Saturday, December 21, 2013

Blog Slacking

Holy Smokes!  Life got busy and we got so many jewelry orders it was amazing!

We want to thank everyone for their support as we start this new business.  Speaking of new businesses, did I mention that we launched our new website?! www.hellosweetlove.com  We had the help of my sister Tiffani Forsey and she did a fabulous job.  This is something that the handsome Mr. Lunnen and I have wanted to do for a while.  Start a business I mean, and more importantly we wanted to do something that helps others.  And what is cool is that you, the customers are the ones who are making that happen.  In the last two months we have made and sold more than 200 necklaces! Thank you for helping us make this happen.  We have added a couple new designs.  My favorite being that simple bangle.
This piece is darling.  It is silver plated and comes with two personalizable charms, and up to three beads of your choice.  I love this one for teacher especially.  It is sold on our website for only $10.99
I also want to run a blog special.  Unfortunately they will not be able to be shipped in time for Christmas, but if you are in the utah/salt lake county area they could be made and picked up in time.  The special is buy one get one free on the stacked squares.  What I will have you do is buy one off our shop on our website www.hellosweetlove.com and leave the details for your free one in the comment section/special instruction section.  

Now, a little update on all our recipients so far.  I saw on Dustin Dickamores blog that he has near perfect vision in one of his eyes!  What a miracle.  Ryan is still doing her Chemo treatments, and so is Ed.  All of them still need our support and well wishes.  Feel free to leave a comment below letting them know they have an army fighting beside them!  

So much has happened lately.  Another semester of school finished and I have the handsome Mr. Lunnen all to myself (kinda) until the first week of January.  This last week I accomplished another of my goals (Hooray).  All it was, was to get a family photo. So I set up my tripod and self-timer on my camera, told the family where to stand and ran into place.  Id say they turned out pretty good for using a tripod!  

Hopefully I will have a better update soon, again we thank you from the bottom of our hearts for all of your support and purchases.

Brittani

Thursday, December 12, 2013

A time to give. Meet Ryan.


Because it is Christmas time and the season of giving we wanted to try and give a little more.  We have chosen to help another well deserving person.  

Ryan helped us design a beautiful piece of jewelry specific to her fight.  She put a lot of thought into what she wanted on the necklace.  We hope that you can find it in your heart this season to help this young mother and her family as she fights for her life.  The necklace is beautiful and can be purchased on our new website www.hellosweetlove.com just choose the Shop/store tab.

Ryan Talbot is a beautiful, witty, spunky, and intelligent 31 year-old wife and mother of 3 young children, ages 6, 3, and 16 months.  Ryan has worked as a 4th grade teacher, and most recently as a Special Education teacher.  She enjoys biking, running, reading, crafting, being outdoors, and spending time with her husband and family.

On October 14th, 2013, just 9 days after running her first marathon, Ryan received the devastating news that she had breast cancer.  Ryan was diagnosed with Adenocarcinoma and had a lumpectomy on October 23rd.  Also removed were 7 lymph nodes.  After more testing was done, a second type of cancer, Ductal Carcinoma In Situ (DCIS) was discovered.  This resulted in Ryan having a second surgery on November 6th and a third on November 27.

Ryan’s first round of chemotherapy began on December 5 and will take place every three weeks for four months.  On top of chemotherapy, she will also undergo weekly Herceptin treatments to help slow the progress of the cancer.  When chemotherapy is finished, Ryan will undergo radiation treatments, as well as five more years of oral Herceptin. 

Ryan’s deductible is $10,000, which she has already reached, but hasn’t paid for yet.  Because it is the end of the year, another $10,000 will likely add up in the first few months of 2014.  In addition to at least $20,000 in deductibles, it is unclear if all of her medications, scans, tests and treatments will be covered by insurance. 

