Why I am not posting much or answering comments

Over the last few days I noticed I had malware on my blogging computer.   It refused to let me flush or clear my network adapters, and I was being constantly logged in to Texas unless I specifically moved it to another place.  Still even then I am not able to flush the network adapters on either the computer nor NordVPN.  I download and open a lot of stuff and stuff that I suspect might be sketchy, but I can normally fix it with minimal effort.  This one took more work and will be a few hours before I am fully back to full speed and power on it.

The video computer, the one I use to play videos on because it is a slightly less powerful CPU but has the same 16 GB of ram and the same medium priced graphics card, is not effected.  When I tried the network flush it works.  The plan for this morning is to reset the Windows and reload my programs.  But … the local Windows reset / reinstall did not clear the issue.  The second reset / Windows cloud based reset where it downloads a new copy of Windows, failed to clear the problem also.  So I got out one of the store bought Windows program install USB and ran it, wiping out the existing C drive entirely and formatting all other drives.  It worked, but this one is out of date by years so it takes a lot more updates and I have to redownload all my 100s of themes from Windows Store.  I also then have to download all my programs, including all my security programs and clean up programs.  So much work so I won’t be getting to comments until later.   I do think I know where the malware came from.  Of course the only way to prove it is to reopen the same files, and then if it is that, I would have to do all of this over again.  Not worth it right now.  I will just watch when I go to that site to see if it happens again and if so … well you know.   Have a great morning everyone.  Hugs.  Scottie

Some changes long past time due

As the title suggests I am making some changes to the way I deal with blogs I enjoy, comments, and email.  I have always signed on, quickly looked at the bell notifications, then got enough read / answered that if more poured in I wouldn’t miss too much.  Then I would do other things like email.  Often during this time or if I was not well I lost everything in the bell notification as it only allowed so many.  I was constantly missing comments, which in truth is more important to me than other things online.  Not sure why it has taken me to come to this change, except that if I am comfortable with something, I am the perfect frog in the pot of the hot water.  Now the water is hot enough I am forced to jump out of it.  

I love the blogs I follow, and I hate being rushed in reading them.   But comments on my blog have to come first.  I love them, I adore them, I am willing to put in the extra effort for them.  I do not want to miss any more of them.  So here is the change.  

What I did this afternoon works for me.  I had to do some other things and when I signed back on I was pissed that all my caught up stuff was no longer caught up, and I lost stuff.  What did I lose?  I don’t know, that is what bothers me.  So I went to the top of the bell and worked down finding every comment and replying.  Then when I got all them answered I went back to the top of the bell and got the new comments.  

Going forward when I get up and sign on, start all my systems, I will start at the bottom of the bell notifications looking for comments.  I will move up the list replying to comments.  Then I will check my email and answer that, something I have not really done since … well at least a decade ago.   Then I will go back to the bell notification and start reading all the grand blogs from the people I enjoy hearing their thoughts and leaving my own on.    During this I will go back to the top to check for comments.   If during this your blog drops off the bell notification list I am really sorry, I do love reading your blogs, but the list has gotten too long, my health is not well, and I just get too upset not keeping up.   To the point I keep hundreds of open tabs, I think the count right now I keep open is near 500.  I doubt I will ever get to them, answer them, or post them … some are news articles I wanted to post, but I save them with a hope.  I will be going through them catching the comment left two or three months ago, then delete the windows.  I just looked I am keeping tabs of blogs or comments from 3 months ago hoping to somehow get to them.  It is past time to stop pushing and punishing myself.  Ron is at his wits end on this.  I set my alarm and got up at 3 am to start today.   Yes I have to take breaks, and go lay down, I can only sit for five or ten minutes at a time, so I am up and down and laying down up at the desk, standing walking, sitting, going back to bed … I am exhausted and my health is failing, and Ron says one of the reasons is I feel driven by the stuff online.  I just am recovering from a stomach virus causing me to vomit all day yet when I could sit I was at the computer.  When my body drives me to bed I do it from my phone and tablet.  I read news and post it.  I put a keyboard on my old tablet to answer comments from there.  It is not the best but it works. 

