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The Road Before & After Surgery
July 1, 2012
Trying Not To Throw In The Towel...
Mood:  on fire
Now Playing: Day 812-The Final Road To Survival

Ahhhh.....The ocean. The sand. The sun...While my friend John is continuing to get acquainted with his new home out on the west coast in California I am still trying to let reality sink into my brain here in Ohio.

This weekend it seems there are a few of us doing the wicked intestinal treatments. Poor Jennifer is up to over 100 bottles of magnesium-citrate and I still have yet to keep track or remember what jug of liquid Drano aka Hell-In-A-Jug I am now on. Since each week it knocks me out for the count one of these days I pray someone out there comes up with a better solution like "IV Drano" so I can finally knock these jugs out of my life for good. AMEN!

We finally have been getting some rain although it does make the heat and humidity a lot worse. The grass and trees sure needed it since its been so dry. Instead of Eric having to take over watering the flower beds the past few days Mother Nature has done it for him. Unfortunately he won't get out of cutting the grass this coming week. We are hoping the drains finally get done this month. Then there will only be one project left for the house repairs. It seems like it is taking forever...

Since this treatment decided to play a harder internal game on my organs than last weeks I have been home sleeping most of the day away. This isn't normal for me because I usually have enough energy to at least keep busy the next day after treatment however this time it didn't happen. At least Eric set an alarm for every two hours to wake me up so I can take in fluids and not get dehydrated. Let's just say after 8.5 years my poor body is starting to get tired and that energy is wearing thin. I don't blame my Idiopathic Gastroparesis on anyone, in fact over the years my heart has grown 100x the size it used to be when it comes to helping others who also suffer from GP and other disabilities. I assume as my friend said this evening via text, "Its because you walk in the same shoes. You actually "GET IT" and what it feels like to suffer." Still on days like today its hard not to just throw in the towel. I struggle sometimes and it isn't easy when your body is down right tired but your mind is still fighting.

We tried to catch up on some other shows Eric taped this evening but my GP won along with a high fever that soon followed. After a Tylenol, Smartwater and an icepack I am hoping to call it an early night. Wishful thinking...


Posted by GastroparesisAwarenessCampaignOrg. at 11:23 PM EDT
Updated: July 2, 2012 2:54 AM EDT
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June 30, 2012
Being REAL-istic...
Mood:  sharp
Now Playing: Day 811-The Final Road To Survival

Sometimes when you least expect it history makes a strange full circle.

There are quite a few specialists who have recently been able to pull prior records from decades ago. Even when I was a baby. Which came first? The chicken or the egg? No one is certain although I guess anyone can try to be Einstein in the confusing world of Gastroparesis. Tanya always said, "She has been given a bad deck of cards in life." It now seems they might had been handed to me at birth. The questions remain in the minds of more than 10 specialists now who have treated me over the past 8.5 years whether I suffered from lack of nerve development before I was even born?. Some questions will never be answered but many prior records are showing a sick infant with intestinal problems that then turned into a sick pre-adolescent with stomach problems. Could the Gastroparesis journey started way prior to 8.5 years ago? The bigger questions concerning my surgeons are the ones during visits to Children's hospital when I was a young child. Was there a surgeon back then who could had heeded the signs? The early warning of things that were to come? The inevitable? No one is certain but one thing they are almost certain of now is that this didn't just suddenly "happen." There were years of GI problems prior to my Idiopathic Gastroparesis diagnosis.

YIKES!

Now it seems that bad deck of cards could had most likely happened before I was even born. It sure has my surgeons who did my prior surgeries racking their brains because its rare to see Idiopathic Colonic Inertia-meaning the nerves in my colon and intestines stopped working not to mention my Idiopathic Gastroparesis which did the same to my stomach. Are they all connected? Yes. Now they are wondering just how much nerve function I ever had to start with?. Not to ponder on the past or drive one crazy to find answers that are not available because the sad part is things that could had been run as an infant are a little too late. Technology back then wasn't as advanced as it is now. This is why the medical testing equipment we now have is able to detect paralyzed organs-dsymotility. We could be here all day, evening and into the following day, weeks and months trying to piece the missing puzzle pieces of my unique medical mystery however it is what it is. "Que Sera Sera."

