weekend.

This weekend was my little Sister’s Bachelorette “day” out. We went on a luncheon cruise (where everyone drank amazingly delicious smelling sangria) and listened to a DJ play some serious wedding tunes. It was really relaxing and enjoyable, even if I did feel like I wanted to yack once or twice. Thanks motion sickness! Afterward we went and got pedicures, and walked around an outdoor mall for a while.

All in all it was a pretty awesome day, and I’m really happy I was able to come home for the weekend and spend it with my sister (and the other bridesmaids).

When I got back to my Mom’s, I was beat. I guess being almost 31 (ugh. ugh ugh ugh.) will do that to you! Ha- just kidding. I know 31 isn’t “old” in the grand scheme of things life, but holy shit…I feel old now. After Kenley died, I immediately aged 10 years physically, and probably 50 years emotionally/mentally. I feel like I look old, I feel like I have no desire to do much of anything (hello depression, you nasty bitch) but I try to make myself look presentable (usually fail pretty well at this and end up in mascara and leggings). I have to force myself to enjoy things (also fail). I have tension headaches a lot these days, and I can feel the anxiety heavy in my chest. Sometimes, I will have an extra anxiety ridden day and I can literally feel it in my sternum. I have the need to crack my chest; until I make it happen, I have an excruciating pain where I can’t stand up straight and taking a deep breath is like knives in my chest.

Anyway, back to this weekend.

Landon has been sick for 50 years (read: 1.5 weeks-ish) and I just figured it was seasonal allergies, or a mild cold. He started to get pretty lethargic and stuff last week so I kept an eye on it and told myself if he wasn’t better soon that I would make an appointment. Saturday he complained of a headache all day, and over night he came into my bedroom screaming and hyperventilating saying that his head hurt so bad on the right side. I tried to calm him down, ended up giving him some Motrin and he laid with him until he fell back to sleep. In the morning he came into my room at 6am complaining again. I got up, and fed him breakfast and we watched Spongebob in the dark until about 7:30. He then started crying and freaking out about his head again.

I didn’t know what to do and honestly he was starting to scare me. I told my mom that I needed to take him to the ER so off we went. Long story short no strep, no ear infection, no anything. They gave me a script for Sudafed- a decongestant. I’m not sure how this will help his intense head pain?…but I’m no doctor. I’m going to keep a really close eye on it, and the second he complains again about his head we’re going to get a CT scan. I don’t really talk about it too much, but when Landon was 3 we had something similar happen to him. He ended up needing an Electroencephleogram (An electroencephalogram (EEG) is a test used to detect abnormalities related to electrical activity of the brain. This procedure tracks and records brain wave patterns. Small metal discs with thin wires (electrodes) are placed on the scalp, and then send signals to a computer to record the results.) because he was having super weird twitches and making random noises all the time. I was pretty sure that he had Tourettes or something.

Turns out he was ok, but has “extra electrodes (or neurons? I can’t remember) firing in his brain” and for people with this, 50% of them have a 50% chance of having a seizure at some point in their life time. So…technically not ok? But again…not a doctor here.  Also they mentioned that children with these extra whatever’s firing are often “gifted”. That’s about the only part that makes sense. If you know Landon at all, you will probably more than likely agree the kid is super fuckin smart.

Ask him anything about Dinosaurs, I dare you.

We got back to my Mom’s, packed our stuff up and went to visit my Dad for a little while. As we were leaving my Dad’s, Shane text me and said he just got breaking news on his phone that there was a shooting on I-71 near the Polaris area.  The Highway Patrol had shut down both north and southbound lanes of the highway, so I figured I would be stuck in traffic. Well,  when I got to the I-71 on ramp in Mansfield, it was a shit show. The traffic lights were all out, there were no cops there to direct traffic because they were all at the crash scene of the shooter literally 2 miles up the road. Landon and I got some lunch, and hung out in the car for a little while to watch the traffic nightmare.