So I am sorry if I miss your blogs.  I am sorry if you post something really grand I think needs to be shared.  I have to back off.  I have to set priorities.  I have gotten myself into a rut, pushing far past what my medications can hold until I am in tears trying to deal with stuff.  I fall asleep at my desk after telling Ron I am going to bed.  Then we argue about it.  

Anyway everyone gets the point, I am just flogging the dead horse and making my self out to be a martyr at this point.  That is not the case.  Sorry if I give that impression, but reading over this I feel I have.  None of what I do is anyone else’s fault.  I do it because I enjoy it and love it. These computers are my ability to move outside the walls of my home, to connect with a larger world.  I am addicted to it.  But like any addiction it is hurting me, so I need to curb it.  For example right now I just got up and walked around the kitchen because my right hip, the first hip I had replaced back in 2004 is burning, hurting, killing me so badly I am having to finish this sitting sideways.  What people don’t know is that how I do a lot of my online posts and comments.  I do a few minutes, get up and move, do more, go lay down, take more medications, get back to the computer.  Ron says my exercise regiment is how much I have to keep moving to help the pain in my hips and back.  

So let us all hope this gives me the chance to answer any comments without missing them.  Please keep them coming, I love hearing other peoples thoughts and ideas.  Plus as Ron says there is a bit of argumentive streak in me from the time I spent soaked in the bile and vitreol of the adotptive family.   Hugs.  Loves to all.  Best wishes to those who understandably don’t want to be hugged I was there once myself.  Scottie

Sweden’s parliament passes a law to make it easier for young people to legally change their gender

https://apnews.com/article/sweden-vote-legal-gender-law-minimum-age-9cfb3c6879ae03c3187f520eed308377

One of the anti-trans haters go to things is that the European countries are reversing themselves on pro-trans beliefs.  It is all selective misinformation and ideologically driven attempts to deny the progress in medical science / understanding over nearly 50 years.  Their goal is to roll society back to when the LGBTQ+ had no representation nor equality.  It is entirely to create the idea that trans kids / people and their best medical practice is wrong and shouldn’t be.  But this article again shows they are incorrect.   Just so those who are denying the progressive trend for trans rights in the European countries, a quote is below.  Hugs.  Scottie

Elias Fjellander, chairman of the organization’s youth branch, said it would make life better for its members. “Going forward, we are pushing to strengthen gender-affirming care, to introduce a third legal gender and to ban conversion attempts,” Fjellander said in a statement.

Last Friday, German lawmakers approved similar legislation, making it easier for transgender, intersex and nonbinary people to change their name and gender in official records directly at registry offices.


 

A view of the Swedish Parliament as lawmakers vote on the new gender identity law, in Stockholm, Wednesday, April 17, 2024. The Swedish parliament passed a law Wednesday lowering the age required for people to legally change their gender from 18 to 16. Young people under 18 will still need approval from a guardian, a doctor, and the National Board of Health and Welfare. The government of Prime Minister Ulf Kristersson has been split on the issue.(Jessica Gow/TT News Agency via AP)

A view of the Swedish Parliament as lawmakers vote on the new gender identity law, in Stockholm, Wednesday, April 17, 2024. The Swedish parliament passed a law Wednesday lowering the age required for people to legally change their gender from 18 to 16. Young people under 18 will still need approval from a guardian, a doctor, and the National Board of Health and Welfare. The government of Prime Minister Ulf Kristersson has been split on the issue.(Jessica Gow/TT News Agency via AP)

BY JAN M. OLSEN
Updated 12:17 PM EDT, April 17, 2024
 

COPENHAGEN, Denmark (AP) — The Swedish parliament passed a law Wednesday lowering the age required for people to legally change their gender from 18 to 16. Those under 18 still need approval from a guardian, a doctor and the National Board of Health and Welfare.

No longer required is a gender dysphoria diagnosis, defined by medical professionals as psychological distress experienced by those whose gender expression does not match their gender identity.

