Showing posts with label YMCA. Show all posts
Showing posts with label YMCA. Show all posts

Monday, August 3, 2015

Why yes, I'm ecstatic!

Sarcasm!

Forewarned this post may be a bit if a rant.

I saw my son yesterday. He's a mess. He has obviously been in the same cloths for a long time. He hasn't showered or even washed that I can tell. He hasn't been taking his medications. I'm pretty sure he has been smoking marijuana.

Hubby and I picked him up to take him and get cigarettes. First we had to go to the bank so that I could transfer him his $314 that I owed him from disability. The whole time we were with him he was clenching his fist with all of his strength. I knew when I saw this that he wasn't taking his medications. At one point hubby said he asked my son why he was doing this and my son replied that he was trying to make his body work right. His brain isn't working right so his body isn't going to. He ended up giving me his bank card so that I could buy the smokes for him because he couldn't 'catch his breath' to get out of the car and do it himself.

I told my son that once we got back to the shelter I was going to go in with him so he could get his medications and put on some clean cloths. He said ok. As soon as we walked in to the shelter... Hello ODD. His defiance came out of nowhere. He didn't want his medications. One of the staff said they have been talking to him about showering etc however he 'bolts' or leaves the shelter.

Hubby and I have been talking about what to do. So far we haven't come up with any solid answers. I try not to get pissy with him when he asks me what I'm going to do. But seriously, if I had the answers I would be doing it. I don't have them... I don't know what to do.

I know how much I wanted to grab my son's stuff and bring him home.

Here's the catch. I'm a recovered addict. If I want to stay a recovered addict then one thing that I need to be able to do is think things through to the end. One of the problems with being an addict is that the mind only wants to see the good parts of using. Not the negative consequences and as long as one can keep blocking out those memories then one can keep pretending that using is ok.

I forget the exact wording of what was said during an ADAPT meeting but something along the lines of: An addict will not change until the pain of using is worse then the pain of not using.

I can bring him home. He has over $300 in his bank account. He is unstable and defiant. He believes he should be able to smoke and drink in his room. It doesn't take a genius to figure out where that scenario is most likely going.

I had already said to my husband that I need to bring him home if I can put some things in place. Before I left I tried to talk to my son. I wasn't expecting it to be an in-depth conversation considering his mental state. I got worse then I was expecting. I went to crouch/sit beside him and he got mad and told me to stand up and talk to him. I don't know why he gets like this with me. I mean the not wanting me to talk to him on his level. It just goes against everything that I have read on how to talk to someone experiencing psychosis. Especially since he gets so defiant with me being the main disciplinary. Yet he still gets mad, doesn't want me on his level and wants me to take the authoritative stance. The only thing I can reason is that somewhere in his head is a recognition that he actually needs someone to take on the role of authority for him. But then his ODD gets in the way...

I asked him if he remembered talking to his Nana about not going out there. Yes. I told him that I want to take him home however I can't if he has control over his money to buy alcohol because alcohol is killing him. I want power of attorney. He refused.

A couple of days ago I received a message from his grandmother stating that she had told him no to him coming there and she hoped that made everyone happy. Needless to say I didn't respond. The sarcastic side of me wanted to answer with: Why yes, I'm ecstatic. Thank you! I figured not answering was the better option.

My daughter calls to find out if I got the message and to include the side-note that obviously Nana didn't really mean it and that she would step in and take him if she felt it was necessary.

As far as I know that plans are/were to have my son go directly into a shelter out there. So switching one shelter for another? Then I guess work on getting him into his own place since this is what he wants. Well it's what he says he wants. He knows full well that once he gets there he can say no to any form of assisted living and that if he does that then he will end up with Nana. The ideal situation for him. He doesn't have to care about anyone except himself. He doesn't have to try to be sober and stable. To be blunt, he doesn't have to try period. He will get his pat on the head while someone else cleans up after him and protects him from himself.

The rant. Can you see my son living on his own?! He can't even keep himself stable when he is living somewhere that is feeding him and providing him with basic amenities. Yet that is what him and his grandmother seem to be concocting between the two of them. Unless he is telling her that he will go into a group home out there. If that is the case and it is being believed I can only shake my head some more.

My son, in my opinion, needs several basic things. Mainly he needs long-term treatment for addiction. By long-term I'm thinking 3-6 months to start. He needs help from non-family, so he can't use and manipulate them, to help him become stable, stay stable and learn to mature and grow up. Until he gets these things. Everything else is just prolonging everyone's suffering, including and especially his own.

