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The Road Before & After Surgery
May 30, 2012
BULLSEYE!
Mood:  sharp
Now Playing: Day 780-The Final Road To Survival

Me:JEALOUS!

Friend: At least I'm not burnt yet.

Other Friend: You need a vacation but I forgot two other people who are suppose to not be selfish are taking it for you but glad you have us sweetie!  :)

Me: Why does the courts make it so darn difficult to do a first and last name change? One would think I was part of the Mob or something. Hahahaha!

Other Friend: Maybe you are?!

Friend: Bring your Dranotini's with an umbrella on over, hee,hee,hee,hee...

Other Friend: You can always move down south and my family insists.

Me: Dranotini's for all! Only if you share with me.  :)

Friend: BAH! I might then actually get burned!

Me: Hey, I need to continue this new lease on life but if only you all lived in Nevada then I would take you up on that offer.

Other Friend: Then moving we shall see Kalyani! By the way I like that name and the meaning sure fits you to a "T!"

Friend: You will always be Kimberloo to me.  :)

So maybe this isn't South Beach but for those of us who suffer from Gastroparesis life is far from a beach to start with in fact some of us like myself instead of walking in the sand I get to drink it. Hahahahaha! Others would never know what its like to suffer but in life just remember no one is invisible when sickness comes calling but make sure you have support. AMEN! I was recently called, "Selfish." I don't know how seeing I am not the one who is constantly vacationing across the great USA. Some folks sure are SILLY aren't they? Then some of us like myself are just plain SMART.

BULLSEYE!

Today was once again a new start doing my best to get some additional walking in order to help prepare my body for the upcoming surgeries. I am also getting the legal side of things finalized in preparing for surgery which includes who can be present during surgery and who my surgeon and surgical staff will be talking to regarding post op and follow up therapy. Me and my friends are just hoping the surgical team down here won't back out and instead have the Cleveland Clinic team take over, YIKES! I can't even last past an hour in the car whether alone hours driving up north. NO WAY! If they bow out of the high risk surgery then this gal might as well start living like I am dying (Isn't that a song?) Hahahaha!! Maybe a bad joke to some but you can't always let serious situations in life take every bit of humor you have left inside of you.

Speaking of NOT a laughing matter...

Poor Oreo puppy hasn't been feeling like himself the past week so I decided its time to take him to see his Veternarian. He has a very hard time laying down and standing up. He won't climb steps anymore so you have to carry him and when he is taken on car rides you have to pick him up so he can get into the car. After his appointment last week at the groomers we all noticed quite a few small bumps located on the side of his stomach, back legs, spine and one on top of his head. His tremors are also getting a bit worse and so has his hearing that started three weeks ago. Oreo will be 14 years old this December but to me he will always be my big puppy. He now sleeps next to Mommy at night by my side while Littleblue keeps my feet warm. I think he likes the feeling of being comforted. I think we all do!

Instead of taking him to see his Veternarian earlier this afternoon we decided to go this evening since it is less crowded. Littleblue also went as moral support. I think Oreo however was more nervous than Littleblue but since she tagged along we also decided to get her weight on the puppy scale. Oreo weighs 39 pounds and Littleblue topped off at 50. WOW! She has become a BIG GIRL! I have been seeing the same Veternarian for years. Actually almost 14 years to be exact and he remembers me every time or maybe its because my sweet Pumpkin kitty decided to bite him during a surgical procedure. Hee,hee,hee,hee! Regardless he knows first hand I treat all my fur kids with the best care. They are my kids. Since getting up in age poor Oreo is starting to get not just one but many cysts. The original one which was found over two years ago and luckily remains the same size but the other ones are new. The Veternarian also said his arthritis has also gotten worse. This would explain why he is irritable and can't get comfortable. After he finished up Oreo's examination we were told he can no longer go up or down steps or jump onto things by himself. He will now need assistance. Since he is an older pup they can not do surgery to remove the cysts/tumors because it is far too risky. Because they are causing him pain they put him on two medications. Oreo's Veterinarian also said he needs to be limited on any activity however I did tell him the past few weeks he hasn't been doing much which is odd because he was always so active. Oreo will continue to be closely monitored for tremors/seizures and will not be allowed near other dogs which is sad since he has a new buddy next door but I know its for the best because he could snap at another fur kid. He said, "Littleblue understands he doesn't feel well. All dogs can sense when another dog is in pain which might be why lately she has been Mothering him." Thank goodness Oreo has his buddy Littleblue and we can still take them together for their daily car rides. For now I must continue keeping stress at a minimum which funny enough I have also been doing it for myself lately.

