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The Road Before & After Surgery
August 14, 2012
LOVE THE FALL-LIKE WEATHER-Day 3!
Mood:  chillin'
Now Playing: Day 856-The Final Road To Survival

Guess what time it is?...LITTLEBLUE SHEDDING TIME! uggggggggggg.....

Didn't she just finish shedding her winter coat not too long ago? Honestly after finding a few clumps of hair around the house I just assumed it might be Oreo's before his day at the doggie salon. That was until I grabbed the brush and when it got to Littleblue's turn five strokes of the brush and it was full! YIKES!! Thank goodness we have a new defurminator rake that really helps with the constant shedding. Looks like this will continue for the next 4-5 weeks. The downside is her Hospice PAWS training will have to be placed on hold because they can't have her shedding inside the hospital. Sure looks like fall and winter is just around the corner but you won't catch this gal complaining one bit! I hope we have monster snow storms this year. I LOVE COLD WEATHER! I LOVE SNOW!!!!

Eric has been taking a few hours each day staining the front porch and ramp. It didn't seem like that big of a job but trust me it is! I have been helping but since I can't do that much stooping I can only assist with eye level pieces of wood that need to be stained. Thank goodness the weather has been cooperating but regardless even with additional help it will still be a 2 week project. No hurry though because fall is still a month away and its better that we take our time than to rush. The porch and ramp aren't going anywhere so all in good time... We are almost done with the first gallon of stain and looks like this project might call for two more by the time we are finished. Its relaxing since the weather has been so nice but all that cool air sure makes one tired. I was OUT early last night-or more like this morning but I needed that solid sleep. My body and brain has been BEAT!

I have received some interesting news via phone today. Eric actually got to listen to it first on the answering machine. A publisher who is also a fellow GP'er has been an active reader of the blog. I was asked not to mention names or the company for obvious reasons however I am very flattered by the offer. This blog has been a way to provide myself some therapeutic relief and I am glad to hear its also done the same for many others. At this point we have not gone over all the details just yet but I am willing to let Eric look further into the offer since it will be his baby so to speak. This isn't the first publishing company to come forward, there have been four so far over the past 18 months. Eric has been doing a lot of the blog writing recently along with five other fellow GP'ers since lately spending over an hour online has been spiking my tremors. My specialists also agree on cutting down online time to see if it helps calm things down. They have all been super supportive in assisting me not just with the blog but also the Gastroparesis Awareness Campaign website. With the third annual "United GP Walk" just a few months away things will be busy so its been a blessing to have all the extra help!

My new fellow GP friend Ruth who lives in the UK was lucky enough to attend the 2012 summer Olympics with her family. She sent me over some amazing photos this evening and WOW!! how neat would that be to see the Olympics! They were right there in London for all the action, events and festivities. She said they all had a great time and so did the kids. Thank you Ruth for sharing with the GP family and CHEERS! to many, many more happy GP-FREE lifetime events!

I officially have three good days left before starting my next Hell-In-A-Jug. Hopefully during the next treatment my flipped intestine will turn itself back over without complications and that horrific pain! So far...So good! If we are to get out and enjoy life there is no better time than NOW. AMEN!!


Posted by GastroparesisAwarenessCampaignOrg. at 11:53 PM EDT
Updated: August 15, 2012 1:47 AM EDT
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August 13, 2012
Sometimes You Just Gotta Go With The Flow...
Mood:  d'oh
Now Playing: Day 855-The Final Road To Survival

 Its going to be one very long week!

Thankfully when I got up around 7am I remembered to set my cell phone alarm but not like that mattered seeing some late night stress that "tries" to surround me in this city once again failed. Its like someone once told me, "After awhile the same behavior becomes so repetitive that you get used to it." If this was Vegas and a game of craps we would be multi-millionaires by now! Its been amazing the amount of support from everyone in order to help me move forward by making important changes in my life. Its hard when you still want to see the good in people. That continues to be my biggest problem. If I am to keep a blog about my life I would be lying to myself if I said it is filled with roses and candy cane lanes. Life doesn't work like that and if so we would all be living in a black & white world with no color to make things interesting. AMEN. Making a huge move out west has always been a dream of mine for when I am in my late 50's however I feel pushed by bad behavior of others in the name of keeping my sanity to make the move earlier so the constant stress doesn't literally kill me. Sad facts.