My son isn't stupid by no means. When I had the police take him, one of them went with him to his room to collect his things. My son was very drunk. Not as drunk as I thought. He made sure to disconnect, unplug and turn off the laptop so that I couldn't have access to it. Before leaving he wanted my phone to call his Nana. I know some may think: Well yes she is the one he knows will support him. Hmm. The one that will support him or enable him. There is a big difference.

Honestly he has support coming out his.... ;) Agencies and people just waiting for him to give the go ahead and they will be right there. PACT has peer support, group support and vocational (job) support. ADAPT has addiction support. Applications have been started for housing. He has an open file at the YMCA for free schooling at his own pace. My son is 21 and says no thank you...

He also has me and my husband. Apparently I expect too much. Expecting Michael to follow basic rules that a 5 year old can follow, clean up after himself, treat me with respect, not be violent, try to be medication compliant and engage is addiction services is apparently too  much for him. How do you respond to that? Seriously if he is that bad off then he really should be in the hospital with 24/7 care not traipsing on a plane across the country!

Where we are at now is not new. He has been here before. He has played the system, played and manipulated emotions until he got what he wanted. Freedom from responsibility, stability or sobriety.

Do you think he doesn't know that if he doesn't participate in recovery plans here that in time he will get what he wants? Of course he does. Like I said he isn't stupid.

Something I had too look at and acknowledge was/is that his masturbation episodes are tied into his alcohol use and not his schizophrenia so yes it is more behavioral. I didn't know until I found out about him calling dial-a-bottle that he was during the time of his masturbating frequently and in public, drinking almost a bottle of alcohol a day. I also found out that one of the ladies at the shelter caught him doing this in public and had to talk to him about it. I didn't tell her that I knew that he had purchased a bottle of alcohol since being there. Just like I didn't tell them that I'm pretty sure he probably has marijuana on him. Maybe that is why he bolts when expected to shower and change cloths? He keeps his jacket on and close to him when he is hiding stuff.

There is also the distinct possibility that if he gets himself kicked out of there then in steps his safety net. I may not be actively stopping this from happening however I'm certainly not going to help it happen.

Of all the blogs that I read. Jagged Little Edges is without a doubt one of my favorites. Lorelie doesn't hold any punches on what addiction is and the truth of it's ugliness is spelled out in black and white. Lorelie's last blog post: Loving An Addict Means Saying No.

A lot of Lorelie's posts are also highlighted on: Addiction Campuses

I know there are a lot of families who struggle with concurrent disorders of addiction and mental illness. I only speak for what I see with my son. He doesn't use to self-medicate symptoms. He uses/drinks to feed/satisfy his addictions. It's doing this that triggers his schizophrenia and causes the rebound affect. Also my son doesn't want to medication his symptoms. He very much enjoys his psychosis when he is in it. Probably another reason why he didn't want to take his medications yesterday. Why mess with his high? I have been around addiction enough to recognize that mind-set. I have been there. Don't eat too much before doing this drug or you will lessen the high...

I did tell the lady at the shelter that my son was psychotic and needed his medications so hopefully they were a little more attentive last night about 'reminding him' to take them. It's not a part of their duties and they get busy. Not sure I buy that. The other shelter had less staff and they did more. They followed up on medications. They searched more for drugs etc. being brought in. I know because I watched them do it. Too bad it was in such a horrible neighborhood. I have yet to see this shelter search anyone including my son. The lady asked what the signs were of my son's psychosis. To me it's obvious but I'm mom and have looked at his face for signs for years now. I asked if she knew what high looks like? What extreme exhaustion looks like? Combine them and you have my son's current face. Again I left out that he was most likely high... Really in the end it was the psychosis I'm trying to nip in the butt before something negative happens and high or not high he would still look pretty much the same from psychosis.

My appointment with ADAPT last week got rescheduled to the 18th of August. Today is a civic holiday here in Ontario, Canada so I'm not working! Hubby is :(. My work schedule has changed. Now I'm 12-6:30 Mon-Fri and I think 10:30-2 on Sunday. So 6 days a week and more hours. I may see if I can switch from Sunday to Saturday as Sunday is the one day I can pretty much count on hubby not working. The hours are being split between me and another lady. I got paid! I needed it to help cover rent due to what I had to give to Michael. I got my hair cut yesterday. Pretty short. I guess it's a bob? shorter at the back and long around the face. It feels good. I haven't had a cigarette in 6 weeks! I'm not sure how long it's been for hubby. I think 3 weeks. My homemade protein bars were a hit. We both like them. Have to make more today. I may even get back on my stepper today and do some exercise.

The above things make me happy. Certainly not the situation that my son is in or the fact that I have to fight so hard to try and get him the treatment that he needs.

