Polar VorSUCKS

Hello, faithful friends.

Last time I wrote, I shared with you the immense struggles I was having. It’s been a while since that last post; my brain and my thoughts and my life are going in circles.

Two Words: Polar Vortex. This cold hurts my joints and my body so, so much. The lack of sunshine, the homebound-ness of it, the depression that accompanies the harsh, extreme conditions; it’s just shit icing on the shit cake. I realize that for someone with my physical condition, living in the coldest fucking state in the country, um sometimes colder than MARS for fucks sake, is probably not the path to my personal happiness. But all in due time.

It’s hard to really get perspective, but there are several feet of snow. There’s a road there somewhere! 

Not much has changed and everything has changed all at once. My sister has arrived and that’s going very well so far. However, this also takes me further away from the life I loved with Michael and closer to a life that I no longer recognize as my own. I feel like a passenger on this planet, and that’s not a cool feeling to me. It’s not a feeling I’m comfortable with, or a feeling I want to settle in to. I don’t like feeling like I’m a victim to the circumstances around me, or that life is “happening” to me. My method is always to push through and gain control of my own situation. I’ve always landed on my feet. Not this time. Not yet.

The newness of roommate living hasn’t been hard for me, at least not yet.  Living with my daughter has been challenging for us both, and it’s brought a level of pain and drama to my life that is damaging to my healing and my process. I’m continually working on myself: working on my patience, my empathy, and choosing my battles. That’s all I can say about it right now.

When I really watch my thoughts and look inside, I find myself consumed with fear. I’m afraid to live without him. I’m afraid because I can’t afford to survive. I’m afraid of the physical pain I feel. I’m afraid of moving forward. I’m afraid of staying stuck. I’m afraid because I don’t know what I want or how I want to live, or with whom, or where, or what I want to do. I’m also afraid to move on and lose the connection, however slim, I have with Michael.

I try to say his name out loud as much as possible. Many, many times a day. I talk about him all the time. I don’t know if people are cool with that or not, but it’s how I choose to live. I choose to still love him with all of my being, and I choose to think that we still have a relationship; it’s just across planes of existence now rather than being a physically present relationship.

I’ve decided against inpatient treatment for now, anyway. I’ve increased my therapy sessions to twice per week. I’m actively seeking groups. A new friend who has a passion and a ton of knowledge about mental health issues turned me onto some resources. Another friend who works in mental health helped me choose a reputable facility if I DO decide to go inpatient. I’m getting better at protecting my process and making this journey through hell my priority. I know things will never look better or feel better if I don’t walk through it. And I’m going to protect my right and my need to process things in my way and in my time. Many people don’t understand that, and that’s okay. Not one person has said a word to me to make me feel pressured. They don’t say it, but I feel as though they expect me to be over the worst of it and in the same brain space I was before all of this happened.  Many treat me exactly the way they did before, not understanding that I might look and sound the same (well I don’t look the same – I look like hell all the time), but my brain and my personality are very different now and without realizing that I’m still very much in mental limbo, evolving and changing all the time.

Having my sister here has helped with some of the depression, as I’m not alone with my thoughts as much as I was before. It’s also helped tremendously in the physical department, as she’s so, so helpful at home. She shovels and I snow-blow. I could never do this alone. Physically I just am not able to function in the extreme cold we were having, and I seriously could NEVER have gotten through these 512 feet of snow (give or take) without her. She has two ADORABLE doggies and all of our dogs have integrated so nicely. We’re making meals and having dinners together. I’m able to take naps when I need them because I’m still not sleeping at night. We’re watching stupid movies and laughing until we cry. It’s been good medicine for us both. ❤

I’m working pretty consistently. Planning rescue runs, working marketing, fundraising, relationships, etc. I was supposed to get a foster dog this weekend, a pregnant momma dog <3! But, the weather postponed her transport. ☹ Hopefully, she will be arriving soon. This weather is just a bitch.  And it stinks because I was SO ready for little babies. Soon, I hope.

My momma dog, hopefully arriving soon! 