OH WELL...Live, learn, move forward and accept that sometimes no matter how many times you try, try, try to work things out sometimes things are unworkable.

This sounds like part of my day with two specialist appointments. What I miss most is working. My job was my outlet and a way for me to feel accomplished and successful. I miss working with others because I was always a huge people person. I am a very structured, organized problem solver so not having the body that my brain demands can be down right frustrating! SSD does allow for a back to work trial period. I "tried" but was denied. Since my seizures have become more frequent and more intense instead of finding a specialist to approve trying to working again instead I was told not to drive. Actually I was told, "You can't drive anymore. You are in a position to not just endanger yourself but others on the road." This is the second time in less than two weeks I was told by my specialists that I shouldn't be driving anymore. NOT GOOD. Not only are the numerous anti-seizure medications not working but the complex seizures with tremors are becoming as well hard to predict. Most of the time I get an aura-warning but lately they just pop up out of no where. My doctors have said it is just part of the progression of my unique medical condition and connected problems. I guess when they said, "There is no turning back" they were not joking, but what they failed to mention was the constant, never ending life changes that are included with the GP deal. Eric knows they mean well but I know they mean business! I reiterated the need for me to keep busy however my doctors feel my expectations of what my body can't do anymore is way too high. I need as they said to find hobbies that won't harm or cause me further physical damage to my fragile internal organs. "EASIER SAID THAN DONE."

Its frustrating and sadly in this GP world I am not alone. I am reminded of that every day when reading a multitude of emails and letters being sent to me from others. Indeed I am not alone. We as GP patients are in a league of our own. This too shall pass. Time heals all wounds. At least I hope so but in the meantime my therapists will be helping me to find GP-friendly activities in order to help me feel better about myself and more productive. Since I am such a hands on gal it will be a challenge but we will take it together one step at a time.

The great house hunt still continues but I must remember there are a few road blocks to still overcome on Eric's end. I pray for the best but know I could expect the worst. I am 110% set on moving full steam ahead regardless of any set backs because they are just that, "Set backs." Eventually those road blocks won't be there anymore and we can continue our path to a better life. For me, a more sain life that doesn't include negativity and bad memories in this city. CHEERS TO THAT!!

Looks like the remainder of this evening will be filled with catching up on so many shows that are on the DVR that I might not have time to think about new hobbies. Hahahaha! The fur gang don't mind though because after Oreo's day at the doggie salon he is ready to CHILL OUT! Heeheeheehee... 

 


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: August 14, 2012 2:42 AM EDT
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August 12, 2012
Houses And Houses And Houses OH MY!
Mood:  d'oh
Now Playing: Day 854-The Final Road To Survival

Good GRIEF! Is it me or have you ever gone house hunting through tons and tons of photos that after awhile they all start to look the same? Sure, houses out west honestly don't look anything like what we have around here since we don't live in the sand. Hee,hee,hee...

Less to me is more and that also holds true when it comes to cleaning. I have found a love of landscaping this year which is totally out of the norm for this gal but giving back to Mother Nature has been very self gratifying to say the least! Landscaping in sand and rocks...Well...It might prove to be an adventure but I do love cactus. BRING ON THE PRICKLY'S!! The nice thing about living out in the desert is zero humidity and very, very cool evenings. With Las Vegas being just a 10 minute hop, skip and jump away it will also be nice with my VAMPIREEEEEEE lifestyle because everything is open 24/7. BONUS! It will be an all around perfect fit. AMEN!

I would love a ranch style house. Lots of windows with big open floor plans have been nice to see for a change. With so many houses to look through I was mentally exhausted by 5pm so we both took a break. Eric has been working on staining the front porch and ramp this weekend. I expect it to take at least two weeks. Since the wood has yet to be stained it might take a double coat so thank goodness for having friends in the city offering to help. We were able to head up to our local park today so I can work this last treatment down my paralyzed insides. I have done my first of many steps learning to mentally tune out any stress which made a HUGE DIFFERENCE when it came to this treatment! Looks like I will have three good days for this upcoming week and just in time to celebrate all the positive life changes heading our way. WOOHOA!!

If this weather continues to stay fall-like I see nothing but a happy, happy upcoming week. CHEERS TO THAT and much cooler weather-no humidity too! Time to let the fur kids outside and start up my favorite DVR shows-Big Ang, Extreme Makeover and Four Weddings.