Once we got home they both got a last walk in for the evening and I got Oreo situated on my couchbed all tucked in with his blankie. He is very good with his medicine and the first round he took with no problem. At least now he won't be in so much pain and hopefully be a lot more comfortable.

Being a fur Mom is the best job in the world and the benefits of unconditional love are priceless!


Posted by GastroparesisAwarenessCampaignOrg. at 11:00 PM EDT
Updated: May 31, 2012 4:08 AM EDT
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May 29, 2012
Thank YOU! :)
Mood:  happy
Now Playing: Day 779-The Final Road To Survival

It felt absolutely GREAT to finally catch up on some solid sleep! I am also glad the holiday Dranotini weekend is over. Now its time to bounce back from treatment and allow my body a few days of freedom before the next one begins.

With it being a holiday weekend and no mail delivered yesterday the mailman made up for it today. Included in a huge stack of mail was another huge stack of papers for my upcoming surgeries. I am still dealing with the first round. This is almost like signing your life away and I am not even in the surgery room yet! Hahahaha! It might be a good thing I still have a little over a week to fill the rest of the paperwork out and mail it back to my new surgeons office. Thankfully there are no other doctor appointments scheduled for the remainder of this month so it looks like I will be catching a bit of a much needed break!

Its been a very, very pleasant day and I feel good vibes ahead for next month. Today was a turning point and one step in the right direction. I asked last week, "Where is the help?" Guess what? It finally called, emailed and showed up today. Maybe breaking down some of my privacy walls is helpful in order for others to understand what I need as far as help. I am not the type of person to ask for help but with a team of 2 its almost impossible to handle our full plate. This afternoon a huge portion of that plate got lifted. It started early this morning in the form of emails then continued through out the afternoon with phone calls and visits to the house. The amount of support given by not just friends within the city but strangers whom I have yet to meet but care enough about us and my overall health and happiness stepped forward one by one. We no longer have to be concerned about anything other than getting my body ready for the upcoming surgeries.

Thank YOU!

There will be a few weeks ahead of us filled with changes but all positive. Its slowing starting to feel like a huge weight and burden is being released off our shoulders. Not that all this amazing help and support from everyone wasn't enough I also got treated from a very talented local hair stylist to a evening spoiling my poor locks. Thank you so much Jennifer! You are amazing and it was so nice to share an evening of conversation filled with smiles, tears and laughter. My hair also thanks you too! Jennifer will now be handling the final transition of going from hair here gone tomorrow but as a step by step process this way she said I don't go into hairless shock, hahahaha! I can't forget Frances aka Sis for all the support you and Roland have given me through this rough bump in the road. Gym Moms and their families who continue to cheer me on from the side line thank you for offering your help. Pam and Mike-Eric said thank you for sending over the home made dinners after hours of working outdoors helping with the house repairs. Big Joe and family for offering their assistance how ever it may be needed. HCSD employees and others who have remained anonymous thank you, thank you and thank you! Its through trying times in life that you realize strength is indeed in numbers. I am very humbled and we can't thank you enough!    -XOXOXOXOXO


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EDT
Updated: May 30, 2012 3:15 AM EDT
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May 28, 2012
HAPPY MEMORIALDRANOTINI DAY!
Mood:  d'oh
Now Playing: Day 778-The Final Road To Survival

Well at least the generic Drano aka Hell-In-A-Jug is staying down far easier than the name brand ever did! I also don't have to worry about gagging on the extra salt chlorine taste with the generic brand. Not that it isn't there but it just doesn't taste as strong and it also seems to stay down without coming back up through my nose. UGGGG!