Sweden joins a number of countries with similar laws including Denmark, Norway, Finland and Spain.

The vote in Sweden passed 234-94 with 21 lawmakers absent, following a debate that lasted for nearly six hours.

Sweden Democrats, the populist party with far-right roots that supports the government in parliament but is not part of the government, opposed the law.

Jimmie Akesson, leader of the Sweden Democrats, told reporters it was “deplorable that a proposal that clearly lacks the support of the population is so lightly voted through.”

But Johan Hultberg with the Moderates of Sweden’s conservative prime minister, Ulf Kristersson, called the outcome “gratifying.” Hultberg called it “a cautious but important reform for a vulnerable group. I’m glad we’re done with it.”

Kristersson’s center-right coalition had been split on the issue, with the Moderates and the Liberals largely supporting the law while the small Christian Democrats were against it.

Peter Sidlund Ponkala, chairman of the Swedish Federation for Lesbian, Gay, Bisexual, Transgender, Queer and Intersex Rights, known by its Swedish acronym RFSL, called the law’s passage “a step in the right direction” and “a recognition for everyone who has been waiting for decades for a new law.”

Elias Fjellander, chairman of the organization’s youth branch, said it would make life better for its members. “Going forward, we are pushing to strengthen gender-affirming care, to introduce a third legal gender and to ban conversion attempts,” Fjellander said in a statement.

Last Friday, German lawmakers approved similar legislation, making it easier for transgender, intersex and nonbinary people to change their name and gender in official records directly at registry offices.

In the U.K., the Scottish parliament in 2022 passed a bill allowing people aged 16 or older to change their gender designation on identity documents by self-declaration. It was vetoed by the British government, a decision that Scotland’s highest civil court upheld in December. The legislation set Scotland apart from the rest of the U.K., where the minimum age is 18 and a medical diagnosis is required.

My wonderful brother Randy sent me a gift

For those that don’t know starting in 2013 my childhood abuse started to crash over me.  I struggled daily to work and keep it together but I had started to again self harm.  I would take a very sharp blade and draw it across my forearms and watch the blood flow.  Yes the feelings when I did that released good endorphins.  When Ron found out, he took to hiding knives, especially all his X Acto tools he had for the crafts he had.  But he forgot about my long time pocket knife, a jack knife I had had for a very long time.  I kept it to a razor edge.  

But in March 2014 I fell into total breakdown.  I wanted the memories to stop, I was reliving them constantly with full emotions and body feels including smells along with tastes.  I was close to choosing to end my life.  I was doing my best to hide it from Ron, but by this time I was refusing to leave my bedroom other than for my pain doctor visits, which Ron who was working 12 hour night shifts would take me to.  

This is where Randy stepped up, became my brother and maybe saved my life.  Randy had entered my life earlier and was a grand online commenter to my first blog and we formed a great friendship.  Randy is a really great writer, and anyone that has read his posts here knows he can write very well.  Far better than I can.  He started to send me his stories and I enjoyed them.   Then he sent a story about a man in a food court saving an abused child.   It triggered me into a bad episode because of the break down I was dealing with.  

I was very upset and wrote back to Randy about how his story was great and so real to life it had triggered me badly, and I was really struggling.  Randy right away reached out to me online apologizing and eventually as we kept talking he asked for my phone number.   This was before my total melt down when I started hurting my self.  Randy and I talked on the phone … which was rare for me.  One of the worst beatings I got as a kid was reaching up to the ringing wall phone and going to hand it to the adults there.   I was never to use the phone.  It was beaten into me.  Never touch the phone.  I now realized they were worried I would report my abuse.  

Randy and I got to be close friends.   Then when I started hurting my self, deeply cutting my arms, refusing to leave my bedroom, and wanted to die, Randy who was working 12 hour night shift in a hard job would have his phone on so if I felt myself slipping I could call him.   Hour after hour he talked to me, denying himself sleep as he kept me grounded.  I could call him anytime … and I did as I was about to use the knife on my skin I would put it down to pick up the phone.  I talked to him about everything I never told anyone.  I poured myself out to him and he was there.  He was the brother I really desperately need but never had growing up.  He became my brother in every way that ever matters.  

