Sunday, July 31, 2011

One week AFTER LAST CHEMO....

It's a Sunday morning and it's actually raining outside in Southern California.  I'm rather happy about this fact considering we always need water down here. Plus I'm not a native to So. Cal.  I'm a NORCAL girl and I am used to the greenery of life.  So it's nice to be listening to the raindrops in the background.  It's started the day with the right tone.

Since I last wrote, I am finally happy to report I am getting my energy back and am beginning to be able to appreciate life better.  I'm not lying in bed any longer; I'm doing very basic chores around the house and have been out a couple times on outings for a couple hours at a time.

The other day my feet and legs and overall body were so swollen and feeling like it was "plugged up" in the sense of flexibility and lack of movement.  My daughter had told me about a Reflexology business she had heard about from a friend. So I said, "Let's do it.  Let's try this place out and see if it can give me some relief from this swelling and overall uncomfortable feeling."    Off we went.  I have never been in this type of business before so I didn't really know what to expect.  We were met by a nice man and he escorted us into what looked to me like a mini movie room that was dimly lit with a TV playing very quietly -- there were 2 very comfortable looking chairs with ottomans situated side-by-side. Ash and I sat in each chair and got ourselves comfortable.  It was a very clean environment.  Chairs were very comfortable as well.  We removed our sandals and waited for the techs to return.  The technicians came in with some herbal bath and placed our feet in them to soak for a few minutes.  Very nice.  They returned and then began a type of massage on our feet and up around our knees.  I wish I could state that it was really relaxing because that isn't the truth of the matter.  For me it was rather painful where he was applying pressure to my feet.  My feet felt really "congested" if that makes sense. They were so very tight. It felt like there were little pockets of built up tension that was being popped.  OMG, it go painful at one point that I had to have him stop for a couple seconds so I could catch my breath, but I knew in the end this would be ok.  So off he continued and eventually (30 minutes on one foot) he was finished with what I was trying not to call torture.  I was sitting there thinking to myself, "And I paid to have this done to me!"  Thereafter, my other foot had to undergo the same thing. My right foot didn't seem to be as "congested."  But it still had it's moments.  Before I knew it, it was over.  But I felt complete and utter RELIEF!  I've never had such relaxed feet, ankles and legs.  I wasn't jelly-like, but it was simply wonderful.  I slept so well that night as well. The biggest change was the next morning when I had reduced in inflammation size all over my body.  My arms had reduced, my belly, my neck and face -- all reduced in the swelling.  I had such relief all over.  Part of the chemo treatment is this awful swelling as you probably have seen by my pics I have posted.  And this last chemo treatment increased my swelling once again even more so.  But the relief in the swelling, I believe, with the reflexology helped. Of course, my water intake continues to be ongoing because I want to be well-hydrated and it aids with flushing out toxins.  So this is a method of relief I will continue with for the time being. 

I had a chance to do a little shopping at the local mall yesterday.  It was so fun to be among the living and doing something so very normal with others.  I hung in there for four hours!  I was very tired later, but it was worth ever second being able to get a few things done and have a sense of norm. 

My next goal for this next week and continuing forward is to get back to the gym slowly.  I need to get my aerobics restarted and to regain good heart health strength and blood flow.  All of this will help with the detoxification process of the chemo plus overall endorphins to be released to help me feel like my old self again.  I continue to eat very clean with lots of veggies and good proteins.  There are some teas I could be drinking more of to clean out my liver, kidneys and intestines, but that will come in due time. I have to pace myself a bit and not to do too much too soon.  I have learned a lot about pacing myself through this whole ordeal and I realize that learning process will never end because I still have so many challenges ahead.

I'm going to sit back today and do little projects I have been putting off due to my lack of energy and overall attention span. It's still raining out and I'm enjoying every minute of it. So cleansing! I guess symbolic for me just a bit --

I'm happy to report today my Cup's Half Full and fighting the fight in my way!  i continue to move in a forward motion of healing!

Ciao! Ciao!
PS.  My youngest daughter will be arriving in late August and I cannot wait!

