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

And Ron made a grand supper and I am falling out.

I love all our viewers and I really love sharing the news / things I know.  But as I often say with the strong medications I take and food working against my diabetes, I tire out in the late afternoon.  It is now 5:30 pm where I am.  And after the wonderful meal Ron made, I am crashing. So after posting this I am off to bed.  Where I have been assured by my 34 year long spouse he will be joining me soon … He made it sound like a promise was implied.  I like that … after I rest a bit and wake up. 

I helped a couple of hours before he got ready to cook, I took out the condiments of many things that one of us puts on their burgers, chicken burgers this time.  I got out pickles of two types.  Both sliced and full baby ones.  I got the lettuce out, I got the condiments out, which for us was mayo, mustard, two kinds of pickles both sliced and whole, ranch dressing, salt and pepper, lettuce, and maybe a few things can not think of such as which cheese either of us likes.  We don’t use the same condiments, but we both hate them refrigerated super cold.  The chicken burgers were wonderful!!!

As there were no potatoes or other ingredients, all I had to do was wait for the food bell.   Ron cooked the chicken patties in our grand deep fryer.  Here is a picture of the two sandwiches I had.  Yes it was a lot, but it was the most I had had all day.  So I did not over eat.   Hugs.  Scottie

Scotties chicken burger.

Bewitched and why

Ron and I are both under the weather.  Yesterday we both had sinus problems, breathing issues, along with stomach problems.  Plus chills.   This morning I woke up at 3 am with my stomach in distress and that soon turned into … well let’s say something not discussed in polite society.  

Wednesday I went to a doctor’s appointment and Thursday Ron went to a bunch of stores.  Also I had to go to the pharmacy.  So of course any time I with my system goes out into the “unwashed masses” I get sick.  We are debating who gave this to whom.

Last night I went to bed at my normal time of around 5 pm, But I was surprised when Ron soon joined me.  He normally comes to bed at around 10 pm or an hour later.   But he explained he was not feeling well.  

Neither of us felt well and did not have supper.  Well today I got up as I wrote at 3 because by 3:30 am I was sitting on the toilet, something that happened for the next few hours.  Ron got up, did the same, and then went back to bed.  

Only now at around 4 pm are we starting to feel well enough to eat.  Ron had made bake and shake n bake pork chops last night that neither of us felt up to eating.  We had them tonight with some leftover potatoes and brown gravy.  

I am feeling a lot better, but still feel worn out.  Ron bounced back again much faster than I did, but that is normal when we both get sick.  I am seriously tiring out.   

I offered to help Ron clean up, he said he has it covered.  I want desperately finish as many bell notifications as possible before going to bed, even though I am very tired.  

Which leads me to the name of this post.   Because I was watching lots of videos and news stories and got tired, so started watching a Bewitched clip that came up on my YouTube feed.   Ron and I laughed at the clip and talked about the house.   That clip lead to full episodes, none I had ever seen before.   I spent the last few hours watching Bewitched and admiring the house and the great actors / actresses.   

Hugs.  Scottie

Saddly it has happened that …

I tried from the time I got up, every minute that I could stand to sit in my chair before the pain drove me out to my bed or to at least move.  But still I am 2 days behind on the notification bell of blogs I follow and more important … My beloved comments.  I simply have run out of steam.  Ron brought me a supper of a huge roast beef / gravy sandwich which he admitted he knew was far too much for me.  He then cut it in half and added a few of the fried sliced potatoes, which are grand when hot, not such when cold.  Yes he loves me but he is on a kick to try to get me to eat more, which I don’t want.  He can eat as much as he likes, I never judge, but he seems driven to get me to eat more all the time.  In our last A1C tests his blood sugars were high while mine were very low.   Oh well.   I am not judging as next time it could be reversed. 

But the point is I have run out of steam.  I am tired to the point where every other key I hit seems to be the wrong one.  I need rest, the medications, pain, and the other stuff have had their say.  Love each one of you but sadly it ends here for today.   Good news, I will see you in the morning.  Normally the pain drives me from bed by 3 or 4 am so I might catch up then.  Hugs, loves. Scottie

Running Without Sound – Gay Short Film

Coming to terms with who we are is hard enough to tell people, but for Sean he must come to terms with his exploration in a world that he cannot hear and a world that does not always hear him. A fascinating story of love, trust, and friendship.

I often wondered what my life would have been like if I had been a kid in the modern age where being gay was so much more accepting than it was for me in the 1970s with Anita Bryant spewing her hatred and lies about people like me.   Then I remember that today there are the Libs of TikTok and the red state governors / republican fundamentalist Christian legislators who are doing to LGBTQIA kids what was done to me back in the 1970s by Bryant.  Spewing lies and hate to make us hated as much as possible.  

But there is another part of my thoughts.  Like the boy in the short video I couldn’t find the spoken words to tell of my abuse and the signs I was showing people either they couldn’t hear or did not want to.  What if I had had the words to say as a four-year-old what was happening when I was asked to go next door, that even though the man was nice, kind even, it left my butt sore, and the hell spawn I lived with would make fun of me for it.  They knew, which makes me now believe the adoptive parents knew also.  Maybe they pimped me to him?  After all, someone had to tell me to go over there, to give me permission.  Yes the man was raping me.  But he was kind and nice to me.  Unlike at home.

Imagine as a 6 yr in first grade, in torn clothing who had bruises all over me who in class just put my head down on my desk and went to sleep because I knew there it was safe to do so because no one would hurt me.  To my little boy mind that was shattered when the teacher took me to what seemed to me a large room with some other adults.  Both male and female.  They asked me to remove my clothing.  I started to obey as I had learned not to disobey that demand … but when they told me to remove my underpants I started to cry, to sob.  I promised to be good, I promised not to sleep in school anymore, I begged them, I even said as I stood there after taking off all my clothing and they had me move in different ways while touching me to make me stand or show what they wanted to see, that I promised I wouldn’t tell as they asked me questions I dared not answer.  I kept repeating that, hoping they knew that I would cooperate and not tell so they would be nice when they used me.  They did not understand what I was saying when I said I promised not to tell.  I knew the punishment for telling, I did not know they were trying to help.  They scared me, because these were adults I did not know and the few times before with adults I did not know first what they did hurt really bad.    I simply did not have the words, I did not understand what they wanted, and I had no way to tell them what they wanted to know, yes I was being abused, I was being hit, I was being …  In a way that was somehow more traumatizing to me because in my 6 yr old mind I was about to be forced to please and give my body to these four or five adults … If I was lucky and they did not want to simply hit me to make me hurt even more. 

If only I could have heard them, and they could understand that which I had no voice to say.   I am really tired, I hate that just watching a short YouTube video can bring back such strong memories, making me feel those feelings, relive those events.    Hugs.  Scottie