PS: Note to those who were concerned I was in the hospital or something happened to me. I don't check my email accounts until the late, late evening hours so I had no idea of any emails being sent nor was I aware of posts that might had some believing I was sick or in the hospital. Please know if you are ever concerned or in doubt I promise to send everyone a text message and by all means you can always check up on how I am doing and feeling via this blog. I wanted to apologize for the slight scare this evening regarding any social network posts from anyone or email from a shared GP account. With the upcoming 3rd annual "United GP Walk" there are many helpers accessing the GP Awareness yahoo email account so I am terribly sorry for any emails that were concerning or distressing.

Xoxoxoxoxoxo  -Kimberly


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: August 13, 2012 2:53 AM EDT
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August 11, 2012
WOOHOA!
Mood:  celebratory
Now Playing: Day 853-The Final Road To Survival

Its been a day of great news! FINALLY!!

My fellow GP friend and Realtor gave me some fantastic news this evening that we got pre-approved for a home loan and it looks like Henderson, Nevada might be coming around sooner than later. WOOHOA! Now we are just waiting on things with Eric's end and the final T's to be crossed. Patience is a must right now but I am getting super excited!! It will be a dream come true for this gal and finally I can be free of this nightmare city by starting on a new life-slate out west. This means I won't have to worry anymore about being constantly/falsely judged around here and I can be ME for once. AMEN! My friends in the city are so happy for us and I can't wait to celebrate soon! We are going to do our own celebrating next week since I am on my second Drano aftermath day which means with 3 good days coming around the corner one will be saved for ringing in a new lease on life. CHEERS TO THAT!!

After giving it some serious consideration we have also decided to take my friend Gabe up on his offer by staying at the beautiful cabin this fall down in Tennessee. We both agree its been long overdue to take a much needed break and at least we can bring Oreo & Littleblue. Three of his close friends have already volunteered to keep an eye on the kitty gang so at least I know they will be well taken care of and safe. If my body doesn't last at least its not that far of a drive back home. When I finally do fly it won't be down south but out west to our new home so I am saving that for a later date. I haven't been on a vacation in 7 years. Yes, crazy isn't it?! I must continue testing my bodies boundaries and by making the trip to Tennessee it will help me figure out my limits.

We have been getting so many kind cards, letters and gifts from my GP (Gastroparesis) family that I wanted to say this evening, "Thank you to everyone!" You are all super sweet and I am very blessed to have you in my life. Thank you GP Dad-Joe, GP Mom's Janet & Arline too for all your guidance and support. Thank you KimAngel and family for the beautiful frames and the fur kids gave a paws up on their treats. I finally got the last one filled this evening. We have one on the fireplace mantel and the other one hanging up in the dining room. They fit perfectly with the decor! Hopefully with the move we will be in a perfect location out west to finally meet many of the GP family. Thank you once again to everyone for lifting my spirits and brightening our days! Xoxoxoxoxo


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EDT
Updated: August 12, 2012 3:40 AM EDT
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August 10, 2012
Life Changes-Ahead.
Mood:  chillin'
Now Playing: Day 852-The Final Road To Survival

Yep, its that wonderful time again. DRANO TIME! UGGGG...

It's ok though because all day I made sure to wear my armor of steel just in case stress or drama came knocking at my door. Even so regardless I am learning the tools it takes to remove myself from the equation. There will be set backs. Isn't that what life is all about? I am proud of myself by taking set backs today with a grain of salt. I am doing my best to not allow people/things to continue getting to me. Why you may ask? Because its not worth it. I must continue to focus 100% attention now to #1-ME. I can't replace organs and the stress/drama just isn't worth losing more vital body parts. AMEN.

Eric called me out earlier this evening about walking into the alligator pit once again knowing I won't get out without being injured. HOWEVER this time around I proved him and myself wrong by handling the relentless stress that surrounds me in this city fairly well. CHEERS TO THAT! In between glasses of Drano I got out my paper and drew two separate columns then started weighing the pros and cons that are a must in order to make important life changes. After finishing I took a step back and thought to myself, "WOW!" On this side I have many negative things and this side I only have one positive thing. Not good! It all makes sense now when you step outside your own shoes and see what your stress/anxiety triggers have been for quite sometime. It didn't make me angry or upset but I felt a bit foolish because as told I have been enabling some very bad and inappropriate behavior. I must now make life changes in order to remove myself from the stress in the city until our big move out west. Thankfully no anxiety attacks today for this gal because when you know your triggers its important to do everything in your power to acknowledge them and then move on.

