Showing posts with label Lupus. Show all posts
Showing posts with label Lupus. Show all posts

Friday, February 10, 2017

I was given a "press release" that I am very proud of ;)m- Goes to show ANY Advocacy Work is well worth doing especially for Chronic Pain and Illnesses


I've really been down and out lately at the numbers that are coming to my blog. Used to I would have at least 75-100 and sometimes 300 or over. But, over the past 4 months, even before I went into the hospital I noticed a huge drop in those coming to my blog.

I know "Google" have changed a great deal of their SEO stuff, BUT, I have many of their ideas and recommendations that I use. I've not went through the entire "book" of recommendations, BUT, I usually post everyday, sometimes more than once. I do miss sometimes, such as when I was "out of pocket" due to the hip fracture, but even then I still posted once I was feeling a bit better and had my laptop to post to all of my social media places.

The one thing that I have not done "much" and continue to try and not do, is get too deep into the "political" issues that are invading our lives DAILY! I know many are like myself and HOPED that AFTER THE ELECTION some of the DAILY CRAP WOULD STOP!

Well, I should have known much better than that. With the "Donald Duck" elected LOL, there is NO way to SHUT HIM UP NOR the NEWS. Everything he does, tweets, says, posts, and probably what he eats for his 3 meals a day are NOW LARGER ISSUES ON THE NEWS, THAN THE ELECTION!!!!!

I am SICK TO the point of NAUSEA hearing about "The Duck" this, that and the other.... I cannot even "type his name" it makes me so ill to see or hear about one damned thing he does.

I was a "voter" and I've voted for many years, without missing many. Of course I feel if we "vote" then we do have a right to GRIPE! But, for those WHO DO NOT VOTE, then you do not have the RIGHT TO FUSS because you did not allow YOUR VOICE TO BE HEARD!


I KNOW that my "typical" daily life may not interest you. thus I "try" my best, to put something useful, fun, information that you can use, new items from The Arthritis Foundation, to WEGO, to other health and human information especially for us that remain all too ill, from Chronic Pain and/or illnesses.

I am HAPPY that although I had TWO HIP FRACTURES, now in 3 days it will be 90 days since that 1st surgery, and I am doing very well. Even without a cane, and in fact, I left it at home yesterday and did not even take it with me.

I realize at times, I am still leery about being almost too cautious, in fear that another fall could even be worse. I also am in fear that if I don't try and do all I can to "never cure" the osteoporosis, BUT try and build "muscle" and "put protein" back into my body, I have a far better chance of not being a "fall victim".

The woman that was in the room at the Rehab place with me for part of the time, had already been in the hospital like 3 times BEFORE CHRISTMAS, IN LIKE 3 MONTHS! She had pneumonia a couple of times and was put in for that. She has also been a "Diabetes 1" victim since being a teenager, which I watched even after all these years, especially without a proper diet like she should have had in Rehab, she was always having way too many problems with her Diabetes. Then she had fallen and been in Rehab before Christmas I guess in August or September, then fell broke her pelvis, WHICH SURGERY OFTEN CANNOT REPAIR A BROKEN PELVIS, thus you have to spend WEEKS AND WEEKS IN BED TO ALLOW IT TO HEAL ON ITS OWN! Her pain had to be horrible. I know HOW MUCH PAIN I WAS IN WITH THE FRACTURES TO MY HIP, and I was yelling, screaming, cussing, bitching, crying and my entire neighborhood probably thought someone was attacking me, or I had just lost the rest of my mind. MANY of them came when they saw my son's vehicle here to ask what happened, that I was SCREAMING AND CRYING SO MUCH, they could not imagine what had happened. No one I guess heard me screaming and yelling and crying, while I was still in the house for over 3 hours, being too stubborn to call the ambulance. I "hoped" I had a "bad bruise" NOT a damned brake to my hip. But, alas dammit the news was worse, because I had TWO breaks in it.

I cannot begin to even express "ALL I LOST" in those weeks and weeks, through the surgery, through being an inpatient in a Rehab Center, from my own self-esteem, pride, I felt unworthy, useless, a burden, and just a totally screwed up person to be going through this and making my kids go through this also.

LOTS played into my issues with the entire thing, because of losing Mom to Lewy Bodies Dementia in June of last year, and having to take care of her, the 6 months prior, I was already more than behind on "caring for me"... I cancelled neck surgery at least 4 times, and just put my RA medication on hold, since I just felt I COULD NOT leave and go to Dallas for a few hours.

I AM STILL trying to "clean up" everything that needs to be done, and actually am totally confused, because I feel I did not "grieve" enough before trying to begin taking care of other affairs once she past away, that now I get to a place I am not sure what, what not, which, how, is done, not done, and my own "Christmas Present" to myself, is still sitting in my hallway, along with the new rug for my living room. But, now with the hip thing, I fear trying to turn the old sofa over in order to get the backs off of it. That is what has to be done, before it can be taken out of the house. Once that is gone, I can once again clean the hardwood floor very well, put the rug down and get my new sofa/futon/chaise lounge finally put up and using it.

So, NO the political issues I speak of are usually tied into "medical things".... whether clinical trials, or laws, or trying to get the government to fund certain research projects, and so forth, my "own personal beliefs" in whom should be or not be President, and so on down the agenda, I feel I did my part, I can now bitch all I want, AND then go on with my life and pray we have NO ALLIES by the time one YEAR has gone by with the "Donald Duck"....



P.S. I WILL POST THAT PRESS RELEASE AS SOON AS MY NEWSPAPER PUTS IT OUT.


Thursday, January 12, 2017

Saturday is "D" Day for me (Discharge Day) from Rehab - Excited,Thrilled, Terrified, how to "move back" into real life yet knowing the Osteoporosis could cause further issues

Finally I knew that day was coming soon - the "D-Day" of my own life, discharging and going home from Rehab...

I've been asking "how much longer" now for months it seems; although it has been "weeks" and not months... Yet, after being told yesterday, I would be leaving Saturday, I felt a "good panic" and a "bad panic" in my head and gut.

I am thrilled to GET HOME! To my life, my eating, sleeping, and living habits, BUT I am still going to be limited as far as "what I can and can't do" - and that scares me. I am so used to doing my own thing, going to the market when I want, cleaning my house the way I want, messing around in the yard, caring for my plants, doing laundry, and all of the usual stuff, from vacuuming, cooking and cleaning, yet just now I figured out with this walker and going home, that even carrying a cup of coffee is not going to be the easiest thing in the world... trying to push that walker with one hand, and carrying the coffee was kind of "difficult". But, I've got to learn to "make my own ways" around, and hopefully I will be on a cane soon, where one hand will be free to carry some things...