The sad part makes me wonder of other young children who start off a life of GI problems that will progress through out their lifetime unless things are caught early and intervention is made by a specialist. I would never want to see any child go through what I have nor would I wish it on my worst enemy and trust me, I have had some crappy things happen by some rude and inconsiderate people through out my lifetime. AMEN.

Today was of course Drano aka Hell-In-A-Jug day. I now dread this stuff because I REFUSE to allow it to be my final demise. We now make it a day full of Drano fun by decorating the jug. Anything for a good laugh because during treatment I will take all the laughs I can get! Eric decided to take another one for the clean-out team. WOOHOA FOR ERIC!! Who else would do this? UMMM....NO ONE I KNOW. Hahahahaha! Willingly anyways.... He did tell me later this evening, "NEVER AGAIN!" I guess the ole jug of salt water and chlorine was even a bit too much for him. If he can't handle a small glass he would never make it through what I do on a weekly basis. It sure made a believer out of him. Maybe it needs to make a believer out of a few other individuals I know too. Hmmmm?....

After careful "Hair-debate" this evening I decided July will be the month I will say farewell to the last of my locks. The bald spots on the side and back of my head is getting worse each week and I refuse to look like Count Dracula from Sesame Street. At least let me have a bit of dignity to choose my hair-less time. Hahahahaha! OK. So, maybe Count Dracula has less than I do but you get the point. If Charlize Theron can do it for a movie role then surely I can do it for the role called, "Life."

As I face the inevitable and end of life I don't consider it being pessimistic. Its called being a REAL-istic person when your insides are progressively going against you. We all make plans each day on how we live our lives but in the game of life there will come a time when we all need to make plans ending it. I am fortunate to have a fair-warning. I call it the past 4.5 years, "Defying the odds."

Que Sera Sera

Que Sera, Sera,
Whatever will be, will be
The future's not ours, to see
Que Sera, Sera
What will be, will be.


Posted by GastroparesisAwarenessCampaignOrg. at 11:43 PM EDT
Updated: July 2, 2012 1:52 AM EDT
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June 29, 2012
FREAKY FRIDAY!
Mood:  don't ask
Now Playing: Day 810-The Final Road To Survival

I don't know why but I had a strong gut feeling this was going to be one of those days. It was going to be, "FREAKY FRIDAY!"

Thank goodness my body and brain got a solid night of sleep because who would had known after today's set of strange events I would need it?.. Once we woke up Eric took care of everything while I got ready for the eventful day. Since the drains have yet to be finished on the side of the house I turned on the weather channel. Although they weren't calling for any rain soon I had a odd feeling we might find the storm up north heading down our way. We only have a 5x5 section near the back door that isn't covered so surely that can wait until we get back home from my surgeon appointment. Right? Well...WRONG.

I hadn't been to this new surgical center yet which is located only 15 minutes from our house. We were right on time and once we got checked in they took me back right away. I told Eric to wait in the lobby and if I needed him I would have the nurse send him back. Needless to say I didn't need him and its a good thing I decided to brave this new chapter solo. Not only did I meet the new surgeon but also another doctor on staff who found my unique medical condition, "QUITE FASCINATING!" This of course isn't a good thing because that tends to always mean bad news ahead. The first part of the visit started on a bad note when they were concerned about my low blood pressure. I am used to it but the surgeons were not and it had them very concerned and same with my low blood sugar problems followed by uncontrolled seizures that don't respond to normal therapy-medications. Of course this is all caused from my unique medical condition-Gastroparesis & connected problems.

While the surgeon and doctor both took turns coming into the room I watched from the window dark eery clouds slowly creeping into the area. The appointment wasn't going any better. There isn't much you can tell me that is shocking. Sadly I have become a pro at taking bad news which might be a blessing because while taking one small step forward preparing for 3-step surgery today I took 10 steps back then it was a complete BUST!

FOR CRYING OUT LOUD! YES. IT DID HAPPEN.

