That hair, that hair, that hair…

 

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Phoebe is on the left in this picture. Is her hair to die for or what? Big thank you to my little Rachel for making her day yesterday. Love you, Rach. You are the sweetest soul. Thank you all who have left such sweet comments on Phoebe’s page. Truly made my day.

Next up for Phoebe is a bone marrow transplant. Please keep her in your thoughts.

http://www.caringbridge.org/visit/phoebe26

 

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“Do this for Ro.”

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Ronan. I survived your 22 months. It was actually an o.k. day. It didn’t start out that way. I woke up, upset, crying, worrying about you like I always do. I swear I worry about you more now than I did when you were here and alive. Your brothers had basketball playoffs. They were the only team undefeated in their league. Your daddy spent all week practicing with them, coaching them, playing with them and their hard work has really paid off. On Saturday, they had an early morning game and if they won that, they would head into the final championship round. Your daddy and I spent the morning giving our usual pep talks and telling your brothers how proud we are of them. Off to the game we went and you could feel how excited they were to be playing in the playoffs. Before the game started, I walked on to the court, gave them both fist bumps and said, “Do this for Ro.” They both smiled and said, “O.k. mom.”

I sat back and watched your brothers as they had the time of their lives as they played their little hearts out. Both of them played the best games of their lives and the first game was won. We took them for lunch after as we had a couple of hours before their next game started. We talked in the car about how great they did, how great their whole team did, and how proud we knew you were. I tried not to get too sad as we talked about you and did my best to keep a smile plastered on my face. It wasn’t hard but talking about you and not having you around, still hurts for me and still takes me breath away. I would so much just rather have you here but beggars can’t be choosers, as they say. Your brothers went into the final game wanting to win it all so badly. That is exactly what they did. I watched them fight for something that they really wanted. I watched the fire and passion pour out of them as they played. I know much of this was fueled by you. It made my heart skip a beat, watching them on the court. Basketball has become their passion and outlet. I truly feel as though it has saved them in a way. The smiles on their faces after the game and the days to follow have been smiles that I will never forget. I know I say this all the time, but I am so proud of them. I am so lucky to have them. They truly are the best little boys.

Things here have been busy, but I’ve been trying to keep things as calm and peaceful as possible. I’ve started seeing Dr. Schwartz every week. Today, we sat in her office and talked. I asked her when she would be able to strip my membranes, to get this baby girl out. She asked if I was miserable. I told her no, that I just had a lot of anxiety. I told her about the support group I went to last week and how pretty much everybody in the room had a baby that had died of still birth. She said she could not believe I went to that. She sat down with me and told me she was sorry. That if I was that anxious we would of course figure out a plan. We picked out a date. I felt a little better after leaving there. She told me not to go to any more support groups as of now. I told her I would not, that I would just continue to see Dr. Jo, one on one. That seems to work best for me anyway. Those support groups have never worked well for me. It’s great to connect with other parents, but having to listen to everyone tell their stories is beyond heart wrenching and I’m not really in a strong enough place where I am o.k. with it. I wonder if I ever will be.

I had a little phone call today. I don’t want to talk about it too much as of now, but we’ve got some crazy big things in the works. I feel very blessed and excited to have such big power houses involved with your foundation. Not only powerhouses but powerhouses with the BIGGEST hearts of all. That makes such a difference to me. After my phone call, I ran to the post office to mail out some bracelets. I’ve become pretty friendly with my post office lady due to being there all the time. Today, she asked me what I was so busy mailing off. I told her the rubber bracelets I wear around my wrists which are for my son who died. She looked at me and bluntly goes, “How are you doing with that?” I just told her, “I’m not.” She told me that it will never get easier and confided in me that she had lost 2 sons. I told her I was so sorry. I thought to myself, another mom who knows this, gets this, and is not scared to tell me it doesn’t get easier. Then to my surprise she told me a sorry wasn’t necessary. That her boys where exactly where they should be, with god. My stomach dropped. A year ago, I would have lost my shit on my blog and ranted about what in the world is wrong with all of these delusional people, that think this way. If somebody tells me this, who does not know what it is like to lose a child, I might still punch them. But when it comes from somebody else who has lost a child, I am not going to judge that or tell them their way is wrong and mine is right. If that is what she truly believes and that is what gives her peace, more power to her. I quietly told her that I didn’t like that saying. That there is no better place for my son to be, but with me. I can agree to disagree with her on that one. I walked out of the post office thinking about her words. Not mad, not sad, just accepting. Obviously this woman has a stronger faith than I do and I am glad that she does. What works for her is not for everyone. What works for me, is not for everyone. At the end of the day, both of us are still here and we are surviving this extreme loss, day after day after day. That makes us both fighters in our own way. We both know how this pain feels. We both know this pain will never go away. We should all be proud of ourselves for finding our own light at the end of the tunnel that gets us through this; no matter how differently it may be.