As far as treatment day...You can't win them all and yes, it will be a long night into the early morning hours but that is something I WILL tolerate and have for years. One can't say living a Gastroparesis life is easy by any means. It honestly took me many years to become my own GP-Pro but I can handle the good with the bad which has made me who I am today. A Fighter & SURVIVOR! If I can apply that same strength to other aspects of my life in order to finally have some peace then it will make a world of difference for #1-ME.

Note To Self: The world wasn't created in one day and even God understands neither can positive changes.

God grant me the serenity
to accept the things I cannot change;
courage to change the things I can;
and wisdom to know the difference.


Posted by GastroparesisAwarenessCampaignOrg. at 11:11 PM EDT
Updated: August 11, 2012 2:25 AM EDT
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August 9, 2012
Coming Full Circle.
Mood:  chatty
Now Playing: Day 851-The Final Road To Survival

Talking about coming full circle!!

 

We both were out like a light last night and slept HARD! Make that ALL of us because even Littleblue didn't want to get up once the cell phone alarm went off. Today is the last of my doctors appointments. WOOHOA! This week has been so crazy and UFO that I can't figure out what day we are on. It seems like we just ended the weekend and tomorrow is already Friday.

Since I "thought" this was a new specialist I was seeing today we made sure to download directions to his office. After a ten minute drive I started to realize this wasn't a new doctor by any means, in fact this is the same specialist I saw in the beginning of my Idiopathic Gastroparesis diagnosis. In fact once we arrived and I walked inside the building it WAS the EXACT same DOCTOR! WOWWWW!! Talking about life making a full circle. Hahahaha! Once I finished filling out all the new patient forms (although I was far from new-maybe new since it has been 7 years since my last visit) they called me back to the room. It was the same doctor and the first words spoken were, "I made a full circle. I seen you almost 7 years to this date when you figured out the great medical mystery. Internally. If it wasn't for you flagging my doctors and surgeon they would had never known my stomach stopped working. After a few nuclear studies I was quickly diagnosed with Idiopathic Gastroparesis." His first reply was, "Wow, that is amazing! Well good to see you again!"

It was a great and extremely informative first or more like second visit however it will be my last because he figured out this other great medical mystery. It didn't take him but under 2 hours to confirm that I don't have any mental problems but I am suffering from PTSD and anxiety attacks due to relentless stress caused by some around this city. Things had finally come to a boiling point and the body as well brain can only take so much. I honestly have been doing the right and healthy thing which is to separate myself from the drama and stress. In my unique medical situation it can be destructive and dangerous. Its also causing me to now constantly change my weekly treatments. Thank goodness I am smart enough not to do treatment when stress is knocking at my door, phone or email. Since we clearly know my triggers, the next step is to get my anxiety and stress under control. This might take awhile because you can't unravel years over night. Patience is a must and together we will come up with a game plan in order to not further jeopardize or risk my fragile health.

What I did learn today is that you can't tell people how to think and everyone is entitled to their own opinions. I have spent far too much time trying to make others understand my medical condition when in all reality who cares what they do or don't believe. The arm length of medical records speak for themselves and its not up to me anymore to force others to see what they don't want to see. Instead I need to focus for once on only one person who matters most. Me. It was nice to hear my brain has conquered and overcome some hellish stress to say the least and Eric was wrong in thinking I wasn't continuing to be in battle mode. Me silencing myself if only for a few days is a way to recharge my brain and allow my body a much needed break from all the constant stress. People handle life battles differently. What works for one person might not always work for another. If anything, I have learned I am far, far stronger than I give myself credit for! AMEN.

We both got home feeling a huge sigh of relief. Its nice to talk to someone who is on neutral ground and a professional who deals first hand with resolving stress, anxiety and conflict when it comes to life. Some things that will have to happen will be hard at first. I must understand that things have to change. I have to now put myself and my health first. I was told to consider it like a physical disability that eventually will get easier over time. I sure hope they are right!

“Your thoughts about your circumstances have you down. On the other hand, you can be in one of the biggest battles of your life, and still be filled with joy and peace and victory - if you simply learn how to choose the right thought. It’s time to think about what you’re thinking about.”
-Joel Osteen


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: August 10, 2012 4:40 AM EDT
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August 8, 2012
What Sleep?!
Mood:  d'oh
Now Playing: Day 850-The Final Road To Survival

I am rotating with the season and so is my sleep. "We" didn't get to sleep until 6am. Me-because I was having a bad GP moment. Eric-because his body is so used to working third shift that he wasn't tired.

