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The Road Before & After Surgery
June 15, 2012
Time To Walk!
Mood:  lazy
Now Playing: Day 796-The Final Road To Survival

After spending lots of time resting my insides are now screaming so its time to walk, walk and walk! I sure hope gravity is on my side over the next few days in order to work this gosh awful treatment out of my system so I don't end up back at the hospital.

I can't believe its another holiday weekend. If feels like we just celebrated Mother's day last week and here we are with it being just a few days away from Father's day. YIKES! Luckily I got my gifts last week when I was feeling fairly well because this weekend it will be low-key for me. Where is the holiday made for us patients? One where others do good deeds in order to help us conserve some energy. Wouldn't that be nice? A day to be pampered and for others to endure our daily struggles for a change. Maybe then people would finally understand our condition. AMEN. Sadly I still firmly believe no one will ever understand Gastroparesis unless they either take a week walking in our shoes or stuff themselves during every meal as if it was Thanksgiving over and over and over and over again. Since this is the first Father's Day weekend with little Erik we decided to do something as a family. I have a fun activity planned but of course with Gastroparesis its best not to plan too far ahead because you never know one day from the next. Hopefully this weekend will bring me a few GP-free days.

Now that the rest of the yard work and landscaping is near completion it was time to bring out the porch chairs and table. The fur kids were so excited that it didn't take long for them to jump up and take a seat with Mom. I had the chairs out earlier this week but Oreo wasn't feeling good so he didn't last that long outside. The weather is going to be in the mid 90's starting tomorrow so looks like we might have to hold off a bit before spending the evenings relaxing on the porch. Between my Idiopathic Gastroparesis/seizures and Eric's horrible allergies it appears we will likely be spending most of the summer months indoors. We sure do have a lot in common just like two peas in a pod. Hahahahaha!


Posted by GastroparesisAwarenessCampaignOrg. at 11:43 PM EDT
Updated: June 16, 2012 4:29 AM EDT
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June 14, 2012
Ok Drano. You Win!
Mood:  down
Now Playing: Day 795-The Final Road To Survival

You know who won the ole Drano game don't you?

Well if this is any guess it sure wasn't me.

Around midnight things got a bit worse. Around 1am I was not only light headed but my pulse started racing. Once the nausea, chills and feeling loopy started kicking in trouble was soon over the horizon. I quickly grabbed a Gatorade and Pedialyte frozen popsicle then started chugging however that didn't work and things then started coming back up. I guess I lost this game of Drano because as fast as I started going down was as fast as I got my gym shoes on and headed to the local hospital emergency room. I wasn't sure if I would make it to the hospital where all my specialists practice. In fact I had another one which was closer in mind however if I planned on surviving this latest ER visit I had better just count my blessings and head five more minutes up north because this other hospital is a huge NO-NO. Why you may ask? Because the hospital staff is just one word: Horrible! I would rather have a stranger blind folded treat me than that hospital. No lie!

Nothing quite like having Drano stuck and it making your electrolytes all out of whack then becoming severely dehydrated. How I drove myself up to the hospital was even a question the doctors and ER staff were wondering but let's just say as I told them, "It was one quick ride!" OK. Once again maybe a bad decision but when you are going downhill fast rhyme and reason is the last thing on your mind. The emergency room and getting there fast is the first and only thing on your mind. Calling someone to meet you up there isn't either but that of course comes into play later when you realize you can't drive yourself nor your own car home. Hahahaha! So after a huge bag of IV fluids, blood work and waiting for my delayed kidneys to start working I was then finally released to go home and continue the Drano treatment waiting game. At least they got me fully re-hydrated and the tremors have calmed back down but I am still not thinking clearly due to all this fluid retention in my intestines.

The fur gang never likes seeing us leave but are always waiting for our arrival back home with tails wagging. They always put a smile on my face even on the worst GP days. Once I let my body rest it was around 1pm before I woke up to the sound of my cell phone ringing. I spoke to my doctor about what was happening with treatment only to be told once again, "Your intestines really need to come out. We can't keep having things like this happening because it is dangerous." Not that this is a no brainer but when you are on the receiving end with any surgery its not that easy. Let's just hope this new surgeon and her surgical team doesn't also scream like hell and run for the hills like the last group from two years ago. Hahahahaha! I am taking it one day at a time. Drano time that is...