I googled and found out that the shooter had shot a man 6 times from a park bench (wtf is wrong with people?) as he was walking back to this car from the restroom at the rest stop. He then hopped in his car, and drove north. The cops found his vehicle on 71 and chased him north of the Mansfield exit where he ran over spike strips and hit the guardrail. He then shot and killed himself in his car.

I was watching the highway as we ate lunch, and I saw the cars that are pictured in the news article I linked to speeding down the highway toward the crash sight. It’s insane to me how close I was to actually witnessing this high speed chase. Thank god I didn’t. Once I got on 71 South, there was no issue and we made it home pretty quickly (1.5 hrs).

So now I’m home and curled up in bed with Shane. What a long weekend!

Here’s hoping that Landon feels better, I feel better and Shane doesn’t catch what we have.

Also, I’m participating in the “capture your grief” photo challenge for the month of October which is Pregnancy and Infant Loss awareness month. If you don’t know what it is,  head on over to my Instagram page (see the side of my blog for the link) and check it out. It’s amazing, and I know that it is such an important thing for myself to do. It helps me to honor my sweet girl, and keep her memory alive.

You can also see a new photo of my beautiful Kenley. I am so in love with her face.

 

 

38+4

Today is another rough day.

Today, the amount of time that has passed since you died, is the amount of time you were alive.

Tomorrow you will be gone longer than you were with us.

I don’t think there are words to describe the way that I’m feeling.

The only thing that I feel like doing or saying is screaming from the top of my lungs that I love you.  That I am your Mother. That you are my Daughter. That you were taken away from our family. That I will always ache for your presence in my life. And that I will never be whole again.

 

unreal.

This whole year has felt unreal; I feel like I am just going through the motions of life in a fog. I know a lot of that is grief and I’m sure someday it will feel different, but for now it still feels this way. Around the 6 month mark I started to feel like the fog was lifting, but now at 8 months out, it feels as if it’s starting to get foggy again.

My brain is pretty much mush anymore, I can’t remember anything, and I know that I’m blocking a lot of stuff out. At the end of each day I feel as if I’ve just finished running a mental marathon. I can’t wait until the moment I get to go to sleep for the night because it’s the only time I feel at peace. It feels like a lot of people’s lives have gone back to their “before”, and that’s ok- I don’t expect people to dwell on my sadness. There are people who randomly let me know that they are thinking of Kenley. They will send us something, text me, email me, or just make a gesture in honor of our family.

Those people are amazing.

I do feel, however, that there are people in my life who think I should be better. Maybe they think that I have too many “bad” days. Maybe they think that I have a grim view of certain things still. But, to those people I ask “Can you really blame me?”…

A friend (you know who you are! xo) who lost her beautiful daughter, but can’t really talk about it openly, sent me this last night. I woke up to use the rest room in the middle of the night and I saw it in my email. I smiled, peed and went back to bed. This morning I was able to read it. It is written to a non-bereaved parent in general, but I think that it can apply to family members, or friends who have no children, also. It pretty much applies to everyone. Please take the time to read it. It is the truth of my life now.

img_7488-707x530

Dear Non-bereaved Parent,

I know you care for me and am so glad you’re reading this. I know that you can’t fully comprehend, nor would you want to, what it means to be a bereaved parent. Honestly, I’m still finding out for myself. To live without my child is not something I ever wanted to learn and yet it’s what I have to.

I see that you want me to feel better. Let me assure you, you’re doing the best you can to soothe my pain, yet it is here and will be here… until it lessens. It won’t ever go away completely and this is ok. Can you be ok about it with me?

I hope you will have the courage to remember my child with me until we part. Please remember this: You may speak her name, you may remember her birthday or anniversary with me, whether that is by sending me a text message, card or flowers – it doesn’t matter, it’s the thought that counts.

Please do not fear my tears or my sadness, it means that I’m thinking of her or missing her. It’s not that I am permanently broken or sick, just broken-hearted and grieving. Please have the courage to sit with me and my pain, without needing to fix it.