Monday, July 25, 2011

Let's Drag this out....

I wish I could report that all is great in paradise, but the fact of the matter is I'm struggling right now getting through this last chemo treatment.  I did so well the first 2 days.  I must have been riding pretty high on the adrenaline from the fact this was my last treatment and the expectations of freedom from Chemo pulsating through my veins. 

My reality is I'm weak again, foggy beyond words and overall achy, sick feeling that I cannot describe to the degree that one would like, but suffice it to say, it really SUCKS!  I know, I know, I will get through this.... But LIVING through this is nothing I would wish on anyone. 

Thank goodness I can zone out and exist without feeling at times. Hard to imagine, but I can do that. 
I also do a lot of meditating which is a life saver.  There is nothing "heady" about this phase of chemo recooperation. You exist.  I'm so done with this right now. I'm sooooo done.  That's part of the mental aspect of this process. 

From what my family tells me, they have stated that this is the best I've been since this whole chemo treatment has started. The difference is that I don't want this any longer to be a part of my existence --- the treatments.  So with that, it causes me to be less than tolerant of pretty much everything.

I have noticed that my eyes are more teared than ever. I can hardly see -- one of the side effects of the chemo.  My hands are hotter than hot.  Not just warm -- I mean HOT to touch.  I'm very swollen all around my body and especially in my face. I'm fire-engine red around my face and neck area. My feet are swollen and HOT to touch.  My head is cool and hot from moment to moment; my throat from time to time closes up -- not sure why that's occurring but it is.  So these are just to name a few of the side effects I'm experiencing at the moment. 

The good news is I don't have to have another chemo treatment. I know I sound like a broken record stating that over and over again, but let me tell you -- until one has gone through something like this process, one has NO IDEA what one could have survived.  I'm so grateful for surviving this. I'm so eternally grateful.

Today, it's humid in my city so I will be laying in my bed resting and preserving my energy drinking my fluids and nibbling on what I need to get my nourishment.  I will meditate and think positive thoughts of Cancer being erradicated out of my body.  I will do what I need to in order to get stronger and stronger so I can get on with my life. Oh, how I yearn for my life back.  It will be here soon and I will be very welcoming as to how it all unfolds for me.  I know this whole ordeal isn't something in vane.  It can't possibly be in vane.  I feel this in my soul.   There is just so much love surrounding me. I feel it pretty much at all times. 

So that's what I have for now. Tomorrow will be another adventure of a day in the life of me -- how extraordinary, right?  LOL!!!  Not really, but it sure helps to write this down.  It's very cathartic for me.

My Cup's Half Full, just want this to move on.............

Ciao, Ciao

Saturday, July 23, 2011

JULY 21, 2011 LAST DAY OF CHEMO --SUCCESS!

I DID IT! I DID IT! I DID IT!

I SURVIVED MY LAST CHEMO!!!

Then I did the side kick into the air in my mind as I walked out of the office from my oncologist!

Perhaps, I should back it up a bit so I can describe to you what I experienced this last day.

Of course it was the regular blood draw to begin with so see what my blood levels were before we began. 
I asked for my results of my genetic test to find out if I have a tendency to clot or not because this would explain some of the reason why I have had the vein issues regarding the port placement, etc. 
Turns out I have one of the genes afterall. So they will have to be a little extra careful with me when I have my surgery in August for my bi-lateral mastectomy.

For some strange reason I'm not concerned. I now know and we can proceed with caution and all the doctors will be made aware of this fact.  And, being the person that I am, i will remind them as well probably a few times just to be on the safe side. 

So the treatments began with no fuss. My nurse was able to administer my chemo without any issues in my veins.  Yeah!  Off I went. There was another woman having chemo for her type of cancer and we struck up a nice conversation. She is a retired gynocologist originally from Manhattan (New York). Very nice lady and one full of knowledge about women's issues. So she enlightened me on a few questions I had. But it was also great to share about what we have experienced. But at the same time we were able to switch the conversation around to our daily lives and relationships and just normal stuff.  That was so very nice to converse about: daily life and NOT cancer.  We laughed and giggled and before we both knew it, our treatments were over.  No fuss -- no big Tah-Dah!  Great ending. Great, Great ending to this ordeal.