I ran and saw your Sparkly for a bit today, aka, my peace. He is the only person that I feel complete and utter peacefulness around, Ronan. It’s been this way since the very first time that we met him, just the two of us. I’ll never forget the wave of calmness that washed over me while I was holding you in my arms and he came bursting around that corner. I knew that instant, that he was going to take care of us, no matter what happened and he has. I will forever be grateful for the bond between the two of you and now, to have him be the godfather of your baby sister… that is truly such a gift. He knew I had a hard week last week and was relieved to see that I was doing a little better this week. We talked about you and your Poppy sister much of the time. He kept telling me how excited he is for her arrival. I am so excited to meet her as well, but I might be even more excited to watch him hold her for the very first time. He has been with me in death and now this new life. I know a lot of people have, but he really has seen me through everything. The worst of the worst and now the best of the best. He laughed at the way I was touching my belly and made sure to throw in some smartass remark about how big it has gotten. I know he only did this to see me laugh, which I did. Your Sparkly always has a million tricks up his sleeve to make me smile. I love that about him. I told him how I couldn’t wait to have a little one to take care of again. I know it is going to be so good for my heart. I know she is going to be so good for everybody’s hearts. Thinking of this always makes me smile. The sweetest part of this for me will be seeing the way she brings a light into so many of our worlds. Especially your Daddy and your brothers. I know she truly is a gift from you and I will find comfort in that. I left your Sparkly with a smile on my face. Just the way he likes to see me. I am glad I was feeling alright enough today, to do so. I don’t like the days that I have to leave him any other way.

Alright my spicy little monkey boy. I have to get some things done around here. I miss you. I love you. I hope you are safe.

xoxo

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You know what is so totally awesome about cancer? Fucking nothing.

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Ronan. Today, I was sitting at my kitchen table pounding out emails, mailing bracelets to people, and missing you. A new email came in and it was an update from your old roommate at Sloan-Kettering, Phoebe. I still check in on her every once in a while. I still try to see her mom whenever I am in the city. We became pretty close after rooming together at Sloan and I know her mom and I both feel that the two of you had this unspeakable bond. I have been keeping up on how well she is doing and watching her get back to her life before she had to deal with that asshole named cancer. I have loved seeing her gorgeous hair come back in and felt really peaceful about the place she is in after she was declared NED from Osteosarcoma; which she developed at the age of 11. Phoebe endured so much, as do all kids who go through this, but her fighting spirit has never wavered. Her smile never seemed to dull. She is stronger than most adults but of course that came with a very heavy price. She shouldn’t have to be stronger than most adults. She should just be a normal girl, living a normal tween life. Unfortunately, that’s not how things have turned out for Phoebe, but you will never hear her complain of a thing. She has handled everything like a champ: much like the way you did.

I think we bonded with Phoebe and her mom for the first time over a bloody nose that wouldn’t stop. I knew that situation all too well. Being roommates in such close quarters, you hear everything. I think I tried to step in and help. Macy was with us. I think Tricia was, too. We will never forget it. Phoebe was scared. Her mom was scared. I did my best to help out because I had been in that situation 50 times before. I was an old fucking pro at the horrific bloody noses that you cannot control. After that bloody nose incident, we became friends forever. You died, Ronan. Phoebe lived. Her mom and I have remained close and her entire family has a special place in their hearts for you. Ellen, Phoebe’s mom, is always reminding me of how much they think of you. I so appreciate that.