At times I might say ‘I need some time to myself’ but more often, I do appreciate you being here, even without any words, keeping me company or doing something with me. Other times I might need distraction and I might even laugh and experience some joy and then feel guilty again and cry in the next moment. It’s ok, this is life and death: complex and paradoxical and not always to be understood.

You probably feel that I have changed. You might even hope and wait for me to return to the ‘old me’ again. I’m sorry but that won’t happen. I’m forever changed. Losing a child is like losing a limb. Even though the scars of the amputation will heal, it’s a permanent change and as much as it sucks, it is what is. I have to get used to it. Will you bear the chance to get to know me as your ‘new normal friend’?

I’ve chosen you as my friend because you have a big compassionate heart, yet I know it’s (almost) impossible to understand the unimaginable. Don’t say things like: “Wouldn’t it be time to move on?” or “At least you have…” I know you might say those kind of things in an attempt to support me. I know you’re well-meaning yet I’ve become sensitive and certain sentences are like shards of glass on an already wounded heart. Even if you don’t understand, would you allow your heart to reach out and trust the sensitivity of my broken heart? (For examples on what to say instead, click here.)

I might not be up to celebrating pregnancy news, I might even feel jealous of those lucky mothers who are joyously carrying their children. It’s not that I’m mean, it’s because my heart longs for my child and seeing those mothers with their children is a reminder of what I don’t have.

With time and healing, I will be sad less often or cry less often as at the beginning. This does not mean I’m ‘over it’. My child lives on in my heart and I will never get over the fact that I’m never to hold her hand in life. Please do not confuse my healing with ‘been there, done that’. My child might have gone with the wind, yet I’m still searching the world for signs of its fleeting presence.

Thank you for being here for me and with me.

Thank you for being my friend and having remained my friend through this.

Thank you for creating a new friendship with my ‘new normal’ self even though we wanted everything to remain as it was…

Thank you for remembering my child and therefore honoring me as her mother.

Every day that I wake up, I am sad. I know I have so much to be thankful for, and trust me, I am VERY thankful. I’m thankful for Landon, because I don’t know if I would have been able to pull through this without having to care for him. I’m thankful for Shane because he  is my rock, and even though he is incredibly sad as well, he keeps a strong face for me. He is the only one who feels my grief 24/7, and also deals with his own, too. I’m thankful for this new baby girl growing inside of my body. I’m so thankful that we were able to even afford IVF with no insurance coverage. I’m thankful for my doctor who is amazing, and always lets me be neurotic, ask a zillion questions, and roots for us.

I’m thankful to be alive, but that doesn’t mean that somedays I wouldn’t rather not be if it meant I could see Kenley for even 5 seconds again. And I don’t think there are many people in the world who really understand that statement.

I’m trying. Every single day. I wake up, I repeat the cycle of the day, except it’s not how it used to be. I’m a broken Mom, and Wife now. I’m a broken Daughter, Sister, and Friend. My heart is broken, and it effects every part of my life.

And it always will.

 

photos.

Earlier this morning Landon handed me a seashell, and said he got it for me. This seashell sits on my buffet next to his baby picture. I said thank you, and acted like I was super impressed for a few, then asked him to put it back on the buffet because I love it there. He walked over and set it down and said ” I’m going to put it next to my baby picture”.

I love his baby picture. I love Kenley’s baby picture too, but in a different way. I got to thinking about the photos we have of Kenley, and realized we don’t have a picture of just Shane holding her. There are photos from NILMDTS of me holding her with him over my shoulder etc, but none of just him holding her. This has been weighing so heavy on me this evening. I will never have a photo of him holding her. Somedays I’m able to look at these things and think “Ok, don’t be so hard on yourself because who the hell thinks of these things in the moment when you’re shocked because your child died”, but other times I think “God…how could I have forgotten to take that photo?!”.