We had work come out just a WEE bit too early this morning. I assume they didn't realize I had treatment so was unaware 10am might be a bit too early to start breaking up concrete on the side of the house. I have come to realize you can't expect or assume that the world understands your medical journey. Especially if you don't speak up. This afternoon I finally decided to break down my own concrete wall and spoke to someone I have known for over eight years regarding my unique medical condition and situation. Let's just say I might share certain things or parts of my life on this blog but I still have details of my life I keep extremely private. I was always known in highschool as the gal you could tell a secret to and trust it would stay as such, "A secret." Now as an adult there are many times I want to be ME and not ME with Gastroparesis. What I have also became aware of is sometimes you can't be yourself minus a medical condition and you need to be both. It would be great to run from Gastroparesis but sadly each time I have tried it quickly found me. Hahahaha! Telling someone you have known for over eight years that your medical condition has changed and progressed since the first and last time they heard of anything can be a bit shocking for them. I saw it first hand today but you know what? It felt good to be upfront and honest regarding my unique situation as well explaining truthfully why me and my ex are no longer together. "When you get sick not everyone can handle or wants to be around it. I am not the first to have it happen nor the last but you live, learn and move on with life making sure to fill it with those who do care and want to help." I have come to realize maybe we both just really didn't know much about each other to start with because two very private people doesn't always make for a very public conversation. It was nice to talk as adults and work out our differences and I finally have a glimmer of hope once again that not all people are the same. Some do care and others don't. Its up for us as patients to decipher the difference between the two. Sometimes it won't happen right away but eventually over time even caterpillars show their true colors.

Me and my friend-Caregiver and the fur gang had a very nice, low key and relaxing Memorial Day. My friend has been serving in the Army for almost 15 years. He not only helps to protect America but also took on the roll to help me. He recently gave up a rank promotion so he could remain in the states to help me medically and continue providing assistance around the house. When people like him give up important things in life not because they were told but because he wanted to shows the utmost support and act of selflessness. If only the world had more people who cared without being asked then maybe it would be a better place. He will not be re-enlisting next year even though he is only five years away from retirement. Why you may ask? Because he said, "Who would take care of you?"

Good point.

Thank you Eric for not just serving our great country but giving a huge part of your life in order to help me with mine.

A team of 3 is now down to a team of 2 as my surgery day comes a bit closer. We are looking into nurse home care options and a few amazing GP friends of mine are also looking into their schedules to see if they might be able to help. My dear friend Kevin who lives here said he would be more than willing to step up to the plate and help too! For now I am going to become like the Bears and hibernate in order to get myself back on track. Stress up here must go back down there. I only have one me and I only go around once in this lifetime. I can't lose anymore precious time for hope in others but instead must now believe in myself.

"Wisdom is knowing who deserves a second chance. Courage is knowing the next time will be the last."    -Mark Amend


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: May 29, 2012 4:01 AM EDT
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May 27, 2012
The Calm Before The Storm...
Mood:  bright
Now Playing: Day 777-The Final Road To Survival

The heat is upon us again today! I can't wait for some cooler temperatures instead of it feeling like August outside. My head issues-Seizures/migraine/tremors are sure not enjoying the extreme temperatures either. At least the dark sheet that plays as a make shift curtain blocking the sun from the back of the house into the living room so far has been working! It now stays super dark so I am not awakened by sunlight or migraines/tremors. Now it takes around 15 minutes to set everything up blocking the windows from any sunlight before going to sleep. Its a routine but after awhile you get used to it.