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: June 15, 2012 1:50 AM EDT
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June 13, 2012
Are You Sure It's Not FRIDAY The 13th?!
Mood:  don't ask
Now Playing: Day 794-The Final Road To Survival

Ever wake up and just "know" its going to be a bad day but you still make the most of it? Well...at least try and do your "best" to make the most of it.

Drano and me just aren't working this time around. Treatment is now consisting of days playing the waiting game. Not like drinking tons of sodium and chlorine isn't bad enough but when it gets stuck in your stomach and intestines it takes things to an entirely different level. I feel for my fellow GP clean out friends who have to endure weekly treatments of mag-citrate only to sometimes also find out things don't always go as planned and it too gets stuck. Instead of laying around "thinking" about it I decided to once again play landscaping Supervisor as my Husband finished up the new flower beds so we could plant the rest of the wildflower and sunflower seeds. Hopefully the squirrel gang won't find this new flowerbed. Hahahaha! Wishful thinking! At least the weather was perfect. Not too hot and not too humid so if we are going to get all this last minute planting out of the way we better do it now before the nasty summer heat is here. I will never be able to enjoy summertime anymore. Not with Gastroparesis and connected seizures. I am slowly getting my body to sleep and rotate with the change of season but even just a little bit of outdoor sun and heat tends to quickly zap my energy. This seems to be the typical norm with GP'ers who have been writing me saying they too would rather just skip summer all together because they can never enjoy the outdoor activities.

Where is GP Island when we need it? Surely at GP Island we could build a huge indoor place with plenty of windows so at least we could see the beautiful summer outdoors. CHEERS TO THAT!

I guess for now I will settle for an evening stroll around the lake at our local park. At least the ducks are happy I am not on GP Island and instead enjoying their lake home. The endless supply of bread doesn't hurt either. Hahahaha!


Posted by GastroparesisAwarenessCampaignOrg. at 11:52 PM EDT
Updated: June 15, 2012 1:02 AM EDT
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June 12, 2012
Drano Day Round #2!
Mood:  don't ask
Now Playing: Day 793-The Final Road To Survival

If you first don't succeed then try, try again. OK. So the first round of treatment didn't work yesterday. It didn't work at all! Make today Drano round #2 and if this doesn't work then forget it!

One day of Drano is bad enough but for the first time I got ZERO, ZIP, NADA relief so today I was stuck with a back to back dose of wicked treatment. UGGG! This might be a reason why my specialists are urging the importance of getting these darn intestines out and if for some scary reason the new surgical team isn't comfortable and they run like hell at least they will perform surgery on an emergency basis. That is "if" I could or would make it into the surgery room. Sudden bowel rupture is deadly and you only have a certain amount of time to make it to the hospital. When you have a very high tolerance of pain like myself it can be tricky to know "when" its time to head to the emergency room but I try not to think too far ahead. I just hope I will never have to go through such a scary scenario but I am a realistic when it comes to my unique and progressive medical condition. "It is what it is."

So....I finished up another Hell-In-A-Jug treatment by early this evening then decided to play landscaping Supervisor while my Hubby got the flowerbeds de-weeded and ready to plant more wildflower seeds. The sunflower seeds we planted last week became a quick snack for the squirrels so I decided to just plant some additional wildflower seeds that way I know at least they won't become an appetizer for the wildlife gang. Hahahaha! Wildflower seeds are great because you get such a wide variety of flowers that come in a rainbow of colors. They are also low maintenance and love the sun and summer heat. The tiger lillie's and roses are doing really good and so are the butterflies bushes however we have only seen a few butterflies so far this year. Hopefully once the first round of wildflowers start blooming that were planted last month we will start seeing more butterflies and hummingbirds since they attract both.

After a long Drano day for me and a productive day outside for Eric we decided to get the lounge chairs out to relax. Seems Oreo and Littleblue had the same idea so we each shared part of our chairs. Looks like the next thing on our list to buy for this summer and fall will be a few more chairs!