Me-So far this is a bust and my blood pressure is low as heck which already had them scared running for the hills.  :-0

Eric-Are you serious? What do you mean running for the hills? They are scared?

Eric-Gees. How low is it?

Me-78/53

Eric-Wow. That is low.

Me-First doctor so far is showing various signs of concern. The more they go over my prior medical history and surgical reports the worse it gets.

Eric-So they might now change their mind?

Me-Yep.

Me-It's like a song, Low blood pressure, low blood sugar, seizures and GP, OH MY!

Eric-This doctor makes 19 on the list of specialists who are treating you but I wonder if the disbelief might be a sign of bad news?

Well...it was. Between them running a few unexpected tests an hour visit turned into 2.5 hours. Not only that but after they took a month looking into my prior medical reports, surgical op reports, photos, specialists letters, etc I was told, "As colon surgeons we only do one extensive surgery like this in a year. Even the best colon surgeons in the world only do one extensive surgery a year. Sadly we can not perform any surgical procedure. We can not remove your colon due to extensive damage and progression of your Gastroparesis and connected problems." It might be a good thing I already expected the worst of the worst today. They went into full detail of the complications I am experiencing due to progression of my condition. Surgery wouldn't help me in fact they said, "Your electricity in your body is causing a host of problems. Your low blood pressure should be controlled by an increase of fluids and electrolytes however your intestines no longer work. Same with your low blood sugar, kidney dysfunction, seizures, etc." Of course they can run two tests that so far after 8.5 years I have "YET" to have done but it will not help the situation. It "MIGHT" provide more answers but it won't provide a cure nor any relief. The damage is done and now there is no turning back.

The last 40 minutes of the appointment we went over prior tests, surgeries and also support from family or from some-lack of. We also went over the amazing care my current 17 specialists have provided for me over the years. The surgeon commended all my doctors for doing an outstanding job including my Gastroenterologist who has continued to go above and beyond for me.

I couldn't agree with her more!

At this point my Gastroenterologist was hoping the colon could still be removed and had started my first steps towards preparing for surgery however it is out of the question. I am now given a life sentence living on surgical/colonoscopy bowel prep weekly and the inevitable of my demise. Who knows in the end which will get me first whether it be my heart stopping due to the low blood pressure or a sudden internal blood vessel busting or as expected by most a bowel perforation. Not a good thing to look forward to but its the real deal for me and now I must get my brain around this new chapter at the end of my life. I am lucky to have so far beat the odds but the weekly Drano or as some call it, "acid" might help me to stay out of trouble and becoming toxic however at the same time it isn't doing the job like it used to because my intestines are getting much worse. The bandaid is running out of strength. The doctors were shocked I wasn't tired all the time or constantly napping during the day due to what my body is going through right now on a daily basis. Honestly as I told them, "I don't know how I do it. but I do." They told me of numerous complaints they get on a daily basis from patients having to do the bowel prep for a colonoscopy. "They are complaining of a once in a life time discomfort when you are doing it on a weekly basis and living it for the rest of your life. Maybe now when I tell them the story about you they will think twice about complaining." After 2.5 hours came to an end I met with another team member who went over the other two tests yet to be run but they know the drill...Why bother? Why not take that money and do something I enjoy. AMEN!

Not that it wasn't already a bad start to a very FREAKY FRIDAY but once we left the building we were finally greeted by the eery clouds that quickly turned into 70 mph winds. Yes, it was a no-end day of bad news. I didn't see Dorothy or Toto but we did see on the way back home the nearest Lowe's to buy a tarp and boards for the exposed side of the house where the drains have yet to be finished. Instead what we found once we got home was a heck of a mess where the winds blew the existing boards all over the place, tarps thrown everywhere and tree limbs scattered through out the yard. Hey, at least it helped to take our mind off of everything.

If there is any good to come out of this FREAKY FRIDAY it was finding an old coin laying right in the middle of the new flowerbed on the side of the house. It wasn't there yesterday so the winds must had blown it in however after research this evening I found out my coin literally did have wings! It was an old 1920 liberty dime in which liberty has wings. They call it Greek wings since it represents being a messenger of news.