For more information on Ryan’s battle and for updates on her progress, visit
www.ianandryan.blogspot.com or https://www.facebook.com/FightforRyanTalbot

To make a donation, go to www.FightForRyan.eventbrite.com

Thanks to you all for all your love and support.  

Brittani.




Wednesday, December 11, 2013

Vendors?

Do you have something amazing that you make?  Are you a vendor of some sort?  Would you like to be featured on our site?  Let us know.  Email me at brittani.lunnen@live.com We have had about 10,000 views in the last month, and would like to give our viewers more options.

Thanks,
Brittani

Monday, December 9, 2013

Update on Dustin and Ashley Dicksmore

The more time I spend reading their story the more time I spend humbled and crying. I wish I had the tiniest amount of faith in comparison to theirs. Trust me I am a faithful person.  But the faith they have shown is incredible. Ashley always has a smile in her face and words of gratitude every time I message or chat with her. It completely amazes me.

We need your help. This family has so many medical needs and have a growing family. I know they would never ask for help. But that is why we are here. To help people that need help but will never ask. And it's not a matter of pride. But a matter of gratitude for what they already have. I saw a picture on Ashley Instagram that made my heart just ache.
"never give up no matter how bad you think it is, someone probably has it worse that you and are making it through their challenge. Just always believe." -Dustin Dickamore. 

Dustin and Ashley put a lot of thought into what they wanted their necklace to say and gave me several ideas. The one they settled on is #faithisstrength. It is perfect for their situation because I truly believe that it is their faith that has continued to bless them and improve Dustin's health. 

This necklace is just 17.99. During this Christmas season, this season of giving there is not better time to purchase this beautiful necklace to help someone who not only needs the help but is truly deserving of it. 

Today I sat and complained about my life.  I verbally expressed how hard it was, how messy my house was, how I couldn't keep up with the children's mess, How I had so many jewelry orders to fulfill...blah blah. Instead as I read Ashley's and Dustin's sorry I instead am grateful for my beautiful and healthy children.  I am grateful for a home to live in and access to food and water. And I am grateful that there are people in the world buying our jewelry and keeping us busy this Christmas season.  

Now I plead with you all to find the time to order their necklace either here on the left hand side of this blog, or on our new official site www.hellosweetlove.com  Any purchase made Will benefit the Dickamore family. 

I am honored to be a part of the fundraising effort for the great examples that the Dickamore family has become. I applaud Ashley for her constant beautiful smile.  She said something to me I will never forget. She said " Brittani, I am just so grateful he is here and that The Lord chose us to witness such a miracle!" As soon as I was able to wipe the tears from my eyes and pick my jaw up off the floor I vowed to be a better more grateful person.  

Tuesday, December 3, 2013

Dustin and Ashley Dickamore #faithisstrength


It is time for us to help another family.  I feel very strongly that we as an internet community can rally together to make a difference in their lives.  Ashley and Dustin have shown tremendous faith throughout their recent trial.  So if you can, purchase one of these necklaces that Dustin and Ashley helped me design.  The necklaces are selling for $17.99.   They would make great gifts as they show us all to believe in things bigger than we are.  The majority of the profit goes directly to help care for Dustins medical needs and the needs of their family.  Grab a tissue because you will need it and read their story below.  


Dustin and Ashley grew up in the same city that I did.  I knew them, but not real well.  It was some of their family members that I knew well.  But when I heard their story I just knew that we needed to help them.  Start out by watching the interview in the link below and you can see their current situation.  Then go ahead and read the story in Ashleys words below taken from their family blog.  


On September 20th, 2013, Dustin Dickamore and his family (along with some close friends) took a weekend trip up to the family cabin in Bear Lake, ID.  At 11pm, shortly after arriving, Dustin was in an ATV accident.  Even though the accident shattered most of the bones in his face and caused him to immediately lose his eyesight, Dustin walked himself onto the ambulance for his ride to the local emergency room.  It was the worst head injury that the doctors in the ER had ever seen.  They didn't think he would survive.  Dustin never lost consciousness.
Immediately after the accident, as they waited for help to arrive, the Dickamores turned to our Father in Heaven in prayer for help.  According to Ashley, as they prayed, the words of Dustin's patriarchal blessing instantly came to her mind.