They are now calling for rain starting tomorrow afternoon into late Tuesday. Now not only do we have a huge hole just sitting there on the side of the house but to make matters worse the foundation cracks have yet to be fixed. This could make for one HUGE basement FLOOD if either its not finished within the next 24 hours or if someone gets doesn't get plywood and plastic large enough to cover the entire area. To make matters worse the workers left huge mounds of dirt through out the yard. This of course was after there was hours spent the past week cleaning up weeds along the fence line which was a waste of time. My friend-Caregiver spent most of the day working outdoors just catching up on the last bit of landscaping and cutting the grass. He now has a Memorial Day filled with dirt removal from one end of the yard to another. WHOA! I "attempted" to clean the cars out later this afternoon which was going fairly well until the heat got the best of me. I am lucky for Gatorade and Pedialyte. Last thing I need is another trip to the hospital so it looks like the great outdoors will officially be off limits for this gal when the temperature exceeds over 83 degrees.

We have still been on the great house hunt with so far no luck in sight. We have lost track on how many properties we have called, emailed or drove by in hopes of finding a new home. People don't realize how hard it is finding a handicap accessible home. Either we find a place that "seems" ok until we see it or we run into homes that were far from being taken care of aka "DUMPS." So far within the past 24 hours I have had two calls regarding properties and sent out 15 emails. This is almost becoming a full time job that I should "NOT" be doing. With us just being a team of two add onto the equation Drano aka Hell-In-A-Jug day which was today. I had to postpone it yesterday due to stress however I couldn't push it off another day longer. Call this holiday weekend:

"MEMORIALDRANOTINI TIME!"

We hope to find a new home soon seeing with the rain moving in the stress with this house isn't too far behind. AMEN.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: May 28, 2012 1:35 AM EDT
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May 26, 2012
Do You "EVER" Really Know A Person?
Mood:  quizzical
Now Playing: Day 776-The Final Road To Survival

We both didn't much sleep last night. My allergies and head were kicking my butt. My friend-Caregiver's allergies were causing him sneezing, headache and severe congestion. We still have three more days to look forward to with temperatures rising to the mid 90's. This would had been a great day to catch up on some rest but of course that isn't possible seeing there was "attempted" house repairs going on that started from 10:30am-6pm. This would had also been my treatment day "however" once again that was interrupted. I think maybe I need to just "sneak" in my treatment days or have someone fly me out to "NO PEOPLE ISLAND" that way no one can interfere in my care.

What started off this very interesting day was seeing a 12 year old girl outside my back bedroom window doing hard manual labor which consisted of shoveling solid dirt to dig a 2X2x12 foot hole. OK. My question is once again what is wrong with people? What happened to society? Are we that in dire need to save a buck by having a 12 year old girl help her poor Dad out in 94 degree temperatures???? WOW! My last question to this sickening scene is where are the individuals who make child labor laws to protect the children? No. We did not hire this help. Someone else did.

Not that the day didn't start off crazy enough but guess what? THERE IS A CURE FOR AIDS! HEPATITIS A, B, C! HERPES SIMPLEX 1&2, RABIES, TUBERCULOUS, PARVO, MRSA, POLIO VIRUS TYPE1 AND ECOLI! THERE IS EVEN A REACTION TIME PER VIRUS IN WHICH STATES HOW FAST QUAT WILL KILL ON AN INDIVIDUAL BASIS!! EXAMPLE: RABIES-30 SECONDS!!! 

"I QUAT THAT!"