Mom
BarbieBF

© BarbieBF and Schizophrenia - Mom's Journey, 2014 - 2015. All rights reserved. Unauthorized use and/or duplication of this material without express and written permission from this blogs author and/or owner is strictly prohibited. Links to blog posts and/or pages as a whole (in there entirety) may be used provided that full and clear credit is given to BarbieBF and Schizophrenia - Mom's Journey with appropriate and specific direction to the original content.

Friday, June 12, 2015

A little bit manic? ADAPT, Camping & Rules

To anyone that follows my blog regularly, my apologies for not writing...

I seem to still be struggling a bit with getting back into my grove and my social media with respect to mental illness. I upped my Venlafaxine on Saturday to what my family doctor wants me taking as I was noticing that my thoughts were going back to that negative loop where everything and anything that I'm not impressed with was auto-repeat in my head ;). It takes a couple of days for it to build up and by Wednesday the sedation kicked in and I ended up napping and going to bed early. So hopefully I can get back on track.

Hubby's family get together went well. Very well actually. I ended up reminding/telling my son that he had money as we were taking him to get cigarettes. I asked him to hold off on buying alcohol until after the family get together as I didn't want him being symptomatic while there. He agreed to wait. I know that he found it a bit tiresome but he said that he had a good time.

He didn't buy alcohol until later Monday afternoon. My bad... but I told him that the liquor store wasn't open on Sundays. I didn't think that it was. Hubby told me afterwards that it was open.

I'm guessing it was the alcohol that triggered it; he went a bit manic on Tuesday. Out of nowhere he was putting on jeans, grooming his beard and looking for his dress shoes. We had an interesting conversation about his teeth that day. Some delusional thinking in that he believed he was 'born' when he first started having memories around 3 or 4 and that he has grown new teeth 4 times. His ODD started to act up a little bit. When I didn't engage he said to me: Come on lets talk about this... Translation, come on lets argue ;). Sorry no. I told him that I thought he was being delusional, that I gave birth to him so I know when he was born, if he had teeth or not and that I wasn't going to continue this conversation. I walked away.

He went to his PACT group the following Wednesday which was golf. He participated and had fun. His new nurse from PACT has taken him out of the house for the past two Mondays. I think he is also pushing at PACT that Michael be more involved with the outings so it doesn't look like I have to question if he is on the list for Wednesday's groups anymore. Now his rides are just showing up. I think Monday's outing to the YMCA is being looked at as well. Last Wednesday was supposed to be a trail hike but due to rain they ended up going to the mall instead.

Camping last weekend went well. He said that he had fun. It's hard to tell sometimes. He looks like he is not really paying much attention to where he is yet he must be. Hubby and I stayed up until around 10 and Michael stayed up after that watching the fire ;). His reason for wanting to go camping is the fire. The store at the campsite sells little packets that causes the flames to go different colors which is kinda cool. We got 2 of them this time. Roasted some marshmallows. Hubby and I froze our butts off that night. Not quit warm enough at night yet...

I have had 2 appointments with ADAPT now. I will be meeting with my counselor once a week until she can get through my history. Also because I'm now a client of ADAPT then I'm able to participate in another program they have called 'STOP' which is for quitting smoking. I meet with a gentleman for that Wednesday morning and he gave me a months supply of patches and some lozenges. Now I just have to set my quit date. Because of my own past history with addiction I'm a little bit of both. I'm there as a family member of an addict but I'm also a recovering addict so I should be able to attend some of the programs for that as well.

Every Friday (today) they have a get together for addiction clients where people can talk about addiction, mental illness and how to have a better life. My son keeps asking if he can come to group with hubby and I and of course the answer is no. I reminded him of a youth thing that happens on Wednesday nights however I can't go to that one so he says no. He seemed open to the idea of going to today's session so we will see depending on the weather as it's supposed to downpour. Also I think his motivation may be the food court at the mall where ADAPT is and I can't keep handing money out to these things. Every group he wants money for McDonald's...

Wednesday hubby noticed that Michael seemed a bit edgy or cranky. A week without alcohol and he was/is probably experiencing some withdrawal symptoms. Being aware of this I didn't say anything that would play into that scenario. You know the one that has the addict pushing for a fight or argument so that they have a reason to drink or use ;). I can't say that I want to go through this every time my son gets money. It may not seem like much, however it's a constant cycle of him feeding his addiction then going through withdrawal when he has to go without. Sadly it's him that is suffering with withdrawal...