"As you stay close to our Father in Heaven, He will stay close to you and He will give you the strength and the ability and the courage to overcome any temptation or hardship or trial that you may face.  You will be given priesthood blessings to overcome any illnesses you may encounter or injuries you may sustain.  You will be blessed and restored to full health and strength."


Dustin and Ashley, along with their entire family, enlisted an army of prayers and fasting with countless friends and family and temples.  Through many encouraging priesthood blessings and discouraging words from doctors and nurses, they clung to their faith and pleaded with Heavenly Father to heal him.
On the fourth night after the accident, though he was told not to lean forward at all to prevent putting pressure on his optic nerves, Dustin knelt on his bed and begged God to help him.  He didn't feel like he could go on this way.  He felt swallowed up in despair and darkness.  He knew that our Heavenly Father was the only one who could help him.

After 4.5 days of total blindness, an eye doctor came in to Dustin's hospital room and told him that the MRI showed that his optic nerve was detached in his "good eye."  He told Dustin that the right eye was deflated and appeared to be blown out the back.  With the MRI, and the fact that he was on day 4 of zero light perception, the doctor said "by all accounts, Dustin, you're blind." 
Immediately after saying this, the doctor proceeded to do his eye exam, admitting that it was more of a formality than anything else.  Dustin was not to expect to see again.  As he did this final exam, through a true miracle from our Heavenly Father, Dustin's vision returned to the eye with the damaged optic nerve.  He was able to see his wife, his beautiful 5 month old daughter and his 2 year-old son.


Dustin now says that "Heavenly Father knows just how much you can handle and just how much you need to be able to go on."  This little bit of vision that Dustin recovered will no doubt help him deal with the long road ahead and get to that day of "full health and strength."
The miracles did not stop there.
During a surgery on his right eye, the more badly damaged eye, the doctors found that the eye was round - not blown out the back as expected.  The blood was suctioned out of the eye and the retina was replaced and actually, still partially attached.  This was not what the doctors had expected to find.  They warned Dustin and Ashley that, most likely, there would be nothing they could do.  They discussed the possibility of needing to remove the eye.  With unwavering faith, the Dickamores told them to try anyway.  
Everything is now in the right place in Dustin's right eye to be able to see, but with zero light perception out of that eye for seven weeks now, the optic nerve is unmistakably damaged.  Damage to the optic nerve is irreparable, because it is brain tissue.  They have been told that there is no hope for the right eye.  In fact, the doctors have said the words, "We have done all that we can do and are bordering on miracles for the vision to return to the right eye at this point."  
The vision in his left eye is very dim and only a small box he can see through.  Dustin and Ashley, however, say that they KNOW what they know and they know that he will return to full health and strength.  They also know that our Heavenly Father has a timeline that has Dustin's best interests at heart.  They trust in Him and His plan for them.  They have seen His hand in their affairs every single day since the accident and this helps them to not be afraid.
On October 30th, at 8:30 am, Dustin went into surgery to reconstruct his face.  A planned 12 hour surgery turned into a 17 hour and 40 minute surgery.  We are grateful for Dustin's extremely skilled and educated surgeon, Dr. Gociman, who took his time to take the bones in Dustin's face, re-break them (they had healed and grown together after 6 weeks), and use all sorts of titanium plates to put Dustin's face back together.  We are thankful that his hands were guided by our Father in Heaven and that he was able to accomplish this great task.  This surgery posed a risk to the vision he currently has, but Dustin was promised that his eyes would be protected.  He currently still has the same vision he went into surgery with.
Recovery from this surgery has not been easy.  His pain level has only once been below a 5 (after the initial accident, he never rated his pain higher than a 4), so severe for a few days that all he could do was shake and squeeze our hands and eventually slipped into what they call ICU delirium.  His swelling has caused his eyes to be swollen shut.  He has a trachea tube in his throat and a feeding tube in his belly, because his jaw is wired shut.  Unable to talk and see at the moment has been a source of anxiety and fear and frustration.  Yet despite it all, Dustin has remained faithful and strong.  
Just a week out of surgery, he wrote,

