Showing posts with label blogs. Show all posts
Showing posts with label blogs. Show all posts

Thursday, March 14, 2019

Thursday's Newest Paper about Pain, Autoimmune Illnesses and more...


Be sure to stop by DAILY and check out my Daily NewspaperbannerLife Chronic Pain & Autoimmune Systemic Diseases & Dementia®

http://news.autoimmunearthriticsystemiclife.com/#/

It comes out new each day with all kinds of articles, news, blogs, information on the latest medications from Dementia Chronic Pain... Autoimmune Illnesses and more...

You Can sign up to receive a copy daily right to your email on the front page of the paper!

Friday, November 11, 2016

WEGO Health Day 11 - Bloggers Challenge a "TOP TEN "must follow" Lists From Facebook Twitter, and Blogs....

This one is kind of a mixed up "bunch" for me. I have those that follow me on Facebook, but they may rather follow my blog posts, or I know I have a good deal of following on Twitter. I really never have "kept up" with the number that come back again and again, but do know those that comment and read often, because they either give me a thumbs up, mention my "Newspaper" yes, I do have a Daily Newspaper I put out, FOR Chronic Pain, Chronic Illnesses and Dementia. I send it out daily on Twitter, Linkedin, FB, plus there is a follow page on my blog, in case you want to joint my daily Newspaper. I will say the newspaper "seems" to be giving people a great deal of information, because the articles are from reliable sources for the most part, I have also "tailored" it for those with the Autoimmune, Chronic Illnesses, such as Diabetes, Heart problems, and so forth, plus Chronic Pain, and all that comes with the controversy on it now, especially on our medications for chronic pain. Plus I added "Dementia/Alzheimer's" after my Mom passed away last June 9th, due to the fact I "feel" that it may run in our family, on Mom's side. Both of my Grandparents had it, but my Grandfather, had full blown very difficult Alzheimer's. Mom's turned into an aggressive, what we feel was the "Lewy Bodies" Dementia, that I watched take a woman of 78 years old, who could still drive, clean her home, and cook, etc... to within 4 months go to being bedridden, in diapers, could not even remember her home, who she was, and mostly had no memory most of the time of who I was. Within 2 more months it took her life. One of the most difficult times in my life, and something that has "changed" me forever, in SO many ways.... some good for the most part, and some may say things that may not be so good... but I know to just roll with the flow of it all, and NEVER take ONE MOMENT of life for granted.

So, Here is kind of a "mixed list" of blogs, Facebook friends, Twitter followers, and those that comment, and are "followers" in one way or the other....

Facebook Followers and I follow them also

Denise 

Venetia Shafer- FB

Amanda Matheny - FB

Cynthia Carr Czaplicki - FB and she really is wonderful about making comments and reading, plus she is a relatively new friend there. 

Betty Walters - FB

Raymond Veditz - FB
Judith Flanagan  - FB
Barby Ingle - FB
Nancy Hershalman Gipson - FB
Jean Marie Ely Breaux - FB
Jane Gill-Wilson  - FB

Blogs I follow (and love to tell others about)
Arthritis Foundation (I know it is a website but they have a blog also)
The Hurt Blogger
Rheumatoid Arthritis Guy
All Flared Up
Little Miss Autoimmune
Barby Ingle (all of her writing, articles, books & more)
Float Like a Buttahfly
Not Standing Still Disease
An Autoimmune Arthritic Systemic Life (of course my own  ;)
WEGO Health's Blog, & ALL of the Help. Challenges (good kind) and assistance they give to all of us!! (Website in general)
Creaky Joints

Twitter Followers

JoJo @SuzieMay08
Told You I Was Sick (Also great blog/writer!)
PajamaDaze
Arthritis Foundation
WEGO Health
Cure Click
Cluster Shade
Patient Power
Elizabeth@themamaspace
A Chronic Voice
 

And there are so many more, that either follow me, or we follow one another on Facebook, Twitter,Linkedin, Blogs, and even emails. There are many URL's that truly "help and guide me" at times.  US Pain Foundation, and International Pain Organization, Med-Page and any "medical newsletters I get and save. they are also a wealth of information.