I’ve been missing her really badly lately. Wanting to hold her more than anything in the world. Feeling extremely sad, and beat down about everything. She’s forever going to be baby; as Landon grows she will remain the same in my mind. I will never know what she would look like as a little toddler, or a 5 year old starting Kindergarten. I mean, in a way I do because she looked just like Landon. And honestly? That makes it harder on my heart sometimes. Landon is such perfection in my eyes, he is so beautiful and perfect that it gives my heart a painful jab when I see him being adorable. She will never be here.

The bad days are still here- still very much present. They aren’t as heavy, I guess? I don’t know how to explain it. Friday night was bad, though. I cried for probably 2 hours after I put Landon to bed, and I don’t even know what triggered it. I just got sad. This sucks. This is unfair. This is not how my life should be. This is not how I should be spending my days- very much alone. I should have my girl with me and I should be taking care of her while her big brother is at school.

Monday she will be gone for 8 months. Eight months. 243 days. I have been on this earth, without my beautiful daughter, for far too long. And the worst part?… I have to continue to be without her until the day I die.

A good friend had messaged me the other day asking if we were still planning to walk in Lydie’s Loop (www.lydiesloop.org) 5k that a loss mom is putting on here in my town for her daughter, Lydie. I was seriously considering going, and I had asked my parents, my sister, and Shane’s parents to go with us- all who said yes. But…the more that I thought about it, the more intimidated I became. I didn’t feel that I was ready to be around that stuff yet. I’m not ready to be around other loss moms right now. Online, it’s different. I can just leave or close my phone or whatever, whenever I need to.

She told me that she was still interested in it, and she wanted to register in honor of Kenley and our family. I cried. Her and her sister (and I’m not sure who else, if anyone) are planning to register in Kenley’s honor, and it just makes my heart burst with love. Knowing that someone is going to be there for the walk in honor of my sweet girl is so amazing. A huge thank you to Nicky and Jessica. It means the world to me, you will never know.

Today has been one of those days where I just want to lay in bed all day. I’m so thankful for my amazing Husband. He came home from another long day of work, at one of the most stressful jobs in the entire world, and let me nap. Then, he ordered pizza for dinner so I didn’t have to cook anything.

I love you Shane. I know you don’t read this, understandably, but I just love you more than I could ever put into words.

Thank you for being my rock.

Today, well, today can suck it.

butterfly.

Today, Landon and I went to the grocery store; the parking lot was pretty empty (thank god).  I always look to make sure there aren’t many cars when we get there. Somedays I just can’t with people. We walked into the entryway to get our cart and- I’m not kidding you– there was a girl, probably 18 years old maybe, with her 8ish month old baby girl. FOR REAL?

It just never fails, you know? Whatever.

Fast forward to when Shane gets home from work. I told him I was going to go lay down for an hour or so. I ended up sleeping from 3-5, so a nice little nap. When I woke up, I walked out into the kitchen and there was an orange butterfly on the INSIDE of our sliding back door! How in the hell does that happen???

Why, hello, baby girl 🙂

She’s been around a lot these past few days.

On Saturday night before I went to bed, I held her urn and kissed it (like I do every night). When I kissed it, I told her to help me. I told her I needed help, and that I don’t know how I’m supposed to do this; I’m not strong enough.

I think she heard me loud and clear ❤

 

blah.

I feel very blah today. I don’t really know how to describe it other than that. I’m tired, I’ve been randomly nauseous all day, and I have a wicked headache.

I know these things are normal, but I can’t help but think about my previous pregnancy. I took a medicine for nausea with K that I didn’t take with Landon–could that have contributed to her death?  I definitely don’t want to take that medicine this time around, but if my nausea gets as bad as it was, how will I function?

I think of how tired I was with Kenley. I remember how amazing Shane was about letting me nap whenever I needed to. Now, I can’t help but think, “Well, you’re going to have all the time in the fucking world to nap while Landon is in Kindergarten, and you are all alone without your daughter”. I know it’s irrational to think like that, I do, but I can’t help but have those thoughts.