I read the headline of Phoebe’s caring bridge journal today. It said, “Bad, Mad, and Sad News.” My stomach dropped. My eyes filled with tears. I knew what that meant, before I even started reading what was going on. Phoebe, after beating Osteosarcoma has developed a secondary cancer. This time, it’s AML- Acute Myeloid Leukemia. I immediately sent Ellen a text that said, “I just read your blog. You have got to be fucking kidding me.” She responded almost instantly and we went back and forth. I told her I would do whatever I could, which normally might mean hopping on a flight to go and help. I cannot do that now so I offered up the next best thing to Ellen and Phoebe which is my little Rachel who lives in NYC. I told them if they were o.k. with it, Rach would be happy to come by to keep Phoebe company, bring them treats, or whatever else they might need. They were very open to it so I called up Rachel who was more than happy to help out because she is not your normal 22-year-old. Rachel is an old soul who has such a passion for helping others that it makes me embarrassed at my 22-year-old self. She is the definition of selfless at such a young age which I admire so much. I asked Ellen if it would be alright if I posted Phoebe’s caringbride website because I know Phoebe tends to be a little more private. Ellen gave me the green light. I just wanted to offer them any and all the love and support that I have. They are a wonderful family and I am so devastated that Phoebe is going to have to go through more of this bullshit which was more than likely caused by the treatment she had when she was dealing with Osteosarcoma. I mean it’s bad enough that kids get cancer, but then to develop secondary cancers due to the treatment that supposedly saved them. That is just beyond acceptable.

I am asking you all to show Phoebe a little love. Stop by, leave her a comment, keep her in your thoughts, prayers or whatever works for you. She has a special place in our hearts here at the Thompson household and we will do whatever we can to help Phoebe through this time. Even if it means just making her mom laugh by my, “You have got to be fucking kidding me,” text. So glad to hear I was able to put a little smile on her face today. I am so glad I have my little Rachel in the city to help out, too. Thanks, Rach. I love you so.

Ronan. Ellen asked me to tell you to keep a special eye on Phoebe. I know you will. I love you my spicy little monkey. I promise to fix this. I promise this childhood cancer world will some day be better. It shouldn’t fucking be like this. This is my last little rant for the night but wouldn’t the world be a much better place if people like Honey Fucking Boo Boo were NOT on CNN? I about shot my TV the other day seeing this. Wouldn’t the world be a better place if people like Dr. Sholler or Dr. Jo were getting the kind of attention they deserve because they are actually doing really amazing work. I don’t understand how these doctors are ignored. How this HUGE problem is ignored. How these kids are just ignored. I guess because it’s easier to live a mediocre life where every day seems to be taken for granted and everybody seems to care about the wrong things. I can’t live in a world like that. I won’t live in a world like that. I’m going to create a new fucking world where shit like Honey Boo Boo or The Real Housewives of Asshole America, do not exist. Because people like Ronan and Phoebe deserve better.

Bye, Ronan. I miss you. I love you. I hope you are safe.

Here is Phoebe’s caring bridge below. Thanks all you lovely souls for stopping in to give her some RoLove. I love you.

xoxo

http://www.caringbridge.org/visit/phoebe26

A date where no pants are required

 

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Ronan. Another week done. Another week closer to your baby sisters arrival. A lot happened this week for nothing happening at all. I’ve spent most of the week doing I don’t even know what. Taking care of your brothers has kept me pretty busy. I feel like I’ve poured everything I have into them just so they know how very loved they are. There is a new baby coming. I am trying to be fully aware of everything they may be feeling with this. How does a 9-year-old process the death of their little brother and soon after that, the birth of their little sister? I have no freaking idea. So all I am doing is talking with them as openly as I can while pouring every single ounce of love and affection I have to give, into them. Liam finally got his new glasses and has been wearing them around the house and when he is out and about with us. He looks so handsome in them. He won’t wear them to school yet and I’m not pushing that on him. I’m just trying to let him get used to them first. I wish you were here to see him in them and how proud he looked when he put them on and looked in the mirror at himself. The first time he put them on in the car he goes, “Wow! I can see perfectly!” It made me laugh and broke my heart all at the same time. My sweet gentle giant. He slept with your daddy last night and I curled up in Quinn’s bed with him. Quinn must have told me 10 times how much he loves me. I snuggled up with him as we fell asleep. I always picture how it would be if you were here. I know you wouldn’t be sleeping in your bed but you would be snuggling up with your brothers instead. You loved being with them so much.