BUT, on the other hand I am totally terrified to go home... since I left lots has changed just within a month tomorrow actually. I fell on the 13th of December and had surgery that night. I got to rehab about the 18th or so, and in the chaos of it all, I lost my precious pup Bub's who I feel grieved himself to death missing me. He was so upset for me to leave for a day, or a few hours, I think he just quit eating, drinking and laid on his favorite spot, and wasted away, waiting for me to come home. He passed away, and he had lost so much weight, I just could not believe it, when he died in my arms a couple of weeks ago. Peanut, is so much younger, so he has gotten used to Jason being there, and he so far seems to be doing okay.

I am going to be getting another puppy soon. But, first I've got to get me at the house and settled in. I need rails built on my front steps, and I need I feel a new set of steps built on the back. The concrete ones back there are so steep, even with rails, I feel they maybe too steep for me to try and bring groceries in, and so forth.

I never thought I would be one to be worried about being alone, but that is not because I fear someone getting in etc...I fear having an accident, and hurting myself again. This hip fracture was a total accident, but I am going to have to try and learn to slow down, not try and take on so many projects at once, and know that "tomorrow" on many thing is another day. After all, I face neck surgery soon, and possibly lower back surgery this year. I have that new car sitting there, and I am so used to doing so much on my own, waiting to have "help" putting on the plates, putting in the sticker and so forth, I am not one to put off something waiting on someone else to do it for me... So, my fear is my own restlessness. I also need to rearrange my kitchen where I can reach things that now are in the top shelves, and I must stand on my little 3 step ladder to reach. But, my kitchen cabinets are not all that great, and trying to arrange them will be difficult. Now I wonder if I should have picked Mom's house, maybe it would be easier to get around in... yet it is what it is and I've got to cope - I also know I am going to owe $$ on this damned fall and hip fracture, plus I'll have to cough up funds on the neck surgery, and lower back surgery also... so those in themselves are enough to worry me. My credit issues I spent 10 years or more getting straightened out from my 2nd marriage and all of the high bills he ran up maxing out credit cards, the last thing I need is to screw it all back up with doctor and hospital bills.

So, YES I am thrilled, and YES I am TERRIFIED to go home at the same time.....

Wednesday, January 11, 2017

Chronic Pain Patients and the "absurd" information on abuse and New Medication for pain with Abuse Deterrent in it

https://www.madinamerica.com/…/stop-the-war-on-chronic-pai…/



 I found this article interesting and more to the point when "chronic pain patients" are attacked for something they are NOT causing. I great example (I was not attacked but) since I had to have surgery yesterday, of course I had to be "NPO" thus I could have have ANYTHING to eat, drink and even my meds were taken away after midnight... all of which is necessary, BUT my surgery was NOT until 1PM the next day!
So, like MOST told me and I know myself, I could have been given my critical meds, such as my muscle relaxer, pain med, & my anxiety med...but I was made to wait UNTIL AFTER 3:30PM or longer, rather than just stopping it at 8 hours...


IF the surgery would have been early morning such as 6 or 7 AM etc then it would make sense.. anyway, same with this... "true and legitimate patients are being "punished" or horrified, because with all of the "crap" out there in the news we fear being without our meds.... yesterday, I was in horrid pain by the time I got to the hospital after waiting so long, then checking in, getting prepped for surgery, & then going under (which I was thrilled to go under anesthesia, knowing then I would be free of pain, plus I would FINALLY get some pain meds for relief.... 
  

It is a nightmare if you live in terrible pain daily, or almost daily, and then are terrified all of a sudden your meds could be jerked away... so those that don't understand, should be "educated" on just how chronic pain invades and takes over your life... and quality of life goes null and void, for the patient, family and way of life...

And from the Pain News Network....

https://www.painnewsnetwork.org/stories/2017/1/9/fda-approves-new-long-acting-painkiller


FDA Approves New Long Acting Painkiller  

 

Just came out a couple of days ago!





Saturday, December 31, 2016

Hoping that 2017 "pushes" out all the grief, sadness and illness and brings peace, wellness and secuirty to myself and everyone!

I have been "quiet" - but I had more terrible stuff going on... Bubba my Chiweenie, got suddenly ill, and passed away in my arms night before last. All of the loss surrounding myself and my family is really taking its toll on all of us. I've had all kinds of complications, from the anemia, to a huge hematoma just where the surgery on my hip was done. I look "deformed" because that hip looks like it is 4 times bigger than it should look, then my liver enzymes and lab work was high and all messed up. 

Then I still have this place on my right foot that I swear has to be fractured. I cannot stand to put any weight on it, which hinders my therapy for my hip. I just want things to get back to some kind of normal so I can go home. Even though everyone is extremely nice here, I don't want to stay one moment more than I have to. I had hoped I would be home by January 1st, but looks like that is not happening. My doctor wants to leave the staples in another 5 days or so, due to the large hematoma where the surgery and the staples are... 

PT is going fine, other than me having such heck with that right foot. They re-x-rayed it last night, and the woman doing the X-rays showed them to me, and said she was not the doctor but it didn't appear to have a fracture, and she mentioned a bone spur... but I still insist that due to the pain, the "redness" where it hurts and the pain and swelling from it kind of around and down my foot, something is wrong, and they have not found it. Anyway, wishing everyone a Safe and Happy New Year's eve and Day... I hope is 2017 brings more happiness, peace, and security, and wellness for myself and everyone.... Rhia

Thursday, December 29, 2016

How to Move forward with severa Systemic diseases, Lupus, Sjogren's, RA & knowing when everything feels so out of sorts, even with the New Year Upon me....

A piece of me feels as if I am blocking out all that we went through with Mom, then losing her in June so suddenly. Then the ordeal of paperwork, and all that happens even after the funeral is over.

Then I've went from one issue such as both ankles severely twisted, to sinusitis, to pneumonia, to Lupus flares, then to take such a horrible fall. and break my right hip in two places... to wind up being in the Rehab on Christmas, and maybe for awhile after the 1st of the year.

I just know that things have to get better. I am so terribly tired of being ill in one way or the other. I tried so hard to NOT allow this to happen to me. I knew my chances of a fall could lead to a break of a bone or joint. That is one of the very last things I wanted r needed. But, when I hit that hardwood floor two weeks ago the coming Tuesday, I knew it was not good.

I wanted to believe that it was bruised badly, yet when I could not drag it on the floor without screaming out in pain, I knew then it was bad.