Hubby and I had group again last night. It was a repeat of the same theme as the last one we attended which was concurrent disorders: addiction and mental illness. Hubby seems to be getting a lot out of these groups. It's helping him to see/hear from others, other then just me. The group last night was through the Schizophrenia Society of Ontario (SSO) and they meet once a month at that location. I was sort of aware however I will make a bigger effort in the future to attend these.

I did speak to the lady from SSO for a minute about advocacy and other things. These are the items that SSO is currently working on: Policy and Advocacy

Rules... It came to our attention on Wednesday night, I think, that my son has started smoking in his bedroom. I totally missed the red flag of my son being in his room all night. Here I was thinking: Yah he's sleeping through the night. *face palm* I'm usually more on top of it then that but I guess between upping my antidepressants and my want to not see the negatives... I totally missed it until hubby commented that upstairs smelled like cigarette smoke.

Yesterday he was smoking while I was upstairs so I smelled it. Of course he lied to me. I gave him several chances to tell me the truth and finally had to go find the 'ashtray' and take it out of his room and tell him to go outside. Once outside I brought it up and of course got the: I pay for my room... I didn't respond right away, waited a bit then said to him that I didn't want it to be that every time I bring up something that he is doing that he isn't supposed to be doing that I have to deal with his ODD. He asked what ODD was? Oppositional Defiant Disorder. He says: I'm not being defiant, ok maybe I am but that's because you won't listen. Listen to what? You want to do what you want regardless of the rules because you think you should be able to. Yes you pay for the room however that still doesn't give you the right to smoke in it. If he rented a whole apartment that was non-smoking than he still isn't allowed to smoke in it. The world has rules.

I let him know that moving forward there would be consequences to him not following this rule. Several hours later it's easy to know that he is STILL smoking in his room as he hasn't gone outside for a smoke. I let him know that I'm backing off on giving him attention until he can learn to follow this rule. This may sound harsh however if I let this boundary slip then every other rule or boundary will go out the window with it.

In last night's group there was discussion on the 'slippery slope' of addiction. Well there are slippery slopes with boundaries as well. My son loves to push them and whenever I don't try to keep them then he pushes them all. He will even tell me: Well this is a rule and you let me so I figure this rule doesn't apply either. Typical ODD behavior which is why boundary setting is so important. Regardless of all this I don't want my home full of cigarette smoke, certainly not upstairs when it contributes to my headaches and guess what? It's my home too.

So awesomely today I have totally triggered his ODD ;) by taking his cigarettes out of his room and putting them in the basement. Not an easy tightrope to walk. Enforcing the boundary without allowing this to turn into something ugly so keeping my tone neutral and not reacting to his attitude which as the moment seems to be staring me down...

I'm off to make a coffee and harass my daughter, if I can, as she hasn't been getting to work on time. All I can do is keep calling her phone...

Mom
BarbieBF

© BarbieBF and Schizophrenia - Mom's Journey, 2014 - 2015. All rights reserved. Unauthorized use and/or duplication of this material without express and written permission from this blogs author and/or owner is strictly prohibited. Links to blog posts and/or pages as a whole (in there entirety) may be used provided that full and clear credit is given to BarbieBF and Schizophrenia - Mom's Journey with appropriate and specific direction to the original content.

Monday, April 13, 2015

How do you stay so calm? Behind the Wall

This is what my husband asked me last night. "When I hear him talking like that my blood boils. All I can see is it all happening all over again." Yes me too...

I'm doing my best to learn to let go of things that I can't change or have no control over. My hubby: "Yes but I have seen you, when you put your mind to it, and you do have control and you are able to stop it." Yes but only for a little while... It's raining outside. I can stand under an umbrella but eventually I'm going to get wet. I'm just putting off the inevitable.

I recently purchased a book: Behind the Wall. Click on the book title and it will take you to it. I have barely started the first chapter and already I have felt a connection with the writers and the families they are writing about. In the preface something stood out for me:

"No parent, for example, ever wants to admit there are times when one secretly wishes her child to precede her in death. No one ever thinks that. But this is not an uncommon or unjustified thought for a parent to have while her child is suffering from a particularly devastating episode related to mental illness."

Widdifield, Mary; Widdifield MA, Elin (2015-03-02). Behind the Wall: The True Story of Mental Illness as Told by Parents (Kindle Locations 175-177). Langdon Street Press. Kindle Edition.

No I'm not secretly wishing my son was dead nor is he going through a bad episode right now. Still the ideal expressed in this quote is somewhere that I have been in the past and most likely where I will be in the future, again...