Now all I need is the beach, sand and seashells. Doesn't that sound nice?! We can always still pretend can't we?...


Posted by GastroparesisAwarenessCampaignOrg. at 11:30 PM EDT
Updated: June 13, 2012 2:43 AM EDT
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June 11, 2012
Living In A Drano World...
Mood:  hungry
Now Playing: Day 792-The Final Road To Survival

I'm just living in a Drano world as one of the unlucky victims...EEK!!

Yep. Its that time again. It's Hell-In-A-Jug day. This circle of liquid dynamite just never ends and I don't think it will ever end in this lifetime. I need to come up with some fun ways to make treatment days go by a bit easier. Maybe something to help bide the time and keep my mind off of whether or not it will work too quickly, not fast enough or come back up. If you think reading about Drano gets old then you need to drink this stuff on a weekly basis. Even the prescription refills have now become their own story with each trip becoming more interesting than the other. It isn't the Drano that makes it interesting but instead the continued reactions of others. I am so glad Eric had to go pick it up today seeing I was too busy chugging my own jug at home. Yes, another interesting audience at the store for him full of strange looks and even stranger questions. Maybe not strange to us because we are used to it. Not that drinking this foul stuff is bad enough but staring down another six jugs was the last thing I wanted to see today. UGG!!!!

With it being less than two weeks away from seeing my new surgical team I needed to finish up the rest of the paperwork. Its like signing your life away. Actually your intestines away. Hahahaha! Maybe my intestines need their own social security number because clearly they are starting to have their own identity. Everything lately has literally been evolving around my GI organs. NO LIE. Between the every other day feeling of not being able to breath due to the intestinal inflammation pushing on my lower lungs and daily energy that quickly gets zapped its been a one thing GI event after another. For those who have asked, "Is that a new hair style in your wedding photo?" and other questions I have honest answers for you but for those who are fellow GP friends you already knew the answers.

*No. I lost most of my hair over the past few years which got even worse after each weekly treatments. It has been a slow process thankfully after having too much hair to start with. Hee,hee,hee,hee...I have my own wig collection at home and although I would love to have my full head of hair back it is what it is. I have learned to accept it and there's no use crying over spilled milk.

*My nails have done the same game as my hair. Here today, gone tomorrow. Not being able to eat normally and staying on a mostly liquid diet is only part of the problem. When you have Gastroparesis your body can not break down nor absorb important vitamins and nutrients properly so your nails get brittle. I do occasionally get nails put on or do them myself for important events however with risk of infection that is caused by nail glue I only keep them on for a week-max.

*Yes. I still have to use a cane and wheelchair if walking for a long period of time. I will always have my good and bad days. In our wedding photo I was able to lean onto Eric to keep my balance and same with a few others taken out of town. After awhile you learn not to pay attention to the reactions of others because at the end of the day does peoples opinions who have no idea of my condition really matter? Same with using masks outdoors. At first it drove me nuts with people looking oddly at me but now I don't think twice about the reactions or children staring. Hey, maybe I should take a few extra masks along with me seeing the smog and humidity in this city surely can't be healthy for anyone outdoors.

I guess my point is, life is clearly what you make of it. Good or bad. While people might spend their time and money buying into vanity and what others believe they should look like I am too busy putting my time and money into saving vital organs in order to just survive. Kinda strange how being sick puts life into perspective isn't it? Wisdom isn't gained by age. Wisdom is gained by survival and learning life sustaining lessons along the way.


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EDT
Updated: June 12, 2012 4:30 AM EDT
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June 10, 2012
Rounding Out Another GP Weekend...
Mood:  hungry
Now Playing: Day 791-The Final Road To Survival

I am so mentally hungry its not even funny! Now if my GI organs would just allow for some food...sigh...Sorry, but even the best liquefied food doesn't cut it. Maybe I found a few new fruit and protein drinks lately that do fairly well staying down but trust me even I have my days when all this Gastroparesis nonsense gets old. Very old! Now I know how Pumpkin kitty feels eating the same ole food day after day so its no wonder now I have to change it up a bit and mix a different variety with his normal food. It has also been keeping him from meowing all hours of the night due to being bored with his food. Yes! The fur gang are one word, "spoiled" but they are well behaved fur kids and worth it!!