I've been in a turmoil over the state our nation is in. Now with the "person" that is to be our new President, totally terrifies the hell out of me. I cannot fathom him having enough tact with out own Congress, much less any other nation.

I am having to almost "hide" my feelings this season. Here I see many families, together, excited about kids, Christmas, and this very special time of the year, yet I feel left in a "dark fog" wondering once again why I feel "punished", why did I have to take a fall as I did, and break a hip. And what are the chances that I wind up having another surgery if this hip does not work without an entire replacement since the osteoporosis could cause issues.

Frankly, this is one of the very 1st times I've been this worried about my own health issues. I watched my Grandmother and my Mom be able especially my Grandmother take care of themselves for YEARS alone. Now, I fear everything, from just getting out of the bed to going home. I've always been so bound and determined to do my stuff myself. Now, between the Lupus, the RA, the Osteoporosis, and now a broken hip, that I will lose some of my independence, which that thought bothers me badly.

The latest is I have a huge hematoma where the surgery was done on my hip. I knew it had been looking like a I had "2nd hip" and was sticking out but I just thought it was swelling. But when the nurse went to put a new dressing on it yesterday she found it was much more than swelling, and they took pics of it, and sent them to my doctor. Sure enough it is probably a  huge hematoma, and they are putting ice packs on it 4 times daily, and I won't even get the staples out for another week.

My foot still hurts and I still think I have a hairline fracture in it. I guess I should ask for it to be X-Rayed again. I am just so sick of being poked and prodded on, I hate to say that anything hurts.

I have to wonder if anything in my life will ever become "normal" again?


Friday, December 9, 2016

WEGO Health Blog Challenge for Monday 28th, 2016 - 5 Challenges and 5 Victories

Challenges and Victories (the WEGO Blog Challenge from November for Monday 28th, 2016)


As many of us have faced, it always feels as if the challenges tend to stick out stay with us, rather than the victories. I feel that is more likely about "Human Nature". As humans we tend to "dwell" on the things that feel lousy to us.

Challenges

As far as "Challenges - the 1st Challenge was truly facing the fact, I DID have not just ONE but "several" possible Autoimmune Illnesses, of which any or all, could cause all kinds of havoc in my life.


2) Facing the tests, all the labs (my 1st go round with lab work, they took 18 TUBES of blood, I am a difficult stick anyway but had to go back 2 or 3 times because some of the blood did not get to the lab quickly enough and was ruined before those tests could be ran.

3) How many so-called "Rheumatologists" do NOT have the "same thoughts and mindset" on Lupus, RA, Sjogren's and all of the other Autoimmune disorders. I found that some did not deal with "ALL' but possibly only dealt with one or two of them. I also found out that MANY doctors (specialists) ONLY went by "blood tests". IF you did not have a "positive lab on RA for example) some of them really were not convinced there was a "sero-negative" RA. I went through at least 7 or 8 Rheumatologists BEFORE finally finding the Rheumatologist that fit my illnesses and needs.


4) Trying to "find" the right medications, then trying to get the doctors to allow me to try them, and the insurance to pay for them, and then finding that medication or medications that even worked for my particular symptoms.


5) Losing my own "caretaker", then becoming a caretaker twice, all the while letting my own illnesses, continue to deteriorate my joints, and body. After putting off surgeries, now I facing further degeneration of my cervical and lumbar spine. I've come to find out that losing all of my teeth, all of the joint replacements, surgeries, many of my other illnesses, are ALL due to the autoimmune diseases and medications also. It seems there are so MANY different health problems that can be caused by AI diseases and/or the medications.


Victories     


1) Finally getting "diagnosed after MANY years of not one physician "getting" that it was Autoimmune related issues. 

2) Becoming aware that I was able to take my illnesses, become a "voice", advocate, Ambassador, for some of these, and that my blog, writing, and my books; along with Social Media really gave me a chance to MAKE A DIFFERENCE!

3) Getting to go to Washington DC in 2014 with the Arthritis Foundation! That was a dream come true. All my life, I had said I wanted to stand on the White House steps, and TELL MY STORY! Basically that is what I truly was able to do. I was able to "tell Congress" what my own personal journey through hell and back was like.


4) Finding the ONE Rheumatologist who has helped me, along with my Primary Care Physician, who Thank goodness was the physician who actually "found" my Autoimmune Issues.


5) Continuing to be able to slowly but surely "move forward". At times these diseases are "dammit the hell" bad, and put me on the sofa for even a week or more. BUT, so far, I am able to put one foot in front of the other each day, and even though the pain, and all of what comes with these illnesses can get horrible, I so far am able to do some things myself, realize when I can't, and be "smart enough" to admit that I need help with certain things. 

continuing with another "Victory"

For the most part, I feel "fortunate" to have somewhat of a "victory" over whatever happened to me in 2010, when I was so extremely ill and in the hospital for over 6 weeks having several surgeries, even a 2nd Heart Attack, yet survived to come home, take months to really "get better" and still be here right now to "tell about it"!! 





Friday, November 18, 2016

Throwback Thursday! WEGO BLOG #HAWMC a "phost" from the past? (Christmas Eve 2014)


WEGO HEALTH Bloggers Challenge for 2016 - 'Throwback Thursday" One of my blogs from the past and why I picked it to go back and "share" it again.



 Many of you know how "messed, mixed, and flat horrid most of my year in 2014 was. This post explains a great deal of what went on, and why 2014 had an incredible start, I got to go to Washington DC for the Arthritis Foundations Annual Summit and although I had been down with a severe Lupus Flare, I had been to our Urgent Care the Friday before I was to leave and the doctor who knew a great deal about Lupus, since he suffers from it also, gave me enough corticosteroids for a horse I think (LOL, well not quite that much but enough to make me feel like I was brand new by the morning at 4AM I left for DFW Airport, for the flight to DC!


Little did I know what would happen that last day of the Summit March 26th, 2014. A horrendous nightmare of an event, that forevermore changed my entire life. There are days it still effects me, even now. So, here is the post from then:

http://www.autoimmunearthriticsystemiclife.com/2014/12/christmas-eve-2014.html

Since the post is pretty long, rather than try to post all of it here, I decided to just post the URL (link) to it. That was a year of hell to say the least, then 2015, was not much better... I DID get the honor of being a "Platinum Ambassador" in 2015 BUT, did not get to attend the Summit that March, for reasons why in 2014, along with other issues that happened due to that "eventful" day. 

Then, thinking I would "start new" for 2016, only to become, someone without their own caretaker, that became a "caretaker" for my own Mom, who up until January 2016, had been in pretty good health. Little did we know what awaited us the first 6 months of this year...