On Saturday while we were setting up the backyard and my thoughts were wondering as they usually do. I asked my son if financially his Nana and I were the same and I couldn't provide him with the things that I do, would he want to stay with me? Of course his first question was: Why are you broke? ;) Over $30000 in debt but that's not the point... I wasn't really expecting a black or white answer and told him that I was just curious as I don't want our relationship based on my ability to be a bank account to him. I purposely didn't say the word love as I don't think my son feels or reacts to things based on love. Not saying he doesn't feel it however it's secondary to his own needs or wants. Anyways he basically said that he is comfortable with me, Dad and Nana...

I use tinctures or herbs to treat my menopause and keep my hormones regulated. My son knows this. He has tried a tincture in the past for anxiety however abused it so I ended up getting rid of it. Just because they are herbs or natural it doesn't mean that they can be abused without harmful side affects.

Because he is struggling with anxiety most likely due to no alcohol now since Wednesday and he knows that he can't get any benzos prescribed, he is looking for another means to self-medicate. I have told him that I'm willing to work with him on things like this to help him with withdrawal and anxiety  however he is not going to find the relief he is seeking through a supplement. He says that is not looking for benzo relief however I know better. So we tried a tincture... Yesterday he tells me that it isn't working and asked if we can try another one. Tinctures are not cheap. They range from $20-$50 CAD a bottle.

What do you think preceding me saying no to another tincture? Maybe it would be best if I lived with Nana. That was the agreement anyways that after 6 months I could do that...

It wasn't my agreement and still isn't. This is from when my son was in the shelter the last time and as best that I can tell the agreement was that after 6 months of my son being in a group home and participating in addiction recovery that his Nana would start saving money for him to go out there.

All fine and dandy... What does this mean for my son though? It means he doesn't have to put forth any effort into managing his own life or trying to get better because Nana is waiting in the wings and life with Nana is certainly a lot easier then life with me. I have rules. I have boundaries. He can't manipulate me the way he manipulates her.

My love for him is different. It can see past his feel sorry for me manipulations and half truths that schizophrenia and mostly addiction allows him to speak without so much as batting an eye... Getting what he thinks he deserves is his priority and what others go through to make this happen doesn't matter to him. He knows that Nana would give up anything to give him what he wants. He knows that she can't say no to him. Whether it's good for him or not doesn't fit into the equation. In his eyes that is what love is... Be his minion and put him on a pedestal and you have proven that you love him...

How can that compete with my version of love that says yes I love you but I love and respect myself too. Yes you are special. So are others special too. Yes you have wants and needs. So do others. Yes you have experienced pain. So have others. Yes you deserve a good life... You get my point. I can't compete and I'm not going to try. He can accept my love for what it is or not. A love that sees past right now to a future that could be so much more then burying himself in the fake euphoria that addiction gives him. I use the word euphoria because two nights ago this is what he told me he wanted and what he was looking for.

So the conversation started to get a little heated. He got mad or upset that he is not getting the money that he thinks he should get. Some time ago we signed a room and board contract stating that he would pay me $700 a month because I pay for everything including cloths etc. Disability knows about this contract. I came to this dollar amount by spending considerable time going over the disability website and how they break down their funding. Because he is room and board instead of rent and paying for his own groceries, utilities etc then his payments are $841 instead of 9 something. While living with his Nana they said that he was paying his portion of the rent plus utilities etc so he got a bit more then here. Because it was rent then he got his money at the end of the month for the following month. Here he is room and board which gets paid at the end of the month for that month. You would have to ask disability why they do it this way however he does now have clarification from disability that it works that way so at least we don't have to have that argument anymore.

It clearly states on the disability website that his personal spending amount or money not for basic needs is $119. Do the math. $841 - $119 = $722.

While he was in the shelter the last time I did tell him that I would consider looking at $600 a month instead of $700 IF he was to start buying things for himself like he was supposed to with that money. Not drugs, alcohol, games... Since March 21st we have spent over $200 on him in extras. Not counting McDonald's, Tim Horton's, Chinese food... or the cloths we have gotten him since he loses items while in the shelter system. We have paid for cigarettes for him. I didn't take any money from his disability payment for February and he got the full payment, so that he could buy items for his room.

Givers have to set limits because takers never do...

So no I'm not changing the $700 to $600. Can you guess what followed? The phone call to Nana.

If what you are doing is making an addict happy then chances are you are enabling instead of helping.

Then I'm being asked to talk to Nana and make arrangements. No I'm not talking to Nana and I will not so much as lift a baby finger to help with something that I am dead set against. Considering what has happened in the past, why would I help make that happen again?



My son's case worker from PACT just left...

The kicker is this... Thursday and Friday my son was asking me to help him get his GED (high-school equivalent) because he needs it to work with my husband in construction and he had decided he wanted to do that. Today we were supposed to be looking into either getting him back with the YMCA or into another school that does adult learning.