No seriously the chemical is called, "Quat" which is not only used to kill all the above but also kill mold and anything else living or breathing in its way at a very cheap price of $97.99 for a case of 12 bottles produced by 3M and banned in the state of California. Wow! you mean to tell me all along there WAS a cure for all the above? Well...if my Idiopathic Gastroparesis or toxic colon doesn't kill me there are individuals who are not licensed that believe you can spray this deadly chemical indoors while people are still residing in the residence. Me, my friend-Caregiver and my fur kids. Not that this isn't crazy enough, oh no it gets crazier by the hour since we were then told the city might possibly kick us out if we don't allow the chemical cleaner "Quat" to be sprayed in our home. Let's just say I don't need to say, "Over my dead body" because Quat could do that for us! YIKES!! After doing extensive research on my own I have not only found out Quat can kill and cure all the above but also has deadly reactions to its active ingredients. Two examples:

Ingestion: Gastrointestinal irritation, abdominal pain, nausea, diarrhea and vomiting.

*I guess instead of weekly treatments of Drano I can just inhale Quat! Or let me figure out if its a Gastroparesis flair up or a Quat flair up.

Target Organ Effects: Central Nervous System (CNS) Depression, headache, dizziness, drowsiness, incoordination, nausea, slowed reaction time, slurred speech, giddiness and unconsciousness.

*Forget going out and having a few drinks. Just stand in the house after being treated with Quat and you will have the same effect.

Yes, there are people out there and those who also work in the health department field who find it "OK" for any individual who is not licensed to treat a home with this toxic chemical while the home is still being occupied. SCARY isn't it?!! VERY!!! 

Now for the end of my adventurous day called, "Do you really know someone?" This goes for those whom you might have known for years but do you really know them? I have found out some very shocking information regarding those who been very misleading about themselves. I "thought" I knew them but clearly I do not. Once again I question the behavior of people around this city. My faith in mankind is slowly dwindling..."The problem isn't the problems. Its the people who are creating the problems." Needless to say this house circus needs to not have anymore side shows. The air needs to be finally cleared. No PUN intended!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: May 27, 2012 1:57 AM EDT
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May 25, 2012
FORGET Any Attempts with Gastroparesis.
Mood:  d'oh
Now Playing: Day 775-The Final Road To Survival

Today was the last day enjoying a trip to the local park. The heat is getting to be just way too much for this gal. My Gastroparesis also dislikes heat along with the connected seizures/migraines.

No. There is no cure for Gastroparesis so if you hear the hype word to the wise: Don't believe it.

Gastroparesis is also not just a condition isolated to the stomach. It is a progressive condition that starts with vagus nerve damage which results with stomach dysmotility. Gastroparesis does over time progress unless it is a result of a virus which "if" caught in time it can be reversed with antibiotics. I am not sure why any clinic or teaching hospital would have their staff contact any Gastroparesis organization telling others there is a cure and always was a cure but they just hide it for years from patients. That is "false" information and very misleading. Never, ever give out false hope to a Gastroparesis patient. As my specialist team of 18 which includes three clinical hospitals and two mayo facilities stated, "If there was any surgical or medication cure for Gastroparesis we would be the first to know." Now only did my doctors clarify the information I also wanted to clear the air with other patients. Just remember Gastroparesis is a condition that results from extensive and severe nerve damage. Until stem cell research makes huge advances will we then have a cure. This includes testing to isolate the damaged nerves and surgical options to take out and replace damaged nerves. If you want to donate $$$$ for a Gastroparesis cure make sure you do so towards a stem cell research facility. AMEN!

Back to the park...

Its always nice to clear my thoughts and mind with a nice walk at the park. I am a HUGE FAN of the wildlife and land that hasn't been destroyed by human hands. Nature at peace! Since this is Memorial Day weekend others also had the same idea getting out to enjoy the day before the heat and humidity arrives. 90's should be left out west-Nevada not out east. Mother Nature is sure confused isn't she? My friend John said, "Its not even that hot out here in California," as he continues his search for a new home.