WOW-NEAT!

Eric was surprised I found it heads up in the new flowerbed. I always believed in signs from above. Maybe the Angels are telling me they still have my back and they will help me during this last chapter of my life. Maybe I won't have to suffer the rest of the way but instead find some peace within. After doing some additional cleaning on the old coin I now call it my peace of "Luck" and closely keep it by my side.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: July 1, 2012 1:10 AM EDT
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June 28, 2012
HOLYMOLY! ITS FLIPPIN HOT!!
Mood:  don't ask
Now Playing: Day 809-The Final Road To Survival

OK. If the weathermen were getting paid per each accurate forecast they sure did hit it on the nail today! WHOA! Its FLIPPIN HOT, HOT, HOT!!

Don't let this photo fool you seeing this was just mid afternoon. This is the time of year when I get into huge trouble. The sunlight is one thing with having a seizure disorder but adding horrible heat and humidity also takes a big toll on my Idiopathic Gastroparesis. Its easy for patients to not only become dehydrated but the heat drains what little energy we have to start with on a daily basis. I need to do lots of walking and with the summer heat and humidity now in full swing its leaving me scrambling for indoor places to walk through out the day into the evening hours. This is the time I must get creative or I run the chance of bowel obstructions by not keeping gravity on my side. Sure, the Drano aka Hell-In-A-Jug works but it doesn't work all the time since my condition continues to progress. This evening we had to start finding indoor complexes where I could walk down the pain and inflammation. Crazy the things Gastroparesis patients have to do in order to stay out of trouble. I tend to think the summer months are the worst for all of us.

My friend John sent me an update on the beautiful weather they are having out in Napa, California. A cool, dry 80 degrees with variable light winds. Gees! Like I really needed to see that and now it only makes me yearn to move out west even faster. I would take the weather out there any day compared to this nasty heat. Better yet, maybe Alaska or even better the North Pole. "LOOK OUT SANTA! HERE WE COME!" Hee,hee,hee,hee... By the time it was 8pm the temperature was up to 104 degrees. I haven't seen any tumbleweed just yet but if this heat continues it won't be too much longer.

Tomorrow is dreaded Friday for this gal. Its the day I meet my new surgeon and surgical team. Eric calls it the day of, "Bad news or worse news." Anyway for him is going to be bad because lately the jolly green giant inside my body has become down right ANGRY. He also has noticed the increased inflammation with my intestines and abdominal swelling so you can certainly bet there isn't going to be any good news coming out of this appointment.

Knowing tomorrow will mostly likely be a long day physically and mentally we just decided to call it another late evening catching up on the last of our favorite recorded shows. The fur gang didn't mind a bit and after hearing Oreo's snoring I don't think he did either. Hahahaha!


Posted by GastroparesisAwarenessCampaignOrg. at 11:58 PM EDT
Updated: June 29, 2012 3:38 AM EDT
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June 27, 2012
Waiting For The Desert Heat...
Mood:  cool
Now Playing: Day 808-The Final Road To Survival

I wonder if the weatherman can get this forecast right or once again be "wrong?" We are suppose to get some wicked heat with humidity starting tomorrow. Today will sadly be the last day enjoying any type of outdoor activity. UGGGG!

It wasn't bad outside this afternoon however my allergies are starting to get worse. We haven't had any rain in quite sometime so the grass is starting to turn a few shades of brown and resembling a bit like tumbleweed. Eric might not have to cut the grass after today for another few weeks. Hey! we might not need to head out west after all and instead the desert might come to us. Ohioada-Ohio & Nevada. Hahahahaha! Since we have no plans right now to move due to a pending three step surgery I want to add a few nut trees around the property. The squirrel gang gave the idea a HIGH-FIVE from the current trees in the front yard upon the news. Hee,hee,hee,hee... Eric said, "Great! now we will have every squirrel in the city living around the house since they would now have an endless supply of food. They might instead think we are NUTS." Hahahahaha! Come on now. They already have an endless supply of food but now it would just make it more convenient for them. Call it a, "Self-Service Buffet." Hahahahaha!