Medical stuff: No change. Neurologist ordered an EEG (already done) and a thoracic MRI (scheduled today but um….WEATHER so I need to reschedule). Then she’ll have a direction to go with the neuro stuff. RA biologic meds are still not approved so no changes there, except that it’s been excruciating in the severe cold. Spinal stuff is all on hold because of the auto-immune stuff, so it’s just a cycle. Everything hurts. My kingdom for a refillable Rx of Vicodin!

So, that’s my update. One foot in front of the other, trying my best to take care of myself, trying to find joy, trying to ignore where I live this month, taking one moment at a time. I miss him. ❤


~ Lisa

6 months; I wish I had known

Tomorrow will be 6 months since I lost my wonderful husband.

I REALLY don’t keep track of this stuff. I was talking to my dad’s wife. My dad died 5 months before Michael. We were talking and figured out it’s going to be a year next month that we lost my dad. I know I’m 5 months behind her, and I counted the months. It’s going to be 6 months, not 5. And for some reason that really upset me.

The more time passes it seems, the sadder I become. The sadness is completely overwhelming, and it’s getting worse. I miss him terribly, and maybe the more time passes, the further away he feels. I don’t know. I just know that the emptiness is too much for me to bear some days.

In talking to my dad’s wife, turns out she went through a really dark time right around the 6 month mark. Another widow my daughter knows went through the same things right around 6 months. What I’m talking about, is a complete and utter breakdown.

Yes, me. The past couple of weeks have been REALLY hard. REALLY hard. Impossible to describe really except to say that there is no relief from the underlying black sadness and despair I feel. I’m getting worse, not better. I can’t look at his photos without losing it. I can barely bring myself to remember him without overwhelming pain. I cry myself to sleep every night. I’ve been recording myself in my sleep to see if I have sleep apnea, and I have discovered that I frequently call out for him and sob in my sleep. I’m forgetful, slow, sad. Stuck.

So last week I reached out to my health care team and told them I was in trouble. I wanted to end my life. I was ready to go. I couldn’t find my purpose. I couldn’t escape my reality. Accepting reality is impossible for me to comprehend. And so, I just wanted to end it. My plan was ready to put into action.

I made my therapist and primary care doctor aware that I was suicidal. I saw each of them in person, and we all agreed that inpatient treatment might not be a bad idea. We also all agree that we all trust me right now, to take myself to the hospital if I’m feeling like I’m in trouble again. We all agree that this is one day at a time.

The past few days have been better. The GK party on Sunday was good for my soul. The setup was fun, and the volunteers always remind me of the good work we do and how blessed I am to have this rescue and these people in my life. We’re rescuing more than 15 dogs this week. We have new foster parents. I got through the worst suicidal feelings I’ve ever had, and I kept my head together enough to seek help. I’m pretty proud of that.

The world was looking a bit brighter and then…I realized it’s 6 months. I don’t know why this upsets me but it does.

In talking to my dad’s wife and learning that she, too, went through this, really helped me and convinced me that I need group support. Not a single person can understand this unless they’ve experienced it. I gain so much comfort and strength talking to other people who have been through it. I am trying to find more bloggers who write on the topic. Today’s neat article find is this one. If I can’t find an in-person group that suits my needs, I may try to create one. Lots of good tidbits in this article, and the one I love the most:

“For months after my husband died, I didn’t want to leave my house. I felt like the whole world was watching me. It’s as if what happened to you is what everyone else is afraid of, so they just stare and pray they won’t become you one day.”

Still waiting on news about my health insurance which is a fricking nightmare and so so stressful. My sister will be arriving next week. And the last stressor I haven’t shared with you guys yet; I decided to take the first contractor that did my floors to small claims court. He just received his summons today, so I’m waiting to see if there’s any backlash. Court is Feb 22 if anyone wants to come and support me!

In other news, this cold is awful for everyone but especially for a newly diagnosed RA patient who hasn’t started receiving the big gun drugs yet, it’s more than awful. I’m just staying inside for the a couple of days. Thursday I need to go rescue some dogs, so I’ll bundle up hard for that.