I saw Dr. Jo today for some therapy which included the chocolate cake she had waiting for me when I arrived. BEST.THERAPIST.EVER. We hashed out the weeks events. We talked about this Poppy girl and her birth. I told her I didn’t think I could make a specific birth plan for her because as with everything I do, winging it seems to be the best and works for me. I know she will be there and that is good enough for me. We have talked about having your Urn in the room with me. My only hesitation with that is that somebody might break your urn and ashes will go flying everywhere. But I think having your urn in the room with me as something to focus on might be good for me. We will see. I feel like I have been crying a lot. Crying when I’ve been hiking. Crying in bed. Crying when I’m driving. Crying over every song that comes on the freaking radio. My tears seem endless lately. It is just because I miss you so much. I just miss my best friend. I just miss my spicy monkey. I just want you back in the worst way possible. Dr. Jo asked me today when I thought I would be ready to forgive myself. I told her I didn’t know. That maybe Poppy would tell me when it is time in a secret way and only I will know what it means. Maybe you will let her know when it is o.k. for me to forgive myself for all the things I hate myself for that I know are truly not my fault. I think your sister is going to bring so much light into our world that I so very badly need. I think she will be able to hold my hand through this darkness in a way that nobody else can. I cannot believe she is almost here. I am so glad because I truly do not think I can wait much longer for her. I know I will be able to breathe much easier once she arrives. Both literally and figuratively.

It’s kind of been breakdown city over here this past week. It’s been one of those weeks where I feel like I have the weight of the world on my shoulders. I walk around every single second of every single day knowing that you, the love of my life, died. I never for a second forget that. I constantly feel like I am just here, doing my best, but blindly stumbling through this life without you. I never forget that I don’t have your hand to hold, your little lips to kiss, your messes to clean up, your hair to wash, you to dress or tuck in at night. Some days, I don’t know how I live without being able to do all of those things with you or for you. What I wouldn’t give to be cleaning up your messes or wiping up your puke from the flu. Even when you were here, doing those things, it was never an annoyance to me. I never got mad or upset or complained about the lack of sleep or things I was “missing out” on because I was just so thankful to have you. Even before you were sick, I knew what a gift you were. I don’t understand how you are now sitting on top of my dresser in a fucking urn. I still don’t understand how this all happened. I promise I am doing my best, Ronan but it feels so hard at times. I still know you miss me as much as I miss you. I still know we were never meant to be apart. I will forever think that this is so wrong and so beyond fucked up.

Today, Dr. Jo asked me if Inferno Fuckwad Bob was still around. Meaning my nickname for my grief. I told her yes, but I didn’t hate him as much as I used to. She told me she knew that would happen as it’s part of this shift. How her grief has become one of her best friends. I nodded my head and told her that made sense as our grief is never going anywhere. She goes “That’s right. So we may as well invite him in for a cup of tea.” I understand now. I can’t spend my whole life angry and fighting with my grief. I live with my grief 24 hours a day, so I’d better learn how to make the best of it. Your daddy went to the Suns game tonight. Your brothers are at a birthday party. If you were here, we’d be off doing something fun. Instead I sit in our house and cry for you, alone, the way I like it. Sometimes I have to take a break from the outside world. It’s still hard for me to be among the normal, happy people of the world. I’d rather sit here with my best friend, Inferno Fuckwad Bob instead. At least I don’t have to wear pants for our date.

I miss you. I love you. I hope you are safe. Sweet dreams, baby doll.

xoxo

 

This is all thanks to you and your votes! Rockstar Ronan won! Thank you!

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http://www.parents.com/parenting/better-parenting/advice/parents-blog-awards-finalists/#page=3

I have a chronic illness and it’s called sadness

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I had big plans today. HUGE plans. I had decided on them last night while I was in my bed, crying. I thought to myself, “Tomorrow I’m going to do nothing but stay in bed all day long.” I got up this morning, hopped in the shower and just as I was getting dressed for my “big day,” I got a text message from Stacy. It simply said, “Can you meet for breakfast?” I didn’t even hesitate as I texted her back, “Yes,” and plans were made. A year ago, I would have told Stacy in no way shape or form, could I possibly meet her for breakfast. That was the state of mind I was in last year. Things are different now.