Monday, November 14, 2016

WEGO Bloggers Challenge for Sunday November 13th - "One of the "BEST THINGS THAT Happened this past week?"

November 13th, 2016 WEGO Health Bloggers Challenge for Friday - "Finding the "good" from this past week"




I seem to not have "many good things" as of this past about a year. So, when those time come along, they are certainly not taken for granted, and I try and hold on to that good memory, so I can get through all of the circumstances of pain, burn out, and pure life's grief it can give to us....

#HAWMC
Having the "most" of the past 5 days of this week, where I was able enough to get some things done in the house, like moving some furniture, dusting, and doing that "deeper" cleaning, even washing the drapes (although I don't have them back up yet) & also being able to do some limb cutting from my trees that dearly need it. The drought here several years back did a number on them and almost killed them. So, they needed to be pruned back really far before winter col, cold hits, so they will have a change to put some "good" new growth on, and not look so "bare" in the inner parts of the tree.

I have a great deal more to do, but I got some of that cut up and put out for the trash collectors this morning, Now the larger limbs I have left I have to get cut down small enough so they will pick those up.

I also made a decision (FINALLY) to order a new area rug for my living room and have my eye on a sofa that will be high enough ff the ground the dogs will no longer be able to have their "peeing contests" when they get mad, and soil the carpet OR the sofa.

I am hurting from head to toe, I am hoping to have my neck surgery done in December, and try to help stop this pain. It is another reason that I am not keeping up with my blogging and writing, I am in so much pain, on my right side, shoulders,hand,wrists, swelling, now a lump at my thumb, and I am hoping that they put me on Xeljanz, because the MTX for one is NOT working, and for 2, I am having side effects again from it...

So, there is what I considered "good bits and pieces" of my week, last week.


Sunday, November 6, 2016

Day 4 - #HAWMC WEGO Health Writer's Blog Challenge - for the Month of November 2016

Day 4 - #HAWMC - A Letter to "Myself" at the time I was diagnosed knowing now what I did not know then....

 

 

Dear Rhia (self),


You had already "figured out" that something must be wrong with your immune system. You had been through enough doctors, tests, had so many symptoms resembling Lupus, RA, and several others like Sjogren's and Raynaud's that you really did not know much about.

When the 1st round of labs came back, from my own PCP (who diagnosed me at first), he knew that you needed to see a specialist. Although you come to find out your PCP has been more beneficial with the Lupus and Lupus Flares, that the Rheumatologist, who concentrates more on the RA than the other Autoimmune diseases.

You now can recall the first Rheumatologist, even though he was quite elderly, had just came back to work after a stroke himself, but his diagnosis, just after a thorough examination gave proof enough to show not only did I show signs of Lupus, RA, Raynaud's, Sjogren's, but had findings of probable MCTD, and that was almost more frightening than the Lupus and the others.

My moments that now I wished I had realized that ALL RHEUMY"S are NOT THE SAME, is something I wished I knew when I was first diagnosed. That caused me going through at least 7 specialists, each of which had a different "edge" and look on my diseases, or lack thereof. Most of them were only "blood work" driven. Not anything to do with all of the symptoms I had for years and years.

I could have saved myself a great deal of stress, worry, and getting nowhere, had I known to search for the "proper" Rheumatologist from the beginning. I've also come to find out my doctors here at my local Urgent Care know more about my conditions, than my Rheumy's for the most part. Plus if I am in a severe flare, there is no way I could get into my Rheumy in Dallas quickly. With those at Urgent Care I can be in and out, have the medications I need, and be hopefully on the road to curving the flare, without having to drive 40 miles each way, and maybe not getting what I need.


When I found out that I had 2 or 3 other 1st cousins, all on my Mom's side with RA, then we each began to piece together that this could very well be "genetic".

I wished I had known more about Sjogren's, for one. Maybe had one doctor done more about the Sjogrnen's I would not have lost ALL OF MY TEETH WITHIN A COUPLE OF MONTHS, requiring severe pain, and many dentists visits, to have all of them pulled that were left, and then try to deal with dentures, and the expense of over 15,000.00! Now I am still left with "pretty straight" teeth, BUT "fake" in nature.

So, I also wished I had more knowledge of how I could have been a volunteer and advocate before I myself had been diagnosed. I think had I been involved in some ways with the organizations who help us I may have felt "better" about myself, and not so ashamed of what these illnesses can do to us, our minds, bodies and souls... plus relationships, friendships, and the way people "see" us after we are ill.


#HAWMC

WEGO HEALTH

https://www.facebook.com/hashtag/hawmc?source=feed_text&story_id=10154656411124254 

 FACEBOOK URL FOR POSTS FOR THE BLOGGER'S CHALLENGE

 

 

Tuesday, October 25, 2016

Dealing with Daily "Issues" that for those who are NOT ILL, can deal with them fine! Take someone with RA, Lupus, Joint Issues and they are Major problems! Here is my Story!

I would have to write a BOOK to tell all I've been through this past few days. First of all, my pup, Bub's who is highly allergic to any type of "bite"... was clawing and scratching himself yet I could NOT find one flea, have not seen a flea, and had been driving myself crazy. He has always had skin issues, especially being hyper-sensetive and itching... and he was whining, crawling up in my lap, and even when I asked him"Bub's are you itchy?" - he would head for the kitchen so I would give him a Benadryl. Anyway, I FINALLY got him where I could really take a good look on Friday, and found a bit of "flea dirt' (which honestly I had not known about) on his bottom...where I knew any flea loves to hide... yet still NO flea's! 

So, I sprayed him, sprayed the other one down Peanut, then salted and and put the washing type of Borax own my rugs, and let that sit. That was after spraying the outside of the house, getting more granules and broadcasting them in the back, front and everywhere I could outside. I sprayed down everything in the house with "Flea Enforcer" which a few years ago, worked like a charm, and you can spray it on even your bed, pillows, sofa etc.... so, I got some of that done, had to leave the salt and Borax to sit for awhile, and went to run errands. I was SUPPOSED TO LEAVE YESTERDAY FOR THE CASINO! 