Nana's intentions may be good and I know are coming from a place of love... When my son pulls on her heartstrings with how much he needs to drink or get high because he is so unhappy, stressed, anxious and there is nothing for him in this world... Will she have the willpower to say no? Will she be able to put aside how much she loves him and how much her heart is breaking for him to make the right decisions? Will she be able keep her home drug and alcohol free even if that means him 'going to the streets' to get it?

My son just admitted to his worker that 30% (I say 60%) of the reason he wants to go live with Nana is because it's easier there and because she won't be able to say no to him...

Today for the first time in a very long time I had trouble getting him to take his medication. He doesn't want to take his Olanzapine any more. Why would he? He is already plotting to get the life that he wants which is addiction and psychosis. Both of those worlds are so much happier for him. It's the collateral damage and who he will take with him when the time comes that I am all to aware of. What if it's my daughter the next time or prey tell some innocent bystander...

Am I calm? Inside I am seething that no matter how hard I try to change the path that two dysfunctional families have set my children on... I feel like I'm losing the battle yet again. Is dysfunctional love better then no love? I don't think so. Without dysfunction one can find healthy love and a better life.

As long as this relationship is part of the picture and my son has the freedom to run away time and time again and hide in his schizophrenia and addiction... For my own life and sanity I have to learn to accept and let go. Maybe send another prayer to Donna, my mom in heaven, to once again watch over her first born grandson and if possible interfere so that I can give him the future he deserves.

Mom
BarbieBF

© BarbieBF and Schizophrenia - Mom's Journey, 2014 - 2015. All rights reserved. Unauthorized use and/or duplication of this material without express and written permission from this blogs author and/or owner is strictly prohibited. Links to blog posts and/or pages as a whole (in there entirety) may be used provided that full and clear credit is given to BarbieBF and Schizophrenia - Mom's Journey with appropriate and specific direction to the original content.

Friday, March 6, 2015

Going blind...

It's been a quiet week. My son seems to be recovering and his psychotic thoughts and voices are going away. He is still somewhat delusional in thinking but nothing major. Yesterday I teased him because he was making a sandwich and cleaning up after himself. He replied that he was feeling healthier. Yes that happens when you are not in psychosis :)

The other day he told me that he thought he was going blind. My gut told me that he didn't mean physically so I asked him what it was that he couldn't see. He is having trouble seeing his psychotic thoughts or imaginings. I explained that this was because he is not as psychotic anymore and what he was seeing was part of his schizophrenia. I spoke about this with my hubby and explained that I try really hard not to use terms like normal as they don't really apply here and for my son the goal is not to be normal. I know that for him it can feel like a lose to not see these things so the best that I can do is approach it from the viewpoint of not being psychotic rather then being normal.

This morning we had another little chat. I try to nicely point out that certain thoughts or ideas are delusional because no I can't help him obtain a spaceship so that he can travel the universe. I may be able to do a lot of things and figure out stuff however I do not have those types of contacts :).

Not surprisingly we also discussed marijuana. Earlier in the week I was helping him find a power cord and looked in his coat... Found a pot pipe and screens. Told him it was being confiscated. He doesn't feel like this world has anything for him so he wants to hide in marijuana. Yes he acknowledged that. At one point he tried the: Can we try and you can give me so much every day. My response was: I am not Nana. He grinned and dropped that approach moving on to the idea of getting his own place. All I can do is remind him that it's up to him how many hospitalizations he wants to have before he realizes that marijuana is not worth it. It's his journey I'm afraid.

He would like to have a girlfriend. Well he isn't going to meet any girls by not participating in life. His case worker from PACT was here earlier in the week. She asked him if he had voices and of course his answer was no ;) I stepped in and said perhaps asking how many voices or what they are saying would get a more realistic answer. My son replied that yes he has voices, entities which is normal for him.

Starting next week I'm hoping that he will be more involved with PACT's outings. When asked my son hesitated and I stepped in and said that I would answer for him and yes. Wednesday is there next group meeting were they discuss what type of outings the group will do and someone from PACT will come and pick him up. Monday's they go to the YMCA which again I said yes to. He can swim, work out or do whatever he wants during that time. His worker said she would look into getting him a pass. I don't think she has heard back from ADAPT yet.

I haven't had him call disability yet :( I really should get on that.