Since I am just 24 hours away from another Hell-In-A-Jug treatment its been a day full of running errands while I still have the energy. Forget hitting the treadmill later because I would rather be outdoors walking at the park. At least Cuddles kitty is getting some use out of it today. Hahahaha! She looks too funny! Poor Oreo has been having one heck of a time with his hearing. Its scaring him so much that I am now literally tripping over him as he stays close near my feet. We have to take him back to the Veterinarian next week to see how much hearing he has left or if maybe one ear is better than the other. Its tough on poor Oreo but I am so glad someone is always home with him.

One of my dear fellow GP friends Darlene recently got the Gastroparesis Awareness Campaign motto I started eight years ago tattooed around her ankle. It looks so neat and its such an honor to have others sharing the saying, "KEEP ON! KEEPING ON!" With Gastroparesis it is indeed a struggle with the wide range of symptoms we all suffer on a daily basis. Support is very important and such a critical key to our over all care! Its been truly amazing watching our GP family grow through out the years and no matter how hard the journey may become we will never walk alone because we will always have each other. AMEN!


Posted by GastroparesisAwarenessCampaignOrg. at 11:42 PM EDT
Updated: June 12, 2012 3:15 AM EDT
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June 9, 2012
Is This A FULL MOON Day?
Mood:  don't ask
Now Playing: Day 790-The Final Road To Survival

OK. There must be a full moon tonight or something because WOW! people acting mighty odd and strange today!

Actually it must be a combination between the heat, humidity and the half-moon tonight. Hahahahaha! Honestly I had to step back this evening and say outloud, "OK. This definitely isn't me. This isn't us. Today's odd and testing day is from the actions of others." Just like my little chipmunk outside who has now made a huge tree stump condo tis best to go back in hiding until people go back to being normal and not werewolves. YIKES!

Remember I went into hiding to keep stress at bay three weeks ago and obviously I reemerged a bit too quickly. Looks like I need to get back to my peaceful retreat for quite awhile longer. This also helps my Gastroparesis and connected problems to stay in check since stress is fuel to GP fire. One would think I should had learned but lets just keep saying, "I am a work in progress."

We all got some solid sleep last night which was well needed. Oreo has still been glued to us and can't seem to get comfortable until the evening after he gets his medication. Its still hard to get used to him not being able to hear as well so we have to sometimes walk up to him so he understands us. At least it hasn't been too hard getting Littleblue back inside the house compared to the cooler weather when she would prefer to be outside all day. With late spring and summer upon us so are all the new wildlife babies. By accident watering the front landscaping we came across a nest of baby rabbits.  Add to the rabbits a groundhog den near the backyard fence line and a few skunks. Now its a huge feat just keeping a close eye on Littleblue and Oreo when taking them outside. All the new wildlife babies usually start emerging this time of the year so its typical to start seeing them around the front and backyard.

Speaking of backyard...

"Just" when the honeysuckle trees and bushes were finally full and providing plenty of shade near the back patio area POOF! they disappeared!! Remember, we built a small sandbox on the patio last fall so this spring and summer once the honeysuckle trees and bushes grew back I could enjoy sitting out there since they provide lots of shade. What I didn't know was while I was sleeping the shade was slowly starting to disappear. Mind you, if I do any yard work that might go into either neighbors side of their yard I always made sure to ask them before cutting. I would assume everyone has some common courtesy to do the same but I was wrong. Instead now having a quiet shaded place to rest and put my feet in the cool sand after treatment days I might as well instead head down south to the ocean because its gone. Yes. That started my day waking up to realize my new neighbors butchered all the beautiful honeysuckle trees and bushes so they could plant grass seed?!! Say what? Another thing was I just planted grass seed for shaded areas where the bushes were and the grass was growing nice and thick. Now it just defeated the whole purpose. So did having somewhere in the backyard I could rest and enjoy after enduring Drano. I guess its that half-moon day or something because I would had thought like the prior neighbors who lived there they would had said, "Hey, since the bushes and trees are hanging over a bit I am going to just trim them back but we wanted you to see it first so we don't cut too much or everything back." Instead there is no shade anymore and if it ever grows back it will take years. Needless to say I was shocked once I walked outside to see the shade had disappeared.After the fact I was then told by one of the neighbors they decided to cut everything back this morning however shouldn't they had said something prior?.