I met up with Stacy and as soon as she sat down she said, “Fernanda is meeting us, too.” “Great!” I said. Even though she just had surgery, she still was popping in for our little breakfast which I was surprised by, but shouldn’t have been since her nickname should be freaking Superwoman. I sat and caught up with my friends and our breakfast ended up turning into a two-hour meal/discussion/sob fest. I listened as Stacy and Fernanda talked to me about some things they know I am struggling with. Mostly about the last week or so of your life. They told me they know how I am regretting not having you die in our home and I listened as they both explained to me why it was that we were encouraged to take you to the Ryan House. I hadn’t really ever heard this from them before. They talked about how scared they were that you were going to die this awful, painful death by basically drowning on your own blood. How for many kids that die of Neuroblastoma, this is what happens. It is usually a very painful and awful death. They talked about how they didn’t want your blood, all over our house. I listened to them, understood and now I feel like I can let this little piece of my guilt go. I do not blame anybody for pushing us to take you there. I know my friends only had our best intentions at heart as they always do. We all sat and cried talking about this. I said something about I only have the guilt because you begged me to go home and I feel like I didn’t answer your one little dying wish. Nobody knew you were going to die so peacefully the way you did. Nobody knew you were just going to fall asleep. I looked up at the girls and one of them, I can’t remember who goes, “But Maya, don’t you think Ronan’s home was wherever you were?” I nodded my head in response. We talked about some more things as we continued to sit and cry at the table.

I told them about the chapter for this book that I am supposed to be working on. I told them about what it is I was thinking about writing about. I watched as the color drained from Stacy’s face. “You can’t write about that right now. You are going to give birth soon. You cannot write about that.” Fernanda’s eyes welled up with tears. “You need to listen to your gut, Maya, but do you really want to write about that, now?” I told them I was having a hard time working up the courage writing about this part of my life, but it was the only thing my mind kept going back to. I listened to them both and their advice. I left our breakfast still unsure about taking on this chapter but I could not think of anything else that I could connect with to write about. I ran a couple of errands after breakfast and cried almost the entire time in the car. I came home and made a decision to head up our mountain to go hiking today. I can’t take another day of not doing a thing, exercise wise. I put on my clothes, threw on your little backpack and off I went.

I didn’t wear my headphones or blast my music while I hiked. I listened to my head instead. I listened to you. I took it slow up the mountain to keep your Poppy sister safe. I felt my head become less foggy. It was as I was coming down the mountain that I decided what I am writing my chapter about. It suddenly came to me so clearly just the way things always do when I am outside, exercising, and listening to myself and you. It felt so good to be free and clear with my thoughts flowing non-stop. I’ve said this from day one; nothing good will ever come from me hiding in my bed. I cannot change the world this way and for sad as I am and for as much as I want to hide, I can’t. Because if I hide then I die and I really don’t want to die anymore.

I said something to your Sparkly yesterday that has been bugging me to pieces. I told him I was working on being less sad. Saying that left a bad taste in my mouth and I have been mad at myself ever since. I texted him today as I was going up the mountain and told him that I had decided that me saying I was trying to be less sad, was bullshit. That my sadness is like a chronic illness. It’s something I’ll always have and it will always be a part of me. I have to accept it, stop trying to change it, and learn to live with it. I will never be able to get rid of my sadness but I can learn to manage it. Managing it for me will come in many different forms and I am slowly figuring out the “medication” I need to treat my sadness. No, not real medication. My medication. The things that work for me and help me through this life. Things like exercising, nature, writing, helping others, surrounding myself with the kind of people who build me up, not beat me down, and trying to live a life you would be proud of. That’s my prescription. It may not be prescribed by a real doctor, it may not work for everybody, but it works for me and that’s what I’m sticking to.

I’m tired from today and the hiking wore me out, but it made me feel good as well. I’ve missed our little mountain so much. I see Dr. Schwartz tomorrow so she can check up on this baby sister of yours. Please keep her safe and sound for me, Ronan. I miss you. I love you. I hope you are safe. Sweet dreams my spicy little monkey.

xoxo

 

This explains why I will never support the American Cancer Society. They do nothing for our kids except use them. Making money off of our kids for your huge salaries!?!? NOT COOL!

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http://www.huffingtonpost.com/jonathan-agin/friends-dont-let-friends-_2_b_2759403.html

Grants, Grants, and more Grants.

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Do you all know of any grant applications that we need to know about? Our board is currently in the process looking for them to help us build our center and continue to help children in clinical trials.. If you do, I’m kindly asking you to forward anything at all to one of our board members, Melissa DiFilippo. Melissa handles all grant funding and nominations for the foundation and would appreciate any leads.

We could use help searching for these grants. These grants could help save children’s lives!
Melissa’s e-mail is melissa@ronanthompson.org

Thank you so much!