So, to those who I may have "missed" here, I apologize, because I do see and read you, your posts, and know much about your lives and what all of you are going through.

 

So, Here are my lists!

 
#HAWMC  
 
 
 
 

and by the way, here is the link to my newspaper and the name of it!

http://news.autoimmunearthriticsystemiclife.com/#!headlines

Life Chronic Pain & Autoimmune Systemic Diseases & Dementia®

"All aspects of autoimmune & chronic pain illnesses, fighting to survive & grow past them"




 
 

 
 
 


 
 





Monday, August 15, 2016

Monday, Rain Finally, Catching Up, WEGO HEALTH 2016 AWARDS! and my Nomination - Check it out!

Rainy here finally, not a hard rain but nice and slow like we need... not a great deal either...but it appears "if" things go as they show, we will be getting more over the next few days... I am concerned about thunderstorms, mainly hail... I am in the process of going to paint for awhile at house #2, but I certainly don't want my Prius hailed on... that would be a disaster... but I don't think hail will be an issue, maybe lightening and thunder but so far this morning, we have not had any of that just lots of heavy rain clouds, much COOLER temps thank goodness, I had to turn off my A/C for a bit this morning... so that is a good thing... anyway, got some stuff done yesterday at home #1 - I had some paperwork to do, had a few other things that were beginning to pile up on my desk, so I got some of that done...

 I've got to take the Elantra over to Wal-Mart - depending on the weather, maybe tomorrow, the battery has had it, and I can charge it, but due to it sitting and not being driven any, it runs down... but it needs to be changed anyway. It already was old and not working as it should... so I need to take back some "horrible" paint brushes I made the mistake of buying at Wally World and I am taking those back , plus I had bought some french onion dip mix at HEB, and two mini rose bushes, that had for $1.99 each last week... it was kind of "odd" to me that they had them marked down so low... they "appeared" to be healthy!!! BUT, within 2 days, one of them just died... no apparent reason, I had not done a thing but put a bit of water on it, and it just died... the other one, was not looking the best, but I decided to re-pot it to see if it would be okay... hell NO, it died also... the onion dip package had a hole in it, so it is hard as a brick... and I believe I had mentioned those things over the weekend... but I threw away the small pots the roses were in from the store... I have the receipt and the little plastic explanations about them, and one of them I still have the paper that was around it, but I only have the one bush left, that is already in another pot, dead... but I REALLY don't want to go the the trouble of taking that dead rose bush in... so I am going to take the receipt, the dip mix, and tell them about the roses... I THINK THEY KNEW something was WRONG WITH THEM... SO THEY MARKED THEM DOWN... to get them out of the store before they died... somewhere someone either put something wrong on them, or did something, and they knew those bushes were going to die... I just can't believe both of them died within 2 or 3 days of me bringing them home... I have two from a couple of years back and in fact both of them are on the porch and both have blooms on them right now... other than that if you have TIME -

PLEASE GO TO THE WEGO HEALTH NOMINEES FOR AWARDS THIS YEAR AND put a "good word" in for my nomination... I have not said much about it, but I am nominated right now for my blog, and there are many other awards that you can be nominated for... so not just me, but anyone and in any of the categories you feel should be recognized and get an award (I would get a special graphic to put on my website, plus they send the winners each year a box full of goodies, balloons, a little award, T-shirts, pens etc... I actually also judged the past two years for them also.. so they may ask me again to judge... that was kind of fun.... Here is the link and I've got to get my butt in gear and get to painting....

Link to my WEGO Nomination and "bio"!

Saturday, March 21, 2015

AS YOU Go to DC Next Week to Represent ALL with so many health issues, may WE ALL do our part to BREAKTHROUGH the disparities that hold back Cures...