So I might be rambling on a bit but I don't expect anyone to understand the little things those who are sick with a terminal condition enjoy because they don't walk in our shoes. They only walk in their own.

After that huge disappointing start to my day it only got more odd after some ragging lunatic woman on her cell phone texting came down the wrong way of the street going around 40mph and almost hit me head on. It was one of those situations where you see the inevitiable happening but all you can do is stop and wait. Thank goodness my Guardian Angels must had been watching over me because half an inch was all that was standing between myself and her car.

Yes. Its been a Friday the 13th, full moon kinda day. So you know what this gal has learned and will be doing from now on in this city right? Going back into hiding keeping to myself in this crazy city that way the only responsible person for any crazy or inconsiderate behavior will be myself. I haven't felt a wild hair coming on yet so I guess I am safe. Hahahahaha! Oh what a day and what an evening but as they say, "There is always tomorrow." 

WinkThank goodness for a new day! AMEN.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: June 10, 2012 4:52 PM EDT
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June 8, 2012
Life Is A Lesson To Be Learned.
Mood:  chillin'
Now Playing: Day 789-The Final Road To Survival

If life is a lesson to be learned then maybe after going on 4 years of the spring and summer sunlight nightmare I would had learned to rotate my sleep schedule with the sun. Instead I ended up with a day of migraines, tremors and a few pop up seizures. NOT FUN. This also put a huge kink into the days schedule crossing off things to do like changing lots of information since we are now a married couple. At least the major stuff got changed yesterday. I call the rest "minor details" so it was up to my friend/Caregiver/Husband to finish the rest. Let's just call him Hubby now for short. Hahahahaha! I am sure to one individual, OK, maybe a few that term is burning a hole in their brains by now but you can't please everyone in life and for once I have learned to please myself. AMEN!

With starting the day having electrical shocks going through my head, spine, arms and legs I finally raised my red flag and called my Neuro doctor so they could try me on some new medication. The other seizure and tremor medications they tried me on didn't work. In fact the last three years worth of trying various types of medication didn't work and the only sure way to calm down the lightening was good ole fashioned Valium. Yes, it does work however since it has such a short life span in the body I only get around 4 hours of relief. What I need now is something that will keep me from getting into trouble when my Hubby isn't home seeing I don't have anyone else here in the city that understands nor has even been around me during a seizure. I do have a few friends that have but I can't put them into that predicament having to drive over and stay here at the house when they have family and children of their own. Hopefully my Neuro doctor and his staff can find one of the new trial medications that might work this time around so I don't have to suffer through the rest of spring and upcoming summer months.

Oreo has been hanging in there and doing a bit better each day. We both got a really cute card this week from my dear Angel friend down south. Oreo is so smart he actually read the part to him. Hee,hee,hee,hee...See, you can teach an older fur kid new tricks! So far we haven't had to increase his dosage on both medications but we still need to continue keeping a close eye on him. He still has occasional tremors and gets scared a lot which is normal they said since he is also losing his hearing. Its hard seeing him not feel well but we have been doing our best to give him lots of kisses and hugs. He continues to enjoy bonding time by my side while I catch up on my taped television shows. When he is ready to call it a night he jumps down to sleep on his huge floor bed. Littleblue has been doing a great job playing fur nurse to Oreo and even takes a few naps laying next to him.

My dear friend John contacted me today and was happy to say the big move out west is finally complete! WOOHOA!! He sent me a few photos of his new home and his fur kid Robie who clearly is enjoying the California lifestyle. It seems both of us are now experiencing the other side of the mountain. We have both been through hell and back and hell again through out the years so its been wonderful sharing all the recent great news with each other! We always joke around that somehow they must had switched cribs at birth because we are just like siblings. I sure wish we lived closer but since he is the first to make it out west it won't be too much longer when we will be following right behind. Hubby is more than ready to make the big move and continue positive changes in our lives. I couldn't agree with him more but unfortunately right now I must ride out this next medical challenge to see what the future holds.