The same irrational thoughts go along with this current pregnancy, and getting congratulations about it. I don’t want congrats. In my mind I’m getting these congrats on being pregnant because a series of really fucking shitty events happened in my life that led me here. My daughter who I tried so hard for, died, without warning and stole the light from my soul. I went through (and am currently/will always be going through) the worst time of my life. I went through IVF, and paid completely out of pocket (how much is IVF, you ask? We’re looking at a cool $23,000 after this cycle is said and done). And countless invasive procedures to get where I am. Yes, I am pregnant. I am so thankful for this pregnancy, and I will love this child (if I get to keep her) with all of my heart.

It’s just hard. I think that people heard we’re pregnant again and immediately think “ok they’re done grieving”. Nope. Not anywhere near what the truth is. I am not ok with being around your baby. I do not want to see your baby bump or talk about your pregnancy. I am not okay with being around large groups of people yet. The pain of these things, is not gone just because I am pregnant. I don’t know how to explain this to people yet, or how I can make them understand this. I know that some people will never understand it; they will always think that I should “be ok” by now.

I know that people are going to expect one thing from me during this pregnancy and I’ll probably be over here doing the complete opposite, but I hope that they try to understand. If I don’t want to come to the christmas get together this year, I hope you understand. If I don’t want to buy a million gifts, and celebrate this year, I truly hope that you get it. If, on thanksgiving, I would rather be with my family at my house, alone, I hope you understand why I need that. This year of first’s is going to be the hardest, and I need people to just fucking understand it.

I think we need to take a vacation for Christmas this year. Santa can find Landon anywhere, so why not, right?

 

screening.

Landon’s screening went well today.  I was pretty nervous because the first words out of his mouth this morning at 6:44 were “I don’t want to go to my school thing today”.  When we left the house to go, he was super excited. We got there and the secretary gave us a name tag with his name on it, and a round colored sticker on the name tag. She told Landon that he needed to collect five stickers and then he would be done with his screening.

She gave me a folder, and some more information and sent us to the Hearing center. When we walked in, Landon said immediately that he wanted to take the headphones home with him — What a dork. She also did the color blindness test. He passed that with flying colors, and the lady gave Landon another sticker, and sent us to the next center. We walked into the vision center and Landon sat down in a chair. The man there showed him some shapes, and placed glasses on Landon that would block his vision in one eye or the other depending on which one he was testing.

Landon did really well with his left eye, but failed his right eye. I am pretty sure that he has no issues with his vision as he’s never once showed any signs to us. They told me that I need to get his eyes tested, so I will be setting up with an ophthalmologist for him (and Shane) soon. He received his sticker, and we were sent on our way. We went to the bus scheduling center, and were given the paper that showed us when he would be picked up and dropped of. He gave us a sticker and sent us to the next center. Then we went and spoke with the Lunch Lady. Landon had to enter his student ID into a machine to practice for his Lunch (doubt he will be buying because he only wants to pack as of right now haha). She gave us our last sticker and then we paid the secretary for his school fees, and we were out the door!

I thought they might ask him some academic information, but they didn’t.

When Shane got home, we went to his parent’s house to celebrate his dads 60th birthday. His mom will turn 58 tomorrow, too! Then, his grandmas birthday is the 11th. Too many birthdays- I can’t keep them straight! After 12 years, you would think I could figure it out…

Therapy tomorrow morning; Landon’s going to my Mother in Laws while we go. I was going to cancel, but I know that’s not a good idea. I’ve really been having a hard time connecting to this pregnancy. I know it’s early, and tomorrow is only 6 weeks, but man…this is rough. I don’t know what to do to make myself feel better. I’ve started to feel a little nauseous, so I’m trying to tell myself that “this is good”, but I’m not stupid, and I know that’s not “true”. I hate that I know so fucking much- I wish I was able to be naive and enjoy pregnancy again…

All I want to do is cuddle Landon, but he won’t let me because he’s too cool for that now.

I’m going to cry so hard when he gets on the bus next Wednesday…gonna be a sobbing mess. Ugh. Where has the time gone? I wish I could have him as a little baby one more time. I miss it, and I want to go back and enjoy him more.

Life. sigh.

 

tomorrow.