"Through all of the first half of this, so up until this surgery, I have felt really nervous and felt like I've needed to plead with The Lord to help with everything, but through all of the second part, even though it was scarier at times, I've known that The Lord will provide a way for us.  I haven't felt the "urgency" to call to Him as much, I've just known.  Because "we" - you, me, The Lord, our family, our friends, got this."

We don't know how many more surgeries Dustin will have to go through, but we do know one thing - Our Heavenly Father loves us, is aware of us and our situation, and will provide a way for Dustin to return to full health and strength.    We are so very grateful for the many miracles He has given us already.  There have been far too many to number, big and small.  
We are indebted to all of our friends and family (friends we have yet to meet as well) who have offered prayers for us, fasted for us, sent us messages of concern and encouragement, brought food, gifts, and have come to visit.  You have been a large part of our strength and we would like to thank each of you from the bottom of our hearts.

Thank you,
Brittani

Saturday, November 30, 2013

iphone and Mobile device readers.

Hi everyone.  So I am hoping to introduce a new person tomorrow for us to help.  So to follow up on the two guys we have helped so far.

But!  I have noticed that a lot of our viewers are reading our blog from mobile phones.  Here's the deal with that.  If you are reading on a mobile device you have to scroll to the bottom and choose to view the WEB VERSION. If you do not choose to view the blog from the web version you will not be able to see jewelry that we are creating and selling.  So, please try reading it on the web version.

Ok, so since we are going to introduce a new person to sponsor tomorrow (hopefully) I will give you an update on our other two guys.  We will still periodically update on them.

Ed, is still waiting for Medicaid to give him an approval.  He has been approved for MediCal in California, but he wants to do his treatment where his family is in Utah.  That totally makes cense to me.  He told us that his Gallbladder is giving him a lot of trouble and he has really bad stomach pain and indigestion and is still very swollen and bloated from his surgery.  But what is bothering him most is the pain in the right side of his head.  He says it really bothers him mostly every night.  Then he said "But other than that, Im going pretty good!"  That made us laugh a little.  I think he may be able to start some treatments on Monday, but it is still up in the air a little.  This is all very frustrating to him to know that he has cancer inside his body and he has to just sit and wait.  I think that would be very scary for anyone.  He did mention that he has been going to the gym and walking on the treadmill to try and get some of his strength back before he starts chemotherapy.  So as always any prayers or well wishes on his behalf would be very much appreciated.

As for Dayne.  Dayne has just completed a week at the Kennedy Kreiger Institute for physical therapy in Baltimore.  He hated it.  Poor guy.  He is just finally tired of being in pain.  Well, they had a "team meeting" yesterday and decided that they would only be able to do a couple more days of therapy with Dayne because he is just too fragile.  They are worried about fracturing him.  They also want his knees and legs to heal more from the surgery before he does such intense therapy.   Im bummed that the therapy center cannot do more for him, but he will do some therapy in Utah when he returns home. They are going to work with him for a couple more days and see if they can't at least get him to a point where he can dress himself without help. Im sure he would like at least that much privacy in his life.  He is a homebody and ready to go back to Utah.  

So, once again, thanks for reading and hooray for another reader in another country...India! Amazing.

Thanks,
Brittani

Wednesday, November 27, 2013

Giveaway Time!!!