So after being taken off my drip, I had my regular exam by my oncologist. I was such a happy camper about this exam. I whipped off my top and wanted him to begin to try to find my tumor in my armpit and breast.

He went really deep up into my armpit and thoroughly examined my armpit.  HE COULD NOT FIND IT!  COULD NOT FIND IT!  COULD NOT FIND IT!!!!! So take that, Mr. Cancer!  He had me lay down to examine my breast and could see how much my breast has reduced in size. It's almost the same size as my right breast.  My left breast has never been the same size as my right.  But it's considerably smaller!  Yeah!
It's also very soft and the tumors have reduced.  They are hidden within the dense tissue of my mass to it's difficult to get an accurate reading on that area.  I am rescheduled for another Breast MRI in the next couple weeks.  This will give the exact size of tumors and tell them how contained the cancer is. 

My doc was very happy to say the least.  And he is one to be very, very conservative because that's his position to be objective.  He is so very thorough and I appreciate all his expertise.  Always educating me and keeping me apprised and answers ALL my questions completely and with great care. He's been pretty concerned about my case and I know he doesn't take anything for granted.  That gives me such relief.

We went out for a celebratory lunch afterwards. I went to Mexican which is the 2nd time I've had during all of chemo.  It was dee-lish. I kept it bland. And no issues with digestion whatsoever!  EEEHHHAAA!
Pleasures in life..........Food!  Love food.

WE got home by 4pm.  My energy was still good. So amazing.  Evening came and still doing well. Not that sloggy feeling.  Went to bed without incident and slept just fine.

So the next day, Friday, July 22:

I woke up just fine. No chemo brain sloggy mess.  No mashed potato brain. My energy was pretty darned good.  I was able get my breakfast done -- no assistance. Fed the dogs!  Up and around which never happens post chemo.  What is going on?  They told me at the doc's office that who know's I may cruise through this last one with  no problem cuz of my attitude and the fact I know it's my last one. I think they may be right.  This is simply a miracle in the making.  But I have been cautiously optimistic as well.  Being mindful.
But since I had this clarity going on, I told my hubby I wanted to go to a few stores to do some errands I was putting off. I would take one store at a time to keep it in check. First store went just fine. I was able to ultimately go to the 3 stores I needed to complete my transactions without incidents. Wow!  This is blowing my mind!  But I knew not to push it any further. So I was taken home and put on the couch.  I stayed there on and off for about 3 hours.  Had my lunch and snack.  I was NOT exhausted.  No post-store mashed potatoe brain!  No major unexpected anything.  Kept on drinking my fluids, etc...  All is good. 
I took one little short nap about 15 minutes is all.  This is not the typical post chemo.  THANK YOU GOD!

I had a small pasta dinner with our home growned tomatoes -- dee-lish.  Just what the doc ordered.

I had a great catch up session on Skype with my girly friends which was a major league highlight of this whole chemo treatment.  What a way to end the chemo treatment -- celebrating with my girlfriends toasting on the other end.  I toasted with my big glass of water and they had their cocktails!  Loved it.  We laughed, giggled and shared.  I can't imagine going throuh this ordeal without the love of my girls behind me.  They are amazingingly strong for me and a constant reminder how important it is to have those relationships especially in times like these.  They really boosted me big time last night. What great women.  I love you, my angels!

So all in all, what a great day and what a nice reprieve.  I hope this healing continues on this path.  If it does, I can justify going to visit my mother up in Humboldt for a short visit.  It's so important for me to see my mom before my surgery.  It's a burn inside of me I must achieve.  But as long as I'm feeling strong I will go. If there is a hint that it's not going accordingly, then I won't take the chance so close to my surgery.  But it's looking pretty well at this point. Keep my fingers and toes crossed that my road continues to be well-traveled.

Needless to say, My Cup is especially Full!  Blessings, blessings, blessings!  AMAZING!!