We have just a few last minute things left to do on the project list. Today I got two of them done. I didn't realize how long I had some of my financial accounts and although all in good standing it was still time to part ways. One was opened over 14 years ago. WOW! Talking about time flying by! It felt good to continue making positive changes and at the same time closing a few old chapters of my life. Bear kitty even let me go through his huge basket of toys in order to clear out the old ones. OK. So it wasn't a lot because once he heard me in the basket of toys he quickly reclaimed them. Fur kids sure are smart!

My insides still remain quite angry and although most of the time increased walking helps but not this time. Once it got dark we were right back outside again trying to walk down some of this darn pain and horrible inflammation. Did it work? Nope. I wish. It might be a good thing my new surgeon and surgical team appointment is in a few days because I am not even sure right now if doing treatment this week is such a good idea. Who knows at this point if it would be safe or not so I will leave that up to the surgeon.

After walking, walking and more walking my body was beyond exhausted so this evening we caught up on our favorite television shows and had a low key night...


Posted by GastroparesisAwarenessCampaignOrg. at 11:51 PM EDT
Updated: June 28, 2012 4:34 AM EDT
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June 26, 2012
Running On Empty.
Mood:  chillin'
Now Playing: Day 807-The Final Road To Survival

I officially ran out of energy.

I literally was running on empty all day. "Trying" to keep a smile on my face while attempting a second day of fishing was extremely hard. My Dad decided to tag along today and must had brought the fish with him. He was the only one to not only get a few bites but catch anything. It must had been the secret bait weapon-a can of Spam. Yes, Spam! and the fish sure loved it! Hahahahaha!

Eric got a few snagged lines in the rocks but luckily he didn't have any problems with his reel today. It seemed warmer this afternoon because we didn't have the breeze like yesterday but I continued doing my best to have fun although I didn't last that long. We left earlier than expected but only because I honestly had zero energy left and my insides were screaming with pain. You can only imagine how the rest of my day went right? Right! A heating pad while lounging on my huge comfy recliner.

One of my fellow clean-out buddies and dear GP friend had surgery yesterday. She has also been having a horrible time with her intestines which keep causing her obstructions. Since her main surgeon refused to listen by expressing her concerns that something wasn't quite right a second opinion provided answers and a new surgeon. I never believed in the gastric pacemaker and rightfully so after she contacted me this evening regarding surgery and what the surgeon and surgical team found going on inside her body. Another reminder is the seriousness of Gastroparesis and complications that exist over time once the condition progresses.

I am going to re-post what I sent the online Gastroparesis support group that I started over 7 years ago. I am now a firm believer against anything experimental and not FDA approved.

Group Post-I was never one who was "for" the gastric pacemaker seeing FDA refuses after over a decade to approve the device in use for Gastroparesis-nausea/vomiting. After hearing AMarie's experience and what her surgical team found out yesterday during her surgery proved that maybe they actually need to place a ban on this device.
I just hope everyone who has a gastric pacemaker demands routine check ups and if you ever have any symptoms or complications go with the gut. Don't take them lightly! AMarie is very lucky and fortunate to had a surgeon take a second look and actually find out what the gastric pacemaker was doing to her insides.

Fwd: 3 open incisions and a drain. Much worse than surgeon anticipated. It was the pacemaker. It was entangled around small intestines causing obstructions. It eroded into the bowel and bowel was extremely inflamed. They had to take a section out of my stomach as it was causing problems there and they did take the pacer out. They think they might be able to save the bowel but it is a wait and see. They said I am lucky I didn't wait any longer. This is the worst surgical pain ever for me. I would never get another pacer. -AMarie

There are many GPer's who over the years have also had a gut their gastric pacemaker was making them feel worse. If this is the case and your surgeon will not remove the pacemaker then I highly suggest going over his/her head and getting a second opinion. Any clinic or surgeon who refuses to remove a gastric pacemaker by a patients request obviously is in my opinion using you as a guinea pig for some sort of research or perks-$$$. Gastroparesis patients are not guinea pigs. We are human beings.