So I really enjoy seeing the stats on who is reading our blog, but we generally don't hear from anyone or get many comments. So I'm wondering how many people are actually reading the post. So here's the deal. All you have to do to enter is leave a comment below. If you want an additional entry you can find us and like our Facebook page www.facebook.com/hellosweetluv . We will pick a winner at the end of this thanksgiving weekend,  the winner will get to personalize one of my favorite styles of necklaces the "Name Plates".
The winner can personalize up to six pieces, and choose two charms/beads. The necklace will be shipped out the following business day. Good luck to everyone and don't forget to leave a comment to be entered into the contest! 
Oh!!! And guess who finally gave me a picture to share... That's right, Uncle Ed! #ibelieve



Thanks again for all your support,
 Brittani 

Festive jewelry set

How fun is this festive set? However, keep in mind that all our jewelry is completely customizable. So you can choose exactly what you want it to say. All for 19.99.

Tuesday, November 26, 2013

Seriously the craziest weekend ever.

So this weekend was supposed to be fun. We were going to put up our tree. (I know, to some that is a little early, but I think it makes Thanksgiving all the more beautiful and special.)  Anyway, so I spent Friday finishing up all current jewelry orders. (We like to have them ship out about two business days after the order, so I stay fairly busy.) well I went to bed at 2:30 am Friday-technically Saturday. When we woke Saturday my little girl let the kale-monster out of his bed and he went downstairs. Everything in our house is child proof so I figured I could lay there for a couple minutes. Well I heard him throw something and ran to see what it was. He had thrown a bottle of 500mg tylenols and broke the cap in half. The pills went everywhere.  He knew he was in trouble so the little stinker grabbed a few and shoved them in his mouth.  So we spend the day in the hospital with him drinking charcoal and having testing done.


So then my handsome Mr. Lunnen came and stayed at the hospital with the baby monster (the monster we are completely obsessed with of course) and I took my little beauties to their Christmas recitals.  I have a hard time watching the recitals because I pretty much cry the whole time.  I am seriously overwhelmed with emotion when  I watch my children do just about anything.  I think I mentioned this before, but I still get a little teary when I take them to school.  I am such a crazy!  But seriously look at those faces!  What is not to LOVE?!

So, sappy mom here put a link to the recitals if you would like the pleasure of witnessing these little angels in action.  

Ellies Performance.

Charli had nutcracker practice in the midst of all of this, and then we had a birthday party to go to.  Good news is that the babies alive, and bad news is that child proof lids on medicine can be broken if thrown...by a child.  Hmmmm.  I seriously could not survive without this little family of mine.  Im obsessed. 

So Update on Dayne, Today he finally checked into the Kennedy Kreiger Institute for his strict therapy regimen.  Today was kind of an orientation day where the give him the rules "Lay down the law" is how he put it, and he has decided that he already wants to go home.  But he is so tough I know that he can get through it.  It is just a matter of getting used to a new routine.  And hopefully once he starts to see some progress and gain some independence his tune will change.


An for an update on Ed, he sounded more positive when I talked to him today.  He said that he had the insurance drama just about completed and was meeting with his doctors again.  I swear I posted this before but I guess that I didn't.  He had to have a couple root canals. Ouch! They were also waiting for all the infection and swelling to clear up in his body before he could start any chemotherapy.  Who knew that even your teeth needed to be in good shape to start Chemo!?  Strange.  I have been begging Ed to send me a picture for you guys, but he just won't do it.  So I stole this off one of his friends facebook pages.  I think they had a quick surprise get together. I have completely enjoyed being a part of the fundraising for Ed because I have been in contact with a lot of neat people that know him well, and have told me so many great things.  I have loved reading all the comments that people leave for him.  #ibelieve
I am told by my mother in law that Ed has lost nearly 30 pounds while he has been so sick.  That he has been having lots of headaches.   However when I did do a little texting with him today he said that he wanted all the names of everyone that donated, or bought necklaces or keychains so that he can thank everyone individually.  

And last but not least I am super excited because I am currently designing some Hand stamped earrings. 