I tell all this because I have been under the weather and Ron just lost his brother.  So Randy sent me a gift.  He is a grand brother.   He sent me an insulated cup.   Here are the pictures.   Randy is one of a kind.  He does have a grand sense of humor.   I love him.  

IMG_0810IMG_0811IMG_0812IMG_0813

Well it happened again

Hi everyone.  It happened again.  With Ron gone, I had to go shopping Wednesday.   Yes I went among humanity or as some would say “the unwashed masses of heathens”, or as I say people like me.  And Friday I started to feel bad, crappy, shitty.  Sure enough I woke at 3:20 am ill.  I was sweating, congested, feeling like I needed to vomit, then have three times today.   I am getting so I hate going out.  Almost every time I get sick.  And it is not like I am going up to people and face snogging them.  I respect personal space, I try not to catch anything.  Well the consequence is yesterday and all day today I have not been able to get to the comments.   I doubt I will get to many today, I can hardly sit here and read.   Ron will be home tonight about 10:30 or 11 pm.  I had wanted to clean the house some.  But I have barely been out of bed.  I already feel the need to go back to bed and I have only been up about an hour.  So again as always if you leave a comment that I don’t respond to in a few days (I seem to be almost always two days behind) please recommend, send me a not telling me, anything.  But if you send me an email please tell me in the comments of any post.  I find email the biggest pain in the butt, just a bit less annoying than fussy cats.   Best wishes, respect, loves, and hugs to all.   Scottie

They left about 4:20 am

Ron’s sister Diane got a flight to our local airport, she arrived Sunday night at just after midnight.   Monday was spent making plans.  This morning we all got up about 3:20 and they got ready, packed the car, and left for North Carolina.   It will take them 12 hours to get there.  They need to collect the brother’s belongings, sign forms, deal with the crematory, get death certificates, and so much more.  Then Diane will fly from North Carolina to New Hampshire, where she has a summer home.  Her husband will meet her there later.  Ron will drive home alone.  Hugs.  Scottie

An update on Ron’s brother and the dryer.

Hi everyone.  First I want to thank the commenters on my first post about this.  I want to get to your comments next but I had to rush through things this morning not to lose older comments.  Plus the home here has been in a bit of turmoil today.  

First Ron’s brother.   Ron and I both woke early.  I woke at 3:30 and he at 4 am.  We both know that is the time a lot of dying people pass in the hospital.  Ron said it has something to do with the body / heart rhythms at that time at night.  But I wonder.  But no call came.   So after hugging each other for a while we got up.   I am trying to be as supportive and understanding as possible, but Ron has slipped in to professional mode on this.  I guess it is because he knew it was coming and made peace with it.   At one point he asked me if he was wrong 3 years ago to have told the friend of his brother who his brother was living with to call the medical emergency services to take his brother to the hospital.   But I reminded him that it saved his brother’s life and once in the nursing home he did get a lot better for a while.  I reminded him then we all knew his brother did not have long to live.  

Ron talked to the hospital hospice staff.  Unlike our hospital system where hospice and the hospital were in separate facilities, where his brother is they have a hospice unit in the hospital itself.   The staff there have been great at keeping Ron and his sister updated on the brother’s condition.  So yesterday I wrote he was breathing once every 3 minutes but the intervals between breaths were increasing.   They have reached the stage of about five minutes apart.   Which means his brother is basically brain dead and his body is running on the brain stem only.    His heart rate is down to 30 beats per minutes.  The staff told Ron that it was only a matter of time, but they did not feel he would last the day and he wouldn’t see the morning if he did.   If this was the ICU I worked in, we would have someone with him as a death watch.  The patient’s bill of rights in Florida says no patient should die along, so we find someone to stay with them.   When no family has been available or other person, I have done that my self.   But I don’t know the rules for hospice.  