So, I as "trying" to get ready for that. I had a million things to do, in the yard, in the house, running errands (this was Saturday) and my "light" to tell me my tires were "under inflated" came on. It does that when the weather changes from hot to cooler, but I checked them and they needed air. But, it was already late in the afternoon, I was exhausted, needed to get home to vacuum up that stuff, pack my clothes, so I decided to wait and I would air up the tires Sunday afternoon. So, I get up Sunday, preparing my meds, my clothes, deciding what to wear, and also when to leave to try and "avoid" some of the rush hour traffic Monday morning in Dallas, headed to Winstar. So, I go and get me some quarters (now it is like 1.00 OR MORE for air) and I went to air them where I always do... downtown, at the station across the street fro the automated car wash. Theirs is on the side, and not a lot of traffic etc... so I can park where I can be as up close as I can be... So I get all of them stem covers off, get my quarters ready, and get the line ready to pull, and it comes on, and I TRIED AND TRIED AND TRIED, but my arms and especially HANDS are so stiff, swollen, and I guess weak from the RA and all the trouble I've been having -

 I TRIED THREE TIMES (3.00) and I STILL DID NOT GET THOSE TIRES AIRED UP! By then I was upset, hurting worse than ever, pissed, off (AND THIS GUY CIRCLED THE STATION 4 TIMES, WATCHING ME, YET NEVER OFFERED ANY HELP! THE FREAKING JERK!) Well, It is Sunday, I have no clue where to go to have anyone put air in the tires, and hell now you cannot get anyone to do it, even when I had my oil changed, I was pissed because i ASKED HIM TO AIR THEM UP, MY LIGHT WAS ON BACK THEN) I GET IN THE Car and the LIGHT IS ON, HE NEVER put the right amount of air in them, they take 35PSI IN THE FRONT AND 233 PSI IN THE BACK! I know I've done it myself and hell been doing my own tire airing up for YEARS AND YEARS! Yet, I just could not pull that damned line, hold it up to the stem tightly enough, and the push the nozzle to let the air in.... my hands, wrists, even neck and shoulders just could not let me! SO, I GO HOME IN TEARS, JUST SOBBING.... mad, and so upset, because I would NOT drive the car to Winstar without the tires aired up correctly. I wanted to leave EARLY Monday morning about 6AM or so, so I was NOT going to find anyone to help me and besides by then I did not want to hassle with the entire ordeal. SO, I wound up COMING HOME, CALLING AND CANCELING MY RESERVATION AGAIN!

 I GOT HOME DID THE vacuuming, this was already 5PM or after by the time I finished all of that, and made me and the pups some dinner, and watched a movie. So, that meant NO TRIP again... I've NOT BEEN OUT OF ENNIS SINCE BEFORE MY MOM GOT SICK IN JANUARY! I've not had ONE break, all I have done, is do paperwork (which is still not finished) paint, clean, cut down tree limbs, spend BUCKS to get rid of bees, get stung by those damned wasps, and do any and everything else, but I STILL HAVE NOT HAD EVEN ONE DAMNED AFTERNOON OF A BREAK! MY NECK IS BAD! I need surgery and now, after hurting my lower back again the time Mom got home from the hospital my lower back is always killing me... 

YES, I GO AHEAD AND CUT TREE LIMBS, AND DO EVERYTHING ELSE, HURTING OR NOT, BECAUSE HOW THE HELL DOES IT GET DONE, IF I DON'T DO IT???? If I allowed myself, I would sit on that sofa, and let myself "wallow" in all of the pain, the upset feelings, the hurt, the guilt, and the MAD PLACE THAT I AM over what I TOLD MY MOM SHE WOULD CAUSE, BEFORE SHE PASSED AWAY! NOW she is GONE, AND GUESS WHAT??? Exactly WHAT I TRIED TO WARN HER ABOUT IS HAPPENING! IT IS DAMNED IF I DO, AND DAMNED IF I DON'T.... I am too tired, hurting too badly, and need a freaking moment that I do not have to DEAL WITH CRAP! So, that is why I've not been "online".... I've not felt like it and not only that I HAVE NOT HAD EVEN A MOMENT TO BREATHE... I HAD TO GO, BUY A 12 VOLT Portable Air "compressor".... it runs off of your car, and I bought that yesterday when I found it in Wal-Mart. 

Although I still had to mess with it, and dammit, I know better, I've got to go and buy some stem covers, I always wind up dropping them... BUT I GOT MY TIRES AIRED UP CORRECTLY YESTERDAY AFTERNOON AND THE LIGHT IS NOW OFF! Plus NO MORE do I have to worry about pulling on a damned air hose, I can air my tires up anywhere.... It is small and fits right into my hatchback, with my car cleaning stuff... so PROBLEM SOLVED FINALLY!

Saturday, October 15, 2016

#OneLineOneDay - the Lupus Alliance Message so Crucial for ALL of us with Lupus







Today is the day. Join the Lupus Research Alliance and thousands in the lupus community today for One Line, One Day as we spread awareness with a simple message:

Join the Lupus Research Alliance in a unified effort to free the world from lupus through the power of science. #OneLineOneDay

The Lupus Research Alliance believes in the idea of collaboration as the way to find better treatments and ultimately a cure for lupus. Today we ask you to join us in sharing this message. By working together with the entire lupus community, we will accomplish our mission.

One Line One Day is your movement. Share this message with your friends and family through Twitter, Facebook, Instagram, email - any way you would like to encourage people to help us to spread the word. Through this simple action, we will increase lupus awareness today and beyond until we reach our mission of finding a cure.

Thursday, October 13, 2016

News From National Pain Report and Dealing with the Congress, CDC, and Government and Chronic Pain, Medications and much more!!!!



Chronic Pain Patient Rally Set for Washington D.C.

by Ed Coghlan


PLEASE GIVE THIS A READ! IT WAS in my newspaper a couple of days ago, and I wanted to post it here, separately because I know MANY of you are TERRIFIED of what us, as Pain Patients, Chronically Ill, and Already been through the mill, many times shall do, if things change drastically in regard to our medications.... So, I felt this needed to "stand out"... boy I need to again, since it has been awhile post my battle since the age of 17 years old with chronic pain, that started with severe migraines, and never stopped, going into all different types of chronic illnesses, that cause horrid pain....

The YEARS I SPENT just "trying" to find a doctor, a legitimate pain physician to treat me.... and it was only about 10 years ago, I FINALLY FOUND HIM IN DALLAS TX! The man is a true "hero" in my book for sure....



http://nationalpainreport.com/chronic-pain-patient-rally-set-for-washington-d-c-8831671.html



Friday, October 7, 2016

Fearful that something is very WRONG & not sure what I want t do honestly....

First of all, I want to see who reads this. Some of those if they do, should "respond" to me quickly.

IF they DO NOT, then I know they lie to me about "reading" my blog posts and FB posts etc.


I've lost something like 24 POUNDS for no "real reason" over the past about 8 months. I "chalked" it up to stress of all I went through with my Mom, the Dementia, then the grief and everything that is STILL going on even after her passing away.

Funny how even "family" can be so damned "selfish" once they "think" they are getting a little bit of the "green stuff"... or if they are NOT, and so forth.