I am in love with your sister and her hicupps

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Ronan. I have no idea what I did this week. Not only do I have grief brain, I have pregnancy brain to go with it as well. It’s amazing that I can even drive a freaking car. I feel foggy, heavy, sad, tired… this is NOT depression, P.S.

It’s hormones, grief, and pregnancy. And no… I do not need medication. Nor will I ever need medication for my sadness which is just that. Sadness from losing you. My sadness will never go away and I am o.k. with that. It will forever be a part of who I am. I will deal with my sadness in ways that work for me and no pill will be required. I have been daydreaming a lot. About popping this Poppy out and being able to be free again. Free to go running. Free to go hiking. Free to blow off some of this crap that I have been holding in due to not being able to exercise the way I want to or need to. It’s the only thing that makes my head less foggy. I have been missing my running and hiking so very much. That is the time I feel closest to you. When I am connecting with nature and myself. It’s a good thing that this pregnancy is coming to an end because I am about to burst not having the outlet I am so desperately craving.

Most of my week was spent playing catch up with some things and taking care of your brothers while trying to rest up a bit. Your daddy has been the best helper, as always. I am slowly getting ready for your Poppy sister. It is still one day at a time with all of this as I am being very careful about trying to only buy the things we will need right away. I’ve been making Fernanda so nervous about everything that she just went ahead and ordered Poppy’s crib for me, and didn’t tell me until after! Leave it to her to just take things into her own hands. I couldn’t possibly love her more. I sat with Stacy yesterday and went over a list of things I do not have, but will need. Things such as diapers, burp cloths, bottles, a boppy. I ran to the mall today to exchange something and talked myself into going to Pottery Barn Kids to look at some bedding. Your baby sister needs some sheets. As soon as I got in there I was so overwhelmed. I snuck back to take a peek at what they had. I am so indecisive that I almost had a panic attack. I was walking past the counter and the sales lady goes, “Do you need help?” I just politely smiled and told her no. She then goes, “Have you registered?” I just laughed and said, “No, I have not.” I knew I was not getting off that easy and sure enough she goes, “You look like you’re about to pop and you have not registered?!” It was obvious that not only was not registering a sin, but that I had 3 heads as well. I just smiled and walked off. I was not about to explain our situation and how I had tried to register for baby things, but could not even get past the first few things that I was going to register for. I found myself back looking at the boy stuff and all the new Star Wars stuff they have gotten in. I was so sad as I ran my hands across the new Star Wars sheet set and thought how I would have totally bought those sheets for you. All I wanted to do was crawl into the Pottery Barn bed, pull the covers over my head and never come out again. I practically ran out of the store after that. Fuck that place.

I came home and finished cooking up the best meal ever for your daddy and brothers. My short ribs and mashed potatoes. It felt nice to do something nice for all of them. They have been taking such good care of me. Your brothers are the best little helpers around. I knew I wasn’t going to be home for dinner so I wanted to make sure they didn’t have to eat out, again. They were so grateful and thankful for the home cooked meal. I skipped out shortly after they left for basketball practice to go see Dr. Jo.

I spent a couple of hours with her. I’ve been trying to spend more time with her, talking about everything now that I have slowed down a bit and have more time. It feels good. As we were sitting there tonight, Poppy kept thumping me in the same spot over and over again. I said to Jo, “Feel this. What is she doing?!” Jo came over and felt my stomach. After a minute she goes, “She has the hiccups!” OMG. Cutest thing ever. I don’t remember ever feeling you boys have the hiccups in my tummy. The thought of this little baby girl, hiccupping in my stomach, pretty much made my night. I spent the rest of my time with Dr. Jo going over a lot of things and now I am so beat I think I have no choice but to end this and pass out now. I cannot possibly form another thought. Our sessions are always a lot of work and always exhaust me. Your brothers are in my room with me and I am going to snuggle up to them. We all miss you so much.

I love you, Ro. I miss you so much. I hope you are safe. Sweet dreams, little man.

xoxo

WOW! This is all because of you! Thank you so much! For our first marathon, this is amazing!

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We are beyond EXCITED to announce that our P.F. Chang’s Rock-n-Roll Marathon and Half “Run Like A Rockstar” Team raised OVER $94,000!!!! Can you believe it? $94,000!!!

A special thanks to ALL involved! We are already gearing up for next year!!

xoxo

 

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