He has been taking his medications and it's fairly easy to tell that the psychosis and voices are leaving him. His face is much clearer. He is eating good. He is watching TV and playing games. Maybe not for long periods but still he is doing it. I do feel for him here as it has to be hard to be in this in-between stage where he wants to interact with schizophrenia yet it's getting harder to do. He can 'think' psychotic thoughts yet can't 'see' them as easily anymore. One day he spoke to me about one of his entities that he thought was his son. Whether they are real or not the lose of them will still feel like a lose to him.

Another topic we discussed today was love. I asked him what he thought love was? To be soft like a baby. Translation being soft on him or lenient ;) There are a lot of different sides to love. Sometimes love is hard. It can be a lot of things at one time. Because I'm not always soft it doesn't mean that I love any less. Sometimes making the hard choices is love.

Mom
BarbieBF

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Wednesday, August 13, 2014

On pins and needles

Due to rain my hubby was home from work yesterday so we all went to see Guardians of the Galaxy. It was pretty much what I thought it would be before I heard that it was a great movie. I think I would probably have enjoyed Maleficent much more. My son seemed more interested in the three Lego figurines I got him at the movie theater, although he did say that he thought it was a good movie. These Lego figurines instigated us making a trip to Walmart for Lego. My son picked out a kit for a house and I picked up a small kit to make a 'power digger' for my hubby since he is in construction and is an heavy machine operator. I actually had fun putting it together and he put it on our night table.


My son had fun putting together his three figurines and moving furniture around looking for the pieces he kept dropping. He had stated that he wanted to put the house together with me however I think sometime in the middle of the night he must have changed his mind...

On Monday one of my son's workers stopped by for a quick visit. I told her that at the moment my son is the least of my concerns however he is still a concern :) He has been doing good. Still sleeping in his own bed, so it's been 10 nights, although I use nights loosely as he doesn't go to bed until sometime between 4 and 6 AM. He is not making as many messes and is attempting to clean up after himself. His room is starting to look like another tornado hit it. He can't seem to manage reaching his garbage can or laundry basket. I had forwarded him an email from the YMCA asking if they should be closing his file with them as they can't keep his file open with no activity or progress to report. I feel that he needs to be the one to respond and take responsibility for the choice to not attend. I don't know if he answered it but I'm guessing that he didn't.

When we did grocery shopping last Sunday my son asked if they had anything in the vitamin section, like a herb, to help him with his anxiety. I have tried in the past to help him with this by getting him an herbal tincture however he abused it so I had to throw it out. I take a lot of supplements and vitamins and have been trying to get him to take them as well however he refuses. He even refuses a multivitamin. He has on several occasions stated that he wants some sort of muscle relaxer. Yes he is still looking for that quick fix. In my opinion it's his nerve system that is causing his muscles to be tense. He is either under or overstimulated or some combination of the two. To treat the symptom and not the cause is not going to help him in the long run. 5-HTP caught my eye and his too. 5-HTP is an amino acid that the body produces naturally and I do believe helps to regulate or produce serotonin which helps to regulate mood. I agreed to let him try it as long as he doesn't abuse it. So far it doesn't appear that he is abusing it. He noticed a couple of hours after taking one that he felt more relaxed. I noticed this too as usually even when he is just sitting/lying on the sofa his foot is in constant motion and that night it wasn't. I am trying not to micromanage him taking his pills however I am counting how many are in the bottles every now and then. I also handed him over his Gabapentin/Neurontin on Friday. The first night 5 went missing. He says he put them in another pill bottle. He seems to be on track with his 100 mg Clozapine however his Invega and Lithium are not adding up. I haven't counted his 25 mg Clozapine.

This morning my son and I butted heads as he was still up when I got up at 5:30. Of course not being particularly coherent myself I triggered his ODD when I told him he needed to take his pills and go to bed. According to my son he doesn't need them and that is why his psychiatrist is weaning him off them because he knows that he doesn't need them. Delusional or manipulative? I don't know. Somehow he pulled his friend into the conversation and it was his friend's fault that he had no friends that his friend treats him like crap... I won't say what else he had to say as I'm pretty sure it was being motivated by negative emotions rather then an honest opinion of his friend. As I said I wasn't being particularly coherent and I managed to hurt his feelings by saying something about me doing what I'm doing because I love him and if he can't see that then there is something wrong with him. I meant this in terms of maturity and I tried to tell him that however he took it to heart. Told me to kick him out because he can't handle being here and he would rather be out on the streets. I told him that I am tired of having to walk on eggshells and monitor everything that I say because he can't handle some truth. I'm not going to kick him out on the streets so that he can use that to manipulate others into feeling sorry for him. If he wants to go then go but I'm not telling him to. I don't know if it was lack of sleep, having not taken his pills yet or something else (psychosis) but his eyes were telling their own story. He did go to sleep a short time later.