My heating pad and heat wraps have sure been put to the test lately and I hope they continue so I don't have to go back to feeling like a Zombie on pain medication. Not that getting to sleep at 6am isn't bad enough but at 9:00am I woke up in a huge sweat. I got up and went to the bathroom only to see the same darn abdominal rash I have been experiencing over the past few years. Since my Oncologist/Hematologist wanted me to take a few pictures and call his office next time I got the same rash I did both. After we got off the phone I was advised to take my blood pressure, temperature, blood sugar and peak flow-measuring my lung capacity. Since the rash was still present as well the sweats and chills he had me see my other doctor who is closer to my house. So....FINALLY today they were able to figure out these strange rashes which are tied to my compromised immune system. Since most of your immunity is based in your intestines and mine no longer work you can experience flair-ups or as he said, "Disturbances-Red flags" that your body is in battle mode and what is happening on your insides can actually show on the outside. Rash. Another dear fellow GP friend is also experiencing the same problem but she gets hers after consuming Magnesium-Citrate/clean outs. I am getting them during and after in no specific order but at least now I have an answer to the strange pop up rashes. So far they seem isolated to only the abdominal area but I was told if they spread I would need to head to the hospital. Hey! I have had far, far, far enough ER visits in my lifetime so hopefully it will never get to that point. For now I was told once again to not do treatment until tomorrow. I was also advised to continue using ice packs through out the day and was given an anti-inflammatory drug. Much like the other rashes it will resolve once my internal battle calms down.

Since we didn't get much sleep today once we did lay back down and my cell phone alarm went off it was already 4:25pm. GEES! Talking about a wasted day! It could had been a short non-productive day but instead we both kept busy so my mind could be free. Eric finished staining the side patio and started working on the front porch. I opted for some projects inside the house and by the time we were both finished it was already 8:30pm. Not bad for a short day. Hahahaha! At least Mr. Drano aka Hell-In-A-Jug got another break but it can't last long enough. Tomorrow is a new day, a new doctors appointment and another round of treatment. Well at least hopefully one out of two won't be bad!


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: August 9, 2012 3:51 AM EDT
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August 7, 2012
Rocky Mountain High.......
Mood:  lyrical
Now Playing: Day 849-The Final Road To Survival

My friend and his Son are having a GREAT time out west! Even having a few Rocky mountain high moments. LITERALLY! They will be spending the next few days roughing it with their camping gear in the mountains surrounded by Mother Nature. PRICELESS. The pictures he sends speak for themselves and its nice to be a part of their adventures. Yesterday they attended a Rockies game with his cousin. I am so glad they are having a great time!

My other friend John who now lives out west is in his first month detoxifying his body. No more cigarettes or alcohol but plenty of natural foods and lots of exercise. He's also enjoying new yoga classes which allow for far better sleep than he has in years. GOOD FOR JOHN! Robbie kitty even looks super content enjoying his new life out west.

Today was my first visit after the insurance company brought some great news this week by covering up to 12 physical therapy sessions and another visit to the Nutritionist. My intestines still haven't eased up yet but I am doing better adjusting to the pressure pain. I also haven't felt the need to use pain medication. I went back to the same group-Nutritionists I saw 8 years ago at our local hospital. The best thing they could offer me with my unique medical situation was the same game plan I already started. 95% liquids and must be watered down. They also want me to start using more whey protein drinks which are easier to break down in the body. Sugar is going to be a toughie seeing it takes a lot to keep my levels up so that will remain touch and go. They gave me lots of sample powder packets that you just add into water full of vitamins, nutrients and digestible fiber. Since I am a rare breed, they don't see many patients like myself very often that don't already have a tube or IV line for feedings. They do understand the complications and high risks with line infections in which my weakened immune system could not handle so I have to continue consuming the best I can with what my body can tolerate.

It was a long and tiring day so my brain didn't have time to think about any anxiety. Thank goodness for a break!! Keeping my mind busy is important and hopefully the physical therapists might be able to provide me with some ideas/suggests on new hobbies without jeopardizing my health. I have my last doctors appointment Thursday so we are hoping to get additional insight and a better perspective on how to cope with any unnecessary stress.