Anyway, I've been having severe "night sweats", I mean COLD, shivering, soaking wet to the bone, and all onto my sheets, my blanket and so forth. Those have been going on now for about 2 years off and on... but lately they are much worse.

Then I KNOW I am anemic, and have been, I take B-12 injections monthly BUT my RBC IS not BETTER but WORSE, anytime I have labs drawn.

Then there is the bone weary fatigue. I struggle with severe fatigue, and have always felt it was the Lupus, RA and so forth....

I cannot sleep, the lymph nodes in my neck stay swollen and the Left one under my ear is like a rock, and sore all the time.

THEN, I developed this one "lump" about the size of a LARGE marble on my L. Butt cheek about 6 months ago... rather than go away, now it appears like it is "sunken in" around it, with a bluish tint, almost looking bruised YET it is NOT bruising... I've had NO trauma there and now this past week up and down my outside right thigh, I began to "feel" the little lumps, about 4 or 5 of them...

I've looked and researched, and although we know often these things may mean nothing, YET I fear I may have "Non-Hodgkins" Lymphoma.

The "symptoms fit"... and with my other issues like Lupus, RA, Sjogren's, Raynaud's and so forth, my chances are much greater of having something such as this... I shall say no more for now... and see if anyone reads this....

Wednesday, October 5, 2016

Surviving - Being a Caretaker even after the person passes away, dealing and coping with loss & still "feeling" someone still having a hold on you from the "grave" - Decisions when you are chronically ill, in pain & trying to make everyone "happy"

I've been trying to "get over" what all has been left behind for me to deal with since June 9th, 2016 - Actually more like the start from about 9 or so years ago, when I came back to TX, to help my Mom.

Most of you that follow me, know I was an only child, my Dad passed away in 2005, and by December 2005, I moved back here from Seattle, to help my Mom. I've talked about due to Dad's upbringing in the "Depression" back in the 20's and 30's Dad's "way" of handling life was much different than those who were younger. Not that he had "bad ideas" but there were many things he could never accept, that were just a part of life, as it evolved and changed.

We each know life does not remain standing still. Each day, there is something new, whether it be something horrible like the "wars" overseas, and innocent lives, even children suffering for no reason but greed from others who want to "rule" over people,

There are also many good things that almost change daily, from cell phones, to technology, jobs, the way our country is ran, and all types of good things that can change within a breath's space.

My life, as well as many of yours have changed, evolved, grown, fallen, gotten up, and tried to march on, even through the pain and suffering, the embarrassmentand the good, bad and indifferent of this world.

Speaking of, our nation and world are in such a torment, chaos and it's hard to fathom other humans can do some of the things they do to those like them, humans. Each day the news seems to worsen over not just all of the overseas fighting, hatred, war, and such, but right here in our nation, each evening, I watch almost in horror of what act of violence has happened that day.

I was left to "take care of" all of Mom's affairs, of course Executrix of her Will/Estate, as you can call it.

Mom had made some really "bad" choices when she was alive. She did some things that as much as I had tried to help, explain, and give her insight along with her financial advisor at the time, to get her to understand, some of what she was trying to choose, could cause family issues someday after she was no longer here.

I never "told" her what to do or not do, but helped her, by explaining why I felt one way or the other, as well as her advisor also helped to guide her into not causing family grief, anymore than we would already have after she had passed away.

I had been here over 10 years, and for most of that time, I helped her with just about  everything, from bills, to putting gas in her car, to helping her and doing her taxes, explaining things she did not understand, you name it, I did it... I am an only child, and I felt it was my responsibility to help her in ALL ways, that I possibly could. I can hope that I did for the most part a decent job at it.

Although a couple of things fell through the cracks, and as I said years ago, NOW, we have a family "uproar".... that although one member "seems" to not be hurt by what has taken place I feel badly that it has, and even more upset that the other 3rd party is NOT helping, and is acting like a damned toddler, rather than a grown up adult.


I am going to go ahead and publish this although it is not finished... I will finish it and post the rest very soon...

Wednesday, September 28, 2016

Just a look at what I've been working on, even with a right hand so swollen I can barely move my fingers - NEVER let ANY DISEASE make YOU think YOU CANT - YOU CAN!!! (or most of the time you can)



WELL!!! The Living Room is almost done. Of course the ceiling is not painted, and I still have to do the floor, but I got it all painted, and the chair railings all up and finished this afternoon! I am quite proud of my work, although I can see the “mistakes” hopefully no one else will notice. Then the kitchen wall, and I got it almost finished and have the chair railing up in there. Now the “red” blob…

DO NOT make fun of me yet… LOL, When I finish, I hope it will turn out half as well as the hallway did in my house here… I found the “glitter” to go into the gold paint, so I will paint the upper half red, and white on the bottom, same as the others, but I am going to “sponge”, use newspaper, paper towels, possibly rag roll the gold over the red. If it turns out like I can picture it in my mind, along with my red and yellow curtains, plus my bedspread that has all of those colors mixed in,


 I think it will turn out awesome… if not I guess I will be repainting the bedroom! LOL!! That is the ONE thing I figured out after all of my years of DIY at homes, whether painting, fixing, repairing or whatever, if you feel you do not like it, like coloring your hair, just do it over another way! It can be “fixed” ….. anyway, I am exhausted and my right hand is so swollen you can barely see my knuckles.. and that “sawing” was all done by ME, by HAND with a “miter saw” by the way… no electric saw of any kind, it cut all of those railing pieces by hand…. :)


I know I shall "suffer" the pain and swelling, and all that comes with undertaking a project when you are in chronic pain, and living with several chronic illnesses.., BUT AT LEAST "trying" to partially do something you love, whatever that is, is a WIN WIN even if you Can't FINISH it, you are still a winner because you TRIED! We "try" to never allow chronic pain and illnesses to ruin our "want to's" and joys in life...although at times they take over, when we have a fighting chance, we FIGHT!!!!