So, for now…I guess for always…one day at a time. But especially now. I’m making it through, I’m in tune with my state of mind, and I’m not afraid to get help or check myself in if I need to.

I told you in the beginning that this blog was an experiment. I didn’t know what I would write or do with it. I wasn’t sure how open I would be, but I decided if I was going to hide things I shouldn’t blog. I really hope this post doesn’t make me regret that. I don’t think many are actively reading the blog, but if you are – I’m not suicidal so I don’t want or need anyone to be alarmed. I’m just being honest. This shit is hard and I wish I had known from those who walked before me! It’s not okay that people who are going through this feel they have to hide it. We’re better than this. Aren’t we?

I wasn’t going to talk about this because I worried that the gossip train would start rolling, or that my volunteers may lose faith in me, etc. And then I decided I’m going to talk about it. Because people NOT talking about it is the reason that there’s this whole fucking stigma about mental health. It’s NOTHING to be ashamed of. You would treat a broken arm or an internal illness, why wouldn’t you get treatment for psychiatric issues? And why aren’t more widows talking about this? If this makes people lose faith in me, then they don’t know me at all. At all. I have survived and walked through literal hell on this earth. I’m waking up every day and choosing to walk through a fresh new unknown hell. I’ve gone through more than most people can begin to imagine. And I’m still alive. I am actively involved in the rescue, and this week we are saving more than 15 dogs.

Life goes on. Even when we may not want it to. One moment at a time. ❤


~ Lisa


Subtitle: It’s not what you think.

It’s been a long and hard week at the casa. I saw a neurologist, my regular doc, had a sleep-deprived EEG so I went almost 40 hours with no sleep, saw my grief therapist, the polar freeze is just absolutely unbearable on my swollen joints, some painful relationship stuff with my daughter, and last night I just has a breakdown of epic proportions. The biggest one I think I’ve ever had. I just absolutely lost control, could not calm myself down, and had to reach out to a safety-net person to talk me off the ledge – or rather, to listen to me without trying to fix anything, until I talked myself down. I passed out from pure exhaustion before 8pm and slept for 11 hours. Woke up today in a fog. Head throbbing, nausea, swollen eyes. I feel like I’m hungover.

Let me back up. I’ll start with the neurologist. I like her very much. She has a great bedside manner and she is very attentive. She isn’t willing to say I have MS and she isn’t willing to say I don’t. She ordered a sleep-deprived EEG and an MRI of my thoracic spine. That’s the only thing they haven’t imaged yet. Ugh. She said my symptoms could also possibly relate to something damaged in my mid-spine or a number of other auto-immune conditions, not just MS. The MRI isn’t until mid-February, but I already had the EEG done. The results of that combined with my soon-to-come MRI will dictate next steps. In the meantime, I’m still putting any spinal fusion on hold until we can figure this out.

Therapist: She’s providing me with some really useful tools for working through the moments that feel unbearable, how to get myself unstuck if I feel stuck. We talked about cumulative grief and secondary grief. And then, there’s also complicated grief which seems to be more about the DEPTH of your sorrow and your ability to manage it.

  • Cumulative grief is experienced when someone experiences multiple losses. especially in a short period of time.
  • Secondary grief relates directly to the loss of the person who passed away; but it’s grief for the LIFE you had, not the person himself. It’s grieving the loss of a partner, the loss of someone to plan things with, the loss of your lifestyle, the loss of your memories and inside jokes, the loss of your identity, the loss of your faith, in my case the loss of my health…I think you get the picture.
  • Complicated grief is basically grief x 10. It’s more about the griever’s process and how it affects them.

We discussed my very newfound extreme sensitivity to anything Michael-related and my uncontrollable sadness. I’m having a hard time even seeing his photos right now. And then she said something that hit me like a 2×4. She told me to brace myself, because I haven’t even begun to grieve Michael.