Landon will be starting Kindergarten August 18th, but first he has to attend the standard Kindergarten screening tomorrow afternoon. We have to be at his school at 11 am, and check in at the office. I’m not exactly sure what will happen, but I’m more nervous than he is I’m sure. We still need to get him a few things for school; a beach towel for quiet time, and a snack for his entire class (need to find out how many kinds are in his class first…).

I hope that tomorrow we find out the class list, and maybe his bus schedule. We live about 5-7 minutes from his school, so if he will be on the bus for 40 minutes I’m just going to take him. On the other hand, I’m scared to start taking him because I know that once I do, he will never want to ride the bus (can you blame him?). It’s not like I have anything to do in the mornings, so I guess it’s not a really big deal.

I just can’t help but think that I should be stressing out about getting Kenley ready in the mornings in time to get Landon to school on time. It’s so frustrating to think about. It makes me angry and sad. I hate what happened to her, and I hate the way our family has become. I don’t like that I will never be the same. I was doing so well. I was happy. I was focused on my life, my family, our future, and in one second it was all ripped away from me- from us.

Our next ultrasound is 8/16 with the RE. He said we should be able to hear a heartbeat (with K I heard it at 6+2, I will be almost 7 weeks at this appt). It is starting to scare me to think about not hearing a heartbeat. No matter if I’m struggling with feeling attached to this current pregnancy right now, I still want it to go right. I want this pregnancy, I want this child born into my arms, and to be in my life until the day I die. I might not be able to fully digest the feelings right yet, but I know that I’m doing everything I can to make sure this pregnancy is healthy, and that I am healthy.

The past few weeks have been a crazy emotional time; I’m so thankful that I have my husband by my side. He truly understands me and allows me to feel whatever I need. He allows me to be on my grief timeline, and that’s what I need.

Tomorrow is also Tuesday- ugh. I was driving in the car the other day by myself and I thought “I’m doing better”. I’m able to control my random crying. I’m able to function on Tuesdays. I feel very empty still, but I think that is simply a depression symptom that I am aware of and work every single day to control.

I like to think I’m doing better. Maybe I’m lying to myself, but maybe I have to until I’m really doing better.

Whatever, I am doing what I have to do to survive.

PIO.

I started my PIO (progesterone in oil) shots the other day, and for some reason they hurt really bad this time. After my egg retrieval my RE had me start the same shots “just incase” our embryos sucked and didn’t make it to day 5 for PGS (can you tell my  Dr has like, zero faith in my body? I don’t blame him, really) and they didn’t hurt at all! Shane was a pro then, maybe he’s just rusty. He says when he’s doing it this time there is resistance. Yeah…I know. I feel it.

I watched a few videos today of others giving themselves the shots, and I feel like I could do it but I figure we’ll give it one more shot with Shane doing it. I think tonight when he gets home, I will warm the oil by rolling it in my palms for a few minutes, and have him give me the shot while I’m laying down.

 ( * I ended up holding the vial of progesterone for a while to warm it up, which made the withdrawal so much easier. Once the syringe was filled I held it in my hand for another 5 mins and laid on my bed when Shane gave me the injection. Perfection! Didn’t even feel the shot at all *) 

For those who don’t know about PIO, it’s to support the uterine lining during the luteal phase of a FET (frozen egg transfer) or a fresh transfer.

The set up looks like this (not my photo):

needles

The one closest to the bottle is an 18g needle. It is used to draw up the medicine. The one on the right is a 22g-1.5 inch needle used to administer the injection. The shot is intramuscular.

And the shots go here:

shotsite

Um Ouch.  

If our embryo sticks, and we are indeed pregnant, we will continue this for 12 weeks. TWELVE. Every. single. night. I’m sorry – I know I should feel so pumped and excited, but it’s just not that simple anymore. I’ve lost my naivety toward the situation; I know too much.