Side note.  One of the last functions of the body to go when dying is hearing.   So when I would stay with a person dying I would talk gently to them, saying things like it was OK, they could rest.  I would hold the person’s hand.  I would just be there until they died.  It was the best thing I could do for them at that point.  I am not religious and I believe the dead no nothing, what we are ends.  Others have their own beliefs.  But I do believe that it is a comfort to people dying if someone is there and offering loving comfort.  I once told someone who was holding on “I talked to your family, they are safe, it is ok for you to go”.  The person passed right after I said that.   Coincident?  Well science says so.   Me … Kindness to those in need is its own reward!

The dryer we were able to fix this morning.  Ron went to an appliance parts store.  The person he talked to said the dryer we had was one of three national brands that seem to last forever with only minor things like this 20 dollar switch going bad.  But because both Ron and I struggle these days I had to help him get the new switch in, get the dryer vent hose on, and get the dryer back in place.  It tore me up and I wouldn’t have been able to do it without just having a steroid shot, the spine shot I got.  But after I struggled to breath, my back muscles are so tight I struggle to stand the pain, my legs right now are very shaky and can’t support me more than a few minutes.  I am using my canes in the house, something I don’t always have to do.  When we got done, Ron was very concern, he was thanking me but insisting I sit while he watched me.  He said my breathing sounded like a steam train.  Rapid in and out with difficulty.  That was true, I was struggling to get air into my lungs, my breathing very labored.  He wouldn’t leave me alone until my breathing became more normal.  

But the dryer works including the light which stopped working months ago due to the switch malfunctioning.  But before I can use it to fix / finish the bedding I had been washing, I came out of my Pink Palace to find Ron sound asleep in his recliner and he did not have his C-pap on.  That is very dangerous for Ron.  He has sleep apnea.  He stops breathing in his sleep.  I struggled to wake and then we got him into bed.  It has been a very stressful time for my wonderful 69 year old husband.  

Thank you to everyone who follows my Play Time, to everyone who cares for others and for Ron and me.  To everyone who comments.  And generally I am thankful for people who care about others and show it with kindness.   Best wishes, hugs, and love.  Scottie

Life by crisis, another clod hits the fan.

Long time followers / readers may remember the struggle we had getting Ron’s older brother in a nursing home as he lost touch with reality and couldn’t care for himself.  He actually knew it was happening and drove himself to the VA to get help, but it progressed so quickly.  The VA stabilized him and sent him home, but he got both physically and mentally worse.  He is a long time cancer survivor from the time when they over radiated cancer patients, causing his intestines to harden and die, requiring many surgeries to remove them to stop internal bleeding.  So he got so bad he was constantly bleeding out from his butt and pooping everywhere along with not being mentally able to clean himself, up after himself, or even understand the issue. 

Ron and his sister worked hard to get him into a nursing home that could care for him.  It took a lot of money, his sister had to pay over 5 grand for the first month to even get him into a nursing home.  Medicaid rules said a person had to be in a nursing home for a month before they could be covered my medicaid and medicare.  Ron’s brother is very low income so he got a small $100 supplemental income from the military for his illness in the military, and had medicaid.   But because he was on medicaid he couldn’t have a lot of assets and the nursing home would take all but 30 dollars of his income.  Which meant Ron and his sister would have to put money into his bank account every month to pay his credit card bill, other expenses, give him extra money in his home account to buy treats and stuff, and his car insurance.  The other siblings despite having far more money than Ron and I simply couldn’t find it in their hearts to help pay their brother’s bills.  One sister tried a few times to help, but she was losing her own grip on the world and couldn’t figure out how to do it or would forget, so Ron and his other sister just started covering the entirety themselves.  The paid off his card and sold his car.  They had to stop his military supplement because that would have put him a few dollars over the Medicaid limit, and Medicaid was paying for his care.  His brother went into the nursing home the end of 2019 or beginning 2020.   That required twice a year expensive trips to NC.

