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Rebounder Set Up, New Stability Bar, and Cake the Kitten (plus video) and 10% off!

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Cake the kitten went wild when he saw the new rebounder and wouldn’t get off! He likes to bounce around, too- and will often get under the thing while we’re bouncing. He’s a little hellion. LOL.

Since surviving pulmonary embolisms and covid, I have to use a rebounder to keep my hear rate stable and my immune system going smoothly- will be writing more about that on the blog at missmaisieandme.com (I know, I am a tad bit late, but homeschooling this kid has turned into an all day thing this week). We even keep one in our RV at the farm! 

Currently, we’re using a 48” rebounder from @leapsandrebounds, but now we will be putting another smaller 40” rebounder in the RV instead (which should save precious space).

I have a new stabilizer bar for when I get dizzy spells or for when my father, who is older and has essential tremor, needs to use it.

❤️In this post, you can get 10% off Rebounders from @leapsandrebounds! ✔️Follow their page! ✔️use MissMaisie10 at checkout for your discount OR go to this link: ✔️https://leapsandrebounds.com/discount/MissMaisie10 💋🎈💗😘

#rv #rvliving #rvliving #rvexercise #rebounding #rebounder #covid_19 #covid #covidsummer2020 #covidsurvivor #pulmonaryembolism #pulmonaryembolismsurvivor #lupus #essentialtremor #vertigo #leapsandrebounds #healthylifestyle #chronicillness #kitten #kittensofinstagram #kittens #cat #catsofinstagram #catsofinstagram

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It wasn’t a difficult set up, except for the part where the man boinged himself with a bungee… absolutely LOVE the new rebounder and can’t wait to get it into the RV.

(also, to get it out of the little house. I have no room in here for 2 rebounders)

Cake the kitten was RIDICULOUS about the new one. He was bouncing and dancing all over the thing for a solid 2 hours.

I really LOVE the new stabilizer bar. I thought I ordered one for a larger trampoline, but I was mistaken. Keeping it, though. It’s great to have something to hold onto when one is feeling off balance or dizzy.

I got the bar for my dad’s rebounder originally, but it doesn’t fit the 48″ ones (It only fits the smaller ones). It really improves the experience, even for me. It makes me feel safer when I am wobbly. I suffer from vertigo and weird dizziness leftover from being sick still. My dad has essential tremor and balance issues (thanks, Vietnam War). Having a stability bar is a must for those of us with issues such as these.

The bar has 3 height adjustments, with the highest being comfortable enough for someone about 6′ or more.

I really love this new addition to our rebounder, I will probably order a big one for both dad and me.

I haven’t had time to write the lonnnng (and it will be long) PTSD filled trauma surrounding my covid and pulmonary embolism recovery, due to beginning home schooling the kiddo and other weird snafus (like 3 people in my family, including the kitten, injury their right legs/paws).

I am still offering the 10 percent discount from Leaps and Rebounds for any of these purchases if you would like one of these for yourself.

In this post, you can get 10% off Rebounders from www.leapsandrebounds.com

✔️Follow their page at https://www.instagram.com/leapsandrebounds/


✔️use MissMaisie10 at checkout for your discount OR

✔️go to this link:
https://leapsandrebounds.com/discount/MissMaisie10
💋🎈💗



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Rough morning after 2 weeks of smooth recovery

Been feeling better than anyone could have imagined, with having pulmonary embolisms in both lungs. My lung sounds and functions were clear, my ‘spells’ less so- I felt fantastic… until this morning when I woke abruptly this morning.

I woke up at 6 am, sweating and not able to catch breath. It’s 2 weeks since I was diagnosed with bilateral PEs and I haven’t had a ‘spell’ like this in over a week. I’d been feeling better.

I feel like it burns all the way into the middle of both lungs, hard to catch an inhalation, feel like I have to cough phlegm, but nothing.

My bp is lower than normal 102/80. I woke with tachycardia (fast heart rate) over 120, that went down to the 90s.

I’ve not had spells this bad since the hospital. My pulse ox reads anywhere from 93-98, depending.

I still can’t take a deep breath right now… it’s getting better, but it’s scary nonetheless.

I don’t drink, don’t smoke. I just started getting my steps back up from nil to 7k the last three days. I’m on the ketogenic diet.

When they said recovery is a process with pulmonary embolisms, they were not kidding. I can have relatively normal, excellent days- then BAM! Scary, back to square one.

Some folks in my support group say it takes months to years to recover.

My stubborn self was hoping for WEEKS. I push myself too hard. I am depressed, as much as I can be. Mostly because I don’t like to be idle.

Saw my gynecological oncologist this week and everything in that area is looking great since the hysterectomy. This surgery caused my PEs, btw.

I am too ornery and cantankerous to die. Too much to do… and I have a child to care for.

I refuse to succumb, but if anything happens to me, tell my baby I loved her.

So far, I am told I am lucky to be alive as it is. For this, I am absolutely grateful.

I have so many people I love and have loved. I don’t want to go anywhere.

I want to celebrate being alive. 2018 was rough. I am not the only person in my family to nearly lose their life in a sudden accident this year. We are blessed to be here right now.