This evening I finally felt comfortable enough to go back to the local park. Once we pulled up and started making our way to the side walk we were greeted by two feather friends. Frank & Mike. My how fast they have grown! It was so nice to see them along with the other geese. I still feel horrible that they could not rescue and rehabilitate Miss Goose but I know she is no longer in pain. Eric says, "That one single goose the other day was her finally flying free because you let her live again." I hope she is watching over the baby rabbits too in a safer place called, "Heaven."


Posted by GastroparesisAwarenessCampaignOrg. at 11:23 PM EDT
Updated: August 9, 2012 3:05 AM EDT
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August 6, 2012
I Need A Break.
Mood:  chillin'
Now Playing: Day 848-The Final Road To Survival

If only us GP'ers could get this excited over food!

Hahahaha! Well...at least the fur gang and Bear kitty who "thinks" he is part dog agrees that this new food is DELICIOUS! This is also why at night we now have to put the food bowl up. Put a bag of food in front of someone who has Gastroparesis and we might as well start the barfing a bit early!

Its already starting to be one strange week and even after having a good first of two doctors appointments today stress was waiting for me once again when I got home. I give up and must admit I have had quite enough of this nonsense! Its time that maybe I take a break and get away for awhile. Since I can't get out west just yet for the big move my fellow GP friend Gabe who was in town this past weekend instead offered us his rental cabin in Tennessee.

HOW NICE WAS THAT?!!

It would only be for 4 weeks but heck! 4 weeks would give this gal enough of a break to revamp/recharge my tired body and brain. My doctors also agree that I really need to clear my head and maybe that will help the horrible anxiety caused by this cities relentless stress. For now they don't think its a good idea flying but when it comes to driving they are leaving that decision up to me. We would have to stop every hour and walk around so my spine doesn't lock up but I really should give this amazing offer from my dear friend some serious consideration! Eric has plenty of vacation time and we could bring the fur kids. Two of his friends in the city said they would come over and watch the kitty gang. We could even leave early if need be because I highly doubt I could stay the entire four weeks. Maybe one if I am lucky! Gabe left the offer on the table and said, "Its all yours if you want to get away because I think you both really need a break."

AMEN! AMEN! AMEN!

I have my last doctors appointment later this week so that should give me a better idea if its a NO or GO! I am hoping for the latter. Since fall and mid September is just around the corner it might be the best time to break away from the city. It will also "HOPEFULLY" be much cooler by then so my GP won't be so volatile unlike the constant heat and humidity over the past three months. I also have GP family and friends who live within an hour drive from the cabin. It would be very nice to finally visit with them.

THANK YOU SOOOOOOOO MUCH GABE for offering us a beautiful cabin get away and like always, time will tell (and my insides) if we can take that much needed break. Xoxoxoxo


Posted by GastroparesisAwarenessCampaignOrg. at 11:59 PM EDT
Updated: August 7, 2012 3:57 AM EDT
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August 5, 2012
Feeling B L A H...
Mood:  down
Now Playing: Day 847-The Final Road To Survival

This is going to be a short blog for today... Just feeling drained out, stressed out, anxiety overload and B L A H... It might be a good thing I have two appointments this week and one is a new doctor who will help to get my head back on straight and better control the horrible anxiety attacks that seem to be taking over my life. They believe there was a significant trigger that started the attacks almost two weeks ago and sadly they haven't let up. The new medication for my seizures is suppose to calm down brain activity which helps control seizures but of course, "No Dice!"

We tried taking a short walk at the park near our house but I was feeling so dizzy that it didn't last that long. I haven't felt safe enough to start treatment either so it seems to be one thing after another and I am just hoping both doctors can get my brain and my body back on track sooner than later! CHEERS TO THAT!! Eric keeps thinking I am starting to lose my fight mode but I keep telling him its not that, I just have way too many battles on my hands right now and its gotten to be farrrrrrrrrr too overwhelming. Sure, drinking Drano isn't fun and I won't lie by saying, "I have also had enough of that nasty stuff too!" Instead of the two doctors appointments this coming week maybe I just need my dear friends from Texas to send me ONE HUGE BOOT! then give this gal a good swift kick! Hahahahaha!

Here's to a UFO upcoming week-full of strange things...


Posted by GastroparesisAwarenessCampaignOrg. at 11:45 PM EDT
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