Ron would drive up to NC and get a hotel room just outside the airport.  Ron’s sister would fly into the airport and they would go to the town that the nursing home was in and get a hotel room.  They would spend a week or so with their brother, buying him clothing or things he needed / wanted.  At first they bought him electronics like phones but he was unable to use them and they realized that was useless.  A year ago they moved Ron’s brother to in nursing home hospice care.  And at some point they started doing Zoom calls every couple weeks first with the brother and family done by the home staff then hospice staff included.

While writing this Ron was heading for a nap.  I went to restart the 17 year old dryer as it had stopped.  It wouldn’t start.  I looked and the door switch which had been getting flaky the last year gave up the ghost.  It had all our only deep pocket bedding for the Purple mattress we bought.  So no nap for Ron, he got up, together we pulled it out, he is cleaning it and trying to figure out how to get to the switch.

Over the last 3 and half years his brother got worse.  Sometimes he would go months tracking reality, but then he would slip and lose touch with the real world.  This year he has been out of reality, and a lot of the time his health was so bad he couldn’t really hold himself upright and needed support.  Ron and his sister started getting calls this last month that his brother got out of bed during the night without calling for staff and tried to go to the bathroom by himself.  He can’t walk.  So he falls.  It has happened I think three times.  The first were minor but this last time was serious.   Remember this is a nursing home, not a prison and they couldn’t restrain him in bed.  

This time he fell and broke his leg bone right at the hip joint.  The home and hospice people called Ron but they did not know how bad it is.  He was so bad that when Ron authorized him to be taken to a hospital, the hospital called him and said he would only last a couple of days and that he had internal bleeding they couldn’t trace that may have been going on for a while.  His brother had the issue with his intestine hardening and getting so brittle they would tear apart.  The last few years the doctors removed as much as they could, but it was dicey if anything they stitched to would hold.  That was yesterday.  Ron and his sister were making plans to quickly go see him.

They may have just run out of time.  As I am writing this at 2:32 pm on 4/10/2024 and while Ron was working on fixing the switch from the dryer the hospital called.  His brother was stopping breathing and then after a few minutes would suddenly take a breath.  The intervals are increasing as they watch him.  Remember that he is on hospice, we knew he was dying for the last few years and so while all comfort measures can be given, no lifesaving care can be.  No intubation nor resuscitation.  We just had no idea it would be this soon or Ron and his sister would have gone to see him again.  But normally a hip or upper leg break is hard for an elderly person to come back from, most people in their 80s who break a hip die soon after.  

Ron is on his phone, but 17 years working in ICUs tell him his brother has only hours to live.  The nursing staff at the hospital agreed.  There is no way short of a Star Trek instant teleporter that Ron could get there in time.  He so far is calling people and holding it in.  But he is going to need all my sympathy and support tonight.  Thank you everyone.  But I may be a few days before I get back online depending on how much Ron needs me.  He comes from a large once very tight family, 8 siblings.  He has handled the loss of the older ones but it gets harder for him as he ages and more have died.  He may need a lot of support.  Best Wishes.  Hugs.  My love for all of you.   Scottie

My spine shots (epidural steroid injection)

I take epidural steroid injections in between my steroid muscle injections.   It is a hard choice for me.   I have weird bones; in some places they grow too thick. in other places my bones are way too thin.   I try to limit the spine ones until I cannot stand the pain and must do it because they are so painful.  I have had to have three in the last 4 months.   This time was the most painful epidural I have ever had.  It was the first time I have ever cried out on the table.  I was struggling so hard not to move despite the pain.  Remember I take 2 kinds of morphine and muscle relaxers at the maximum dose allowed by the state of Florida, along with 800 milligrams of Ibuprofen.  I used to take stronger ones before state legislators felt they knew more than my doctors.  

First I waited more than an hour and a half before the doctor actually came into the room.  They are horribly understaffed, and the state of Florida makes providing pain relief care as impossible as possible.  Everything from restricting medication to requiring frequent visits, which means more costs for the poor people needing the service.  I used to go every three months, get my medications prescriptions.  I now must go every two months and my medications are restricted causing me to be in even more pain.   Since the next pain medication level for me is Fentanyl and I talked to my doctor again today and told him I am very scared of it.  I need more pain relief, but he understood.   He thought there might be one kind of muscle relaxer that might help me more.   I am already on maybe the most powerful one that the state will let them give me at the max dosage.  I was on one that worked great and helped me a lot but again the state legislatures make it illegal for doctors to prescribe it in their attempt by republicans to look tough on drug crime. So he changed that medication after he gave me the shots.