Since my holiday weekend will consist of me, a few glasses, red Hawaiian punch and a large jug of liquid Dynamite (Drano) my friend suggested we go out and do something. I couldn't agree more and lately with surgery on my mind and the house mold repair problems still lingering I flippin need a break! CHEERS TO THAT!! What seemed like a great idea didn't last but a few hours. Same with driving. Once we walked outside and started driving my head games began. I took all my medication but even after arriving at our destination it didn't get any better. The air indoors was musky, stuffy and humid. I was bummed because we rarely get a chance anymore to go out and have some fun. My good days are few and far between. We had an early night but the fur kids didn't seem to mind. After a disappointing evening and trip it was nice to see happy tails greeting us when we got home. This is going to be a very, very long weekend with no relief so far between medical/house issues in sight.

Where is the help when you need it? This is getting to be way, way, way, way, way, way, way too much for two people to handle. One sick-Me. Another being pulled in a million directions-my friend/Caregiver.


Posted by GastroparesisAwarenessCampaignOrg. at 12:41 AM EDT
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May 24, 2012
It's Bluey's Day! :)
Mood:  happy
Now Playing: Day 774-The Final Road To Survival

Where has the time gone? It feels like just yesterday when I bought Littleblue's first little pink dress. Now the only part of her that fits into the dress is her front paw. Hahahaha! Maybe "HUGEBLUE" would had been a better name!

Since this has been Littleblue's week she has been treated to plenty of walks at the local park, new chewies and lots of new toys and treats. Oreo hasn't complained one bit since Littleblue has been nice enough to share. Even her birthday shirt from last year barely fits. She has grown up to be one beautiful "BIG GIRL!"

Since the heat is on its way starting tomorrow my friend-Caregiver finished up the landscaping and I assisted planting the traditional sunflower and wildflower seeds. We planted some in another flower bed earlier this week and they are already starting to grow. I love wildflowers because they attract so many hummingbirds and butterflies. Sunflowers are my favorite flower so they are a must to plant each year. I wish my Gastroparesis would allow for more outdoor time but the sunlight and heat continue to easily get the best of me. We are suppose to have work started on the house repairs this weekend but we will have to wait and see. Thank goodness for no rain in the forecast but I sure won't be enjoying this crazy heat!

My dear friend John finally made his first trip out west to look for a new home since getting his new job with the government. He will be living in Napa, California and I couldn't be happier for him! We have been friends for almost nine years and had a bet for the past eight to see who would be the first to move out west. He always wanted to live in California and me-Nevada. Looks like one down and one left-Me. Hee,hee,hee,hee... So not fair the amazing photos he shared with me today. SOOOO  NICE! John is hoping to finalize his move by the end of next month and if anyone deserves true happiness its him. CHEERS to John in finding his dream home!

This evening me and my friend started the process of filling out the huge stack of papers for my new colon surgeon and surgical staff. With so much information needed it might take us a week to finish. So far its only a team of 3 for after surgical care and help taking me to my follow up appointments and therapy treatments. Its going to be tough but where this is a will there is a way! If need be we might have to look into home nurse care but so far we are taking things one day at a time. I wish I could say the same thing about my poor hair. After straightening and trying to style it this evening the only thing I could say was, "EEK!" It hasn't grown for the past six months nor has it stopped coming out. Indeed next month I will have to say goodbye and farewell to my locks. Gastroparesis sure bites doesn't it!...

HAPPY 4TH BIRTHDAY MY LITTLEBLUE  XOXOXOXO


Posted by GastroparesisAwarenessCampaignOrg. at 11:29 PM EDT
Updated: May 25, 2012 3:29 AM EDT
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May 23, 2012
Happiness!
Mood:  chillin'
Now Playing: Day 773-The Final Road To Survival

Happiness to me is new emery boards and clothes that ACTUALLY fit! Its also finding a way to better darken my sleeping quarters so the spring/summer sunlight doesn't get the best of my head.

