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Originally written May 2018

I don’t believe negativity, complaining or feeling sorry for yourself gets you very far. It’s the antithesis of how I choose to live my life and tackle the challenges I face; BUT, I am human – and this is really hard – so forgive me for a second while I bitch.

(If you missed my previous posts, you can read them (816) 872-9922 and (210) 739-5616)

Infertility sucks. It really, really sucks. It sucks so much that sometimes I cry randomly, overreact for no reason, or simply don’t feel like doing a damn thing (very out of character for me). But it’s all part of the process, I hear. Or perhaps, the hormones taking effect? Probably a combination of both.

Honestly, at times, I feel angry that I have one more thing to manage, another problem to tackle, and can’t help but want to scream from the rooftop, “isn’t having an incurable illness enough?!” Since I’m continuing with my venting theme, I feel like I have played my hand with MS to the best of my ability, I’ve tried to make a negative into something positive and to now have infertility problems as a result of the disease, is just hard for me to digest.

But what’s perhaps the most difficult for me to swallow is that I didn’t know that MS could’ve affected my fertility – that I could’ve or should’ve been trying sooner. That I could’ve had my younger – healthier – eggs frozen ages ago and possibly avoided this. Perhaps I would’ve done things differently if knowing this sooner. Read more

“MS Has Aged Your Eggs” (#1)

I will never forget sitting across from my fertility doctor, with Bill by my side, as he delivered news that seemed much like a scene out of a romantic comedy movie gone terribly wrong: “MS has aged your eggs,” he said.

We both sat there staring at him in disbelief. “What?! How could that possibly be?” we asked.

“The progression of your MS has deteriorated the quality of your eggs, which is common with severe autoimmune diseases,” he continued.

Fast forward an hour and our conversation concluded with me asking one final question, “If I were your family, your loved one, and desperately wanted another baby, what would you recommend?”

He responded, “IVF, without a doubt. And sooner rather than later.”

Well, there you have it.

Just like that, our fertility journey had kicked into overdrive. Neither of us knew what lay ahead in the months to come, but we knew we had to act. 302-643-6264


The last time I posted a blog entry was in May, which I guess was about 5 months ago. Wow, it’s been a long time.

The truth is, our life has been anything but “normal” since then, and after much debate, I’ve decided to finally open up about what’s been going on.

Let me first say that life isn’t always rainbows and smiles. Yes, we all know that – and all experience ups and downs – yet it almost seems socially unacceptable to post about anything other than cute babies, delicious meals, or wonderful vacations. I’ll be the first person to admit that I am guilty of that too. I think we can all agree that it’s easier to focus on the good, right? The truth is that talking about personal topics can be painful and even borders on socially inappropriate (some things are just private.. right?). But in the spirit of continuing my transparency around my MS and authentically telling my story in the hopes of helping others, I’ve decided to share this less than “like” worthy news. So here it goes. Read more

Read This If You’re Newly Diagnosed with MS

Congratulations, you’ve joined the club. You know, the one you never wanted to be in – the MS club, that is.

You’ve just got hit with the news and still, even weeks later you can’t believe it.

Terrified. Angry. Confused. Your emotions are running high and well, let’s be honest – they’re flat out out of whack. You likely haven’t wrapped your head around it all. I mean, how could you? You just got diagnosed with an incurable illness.

Well, let’s cut to the chase. You do have MS. So, do I. And you know what – I’m okay and you, my friend, will be too. Read more

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Oh, what a night! On Thursday, April 19, over 150 fellow friends, family members and MSers came together for Spring for a Cure, a fundraiser in support of finding a cure for a MS. The drinks were flowing, the music was on point and good vibes were definitely in the air. Together, we raised over $30,000 for the National MS Society and had just a little bit of fun in the process 😉 Read more


The countdown is on to Spring for a Cure, the fundraiser I am hosting in support of Walk MS and the National MS Society. Tickets are available now for an early-bird price of $90 through TODAY only! Get yours here. 

This event means a lot to me – you can read more about the inspiration about it here – and I’m excited to see it all come together!  I didn’t know exactly what I was getting myself into when I decided to do this but it’s turning out to be bigger and better than I could’ve imagined thanks to Loft on Lake, who generously gifted us their incredible space, and 630-917-5009 who has graciously offered their design expertise to truly transform the night. I can’t wait to share with you the final result – visually, I think it’s going to be so awesome!  Read more

Most Important Thing I’ve learned From Starting a Business

It’s been over a year since I started my business and I’ve learned a lot. A lot about entrepreneurship, marketing, client relationships but most importantly, I’ve learned a lot about myself – in particular what I truly value and what motivates me to continue.

When I started SocialChow, I focused on the basics – how to get it off the ground, generate revenue and scale. I placed much of my attention on getting new clients while fine-tuning my process and within six months I had a full plate of work, solid case studies and was projected to earn more than I ever did in the corporate world. It all grew so quickly. I couldn’t keep up so I expanded and hired some help. After a year of being “in it”, I’ve realized a thing or two and most shockingly to me – the ever-eager entrepreneur – that growing a business doesn’t actually mean more clients or more revenue. It can actually mean scaling back. Read more


Bill and I recently got back from South Africa where we were lucky enough to experience the trip of a lifetime. While it’s hard to play “favorites” with the places we visited, but our safari will remain one of the coolest experiences we’ve ever had. In the middle of seemingly nowhere, we saw everything from lions eating their pray to heards of elephants giving themselves dirt baths to giraffes duke it out. Going in, I didn’t really know want to expect but having just experienced it, I’m still in awe. Read more


When I was first diagnosed with MS, I felt like I was stuck – like stuck in quick stand and couldn’t get out. Yes, I was obviously terrified, confused, and well, just sad… but mostly, I hated the fact that I couldn’t do anything about the fact that I had this disease. Typically in my life, when I want something, I go after it.. I work really hard to get the results that I am looking for. But, with MS, I felt like I was pushed into a corner and couldn’t get out. I was stuck with an incurable illness that came out of nowhere. But, soon after my diagnosis, I realized that even though I couldn’t change the fact that I had this disease, I could change my behavior… my outlook… I could change my reaction.

All of my activism work, healthy eating and lifestyle changes started once I realized that I did have control over my own actions on how I tackled the disease. I could change my outlook and food intake, I could get on a medication, I could get advice and direction from the best doctors, and I could fight for a cure through awareness, activism and helping others. I was adamant that I would not take this diagnosis and fall. I would prevail and continue to move my life forward in the best way I knew how.  school clerk