CIAO! CIAO!


Wednesday, July 20, 2011

DAY BEFORE LAST CHEMOTHERAPY

TODAY is the day BEFORE my last chemo.  I hope this will be forever meaning I never ever have to go through this process again in my life.  I'm banking on it.  I'm only thinking positive thoughts. I have to -- I must!  This is where I am becoming the warrior so many have said I already was.  Until now, I haven't felt this determined -- this committed -- this intense in beating this thing.  I know I have been doing all I can to fight back in my way.  I've been LOVING this cancer to it's death. I've been pushing it diligently out of my body the best way I have been learning -- through prayer, meditation, constant positive affirmations, through sense of humor and only being around loving people.

One of the greatest comforts I've had has been  my listening outside of my home to the voices of all the children in my neighborhood playing, laughing, yelling at one another, their constant great YOUNG energy.  I found myself giggling, laughing out loud at times because they give me hope.  They fuel me with life's great energy.  They are fresh and free and enjoying their childhood -- whatever it may be -- they are living. And that's exactly what I want to continue to do myself.  I want my life back and to continue to grow more and more as a person (hopefully, a good person -- bettering myself).

Through this process, I have found out who truly loves me.  I have found out who are my TRUEST of friends.  I thank you so much.  Yes, I have been disappointed by only a couple, but they have their reasons, I'm sure.  But the bottom line is this:  those who have shown themeselves to me are so much more important and are worth getting the best of the best in return.  It's been said you find out who your true friends are in times of trouble -- I never knew I was so loved.  It's humbling and overwhelming.  I have people praying for me all over the world.  Literally ALL over the world.  It's humbling.  Once again, I don't know how to thank them all.  I guess I do it through my prayers as well. 

Tomorrow at 10:30am - 1pm I will be at my oncologist's office being administered my chemo for the last time! There won't be a big fanfare but I will be meditating and praying and doing my best to allow this substance for the last time to be administered into my body.  As it flows through me, I will be visualizing my little space invader ships doing their best to kill off the last of those nasty little cancer cells!  They are killing them dead.  They must be considering what I have been experiencing in my body.  Even though I've had serious side effects, it will be worth it in the longrun.  Once again, I do my daily body checks.  I cannot for the life of me feel or find the cancer tumor under my left arm.  I cannot find it.  I've had Jim try to find it.  He cannot find it either!  WHHOOAAA!!!! Also, the same in my left breast.  I cannot feel the mass the way it was.  It has shrunk overall.  My breast is back down to almost the same size as my right breast. There is a slight difference in size, but OMG, it's so reduced!  My left breast is very pliable and soft where it hasn't been forever.  Tears do come to my eyes because I know in my heart of hearts I am beating this thing.  Yes, I continue to be cautiously optimistic, but I have to allow myself to get excited at the prospect that this cancer is contained.  I just "feel" it.  I know it to be true.

I cannot fathom that any other cancer is surviving elsewhere in my body.  I cannot accept that it will survive due to the fact chemo has been so toxic everywhere else.  I pray for CLEAR PATHOLOGY. It will be. It will be.  It will be.......................

Tomorrow I will be driven down to Scripp's and will walk in with my dignity in tow -- I will also have my prayer shawls, special spiritual trinkets that make me feel comforted and will go through what I need to in order to continue on my journey forward.  I am ready for my surgery on August 29.  But first things first. I must finish this...........I will with my head held higher than normal and my step lighter than light!

Oh, yeah, bring it on!  Can't keep a good girl down! (what song? or is that even the correct words? Sounds good...LOL!) 

Oh, yes, I have to acknowledge I just uploaded few more pics because I finally figured it out as to HOW TO UPLOAD pictures onto my blog.  I'm so proud of myself.  Anyway, this is the good, back and the ugly truth as to how I have changed.  It is what it is...My face is full from the Chemo. I've been told I will deflate.  I have a few eyelashes & eyebrow hairs left but should be interesting to see if I lose the rest. You should see me trace around my eye's with make-up.  Hilarious, but I still do it.  LOL. Gotta laugh!