It is extremely scary that AMarie had to go through hell and back to prove that these pacemakers are not FDA regulated for a good reason. They are dangerous. I am sending this post as a special notice because I know there are many in our group who have the gastric pacemaker or are in the process of getting one.

*Please remember there is no cure for Gastroparesis. There is currently no specific medication on the market for Gastroparesis. There are medications to help "possibly" ease one symptom or two however they are not Gastroparesis medications. A gastric pacemaker is an experimental device that could "possibly" ease some nausea or vomiting associated with Gastroparesis however it is not FDA approved. It is also not approved by most insurance companies because it is not an approved device. Sometimes with Gastroparesis "LESS" is truly "MORE." This means the more you place into a paralyzed GI tract via mouth or surgically implanted can actually cause further complications and problems. It is always an individual decision with each Gastroparesis patient however please make sure to carefully think things through no matter what plan of action your doctor or specialists suggest because we only have one body.

-Kimberly/Gastroparesis Awareness Campaign-Founder & Idiopathic GP patient


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: June 27, 2012 2:38 AM EDT
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June 25, 2012
Going WAY WAY Past My Comfort Zone...
Mood:  lucky
Now Playing: Day 806-The Final Road To Survival

Today was one of those days when you let the winds pick you up and take you some where you haven't been in years. After almost a decade for me it was:

FISHING! WOOHOA!!

My doctors continue to be adamant by saying, "Things are progressing and getting worse. Your insides are slowly becoming toxic and there is no turning back. The temporary bandaids are no longer working." Today also made me realize what my specialists are seeing during scans which is one huge megacolon that has not only stopped working but has stretched and is applying pressure to my lungs. My intestines are so darn inflamed I am now feeling the shortness of breath more frequently. I also noticed in some photos taken this afternoon at the lake the severe inflammation it is causing around my abdominal area. Did it finally scare me? Yes. A bit.

So after getting some bad news that this surgery will mostly likely become a 3 stage process that will be discussed with me this coming Friday I finally realized that just talking about life is too short isn't enough. Now I am literally scrambling to do what I love the most. Being around water is one of them. Ahhhh....There is nothing quite like hearing waves hit the shore, even if its not the ocean but instead a really huge and nice lake.

Call me, "SUPER SPONTANEOUS" now because if there is anything I want to do I am willing to run a risk to do so and if that means going way-WAY outside my comfort zone then so be it. AMEN! Eric knows how much I miss being near the water and since right now we must wait to find out the next step towards surgery we can't head down south right now. I wouldn't be able to drive with my deteriorating spine however I would risk it all and fly if it meant seeing the ocean one last time. You ever have that feeling that things aren't looking so good with your health? I have had a rude reality check lately with my specialists and of course today after my first fishing trip in years I found myself taking more frequent breaks in order to catch my breath.

DARN GP!

The lake was only a 15 minute drive from our house. I hadn't been there in over 10 years. So many things had changed but it still remained crystal clean and the water was perfect! They added a few new docks, picnic tables, gazebos and new walking trails. Not only is this a great place to fish but could even be a new place to walk. It wasn't even five minutes once we found a spot with lots of shade that two malard ducks made their way up to us. Do they know I will feed them or what?! Eric said, "Ok, Wildlife Mom I guess they know you have a stash of bread with you. How they know though I have no idea?.." Hahahaha! They just "know." Since it was only 82 degrees today with lots of wind and little humidity we stayed for a little over two hours with lots of breaks in between so my back didn't lock up. Thank goodness for the walking trails. Eric spent more time messing with his fishing pole and changing out the floater and weights. Hahahaha! Let's just say the last time these fishing poles were used was in Florida on a pontoon boat out in the middle of the ocean. The reel was full of sand so his pole kept locking up on him so it was smart to bring two extra fishing poles. I used the one I bought on my last trip down south so it was smooth sailing for me although the only thing that was biting at the lake was the ducks and geese who were eating the loaf of bread I brought with us. Who cares though because I had a great time! I forgot what fun it was fishing and how relaxing too!