Huh? Are you fucking kidding me, lady? That’s all I do. ALL. I. DO. And then she reminded me, nope. I was supposed to take 2 months leave, but I was working/ connected the entire time. I moved my daughter in amidst a lot of drama. I learned I have a painful disease that’s impacting my quality of life dramatically. I also learned my spine is a hot mess and I need surgery. I dealt with floormageddon. I pulled off standing in front of 130 people at a Gala 2 months after I lost him. I’m sure I’m forgetting stuff but again, I think you get the picture.

She talked and I believed her. I think the real pain is yet to come. When I came home and looked up complicated grief (the article linked above), the description fits me to a tee. And while I KNOW it’s still fresh and I KNOW this process will take a lifetime,  and I’m not looking for or desiring shortcuts,  I also know I feel stuck/ like I’m moving backwards. This is literally the hardest, most painful experience I could ever imagine. There’s no textbook. There’s no escaping that the core of your being is just gone. There are no instruction books for starting your life all over again, against your wishes.

My loneliness is pretty intense. My sister will be arriving soon and that will help a lot. Nights alone are dangerous for me sometimes. I let my mind go to really dark places and have nothing to distract me from it all. I’m not really comfortable going out in this cold – it REALLY fucking hurts. I’m also super stressed about my health insurance. Long story but it’s very stressful. I’m headed towards some trouble if I don’t find some solutions soon.  But the flip side is, I AM trying to find those solutions. I haven’t given up.

In happy news, I’m looking forward to Sunday. It’s our annual GK holiday party and I have some super fun stuff planned for the volunteers. It will be a double-edged sword: I’m really looking forward to it because I love love love my volunteers, but I’m anxious because I KNOW it will call so many memories to mind. Last year, we held our holiday party in our new office space that was still under construction. We surprised our volunteers that this would be our new home, and Michael was SO proud. When he got diagnosed, he said he was going to beat this because he couldn’t wait to see what Good Karma was going to accomplish. Last year was a huge celebratory time in our lives. If only we’d known. 😥 But I will do my best to face the day and enjoy the company of these wonderful people, and be grateful to be surrounded by my tribe for a short period of time.

So, the recent mantra: “I will get through this.” I no longer say I’m okay, or I’ll be okay. Because NOTHING is okay. But I WILL get through this. Even if I can’t take a step, I will hold my ground and stand on both feet. Most of the time. ❤

When will I get it?

I’m going through something fresh where I cannot stop thinking about him. I wonder what Michael would think of this, or I remember when Michael said that. I should text Michael. I should ask him what he wants for dinner. At the store, I still have to stop myself from buying his favorite things. I need to ask him this. I need to tell him that. Why can’t I get it through my head that he is GONE? He has disappeared. He no longer exists. His ashes are in our bedroom. He’s gone, Lisa. Just gone.

So, I paint. Woodwork is coming along. This is my living room window.

My last post about PTSD relates to this pic. My daughter has the full-blown flu. She’s staying in her basement apartment for the most part, and I got the flu vaccine so I think I’m safe, but my immune system isn’t worth shit so I can’t take chances. The first time I wore one of these was last January when my dad was dying. Then I didn’t see them again until Michael was dying. Putting them on now brings it all back. And honestly, how much does it suck that I happen to have a stock of these?

As promised, my dogs for those who don’t know them yet. All rescued of course.

Cass: My troublemaker crazy minpin. She’s about 9 we think. She came to us about 7 years ago now ❤️. She was pregnant when she arrived and had SIX gorgeous puppies.

Rosie: my sweet girl. She died on my guest bed and I gave her CPR. Two vets told me to euthanize her, I obviously told them to go to hell ❤️

Bella: my grumpy old lady. She’s ancient, partially deaf, losing her vision, and I think she’s going senile. She came to us 7 years ago and seemed old then! Lol She’s very sweet and funny. ❤️

And Baby Faye, my superhero puppy. Her story is too long to tell tonight, but she’s a miracle puppy.

I see the neurologist this week and I’m also going to try to get back to therapy.

I’m finding myself feeling cautiously hopeful about the rescue. Good Karma rescued two dogs this weekend, and we are planning a rescue run in a couple of weeks. We’re saving again and it feels good. I questioned whether my heart would be able to get back into it, but that’s no longer a concern.