Looks like we have gained viewers from a couple other countries.  This just thrills me! So whomever you are in the Philippines and Iceland...Welcome and thanks for stopping by to read our stories!

Once again, thank you from the bottom of my heart for all of your support!

Brittani

Monday, November 25, 2013

KUTV 2 News

Shauna Lake from Channel 2 news was kind enough to choose us to be a part of her "Favorite Things" segment.  The segment runs every year and are her personal recommendations on what to buy for the holidays.  We are very excited and honored to be featured on this segment. I guess there has been some confusion though.  It is a really easy process to order.  Just look at the styles on the left hand side of the blog, Choose the "add to cart" or "pay now" button and you can customize in that screen.  You also have the option to choose the length of chain you would like.  Just let us know.   It first asks for a payment by paypal, but if you do not have paypal you can pay by credit card.

Also, confusion on the last post, it is missing several pictures and a bunch of information.  Looks like the computer/blog was having issues. Hopefully that won't happen again.

Next exciting thing is that we now have viewers from Iceland!  Wow!  How cool is that!?

Thanks again for all your support.

Brittani

Quick update on two handsome gentlemen in two very different situations. (And the Elf on the Shelf. Ha!)

  First of all I am so excited to announce that we now how readers in the Czech Republic and Indonesia! Holy cow! That means we have readers in more than TEN countries, how exciting is that?! We are so happy to have support from literally around the globe.

It seems like we have had a week of positive things happening. First of all shout out to my 2nd grader who took fourth place in the "Turkey Trot" which is a half mile race. She won a medal and hasn't taken it off for over 48 hours. I'm such a proud Mama.

Along with our positive things we also have been so very busy. Between programs at school, food drives, dental, and doctor appointments, and making like a hundred necklaces (YESSS!!!!!)  So thank you again for your support.

Now. An update on Ed.  We finally after much anticipation got in our #ibelieve silicon bands ...
Awesome right. Check out the one on the left.  That would be the ever so manly  wrist of the     handsome Mr. Lunnen wearing not only his brand new #ibelieve band! but his "unbreakable spirit" one too. (Refer to the more feminine wrist on the right for what the band should actually look like). He has been wearing that band literally non-stop in support of Dayne for over four years. That's LOVE. I say that is deserving of a hashtag or two... #thatslove #superdayne #myhusbandiscoolerthanyours < just kidding. Anyway we have ordered several hundred of these bands is adult youth and child size thanks to my wonderful MIL.  

Monday, November 18, 2013

Update on Dayne

So I have been asking Ed for an update but unfortunately he is not ready at this point to do any updating.  So we will give him his time.  But while we are waiting I will personally thank everyone for the generosity shown.  There are truly good people in the world.  The one thing that Ed has mentioned to me while discussing the amounts of donations or as we talk about the jewelry purchased on his behalf he says that "this is good enough news that for just a moment he is able to forget about his diagnosis and find a moment of happiness." So thank you all for that.  It is truly overwhelming to witness first hand the love that has been shown here.

Now,  While we wait for Ed I think an update on the Dayner-Man is in order!  First lets start with pictures.

So as mentioned before, the surgery was a success and the doctor was able to take the rod in the tibia and replace it and do some bone grafting.  It is in place and appears to be stable. And his legs are nearly straight! Yay!  The bad news is that my mom had noticed in recovery that Dayne did not have a incision on his hip.  This was so discouraging for my mom because the incision on the hip meant that the surgeon would have taken a piece of Daynes bone out to be tested that way they could find a way to hopefully "type" his condition, and find further treatment for him.  When my mother asked the surgeon why there was not an incision on his hip indicating that the bone biopsy was done the doctor simply said "I did my part and it was succssful".  Then walked away.  