Cuddles kitty is doing a bit better each day. We still must keep a close eye on her in regards to her heart murmur. I can tell when it is bothering her because she hides in various parts of the house. Oreo has his moments with his seizures so we continue to do our best making his surroundings stress-free and comfortable. Since its been fairly nice outside and the temperatures haven't been too hot Oreo and Littleblue have been enjoying plenty of time running around in the backyard. Since Littleblue's summer coat is now fully grown in she gets tired easily. After ten to fifteen minutes outdoors she is ready to come back inside. Oreo has a day at the groomers scheduled for tomorrow so he can stay cool outdoors when the temperatures start to rise this weekend. At least the groomer can shave his hair super short but since Littleblue is a Husky hybrid her hair must stay long. If you cut her hair short it won't grow back so she only gets an occasional trim but plenty of baths.

Its been a tough time lately finding clothes that fit. I wear a size 2 in juniors and a small in tops. The average "healthy" woman is not a size 2 nor still has to shop in the juniors department but I have no choice. Same with my hair that is barely there... Soon I might have enough wigs to open a shop in my house, hahahaha!. Most department stores don't carry juniors size 2 in pants or jeans so I was very happy today to have FedEx deliver some clothes that my friend bought me as a late Mother's day gift. Guess what? They fit! Finally pants and jeans that are size 2 and new tops to boot! WOOHOA! Add onto that other little things such as new emery boards that now cut the time doing my nails in half. Thank goodness! Just a few things most people take for granted but to me they mean a lot.

Since I am getting horrible tremors and seizures with migraines lately my specialist suggested I make my sleeping quarters a bit darker. Not that having room darkening curtains with dark colored towels hung up at night aren't enough but now the sun is starting to beam into the back part of the house that lets in light through the dining room. Of course the dining room is right by the living room thus my sleeping quarters/couch bed. The spring and summer sunlight also got to me around this time last year and usually makes my seizures worse. Arm tremors drove me nuts today so if I need to make the front part of the house darker then welcome to my new bat cave. BOO! Talking about literally sleeping with the VAMPIRES...My friend-Caregiver said this evening, "Wow! this is going to make the room so dark that I might have a hard time now waking up." Hahahaha! The things you must do being sick. Crazy isn't it?

My new surgeon called this afternoon and it seems we now have to set my appointment back a week which might be a good thing. Its been so crazy this month that waiting until early June might be a blessing in disguise to start working on the next step for my upcoming surgeries. This evening we finally made our way back to the local park so I could get some exercise. Boy did it feel great to get the heck out of the house! Sure, I got some more strange looks from my mask but its nice sometimes to be incognito. Who is that masked/sunglass woman anyways? Hahahaha! My joints and muscles are still sore and recovering from the last round of seizures so walking is a win-win for this gal. Hopefully I can catch a longer break and get back into some sort of routine but with Gastroparesis you don't live for tomorrow. You live for today.

"Courage, is knowing that something scares the hell out of you, but you do it anyways because you know it will change your life forever."


Posted by GastroparesisAwarenessCampaignOrg. at 11:52 PM EDT
Updated: May 24, 2012 2:20 AM EDT
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May 22, 2012
Feeling A Bit Like A "JACKASS!"
Mood:  celebratory
Now Playing: Day 772-The Final Road To Survival

As a Idiopathic Gastroparesis patient I have found through the years that when there is bad news ten times as much good news soon follows! What has been pouring into my mailbox, email and cell phone has been an amazing amount of support from those who have decided to step forward helping to raise Gastroparesis Awareness. This blog that I started over two years ago has not only been a way for me to express myself but also a means to help others understand the many ups and downs living a life with Gastroparesis.

I am happy to say my blog continues to inspire many and even those whom I would least expect. I am honored to say some of my readers continue to step up to the GP plate as I am excited to announce: 

BAM MARGERA & THE CAST AND CREW OF THE HIT TV SHOW AND BLOCKBUSTER MOVIE SERIES "JACKASS" HAVE JOINED ME & THE GASTROPARESIS AWARENESS CAMPAIGN TEAM HELPING TO RAISE INTERNATIONAL GASTROPARESIS AWARENESS!