I love you like no other, Jim, for telling me today on our lunch date how  much more you love my chocolate brown eyes even though I'm without lashes! When I saw your tears welling up, you melted me. You still give me that feeling in my tummy when I see you drive up or walk in the door. We are a couple of sappy people who refuse to give up on each other; you are the love of my life: THROUGH GOOD TIMES & BAD; IN SICKNESS & IN HEALTH!! I love you FOREVER! The world now knows this.......SWAK!

Yes, my Cup is Half FULL.  So long CHEMO!

Ciao! Ciao!

Friday, July 15, 2011

One Week before LAST CHEMO

For the last 5 days I've been feeling very strong.  I have taken myself off sleeping pills to aid me at night.  I'm sleeping much deeper and am able to dream once again, which is a good thing for me.  I wake up well-rested and have started walking my dog, Woody, again out into a field beyond my neighborhood.  I don't as far as I have prior to chemo, but at least I am walking more vigorously than I have been.  It feels good to sweat because of good exertion.

My digestion continues to be a normal level which is a great thing for me overall.  I have had no issues with heatburn which was pretty bad at the beginning of the 4th chemo, but have been able to watch the types of foods and liquids I've been ingesting.  Surprisingly enough, I took a chance last night and went for Mexican food at a little restaurant in my daughter's town.  I had a chili relleno and little rice and beans.  I'm sure some are horrified to think I would try such a plate -- but I did.  I was craving a good chili relleno and this particular restaurant:  La Unica in Lake Elsinore has amazing food.  All authentic and  freshly made.
DEE-LISH!!! It is so wonderful to be able to TASTE the flavors.  Sometimes during chemo patients will lose a sense of taste or things become very metallic tasting.  My tastebuds have never gone to the metallic side, but have been very dulled and  flavors are distorted.  These days, I'm seemingly back to a sense of norm which is so exciting for me.  That was my great dining experience for the night.  But I won't do this often, but it felt good to be able to enjoy something I truly love. 

I've still been taking rests when needed but I've noticed, once again, that I don't have to nap or drink as much fluid as I was needing.  I'm still well-hydrated, but I'm not adding the extra because my body is not requiring it. One thing that is apparent, one must always listen to what their body is telling it needs.  I've always been listening, but of course, through this process, it's been most imparative to do so -- if not, I have paid the consequences.  I don't like to do that, so I continue to learn. 

I was checking my underarm last night and still cannot find the tumor.  So I'm pretty excited about what the chemo has done, but more than that, I'm sure all the prayers and good thoughts and positivity has been helping as well.  I still get my feeling of big hugs coming my way.  I still know I'm being supported big time by something bigger than me. It's very comforting for me. 

Next week will be here soon enough.  It's such a double-edged sword for me.  I don't like the side effects from the chemo especially those first 4-5 days -- they are brutal -- but then again, it is my last one. I will get through this!  I pray this will be the last chemo I ever have.  I pray for clear pathology.  Some people have to go through another few chemos in some cases. I pray I'm not one of them. I pray with all my being that this will not be the case.  I pray for only CLEAR pathology!  One would think that this poison called Chemo could get it all, but one never knows. I pray my cancer is almost gone and/or dying quickly.  It will be gone after my bi-lateral mastectomy -- let it be contained and in a nice neat package for the surgeon to remove.  When I had my breast MRI results given to me, my surgeon had stated to me that it was "uncomplicated". My tumors were within the confines of my cystic tissue of the left breast -- I have to pray that it's still like this.  I do know the tumors within the breast are much smaller! I have to keep that forward motion of positivity to get me through this.  It's difficult at times.  Perhaps, I'm needlessly worrying -- I hope this is the case. I just have to hold onto the fact I'm in great hands, I'm healthy other than the cancer, I have a willingness to beat this and the most important thing of all:  I have LOVE all the way around me. With those odds, I don't see how I can go wrong.