 I know what can go wrong if your hormone levels are off, or if you start spotting. I know that you can have an ectopic pregnancy and lose a tube, or an ovary, or fucking die. I know that your cervix can “not do it’s job” and you can lose your baby at any time even when you think you’ve past the scary points. I know that, even a week before you’re scheduled to have a normal repeat C-section, you can hear the words that will shatter your world forever; “This is where her heart is, and unfortunetly there is no heartbeat”. I know that you can truly feel like you want to die for the foreseeable future because your child died inside of you when you were in the clear; your daughter died when she shouldn’t have.

Those things could happen to us again. Any of them could be a possibility and I hate that I even have to worry about it.  I know that we will be monitored so intensely, but my mind just goes back to “well, shouldn’t I have been monitored this well anyway? I am growing a human for fucks sake”. Sadly, that’s not the case. Monitoring for normal pregnancies is a joke. I had a shitty NINE MINUTE (yes, nine minutes…normal scans can range from 20 mins to an hour for some people) anatomy scan, an intake scan at a new OB that was probably 25-30 minutes long, and a scan at 36.5 weeks…and somehow, no one detected a possibly anomaly with Kenley’s cord. Maybe, just maybe, if a Biophysical Profile Ultrasound was done on me my daughter would be here. Maybe, if my doctors sent me to an MFM because of my history with Preeclampsia, they would have done one on me. I should have been sent to an MFM. I was failed by doctors. All of my doctors failed us during Kenley’s pregnancy.

There is a standard of care, and a general guideline to follow when sending your patient to an MFM…and I ticked many boxes, yet I wasn’t sent.

I will never forgive myself for not advocating harder for my Daughter.

The medical field needs to get their shit together. 26,000 stillbirths a year, and yet we just can’t figure it out?

Unacceptable.

Medicine failed my sweet girl, and it’s hard to believe that anything positive could happen for us now.

tribe. 

Since Kenley’s death I have truly realized who my true friends are. Totally clichè, right? Nope. It’s true. When she died, I received my first card from Megan Ricahrdson. I love this girl, to this day, and I haven’t talked to her in probably 10-11 years, yet somehow she was the first one to send us a card. 

We received flowers from my graduating class (thanks guys), and cards from people I grew up knowing, worked woth through the years, and some I just recently met. All these people were hurting along side us.  The outpouring of love was amazing. My best friend from high school’s mom sent us a sleeping angel garden statue just very recently and it’s so comforting to know people are still thinking of us…of my sweet girl. It doesn’t hurt us to talk about her, or receive cards, or letters about her. We love these things. They make us feel closer to Kenley. 

The greatest amount of love has come from my tribe. The women who have been there through it all with us. The women who, no matter what, get it. They understand if I can’t talk to them because I’m guarding my heart, or if I want to just talk about Kenley for hours on end. They will listen and reply to me until I am talked out.

Immediately after K died, numerous people offered to fly to me from all parts of the states. Just to be with me and let me grieve the loss of my daughter. 

 These women tell me to protect myself and remind me that I am a good person. They sent us the most amazing package after Kenley’s death. The amount of love and kindness that went into this gift was far beyond anything I could ever imagine. 

They have held me up, held my hand though tons of things, and continue to walk beside me through these terrible days. They don’t need to reach out to me every single day, yet they do. They don’t need to send me random “thinking of you” gifts, yet I’m always getting lovely things in the mail. Someone always lets me know they’re thinking of my sweet daughter. 

They could have all left my side after things got hard, but they haven’t. They tell me they miss Kenley, too. They tell me how much she is thought of, how much they love her. They treat my heart carefully and come to me with such care about certain things in their lives that they think will trigger me. 

And I’m so thankful for each and every one of them.

 If you are part of/have been a part of TCF, or the old place, I want to thank you from the bottom of my heart. 

CAL, CAR, 3T, LTL, PAIF, PAL…and my amazing Jan 16 BMB…

Your love and support has meant more to me than I could ever explain in a million lifetimes. 

I am so thankful to be part of a community of women who are the best on this planet. I truly believe I will have you as friends for the rest of my life. 

You are my Tribe, and I love you.