That’s all my news for now. Thanks for following and caring. ❤️


~ Lisa

PTSD 101

PTSD is most often associated with those who have seen battle and war. But it’s a very real condition that anyone can experience after a traumatic event.

My PTSD started almost immediately after Michael passed away. My mind was flooded with images of my father and Michael in their worst dying times. My heart was overflowing with what if’s and omg when I rolled him over did I kill him and wondering if I did a good enough job caring for them. My mind raced all over the place, searching for things I didn’t say or didn’t do. Wondering if our last goodbyes were what they should have been (yes). Wondering if I helped them leave this life peacefully (I hope so). Wondering where they are. And when I would close my eyes, the haunting images and memories of very painful and difficult times overtook me. Then, the panic attacks started (first time in my life I’ve had panic attacks or anxiety). The middle of the night wake-ups to Michael screaming, even though he wasn’t there. Jolting up in bed because I think I hear him calling me. Reliving the horrific hell that was the last few weeks of Michael’s life. Images of my dad thrown into the mental slide show just for fun.

This ticker-tape slideshow runs constantly in my brain. Every time I close my eyes, the movie is playing. Even if I blink too long. The horror movie is always playing if I just pay attention.

My crazy energy is back, for now. I’m painting in the middle of the night again. PTSD. I have a hard time falling asleep unless I’m pretty medicated. I wake to horrific sounds, and then can’t sleep. Get up. Make coffee because why not. Paint. My hands can’t hold the paint brush for more than a few minutes, so I’m switching hands a lot. This woodwork is going to take me forever!

Here’s the bitch. Studies have shown that therapy and medications are the best treatments for PTSD, but nothing cures it. PTSD CHANGES your brain. First, the area of your brain that helps you make decisions, the pre-frontal cortex, is altered in people with PTSD. It’s the part of your brain that calms you down when you realize you aren’t in danger.  Cognitive therapy can teach me how to put those memories away and find a mental place for them, but I personally believe I need to experience this in order to move past it. I know I’ll never forget, nor do I want to. But I DO want to get to the happy memories and move past the pain that we all endured.

Secondly, the part of your brain that alerts you to danger, the amygdala, triggers the “fight or flight” response and is there to ensure survival.  Those with PTSD tend to have an overactive response, making it hard to think rationally.

And finally, the part of your brain that regulates memories, the hippocampus, is working to remember the event accurately and make sense of it. People with PTSD often times find they cannot stop thinking about the traumatic event because they cannot make it make sense. It’s an involuntary obsession that you can’t stop.

I think it’s important to acknowledge this component during my journey. I think people use the term PTSD too lightly. It REALLY is a real condition. It’s MORE than having bad memories of an event or struggling with understanding something tragic. It’s more than “just” an emotional condition. It’s a mental AND physical manifestation of pain and trauma that’s so unbearable, that your brain changes to help you accommodate it all. And it’s lasting. It’s not the sadness that comes after any loss. It has very little to do with Michael being gone, and everything to do with watching him and caring for him while he died. It’s deeper than grief. It’s the real deal.

And along with everything else, I take this one moment at a time. I’m doing the best I can, and that’s all I can do. I tell myself this every single day. ❤


~ Lisa

Thrown into the Ocean

Well, this week really feels like the week I’m back at work full force. I never really took complete time off; it was just time off of Facebook and the day-to-day operations. It doesn’t just feel like I was thrown into the pool. It feels like the ocean. 


Board meeting, volunteer survey, lots of things that need to be addressed as a result of the aforementioned. 

It feels like everyone has forgotten. My entire life is different than it was just a few months ago. But for everyone else, life is normal. Everything is back to normal. People who are upset are not afraid to tell me so. One volunteer who quit this week told me I was an awful person, when I had been back at work for mere hours. Something that happened when I was away somehow became my fault. But I digress. 