For now, I continue to live my life freer than I have pretty much ever-- and I will move forward and cross that bridge soon enough.  I once again continue to ask for prayers and positivity and great energy to come my way and to my family.  It's all felt and greatly appreciated.  I thank my God everyday for all the LOVE I feel -- and I do feel it.  THANK YOU!

My cup's half full!

Ciao, Ciao!

Friday, July 8, 2011

Surviving Chemo #5

This is going to be a relatively short blog today.

Today is the first day (one week after chemo #5) that I feel semi human like.  It's been a tough 7 days.  I thought I have experienced true darkness weeks ago, but apparently not.  Never have been so low (depression wise) in my entire life.  It's not me. Totally not me, but it's happened.  Chemo is a challenge beyond all others from what I've heard and read. Now, I have firsthand knowledge it's nothing short of AWFUL -- FRUSTRATING AND NIGHTMARISH.  This go-around I have been feeling like a bubbling tarpit.  There is no other way to explain it for me currently.  Heartburn doesn't suffice in the description -- it's just this percolation inside my body.  Lovely visual, but maybe that's what we all need to see and understand. 

There is good news:  One more CHEMO!  One more.  I obviously will do this, but I know I will succeed in beating this damnable Cancer.  I just have to.  There are no other options for me.  Maybe unrealistic for some, but not for me. 

I pray so much especially these days -- amazing gifts I'm being granted. 

Speaking of amazing gifts:  I met my soon-to-be plastic surgeon yesterday in La Jolla.  I did not want to be there. My emotional state of mind was not where it needed to be.  But I had the appointment and I must go if I want to get prepared for reconstructive surgery along with my mastectomy.  This man, Scott Barttelbort, is such an amazing person.  He is premiere in his field, understands women with Cancer because he specializes in reconstructive surgery.  We were in consultation for over an hour -- right down to the hellish pictures that were needed to be taken -- oh, well, add it to the list.......... Never, have I been in such an elegant and upscale doctor's office -- he's done well obviously and makes it very, very easy for his patients.  My gown was a spa robe -- no paper here!  LOL!!

At this point my very over-simplified discussion with Scott was this:  It will take about a year for my particular reconstructive surgeries to take place.  I will explain in more detail later as to what I will be going through, but suffice it to say, I'm in for the haul.  He told me and assured me that he will hold my hand through this whole process and that he will give me back Lynn WHOLE.

Needless to say, I got emotional about this whole consultation.  It's going to happen. It's coming up relatively soon. Time is going relatively quickly. 

Like Dr. B stated:  We want CLEAR Pathology -- that is the priority here!  That's what I dream of. That is what I want and require.  I'm all about goals -- this is my goal -- CLEAR PATHOLOGY!!!

Gotta quit for now.  Need to rest.  This feeling of being miserable suddenly hits so I will conitnue later.

I continue to please ask for PRAYERS, GOOD ENERGY and POSITIVE THOUGHTS.

This Cup is Half Full, just need a rest........................

Ciao, Ciao

Tuesday, July 5, 2011

Post Chemo #5

I hope everyone's 4th of July was fun and relaxing.  Down in Southern California it was certainly HOT, HOT, HOT!   I, myself, stayed covered up in the house in the air conditioning.  I, personally, do not like to live in air conditioned situations, but I had no choice.  It was way too hot for my body and considering the chemo, it makes my body that much more sensitive to changing temperatures.

This time around with the chemo has been most challenging.  I cannot believe how wiped out I am.  I mean beyond being hit by a Mack Truck.  Saturday I was in bed almost all day.  I am very much aware of my body's needs now and am doing the best to listen to it; otherwise, I do believe I will pay the wrong kind of price for my stubborness.  Don't want to go down that road at all.  I have spoken of the "mushy" head feeling or the "no sense of concentration."  This time it seems to be doubled that amount.  Wow. I didn't realize it could or would get any more intense to this extent.  Wait a minute, maybe theoretically I have heard and read that the chemo can compound on top of one another, etc.  This is simply awful. At this point, I have one more treatment after this one to go and I pray to God that it won't get any worse, but I somehow I think it might get worse. 