Back to today’s procedure.   I got there and checked in.  I have been going there so long I am very friendly with the check in and check out people.  I talked at length with (name redacted … out of respect for others, I won’t use their names.) the check in woman.  Because I really genuinely care about people, I often get in to conversations and become very friendly with people I interact with.  I noticed she seemed tired and bothered, so asked her if she was OK, was she sleeping Ok.  She told me no.  She had another death in her friendship circle.   She has suffered that a lot over the last year with many deaths of close friends and family.  A friend of the hers had been walking at night, got hit by a car that did not stop to check what they hit and simply called the police to say they thought they hit something.   An ambulance crew found the man just in time, he had to be resuscitated and returned to life, but he is in critical care.  She, her husband, and some friends went out and found some of his stuff but by the locations of his things including parts of his bracelets he was hit hard and maybe dragged.   She couldn’t sleep because her mind wouldn’t disengage and let her sleep.   Boy do I know that.  So I let her talk and express her fears.  I expressed my deep well hopes and well wishes.  It doesn’t take being religious to care or empathize with others.  

After being in the waiting room for a while which I think was not too long, I read some news, posted a few news stories, read some of my books on my tablet I was called in.  

I was not given the normal check in where they do your weight and your medications, so I had to make sure that my restricted medications were reapproved.  As I talked with the woman doing this I complimented her on her purple colored hair.  It was clear she struggled to grow hair and she tried to make the hair she had stand out, so she was delighted to talk to me about the color.  I told her I thought it was great, that I loved the color, which was the truth. I enjoy people exploring being different.  It shows personality and style.  She was delighted and happy.    I waited in that room a bit over an hour.  

Now many might be upset with the time I waited, and it is not right to make patients do that.   But the truth is, it is not the doctors and providers making us wait.  It is the constant need for more profit by corporations.   It was not like this before my doctors were forced to sell to a large health company in California.  They are always pushed to do more, see more patients, and always short on staff.   While I understand that people who work cannot tolerate such waits, most of those in my condition don’t work so our time is our own, so we can give it when we need to.  The only problem I had was the sitting in their chairs was painful, so I had to stand, sit, readjust, and so forth to deal with it.  

Short side note.  One time I was there I waited more than an hour.  My normal provider I love and have followed to every office she moved to was covering for three providers.  She was running an hour behind because of this.   This is the same woman who is the only doctor who gives me a hug both when coming in and when leaving.  She knows the most I have ever told any doctor of my abuse, and I needed to because she noticed the self-abuse on my arms.  When she opened the door to my exam room, I heard a woman come out into the hallway and yell at her / everyone that she had been there almost an hour and shouted abusive language demanding to be seen.  My favored normal provider is elderly, she had already gone to semi retirement of only part-time, she stays simply because she is like me, she cares. She had returned to full time to cover for a fellow ARNP who had gone out on pregnancy leave.  She told the woman the situation yet when she came into my room she was visibly shaken and stressed.  I told her immediately to take a few minutes to decompress and relax, as I was not in a hurry.  She smiled, relaxed and we hugged.  That is what it means to see others as people, as humans like yourself, to accept and acknowledge their needs.

Back to this morning.  When the young man … so many people in professions are to me these days.   Young I mean.  I followed him.  I had to remind him I couldn’t walk fast as he raced into the room, but he came out and apologized and told me to take my time.  As it happened, I had a lot of time.  He got stuff ready; I took the stuff out of my pants pockets along with taking off my glasses, put my hair in a ponytail, and he told me I could get up on the table.  Damn if I knew it was going to be another thirty minutes I would have waited as the table is painful for me.  He went out twice to check on the doctor and said the person the doctor was seeing must have lots of questions.  I told him that was OK as I appreciate it when the doctors / providers take their time with me.  There is simply no way to do the 10 minute visits the corporations demand to increase profits and give decent care to those in need.  