I am continuing to embrace these winds of change and with it comes being a new Mom to little Erik who is five years old. We are taking things one step at a time but I am super excited to see what the future holds for all of us as one big happy family!

"Life comes with no guarantees, no time outs, no second chances. Don't be afraid to fall in love because every second wasted is a second of life you can never get back."


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: June 9, 2012 4:37 AM EDT
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June 7, 2012
Adding To The List Of Things To Do...
Mood:  d'oh
Now Playing: Day 788-The Final Road To Survival

This has been an exhausting week! So far the short list of things to do has now turned into a huge list. Thank goodness for both of us now tackling things together which hopefully means cutting the time in half!

Not that I don't have enough things to do my doctors have their own list now due to the inevitable surgeries. Today one of my specialists said, "I have to be honest with you. Either your colon comes out now or it comes out in an emergency surgery because it can't stay in forever. Your new symptoms show us the condition of your colon and parts of your small intestine are rapidly progressing and to be honest thing aren't looking good." One would think having any surgery whether major or small wouldn't be that difficult to prepare for but trust me, there is a huge difference between the two! Add onto the problem that I didn't do too great during and after my last surgery which has me once again concerned. They wanted to remove my colon three years ago just a year after my last surgery "however" the nightmare experience my two surgeons and their team experienced when they opened me up wasn't too pleasant. In fact the surgical op reports with photos and video scared the next surgeon right out of the next surgery. I fear this new surgeon and her team might react the exact same way. Honestly I just don't want to be put into any emergency surgery position without being prepared. Sadly I have learned living with a chronic condition is just that, "Living unprepared."

With the heat upon us starting this weekend its our goal to finish the big "To Do List" way ahead of time before my next treatment which is right around the corner. We haven't had much time to celebrate being newlyweds however there is plenty of time for that later on. Right now we are just enjoying some peace and quiet by tuning out the reactions of some individuals in the city who were never supportive to start with and instead surrounding ourselves with those who were always there for us and cared about my happiness and over all well being. Thank you my dear friends! Thanks to the never ending kindness and support of strangers our fairy tale wedding will continue later this summer at Indiana Downs horsetrack as we re-exchange our wedding vows in front of friends and GP family.

What did we do the rest of the evening? Our top priority was changing our Medical Power of Attorney and Living Wills. Out with the old, in with the new. I have lived a lot and learned a lot but one thing will never change is the true importance of happiness. Marrying your best friend and someone who always stood by your side when others were causing you nothing but harm is very surreal. Love sometimes is blind but eventually you wake up then realize you truly deserve unconditional love with no boundaries. A coward will stand and take the heat but the honorable will fight back and protect you.

Thank you for protecting me and loving me unconditionally!

"Happiness Is Being Married To Your Best Friend."


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: June 9, 2012 4:54 AM EDT
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June 6, 2012
SURPRISE EVERYONE!-JUST MARRIED!!
Mood:  celebratory
Now Playing: Day 787-The Final Road To Survival

So the story goes about two people who became best friends who ended up falling in love, got married and lived happily ever after.

YES! That's me. That's us! That's my best friend/Caregiver who is now officially my beloved and wonderful, passionate, caring, nurturing, loving, supportive Husband who always saw past my Gastroparesis and accepted me for who I always was. Me-Kimberly.

I finally turned over a new leaf and with it I also turned over a new life. I finally found true love and with it my life partner and best friend. Life doesn't feel good. It feels GREAT!!

JUST MARRIED!  :)
Deputy Eric &
Kimberly Stegman-Dieckmann
Thanks to Indiana Downs Racetrack we will be holding our vow renewals derby style in the winners circle for our family/Gastroparesis family, friends and loved ones-September 2012.
www.gastroparesisawareness.com
*For future invite and details


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EDT
Updated: June 9, 2012 3:22 AM EDT
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