she walks (with support) and is able to do things I can only dream of doing! I can only hope to walk myself in to my first day of school and not be wheel-chaired in to class, to go to my high school prom, to walk down the aisle at my college graduation and most of all to have that first dance with my daddy when I get married.
My mommy and daddy aren't ones to ask for financial help so I figured I would give it a shot. For my second birthday I made a wish to help my parents raise the money that is needed for this procedure. The blood transfusion is going to cost $17,000 and the intensive physical therapy which accompanies it will cost $4,000. There is no guarantee that this will work miracles, but we have to try! With your help and generosity I may gain some independence and have an easier, more fulfilling life.
I would personally like to thank you for your help in making my dreams come true. I will leave you with a truism that my daddy reminds my sister and I all the time, "Your worst day is someone else's best day." Life is what you make of it!