Thursday, September 22, 2016

From Running, to walking, to running, and trying to get my body to keep up and the Lupus and RA to "behave" - Remodeling, Houses, Contractors, and Coping


Well I did have one contractor come over yesterday afternoon, and I got tickled - he was impressed how much work I have already done! I told him I would continue to do what I can, what my body and hands allow me to, and that way when they get where they can come, they can do the larger things like the railings, and the fence... and later side that garage and put a new door on it. I am in a mood I guess I cannot describe.... I have not really been here very much, it seems all I do is run, run and run... I had to take a huge amount of shred stuff to Waxahachie yesterday, so I drove the Elantra to get those miles on it so the computer will register correctly for the inspection. Then I went into Lowe's, bought a couple of "toggle" switches, I really want to use those in that house also... and then some plates for the outlets, again several need the updated outlets in them... I looked at flooring, the laid linoleum... even though I would love to do something else, with the pups, I think I am going to have to stay with that, and actually the one I like is a "standard" at Lowe's... plus they would even lay it very reasonably, if so happen something went awry and my contractor could not do it... I FOUND MY GLITTER FOR THE PAINT! I knew they would have it! I had to search and search, then finally asked two people and one lady knew exactly where it was (which was in a very stupid spot if anyone wanted to find it).... I priced fencing, and I did 5 5 pieces of chair railing... that should be enough to finish the living room! So, a few touch ups with the paint, and putting those up.... I have a new door knob for the front closet... that stupid thing broke about a month ago, and there was no way to get into the front closet, I beat on it, I pried on it, I even took the pins out of the door, and I thought I would never get it open... so finally when the plumbers came, they thought they may need to get in there, and they were able (with a great deal of elbow grease) to get it open finally... of course between myself and them we destroyed that door knob... NEVER in my life, have I seen an "inside knob" that damned sturdy.... I never thought I would get it out... so I bought one with the plates and a glass knob on it... I wanted to do that in this house to all of the closets and never got around to it... and on Amazon I can get the whole thing for about 14.00 including the back plate... so I am going to put that up after I get that closet painted... those closets have NOT been painted since we moved in which was about 1964 or so! Dad painted and did everything else, BUT not the closets, they are horrible! So, paint that is left over, that is okay colors I am going to use in the closets.... anyway, I still have lots to go... I am having him build me, kind of like a cedar platform off the front porch, so it will be large enough to hold my inside plants when I put them out during the spring and summer months.... the porch... OMG those rails were so rotten... I took all of them down myself earlier this week. I only like one post, that the concrete bolts had paint on them so I had to WD 40 them and now I can get those loose also.... I hope between me working until the other guy can come, I will have him paint the ceilings also... no way I can do that... and finish up the stuff I cannot do... I will be moving in by the end of October, first of November... I hope... depends on my own health, the weather, how quickly he can come and get on it... like I told him the garage siding can wait for a bit... mainly the fence, finishing up the painting inside, and I've found a kit I maybe able to help the inside of that damned old tub look better... I am going to order one and try it... it is hideous, but having someone come and redo the porcelain on it would be thousands of dollars... I still want to break that sucker into pieces, get rid of it and put a walk in shower in there... but I know the work trying to take a sledge hammer or a saw to that tub and cut it out of there, it takes lots of work...... Anyway, again I am in a "funky" frame of mind right now... I thought moving over there would be what I wanted, especially after the remodel, now I wonder if that is a good decision, but I cannot do the work this house needs... I cannot roof it, and could paint it outside, but only so much, and it just needs someone who can do the things it needs themselves... a time ago, I could have done it all but the roof! LOL! but that was when I was in my 20's and 30's..... I have painted an entire house outside more than once for sure.... but at my age and with my health issues, my body is already mad at me... my right hand keeps swelling up, and my right ankle is still not all the way well.. and my neck NEEDS SURGERY! I was so hoping to get that done before the end of the year... once again I face whether to keep my insurance or go back to another, and that is coming up soon...more stuff that needs to be done!  Rhia

Thursday, September 8, 2016

Knowing After all these years, that I should have been born a few years later, and I know I would be my dream job...

It has taken me 56 years, well guess a bit less than that since as in infant I would not have known this - :) to FINALLY KNOW why I WAS put on this Earth, and what my "calling" was - that I missed! It just "hit" me yesterday while in the quiet over at house #2 I painted.... first of all, I was born about 10 years or so too early. Had I been born in probably the 70's or so, then our knowledge about technology, computers, the advanced sciences we have now, from medicine, to phones, and you name it, I was a "bit early" on the scene to have those things readily available to me, unlike if I was about 30 years old or so right now. Or even out of High School a few years and then headed to college.

 I should have been AN FBI part of a team that does the "profiling" for our worst criminals, serial rapists, people that in their minds (and you must "get into their minds) to be able to capture why, where, how, when, and so forth they do what they do... their is always or usually a methodology to their "madness"... whether it be just pure evil, or having been abused, causing irreprible damage to their psyche, or they have multiple personality disorders, psychopaths, and so many other things that they either may have been born with, taught, brainwashed, or a numerous specific reasons why some do as they do harm to others and themselves.

 I know that may sound ridiculous, but I of course knew I would always be a writer, yet my true "profession" had life been a bit different, and I had been young enough for the technology that is now available to be here so I could learn about all of these, I surely would love to be one of these types of "profilers" that could help protect innocent victims from the harming of such horrific others. I am too "old" now, and with all of my own personal health issues, I would even if trained, not be eligible to serve at the FBI or such...BUT, I DO KNOW that LIFE gives you WHAT you NEED.. we are born for certain reasons, at certain times... and there is a reason I was born in 1960 - and at that time they did not even know much about "DNA" and the like.... 


http://www.apa.org/monitor/julaug04/criminal.aspx


http://www.forensicscolleges.com/blog/htb/how-to-become-criminal-profiler




 

2016 Flu Vaccine and the New Pneumonia Vaccine - Lupus and those with other Chronic Illnesses..,


 
 
 
I know some of us question if we SHOULD or SHOULD NOT get these vaccines....I get mine, and I also got my new Pneumonia vaccine, because it provides coverage for hopefully 23 types or pneumonia - the 1st day after I had them both (in the same arm due to my right shoulder being completely replaced, so my muscles are not very big on that arm) my arm itched and felt like it was burning. BUT, the next day, all of that stopped, and my arm is sore, but it does many of us that way. 
 
My pharmacist as well as my Rheumatologist recommended I get BOTH! Although we with chronic illnesses may not get "as much protection" as those without chronic illnesses, we still get SOME... since I have had "double pneumonia" at least 2 times in the past year or so, and then twice before, I decided I had better at least try and give myself a bit more immunity if possible.

Sunday, September 4, 2016

Happy Labor Day - Journey's and How Our Lives Change Within Moments - Coping with Grief, Chronic Pain, Lupus, RA, Sjogren's and taking one step at a time....