Bam, you made my day and so many other Gastroparesis patients that I wanted to personally say, "THANK YOU!" I want to also thank his loving family April, Phil, Don Vito and Jess Margera. An extended thank you goes out to Johnny Knoxville, Matt Hoffman, Loomis Fall, Manny Puig, Rake Yohn, Stephanie Hodge, Tyler Newton, Dave England, Steve-O, Brandon Dicamillo, Preston Lacy, Chris Pontius, Ehren McGhehey, Jason "Wee Man" Acuna and many blessings to the Dunn family.

I can't wait to start working with everyone later this summer bringing some of the Gastroparesis Awareness Campaign ideas from paper to life. CHEERS & KEEP ON! KEEPING ON!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: May 23, 2012 3:17 AM EDT
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May 21, 2012
Sometimes Life Doesn't Always Go As Planned.
Mood:  chillin'
Now Playing: Day 771-The Final Road To Survival

You can write it out, map it out and even plan it out but sometimes life doesn't always go as planned.

Take today for example!

This was "suppose" to be the day of new beginnings. That next chapter in my life was "suppose" to begin today. I was super excited and looking forward to taking the first steps in closing one door and opening another but guess what? Things didn't go as planned. The day didn't go as planned nor anything else today went as planned. Even all the post it notes in the world couldn't had predicted today's events.

I laid down on my couchbed rather early last night. 11pm to be exact due to my head was pounding and I had a rather strange aura/sensation. What I should had known was this "aura" was a migraine with seizure waiting to happen. I took two Tylenol and put one ice pack on my face and one on the back of my head. I then got my extra large heating pad out to place on my upper back however I was already a bit too late. When seizure aura comes on you only have so much time to take your seizure medication. I was unfortunate when my seizure problems started four years ago to get the double whammy-seizure with migraine. Its hard enough dealing with any seizure disorder but worse trying to decipher if its a migraine aura you are feeling or a seizure aura. Mine last night into the early morning hours was both.

Let's just say if I didn't have my dear friend-Caregiver living with me I would be SOL! Even with me laying on my couchbed and him sleeping two feet away on the recliner still doesn't prepare you for a seizure. My warning should had been the two hours worth of tremors that would come and go, come and go but didn't actually "go" anywhere. Instead where they went was into a horrible seizure. So to make a long story short around 4am my body went into a full seizure in which I accidentally knocked over my side table full of liquid drinks then since I had my seizure laying on my back I vomited what fluids were in my stomach. My friend luckily was right next to the table that knocked into him so he quickly woke up until the seizure and waves of tremors subsided. Unfortunately after you have a seizure your body locks up and muscles are tensed up so there is no walking. 

Needless to say instead of me attending the meeting/appointment that was scheduled two weeks ago my friend had to go in my place. I won't be opening that new chapter in my life just yet and heck with closing any doors. I couldn't even come close enough today to reach the handle. Hahahaha! Instead I must wait another week and pray my Gastroparesis and other connected problems like my head-seizures calm down over the next several days. Its a good thing I have an amazing team of specialists who are quick on their feet and called in refills of my seizure medications since they now need to increase the dosage. Spring and summer has always been the nightmare time of year for me because light is my seizure trigger along with allergies that my compromised immune system has to endure.

With any bad day there is always a silver lining! My doctor called later this afternoon with my lab work for my kidneys. Luckily I won't have to see another new specialist to add to the current list of 18 and instead I will just have to follow up additional testing with my Nephrologist. My friend also upon getting the mail brought in a package filled with amazing news in the fight for Gastroparesis Awareness. Indeed the Gastroparesis Awareness Campaign Team and GP family should be very proud!

Gastroparesis+Drano aka Hell In A Jug+Relistor+Migraines+Seizures=A Very Bad Day.


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: May 22, 2012 3:53 AM EDT
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