When Dayne was little he was told that he had Osteogenesis Imperfecta type IV as well as Spina bifida Occulta. Now over time Dayne has kind of fallen out of the category for the Osteogenesis Imperfecta type four.  He still has the Spina bifida occulta.  As of now there are no treatment options for Dayne.  Can you believe that?  Nothing?  
 So this day was a particularly hard day for Dayne.  Ya know, growing up Dayne has never said "Why me?", or "Why did this happen to me?" or even "Why can't I be like everyone else?".  So we all kinda just kept quiet and thought that maybe Dayne didn't really realize just how different he was from us all. Well boy were we wrong.  Today was Daynes breaking point.  He cried and cried for hours before leaving the hospital.  He was tired and in  more pain that you could ever imagine and he said that he was so sad to be him.  He never wished his situation upon anyone else, but he said that he wished that he could walk.  That he could have a girlfriend and be like everyone else.  Drive a car, go to the movies with friends, whatever, well right now he just can't.  He is so weak and so fragile and requires my moms help for everything.  He told her that the reason he plays video games all day long is because it is the only way to get away from his "head".  To get away from his "mind".  He told my mom that the thoughts that go through his mind are so terribly depressing that he just has to keep himself busy so that he isn't miserable.  This is the night that my mom did exactly what a loving mom should do and she snuggled up to her baby and kept him comfortable through the night.

 Dayne has had a hard time making friends because he is different from everyone else.  I was under the impression that kids were more kind than they are, but I was wrong.  When I took Dayen to get his yearbook signed last year I spent most of the time crying because there were maybe only a handful of people that talked to him.  It broke my heart.  Anyway, this kid has been through so much.  I was going through pics last night and ran into this one that nearly killed me ...
We almost lost him during this surgery.  
Here are a couple more current pics from the surgery this time.

Looking so much better!  
And you are welcome!  A video of the Dayner-Man dancing to his music! Talk about making the very best of a bad situation.  Now I talked to Dayne the other Day and I posted it on here before.  Dayne has this wish to meet SHAY CARL.  So SHAY CARL, wherever you are, for the love...would you please send this ever deserving boy a message or something! It would make his life!  Or if anyone reading this is able to get in touch with Shay Carl from YouTube, please, please help us out.  This is his wish.  

Now my quick little message to my brother, Dayne, I miss you so much and I am so proud of you for being such a champ through all of this.  It is all painful now, but in the end it will all be worth it.  I am so blessed and privileged to be your sister.  

Oh, and a favor to anyone who reads this...Dayne could really used some encouragement.  His spirits have really been down.  If you have a little message you could send to him to give him some encouragement it would mean the world to not only him, but to me as well.  Please send Dayne a message to hellosweetluv@gmail.com and I will get them all to him.  I am hoping to overwhelm him in the best of ways with all of your messages.  How cool would it be to receive some letters from some of the countries that have been reading our posts...Canada, Nigeria, Japan, South Korea, Nepal, Australia, Russia, France, Germany, United Kingdom, Malaysia, Mexico, Ireland, Israel and Granada,  Holy moly that would make anyones day and give them a little more fight to carry on with their life long battle of pain.  

Love to you all and Thanks for caring enough to read about my baby brother and to keep him in your thoughts and prayers.  Please, please send him a message at hellosweetluv@gmail.com

Daynes Sister, 
Brittani


Thursday, November 14, 2013

A message from Nick (Eds nephew)

Hey everyone, Brittani said it was my turn to blog tonight and asked me to tell you all about my Uncle Ed.  Ed and I are two and a half years apart, so a lot of the time he felt more like my big brother than my uncle.   When I heard Ed had cancer, I could barely believe it. Ed? That's crazy!  I immediately went through the full gamut of emotions, just like everyone else that found out.  And since finding out, it has continued to be an emotional time for me.  We have had so many calls, texts, emails, messages from people who care so much about Ed.  Most people tell us that the news has left them crying for hours.  Which is why we have been trying to help in any way we can.  We have been overwhelmed by the outpouring of love and support whether it be financial, kind words, and jewelry orders to show support.  We are so grateful.  All of this has left me reflecting reflect a lot about Ed and who he is to me.