My skin is so very dry from our climate. My water retention is awful.  The doc had to place me on a diuretic for a short period of time to eliminate the 6 lbs that I have retained since the last chemo!  That's a lot of water!  So I pee a lot which is par for the course at the point.  My attitude is this:  So what?  Just add it on.  The diuretic is giving me great relief from the water retention especially in my hands, arms all over body.  My face has been pretty flushed -- chemo related and heat related.  I have a huge glass of water or some fluid with me at all times.  I never deviate from my fluids.  I also am very mindful of the fact that this diuretic can wipe out good bacteria in my body so I have to make sure I'm replacing it with the potassium that I am losing   -- not through pills.  My poor body is already working overtime processing the chemo, so I replace through diet and that means eating lots of foods high in potassium.

My emotions are all over the page currently.  Not crying but just too much up in my head.  I have so much time to lay around a process and think.  Not so sure this is a good thing. I try to read, but like I stated earlier, I have no concentration.  My words go into the great abyss!  They disappear. This chemo brain is something else.  I have a friend who is always so concerned about her memory issues; well, don't mean to be doing the one-upsmanship, but please, chemo brain is BAAAAAD!   I've been calling it "Mash Potatoe Brain" this weekend.  It fits very well.

My sleep pattern is very deep -- I really go into a deep sleep once I'm there.  I find it remarkable how my body will sink deep into my mattress.  My body is working so hard to get well. All I can do is go with it.
I still find the irony in the drugs -- chemo-- how it works, but it's so toxic and horrible for the body. Meanwhile, the cancer just lays there quietly doing it's thing.  Really creepy for me. So I try very hard not to think about it. I have to think on the positive side of things otherwise I would be in constant panic mode and that is very counter-productive.

On the 4th of July, I stayed in bed yet again. My body is being kicked beyond belief. It's really frustrating and challenging.  It truly makes me feel like this will be always. When will I feel the strength recharge my body?  I do state my affirmations I have been working on to help me cope.  It's so hard to communicate all the stuff that is happening at one time to people around you. Then you attempt to try to communicate this to others and I might as well be talking about rocket science with them because it goes in one ear and directly out the other.  I can't expect anyone to understand.  They have not a clue!  Not a clue.  How can they unless they've been down this road? I guess I hope that maybe someone will have a little empathy. Learn empathy and understanding.  But at this point, I keep it generic because no one understands truly. 

I did get out of the house for about 15 minutes last night to join in the festivities of the neighborhood. What a nice group of people and their children. I feel very blessed.  It was so wonderful to watch what the kids were doing as far as their activities. They were all painted up and having so much fun celebrating the day. That's what it's supposed to be about -- the joy of family and friends. I loved their little voices and their laughter.  It gave me such hope and took away my isolation even if it were for a shirt period of time.  I'll take it.  After awhile, my body gave way and I needed to get back to bed.  Oh, if I could scream, but it would take way too much energy to do so -- so I won't scream. 

I was up a lot last night waundering the house. I ended up on a couch in the living room trying to think positive thoughts and get out of my funk.  I ended up finding myself ultimately completely turned around in my bed. I was sleeping opposite of how I began -- my feet were placed where my head should be -- hilarious.  Oh, well, whatever works.  It doesn't matter -- does it really?  As long as I'm sleeping and resting.

So far this morning I'm functioning but with lack-luster. At least I'm up and trying to move and get some circulation going. It's very muggy outside so I'll be mindful. The dogs, including my daughter's 2, are all about the adventure of this new day. They've got their agenda going on - sniffing every conceiveable nook and cranny around the house and property.  Meanwhile, I'll make the effort to move forward somehow.  My goal:  To listen to my body's cues.  To keep my fluids up and to eat cleanly. 
I pray at all times I will get through this.  I WILL get through this.  I WILL!!! I don't wish this process on anyone.  It could be worse!  It could be. I'm convincing myself a lot today. It's just one of those day's, I guess.

The Cup's Half Full and learning more and more.

Ciao, Ciao!