It’s as if I’m expected to be the person I always was; I’m expected to say and do the exact right things. I am expected to have everyone’s answers and solve their problems. I’m expected to jump back into the rescue and make up for months of decline, and recruit new volunteers. People have needs that they are expressing to me. My sister sold her home and is asking for a lot of my suggestions and help in planning her move. My daughter is trying to sort things out in her life. And I don’t have the answers everyone seems to need from me. 

My health is very much up in the air. Nobody asks about it. Nobody talks about Michael. Nobody asks how I’m doing without him.  I can tell they’re tired of my story, tired of my situation, tired of feeling awkward about it, and no more “special” treatment is due me.

While everyone else is ready for Lisa to be back and everyone else expects complete normalcy, logic, and unwavering leadership from me, I’m nowhere near that place. I may never be. But regardless, we keep fighting.  All I can do is what I can do. I will do my best, but it requires more than that. Time will tell. I can’t speak for “them”, but MY vibe is that “they” all think I’ve had enough time. I need to get over it and move on. Life keeps moving and I better keep up. Or something like that. 

Here’s a newsflash. I don’t want to keep up. I want my husband back. I want the life we had. I want to eat dinner with him. I want to sit on the couch and do nothing with him. I don’t want this new reality without him, and I’m not the person I was before I lost him. I have no desire to be part of this post-Michael world. 

Nothing new with my health. I have a neurologist appointment next week and hopefully that will point me in the right direction. The neuro issues I’m having are tough and not improving.  Emotionally, I’m struggling. I saw Michael in Target the other day. He was across the store…I whipped my cart around to try and catch up to him, and ran smack-dab into my estranged son, his pregnant wife, and their children. I feel he was there to be my strength through that encounter. I’m feeling him around a lot lately. I can hear him warning me to keep an eye on myself and keep myself in check, and telling me not to take on more than I can deal with. 

I have to do better at saying no. Not “no”, as much as “I’m sorry, I can’t help you with this. You need to figure it out without me.” I guess I’m just bummed that I have to say it at all. 


~ Lisa 


Health and Home

Hi friends 🙂

There’s a lot going on right now. We’ll start with my health.

Rheumatologist appointment on Tuesday and that was kinda bad news. My RA is not improving (which I knew), so now it’s time to add “biologic” drugs to my treatment. There are two to choose from, and they are running things by my insurance company because they are very expensive (the nurse told me as much as $3000/month?!?). But, if the insurance company doesn’t cover it, they have copay cards to give out. Both of these drugs are pretty hardcore with a horrifying list of side effects per usual, so that sucks.

Rheumatologist increased my poison pills to 7 a week instead of 6. So I took those tonight. I’m tolerating them pretty well. Some nausea and sickness sometimes, but overall not too bad.

Which drug will it be? Both of them have several-page pamphlets filled with medical jargon and warnings… Hmmmm…..

I’m also still experiencing a wide range of neurological symptoms so I’m seeing a neurologist in a couple of weeks (first available appt).

And through it all, I’m reminded that all of this is grief. Losing Michael. Some people die of a broken heart when their mate passes away. I guess the powers that be don’t think I deserve to have that peace yet. So, instead of dying of a broken heart, I’ll live with a broken heart and broken body. The stress of losing him was just too much for my system to bear. It had been pushing back these diseases when I was a stronger person, but the overwhelming loss and stress that came with saying goodbye to the love of my life finally broke the dam. Happily or sadly, depending on how you look at it, none of my conditions are life-threatening. Just life-sucking and life-ruining.

In other news, my daughter is moved in and settled. I’m making friends with her kitties. I’ve introduced Baby Faye and Cass to them and both dogs did GREAT meeting them. The cats aren’t so sure yet. I’ll post pics of my pups in a new post soon so that those of you who don’t know my dogs can meet them.

Charlie (orange) and Lucy

My sister is officially putting her house on the market this weekend and will be moving out to MN soon. She’s going through so many life changes and it’s understandably overwhelming for her at times. She’s lived in the same state all her life and she’s 9 yrs older than I am, so this is a big deal. It’s a big deal for her and for me.