When you're a kid, there's always people you idolize.  For me it was just Ed.  I didn't actually meet Ed until I was 8. My dad, had just finished up law school a few years earlier in New Orleans and we took a trip to see our family in Utah. Until that point we were  pretty far away from  all of our relatives on the Lunnen side.  That trip to Utah was really the first time I met my Grandpa and Grandma Lunnen as well.  Ed was ten.  I'll always remember that trip.  When your'e a kid everything is so amazing.  Grandpa's house had this really cool loft up on the second story.  That's where Ed's room was, the loft.  I immediately thought Ed was the coolest person I had ever met.  We played games and army with the little green troops and told ghost stories all night with flashlights.  It was a blast.  After that trip, I thought Ed was the greatest.

Years later, we moved up to Salt Lake because my Dad had found a job there.  When I was 12, my Grandpa Lunnen's health started to decline. So my Dad and Grandpa agreed that  Ed and Doree would come live with us.  They lived with us for 3 years.  It was the best.

As I said before, when they moved in I was 12.  Being twelve, I was just starting the tough years where you try to figure yourself out.  Ed was there for me.  I am the oldest of my siblings and so he was the older brother I never had.  I idolized Ed. It's pretty funny thinking about it now, but I wanted to dress like Ed (at that time it was wearing super baggy jeans past your butt and 3-4 pairs of boxers. LOL), I cut my hair like him, I talked like him, and pretty much anything Ed thought was cool, I did too.  Ed was the popular guy in school.  It seemed like he had everything going for him.  A lot of teenagers might get annoyed  having their nephew follow them around all the time and want to be just like them.  Not Ed.  He always included me in things, never made me feel like I was annoying.  He just made me feel accepted, it that was exactly what I needed.  He would let me tag along wherever he went.  I went to all sorts of high school parties even though I was only in the 8th or 9th grade. (probably some I shouldn't have gone to. Ha!)  There were plenty of times we got in trouble for missing curfew. But I didn't care because we always had fun!
We have already established that Ed is a professional volleyball player.  Growing up with Ed he taught me to play volleyball.  From the moment he started teaching me I shared that passion with him.  I too wanted to someday be a professional Volleyball player.  I would always go play with him and his friends.  That was one of the things I looked forward to most.   Looking back, I always wonder why he was so cool and willing to take me to do all these things with his friends.  Well, it's because that's the kind of person Ed is.   He's one of the most genuine and caring guys I know.   He had the coolest friends around, they treated me like a friend too, not like Eds younger nephew.  I always looked up to these guys. Aaron Sanders, Amora, Salman, Danny Chi, and many others.  I think it's just that great people hang around with equally great people.  It's been amazing to see all of Eds friends come together to support him at a time where his world must seem to be crashing down around him.

Anyways, I just wanted to let everyone know what kind of person Ed is.  Chances are if you've met Ed for even just a few seconds, you'd know that he is a special guy.  He accepts you and makes you feel important.  He's always joking around and making the mood a little lighter.  Well, I won't ever forget how Ed made me feel important.  I only hope I can return the favor and pass it forward.  You've got this Ed. #ibelieve. Love ya man.

Nick

(Just a little update on Eds current situation.  Before Ed is able to start any Chemo treatments for his cancer they have to make sure his body is free from any infection.  Because of the severity of the ruptured appendix that required the lengthy surgery this is taking a little extra time.  They also have to wait for the swelling (also a result from the ruptured appendix) to go down.  )

If it isn't enough to have to deal with a serious illness, and a devastating diagnosis, we are finding out that applying for any type of health insurance has become quite discouraging itself.

Thank you, Thank you for all your support and kind words.  Ed wants to post and thank you all himself and give a little update, we will wait for him to be ready to do that.