As for why I am on pins and needles... I think I have spoken some about my downstairs neighbors and their excessive noise. I don't know if I have spoken about the verbal harassment. Saturday I got a pretty big scare. The lady from that unit tried to forcibly enter my apartment as she thought that I had called mental health services on her and freaked out when they tried to contact her. It turns out a police officer that had attended for my previous noise complaint had contacted them. Accusing me of putting an eviction notice in her mailbox that was obviously from the building management and not me, among other things, made them question her mental health. Long story short this has been going on for some time now and whenever I try to get it to stop I'm being verbally harassed by them and having to deal with physical outbursts like banging on walls and what happened on Saturday. Saturday being the second time she has approached my apartment in an aggressive manner. After me almost losing it in front of a police officer and him seeing how afraid I was, something is finally being done about it. I think the charges will be criminal harassment and mischief, once they arrest her... She has been avoiding being arrested since Sunday. The quiet is somewhat unnerving and not knowing where she is has got me more then a little tense. As grateful as I am that something is being done I'm more afraid to leave my apartment alone then I was before as she and her husband have to be pissed at me. On the bright side, they have both been warned to not communicate with/at me and my family or they could both be facing further charges. So now it's a bit of a waiting game and if she doesn't appear they may have to issue an arrest warrant. Hopefully for her sake it doesn't come to that. In the meantime I'm jumping at every sound in my hallway... *deep breathes*

The YMCA called me a little while ago. I told them to close his file for now since he obviously isn't going to follow through on dealing with this. His nurse also dropped by about an hour ago and he went out to talk to her and grab his Clozapine that PACT picked up for him. I'm waiting for some dough to rise and telling myself that I don't need another cigarette! I have been smoking way to much lately. I think it's time for a herbal tea before I start making dinner.

Mom
BarbieBF

Monday, July 21, 2014

Schizophrenia. I wear my sunglasses at night...

I got up this morning at 5 to my son sitting at his computer with his sunglasses on. What else can I say about that!? Yes he had been up all night again. Got his pills from the living room where I had left them for him the night before, told him it was 5 o'clock and time to go to bed which thankfully he did. I myself crawled back into bed until my hubby kissed me good-bye a little while later, assuring me that he had made coffee, so I got up and saw him off to work. Perhaps I am PMS'ing still as I had to fight back some tears this morning. Not a usual occurrence for me. Although sometimes I think a good cry would do me some good but I seem unable to let that dam break. Angry tears may sometimes flow but those that may be a reflection of my own internal hurt and frustration are securely locked away perhaps waiting for a time when they can safely be released. I posted an update on me and my son on the Schizophrenia.com forum and was nicely asked by the main admin if I wanted to take a break from being moderator until I can get a more positive state of mind. And I thought I did a good job of keeping my feelings to a minimum... I guess not. I declined. The forum gives me purpose, especially when my own life is not going as planned.

The first thing I did this morning, after my coffee that is, was to e-mail the YMCA and ask them if my son had been asked to not attend. As I suspected the conversation was a little more in depth than that. They had expressed concerns that he is not progressing and offered to have a meeting with both of us which he declined. He does not want to commit to any goal setting and is not working independently or taking advantage of the 1-1 instructing. They did mention another literacy program that may suit him better as it is for people with lower literacy skills. He was not asked to not attend and an interest is being shown in how to motivate him to participate better as at this rate he will be years preparing for his GED. I gave them a little more detail on what has been happening, filling in the 'He's not doing well.' blanks. For now this will have to wait until he is better able to handle it.

I put in a call to his nurse this morning, left her a message and she called me back. I let her know that he is not doing ok. He has not gotten any worse but he is not getting any better. The amount of anti-psychotics that he is on is not cutting it. I feel that she is finally taking me seriously in that even though my son may not be displaying obvious positive symptoms he is still suffering from symptoms of schizophrenia. Maybe that is why I'm finding myself a little choked up. I seem to have been holding onto this misguided idea that maybe just maybe my son was misdiagnosed, since he didn't completely fit into my idea of what schizophrenia is. That if I could just get him over his addiction and keep him clean that the psychosis would fall away. As I said yesterday, I can admit when I'm wrong.

I set up an appointment for his psychiatrist to do a home visit tomorrow morning. I'm guessing that my son will be ok with this since he wants to meet with him too although for a different reason. My son will probably push for a benzo while I will be trying to get another anti-psychotic prescribed since I highly doubt that we will get him to agree to an increase in his Clozapine. Keep your fingers crossed for us that with a little more patience and perseverance I can turn this around.

Mom
BarbieBF