We had plenty of shaded places at the lake to fish so I didn't get overheated or burnt. The sun was behind us so my head didn't suffer and we brought plenty of fluids and "what if" medication. All in all it was a perfect day and it sure brought back some fond memories. It was an emotional evening when even this gal started to finally fully understand the seriousness of my fragile health. Maybe I can visit Florida again one day soon. Maybe together as family we can visit the coast again for one last time by putting our differences aside before its too late. I still hold onto hope because in my life that's all I have left...

To get up in the morning only to know that you will have to face another obstacle takes strength.

To smile when the only thing you want to do is cry takes bravery.

To act happy & laugh when you know that times are at their worst takes courage.

To be joyous when the only good news is the best of the bad news takes support.

To be there & help others through the roughest times in life takes love.


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EDT
Updated: June 26, 2012 3:04 AM EDT
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June 24, 2012
What It Was Like To Feel & Be "Normal."
Mood:  not sure
Now Playing: Day 805-The Final Road To Survival

There is something way, way wrong when you find receipts from your last vacation you ever took in your life. Mine was June 2005.

BAH HUMBUG!

This day sure was one full of reminders of what "used" to be. More like what it used to feel like living a "normal" life with a "normal" body. AMEN TIMES 10!

What would the wildlife gang do without me? OK. Maybe not have an endless supply of food or their new treat Cheerios. Hahahaha! Eric got the squirrelie (new word) scared out of him this afternoon when he went outside to get something from the garage and the squirrel gang greeted him on the front porch. Hahahaha! What can I say? It was past their feeding time and since darn GP kept me up with pain until 8am I didn't get up until 3pm. It was way past their feeding time so they were pretty upset. Sooner or later they might learn how to ring the doorbell. Hahahahaha!

We finally got the dining room chairs finished today. They all turned out perfect and it only took us around 40 minutes. We bought a nice ivory striped table cloth and new placemats. It was our first project together and I must say we did a great job! Next on the list won't be until fall when the upstairs bedroom will get repainted. Same with the front porch and side awning that both need restained. Its just been already way too hot this year to do much outdoors and I don't think with all this heat its a good idea to stain anything wood outside. At least not until it cools down.

My friends sent me lots of photos this evening catching me up on their weekend adventures. Kevin had a huge family gathering out in Indiana at a vacation house-more like farm that his family owns. He has such a HUGE tight-knit family that gatherings are more like huge projects getting everyone under the same roof. I remember going to this same gathering years ago and I lost count of how many family members were there but all of them were super sweet and nice! I sure do miss a "normal" life but what can you do sometimes?.. John of course had to really round off my evening by sending me super jealous photos of the beautiful ocean that I love and truly miss. Sure...I have lakes here in the area but its not the same as the ocean and coastline. He had dinner with friends at a huge marina diner with an amazing view! SO JEALOUS! Of course he said, "Once you all get moved out west I promise to come pick you up and take you to all the big hangouts and the best beaches."

It couldn't come sooner!!

Eric is even starting to get antsy. Life is short and time waits for no one. I have already let over 8 years pass me by due to my Idiopathic Gastroparesis and connected problems. I miss all the vacations down south in Florida but time took over and some lost their true meaning of family. Now I only keep in touch with 2 family members-not by choice but because I have realized fighting with others over petty things just isn't worth it and in the process of all the bickering I wasted valuable time and progressed my already fragile health in the process. Hey, at least I have all the seashells I collected over the years around the front yard landscaping, photos of the ocean and past vacations but as well the long lost receipts of when life used to be carefree, fun and we all had our sense of heart.

This is going to be a busy upcoming week with new chapters opening in my GP life. At this point there is nothing left that is shocking to me except if they made Drano aka Hell-In-A-Jug chocolate flavored! Hahahaha!!