Side note.  After this doctor sold his practice which was required because a large hospital system screwed them out of 8 months of billing hours, the new company required him to see non-spine shot patients between each shot patient, plus do all the medications needing physician sign offs that day.  He seriously almost runs from room to room.  Yet once in the room he gives his all to the patient.  It is what drew me to his practice in the first place, he is like me, we truly and really care about people.  

And in true fashion, that same doctor gave me the time and attention to address my needs.  But this is the first time I ever cried out when given the spine shot.  I have had a lot of these, I knew the drill.  Plus, I am used to pain.  First from childhood abuse and in later years with my body failing, which my first orthopedic surgeon blamed on the trauma done to my body / bones from that abuse.  I never told him of my abuse but by my scans he already knew.  I am paying every day for what was done to me so long ago.

So when the doctor put the numbing agent in, I was prepared for the pain, the sharp sting.   But what followed next was more than I was used to.  My injections seem to be in three parts but that maybe just how I feel them.   First is the sting of the needle to inject a numbing agent.  Then the second needle to drive the guide needle into the spot.  Those are painful on an increasing scale, the stinging needle I handle easily, the guide channel is really painful but I bear it without moving, I have had a lot of experience doing that in my life.  Then comes the largest syringe of medications.  I get to see them draw it up, it is a mixture of at least two different stuff.  

This time when he put the guide in it was really painful, but I took it.  As I said I have known pain all my life.  He is the kind of doctor that seems to feel your pain and discomfort and talks you through it.   I told him I understood how important it was to remain still and not tense up. Like I said, I get these a lot.  He told me the nerves were really inflamed.    But when he went to put the medication in … The pain was horribly crashing over me and increasing.  For the first time I cried out, saying “flocks” as I desperately tried to stay still.  Every part of my body demanded I move and it took all the will power I had to stay there and let it happen instead of trying to run away.    The doctor was talking to me trying to explain why this time was so much worse than the others, but I was struggling to hear / understand him.  I again cried out “Oh good golly miss Molly” Seems the nerves in that spot were extremely frayed / inflamed.  It felt like he had inserted a golf ball into my spine.  When I said that the Doctor agreed with me and offered me comfort. 

As to the choice of words to cry out.  I am not normally a vulgar person, I had enough of that growing up.  While I don’t believe in bad words per say I know others do.  Even in great pain I tend to use the words I like to express it.   After all that is what curse words are, our expressions.  

Being the great caring doctor he is he did not rush out of the room to his next patient.   He talked to me, made sure I was OK, we returned to the conversation I had with him the last time he gave me shots.  We had been talking about my muscle issues and he even took the time to go back into my chart to find a new medication that might help me.  When I told him how painful the two muscles along the side of my spine would get and then told him they were not so painful today as normal, he kept asking me about it.  I described how they can get as raised as my fists and as hard.  What I did not realize is like the last time he gave me spine shots he mentioned how swollen they were, they were also swollen this morning.  I just get so use to the pain I don’t realize how mind numbing bad it is.   As I said he took the time to go through my chart and look at my medications and prescribed the only one left he thinks will help. 

 

I was in so much pain I could hardly drive home.  I had to have Ron help me into the house.  This morning, Tuesday, my leg muscles are so sore from me tensing on the table during the procedure that I can hardly walk.   I will take it easy today.  Ron just took the bandage off my back and he says that the needle mark / hole is really big.  Hugs.  Scottie

Yesterday I almost caught up. But today will slip

I was with in 8 notifications of totally clearing my notifications before I just had to quit.  This morning I will try to get caught up, but I have more spine shots this morning.  So the day might be a wash for me.  But there is always tomorrow.  I hate the spine shots, they are even more painful than the trigger point muscle shots I get.  Plus the position on the table is painful for me.  But it has to be done.   See ya all soon in the future.   Hugs.  Scottie