I’ve felt so many different emotion since June 9th, when my Mom passed away. As I told my daughter Amanda on Friday evening over the phone, I think the entire ordeal is just now beginning to set in as reality. I catch myself wanting to call Mom to tell her something or ask her something… often times a week. Then it dawns on me, I cannot do that via telephone anymore…. I’ve put off really doing ANYTHING for just myself. I’ve been so busy taking take of all that needs to be done, from paperwork, to painting and working on the house there, that I have NOT had anything I really wanted, needed - other than the weather get nice enough and for me to be well enough to feel like going to Winstar in OK for a night. As soon as I can find a Sunday and Monday, here, there and between there is going to be nice weather I plan on going and it will be a “delayed celebration” of what would have been Mom’s 81st birthday on August 28th.

 But, it came to me a week ago, if I don’t find some other way to sit at my computer to “write” I will never get it done. Right now due to my neck needing surgery, and possibly my lower back, I cannot sit here for very long at a time…. plus when I have the surgeries, I won’t be able to sit like this, due to the neck brace for 6 weeks and so on….


SO, I decided I CAN sit on the sofa, with my legs up, where my ankle also does not swell so badly, and THERE in the evening after dinner when these two hellions (Bub’s and Peanut” calm down - one on each side of me, would be a perfect time for me to get some writing done, more on my blog, be able to get possibly back into my advocacy work, but MAINLY WRITE! I desperately NEED to finish my 3rd book, and after what happened to Mom from this past January till June 9th, NOW I totally understand “why” my writing was “delayed”…. it is clear as day, that I MUST include all of what Mom went through along with myself, as a caretaker that needs a caretaker…. and so much that no one even knows happened…the details of each and every day being there with her those six months, even sometimes changing from hour to hour…. I witnessed such an unbelievable change in her emotionally, physically and mentally… and that is why my writing was put on hold…. I have much more to add to that journey, for myself, for her and for my kids… and Grandchildren later and those to come… SO I broke down and ordered an Apply Air Laptop. I didn’t get the “biggest” or most expensive, because some of it I probably may never use. But, the screen is large enough, and I already love the way the keyboard is laid out and back lit….

I just received it late yesterday via Fed Ex, so I really have not had much time to “learn” about it…. I felt much “guilt” and hesitated at first before I bought it, BUT, I recall what my Mom said to me, several times, but moreover just before she began to really show the signs of getting so bad, so quickly, she made me “promise” I WOULD complete this 3rd book, and have it published. MOM was and will always be my “Greatest Fan”…. So, I want to fulfill that promise to myself and to her…

thus then I knew the laptop made perfect sense…besides, as much as I LOVE MY PRIUS! And planned on leasing another the first part of 2017, if I forgo that, and drive Mom’s Elantra, which only has 10,000 miles on it, and just needs a battery and tires (from lack of her driving it much) then I could do away with a lease payment and higher insurance… I have not made that decision yet, because that Prius was the BEST thing I’ve ever had in my life, as far as “items”…. but I have time to decide… so by then things will be more centered, and I will be able to make that decision. So, here are a couple of photo’s of my Brand New Apple Air Laptop!



HAPPY LABOR DAY!

Why Do We Celebrate Labor Day and How It Began! 



For a lot of people, Labor Day means two things: a day off and the end of summer. But why is it called Labor Day? Labor Day is a day set aside to pay tribute to working men and women. It has been celebrated as a national holiday in the United States and Canada since 1894.

­­
Labor unions themselves celebrated the first labor days in the United States, although there's some speculation as to exactly who came up with the idea. Most historians credit Peter McGuire, general secretary of the Brotherhood of Carpenters and Joiners and a cofounder of the American Federation of Labor, with the original idea of a day for workers to show their solidarity. Others credit Matthew Maguire, later the secretary of Local 344 of the International Association of Machinists in Paterson, N.J.

The first Labor Day parade occurred Sept. 5, 1882, in New York City. The workers' unions chose the first Monday in September because it was halfway between Independence Day and Thanksgiving. The idea spread across the country, and some states designated Labor Day as a holiday before the federal holiday was created.
President Grover Cleveland signed a law designating the first Monday in September as Labor Day nationwide. This is interesting because Cleveland was not a labor union supporter. In fact, he was trying to repair some political damage that he suffered earlier that year when he sent federal troops to put down a strike by the American Railway Union at the Pullman Co. in Chicago, IL. That action resulted in the deaths of 34 workers.


In European countries, China and other parts of the world, May Day, the first day in May, is a holiday to celebrate workers and labor unions. Before it became an international workers holiday, May Day was a celebration of spring and the promise of summer. Membership in labor unions in the United States reached an all-time high in the 1950s when about 40 percent of the work force belonged to unions. Today, union membership is about 14 percent of the working population. Labor Day now carries less significance as a celebration of working people and more as the end of summer. Schools, government offices and businesses are closed on Labor Day so people can get in one last trip to the beach or have one last cookout before the weather starts to turn colder.

 Links Below for More Information On the History of Labor Day


 

 

 

Saturday, September 3, 2016

ANYONE LOCALLY - (Ellis County TEXAS) Who maybe able to assist me with some painting and carpentry work!

I "realize" this is not a "usual post" for here, but I felt as many of us that are here from Ennis, may be able to point me, or point someone to me to help me out with these things. Mom passed away in June as many of you know from an extremely aggressive type of dementia. She was "okay" in January, and by May, was in bed, in diapers, and had no clue who I, nor herself was, or even could get out of bed. So, here is my "post" - anyone who maybe able to help out, please let them know to contact me - Thanks so much Pam Ravishing Rhiannon Steele -

I've just POSTED in a couple of Ennis TX and Ellis County TX posts about needing to hire someone to come in & help me finish the inside painting of the house I am working on. My Rheumatoid Arthritis/Lupus are keeping me from doing this myself, as I wanted to.I can barely hold a paint brush right now. by the way, the house is barely 1,000 sq. ft. & is only 2 bedroom, one bath. I've picked out all of the paints (or most of them and have began how I want it to look.)
 I am looking for someone to put siding on the one car garage, put up some new handrails on the front porch (about 4 or 5 steps) and then put one on the back porch (about 2 or 3 steps) down. I am furnishing ALL of the materials. I will want a new garage door put on the garage also. 
Those are my "MAIN" things If you know of anyone is my area, who can paint & do a bit of carpenter work, is reliable, please tell them to message me here, OR send me an email to redstangblonde@yahoo.com. I will keep an eye on that email address for anyone, who may help. I thought I would finish the painting myself, but there is just no way, with my health issues, I can continue to do some of it, but I need help. Thanks so much! 
There are some trees and limbs that need to go and an old piece of bus on my back lot, that is FULL OF BEES! They have been here all of the early Spring and Summer, and I've not been able to see the hive, but it must be huge! So, BEES and BUS can go, if anyone wants to haul it off for the scrap metal to sell.