Well the "day of infamy" is almost upon many of us! That is the packing, preparing, and getting on that flight to Washington DC for several activities going on there this coming week! I believe our Congress will be a bit on overwhelm at times with all of the health activists, Ambassadors, Volunteers, and many that will be telling their own personal story about their chronic illnesses, the different disparities and challenges they face, some daily, and how much more we need in research, in new technology, new medications, more specialized physicians, of course which all take lots of dollars to be able to fund some of these extremely needed actions. Life is already a huge enough daily challenge, to work, take care of family, kids, go to college, and participate in the "daily" life of living. Then you add on top of that, chronic illnesses, chronic pain, being unable to get the doctors and medications you need, further more possibly not being able to even get a "real and proper" diagnosis FIRST so you can receive the treatment you need. The amount of "challenges" that those of us with chronic illnesses face, especially when the diseases are often arthritis, autoimmune, or both, and we still have so many UNANSWERED questions about these illnesses. Are they genetic in nature? Is there something on Earth, in our water, food, land, air, that is causing so many more of us to become ill with these chronic diseases? It is almost unbelievable to actually think about the growing numbers of those (and especially once again women) at an alarming rate being diagnosed with autoimmune, autoimmune arthritic, arthritis, FM, CFS. MS. Myasthenia Gravis, and then the other "ailments" that follow along with these "main illnesses"... brain issues, heart problems, lung problems, bones, joints, spinal issues, and then with Sjogren's the "dental" problems that are so very severe so quickly, that within months, like myself you find you are losing every tooth to this horrid disease, and there is not a thing to do about it, but have dentures. You cannot stop it or even slow it down. I tried. I was meticulous with my dental health, always had been. but, even as meticulous as I was, also using the couple of medications available, along with keeping my mouth moist, chewing sugar free gum, you name it I tried it, yet I still lost ALL of my teeth in less than a year to Sjogren's. So, each and every person, whether you get to go to DC this week and tell your story, or you are sitting at home, possibly too ill to attend, and you do your "advocacy" work from your computer, you send emails, you send snail mails, tell your own elected officials, and not just "federal" but our STATE Officials, and even Local governmental officials need to be a part of this growing, ever enlarging issue of autoimmune illnesses, and rare diseases. All also goes along, with people getting the help they need, so they can afford their medications, they can afford and be seen by the proper physicians, they can afford the surgeries, or whatever their treatment needs to be, even like myself, trying to PAY out of MY POCKET over $15,000.00!!!!! cash for my dentures to be put in properly... there are not many people around with that kind of available money to spend in one whack at a dentist! THIS NEEDS to be PAID FOR MY HEALTH INSURANCE! IT is A HEALTH PROBLEM, NOT DENTAL THAT CAUSED ME TO LOSE EVERY TOOTH!!! But, we ALL need to stand up and say NONE of this is RIGHT, NONE of this is ACCEPTABLE, WE should have the medical, dental, eye and more CARE of PROFESSIONALS and experts that can help us live somewhat of a normal life. The ALMOST INTRACTABLE PAIN I've been in over the past week, SHOULD NOT BE!!! I SHOULD not have to wait, I should have been able to have my medication UPPED the next day, not a week later! I HURT! I HURT to the point, that it's stopping me from doing what I love the best, my advocacy, my writing, my helping others.... my taking care of my own home, shopping. and helping Jim and my Mom... ALL of this is just WRONG! AND ONLY YOU AND I can MAKE IT RIGHT! So, for ALL of you whether you will be in DC next and able to "stand on the steps of the White House" as I used to say, and plead my own case and the case of others that could not attend, or if you are home, and not able to attend you still MATTER! YOUR VOICE will STILL BE HEARD! We must RING OUT, CRY OUT, and say ENOUGH IS TOTALLY ENOUGH! WE are one of the MOST INTELLIGENT NATIONS in the entire WORLD! There is NO REASON that our incredibly talented researchers, doctors, professionals in these fields can't find solutions, but they need funds to get these types of things running and off the ground. Again, I wish ALL next week an incredible and memorable trip to DC. May your voice RING true for all of us... from patients, physicians, family, friends caretakers... researchers... may we FINALLY BREAK THROUGH the "thick headed" thinking of some, and get brilliant things accomplished! As tears roll down my face, I beg of all of you to stand up and tell your story... to stand up and tell a story of a friend, family member.... stand up and be heard!