Things are so, so different now. I think back and realize that in the span of a few months, my entire world has changed. Our home no longer feels like “our” home. In a FEW MONTHS, I’ve gone from a secure, very happily married woman with a partner and a plan and a home and life I loved and a successful rescue – to an overwhelmed widow with soon-to-be two new roommates, two cats, a house that’s completely changed, new health issues that are affecting me greatly, a rescue that is struggling to stay alive, a body that doesn’t work sometimes…just an entirely different life and big picture than it was a couple of seasons ago. How in the hell could ANYONE wrap their head around all this? My mental state is so out of whack.

Work in the house continues, depending on my motivation and ability to hold a paintbrush. Here’s a sneak peek! Our house has a TON of wood. Solid doors, window frames, door frames, banisters, ALL in that lovely 80’s Golden Oak I believe it’s called? Well, I’m taking it white and bright. I tried it with the matching stain, but it’s so much work and I’m not able to do all the sanding and prep work required for SO much staining. I kinda reluctantly decided to go white and quickly realized I freaking LOVE it. Here’s a sneak peek! Old door in the background, new door in progress in the foreground 🙂

door preview

I have SO many doors to do, both sides. the hallway is full of doors. The white is dramatically changing the look of things. It’ll take a bit of time. I’ve been low on motivation and kinda bored with this project so it’s taking longer than it should. It’s just WHITE paint. Boring. And it’s on doors so it needs to be perfect. It’s super easy for paint to pool in the panel insets and then it drips, no matter how careful you are. You have to catch drips and if you don’t, you have to sand them and paint over them again. You have to remove hardware or paint around it. I’ve been using a kids’ watercolor paint brush set for the details and edges. I tried a roller but it left roller marks; almost a “texture” to the door that I didn’t like, so brush it is. It’s a little labor intensive but man…it’s gorgeous when you see the whole picture with the paint and the floors.  Oh and for what it’s worth, for any DIY’er: SPEND THE MONEY for GOOD paint. I’ve been using Sherwin Williams which is super pricey, but it DOES make a difference. This particular paint is zero VOC so there’s NO paint smell, and it’s super thick for doors and cabinets. I also like Dutch Boy low VOC paint. But for projects where you need lasting results like doors, windows, baseboards, etc., Sherwin Williams. Spend the money. You’ll be glad you did, trust me on that.

Here’s another before and after. Golden Oak to White. Also, fresh (darker) grey paint on the walls.

blinds before

Another cool project I did was the banister and the handrail! I LOVE how it came out; do you? Buh-Bye, Golden Oak.

banister before

Other projects include my daughter’s apartment downstairs. I can’t show you the inside yet because she’s still unpacking, but I converted a mess of a basement into a really cute apartment for one. The front door was a fun project. Purple front doors rock. Note the doorbell and the “porch” light? I made the sign myself with separate components.

alyssa front door

So, this is how I spend my time when I need an outlet and when my hands and body allow. I get very cabin fever-y in the winters because I can’t get outside and spend time in the dirt, so I need some sort of creative outlet.

And yet at the end of the day, I sit and I see all the changes…and none of it matters, does it. All the work, all the colors, details, fine lines, accessories, special touches…in the end, it doesn’t matter. It’s just a way to pass time, really. A distraction. And I guess that’s okay too. Anything to get through each day. It’s truly, indescribably, unbelievably, seemingly insurmountable, ongoing horror. Each moment of each day. It’s a bad movie I can’t walk out of. A nightmare I can’t wake from. A reality I don’t think I’ve truly processed or accepted yet.

Lastly, a friend sent me this today. Please take 4 minutes and watch it. It’s so perfectly true. I remember when I first lost Michael. Everyone was saying all the things we say when someone passes away. Everyone was saying what we were all TAUGHT to say. And then, there was my girlfriend Lynn. And she was the true embodiment of this video. She literally just said “OMG Lisa your life fucking sucks”. And at that moment, I fell in love with her all over again. Acknowledgment.

And that’s all my news for today. I will post pics of my dogs soon. Thanks for tuning in.


~ Lisa