Posted by GastroparesisAwarenessCampaignOrg. at 11:47 PM EDT
Updated: June 25, 2012 3:01 AM EDT
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June 23, 2012
Leaving A Legacy...
Mood:  happy
Now Playing: Day 804-The Final Road To Survival

June 23, 2012

 

The Gastroparesis Awareness Campaign Team welcomes from the icon of American Pop and legendary TV show, The Brady Bunch

 "Alice B. Davis"

*From 1969 to 1974, Davis played housekeeper Alice Nelson in The Brady Bunch television series. Since then, she has returned to take part in various Brady Bunch TV movies, including The Brady Girls Get Married (1981) and A Very Brady Christmas (1988). She also reprised her role as Alice Nelson in two Brady Bunch spin-off television series: The Brady Brides (1981) and The Bradys (1990). Davis has appeared in a number of Brady Bunch reunion projects, most recently TV Land's The Brady Bunch 35th Anniversary Reunion Special: Still Brady After All These Years. The Brady Bunch was awarded the TV Land Pop Culture Award on the 5th annual TV Land Awards. Davis and other cast members accepted the award, and she received a standing ovation.

 TOGETHER LET'S HELP SAVE LIVES & RAISE GASTROPARESIS AWARENESS!

KEEP ON! KEEPING ON!

"There is nothing more gratifying in life than knowing you will leave a legacy behind when Heaven calls helping millions of other Gastroparesis patients on their own personal journey."

Gastroparesis Awareness Campaign/Founder-Kimberly

www.gastroparesisawareness.com


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EDT
Updated: June 24, 2012 2:49 AM EDT
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June 22, 2012
DranOVER Day!
Mood:  down
Now Playing: Day 803-The Final Road To Survival

Wow! Do I have a super Drano aka Hell-In-A-Jug hangover from hell!! I think Oreo is even having a sympathy day for me but at least one of us gets to rest. Forget about sleeping all day for this gal because I need to keep moving. It was a S-L-O -W day but heck! at least I did it and even with a smile on my face. Half-smile that is. Hahahahaha! The worst part of the darn weekly treatments is now I have to follow them up with the rest of the injections. Its like getting hit in the AS* twice! OUCH.Someone even wrote to GP Rocky last week saying, "Your diary reminds me of Anne Frank because you both are to the point and brutally honest." I certainly agree because you can't get more honest when the bathroom becomes your second best friend. Hee,hee,hee,hee...

Its also been a busy afternoon outdoors with the last of the house repairs. At least the jack hammer didn't bother me too much. The only annoying sound was when there were breaks in between the hammering. At least the humidifier that doesn't work got taken out so the air duct company can do a detailed cleaning of the a/c system and air ducts in a few weeks. We are getting down to the last of the house repairs and mold correction issues. The huge floor dehumidifiers on each level of the house not only are killing any existing mold but helping the air stay much drier and cooler too! The only down side might be the next electric bill coming in a few weeks. YIKES! I guess we will just have to wait and see... With no mold issues anymore from the monsoon rain we had in May and foundation repairs coming close to an end its enough to make us both JUMP FOR JOY! AHHHHHHHHHHHHH!! Eric said today, "'After everything is finally finished next month we might start getting bored because we are so used to having things to do." He might want to stop while he is ahead because when you live in a house there are "always" things to do. Hahahahaha!

Since this treatment will most likely take three days before I start bouncing back we got some new material to reupholster the dining room chairs. There isn't anything wrong with them but it will be nice to add a bit of new color and pattern. The material we found was on sale so it wasn't that expensive. I am hoping to have the chairs finished by this weekend with help of course from Hubby. HINT-HINT...

This evening we looked online at a few more properties out west in Nevada. I found some great potentials but of course we must see whats going to happen with surgery and my new surgeon and surgical team. Eric has the chance to work with another Sheriff's department in Nevada but had also gotten a few other job offers from fellow GP friends who have companies of their own out west. Its a win-win situation and if it means less allergy problems that is even a bigger bonus! I know my dear friend John would be super excited because that means we would only be a 2 hour drive away from where he lives in California. Life is always changing and life is also short so if you feel the winds of change its important sometimes to see where the winds might take you in the process.

With Gastroparesis its one day at a time. In my world its one jug at a time too! DITTO.


Posted by GastroparesisAwarenessCampaignOrg. at 11:35 PM EDT
Updated: June 23, 2012 2:26 AM EDT
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