I am doing videos on Youtube because of not being able to write. Check out my newest post. Heartbroken in Benzohell
I am doing videos on Youtube because of not being able to write. Check out my newest post. Heartbroken in Benzohell
Today, I spent some time trying to piece together the last 60 days. It’s hard. There are lots of big spaces of time I don’t remember much. That scares me. It’s evident whatever happened freaked out my loved ones in a big way. I was on the phone saying so many things that were not at all what I was wanting to say but my brain just was somewhat frying. It just was what it was.
Which of course adds to my shame and guilt. I have not had that occur since I quit gambling. Yes, I’ve lost control of my emotions before, but I have had no “out of body” experiences like I experienced this time. I sure am glad I write tho, because I can go back and somewhat piece together the build-up, the blow, the loss of time, and then I went straight into detox for the Xanax withdrawal. Not the smartest idea in the book. But hey….who said I was thinking in any congruent way during this time?
Although extraordinarily fatigued with pain increased, I think I’m doing pretty well. I am stronger than I remember sometimes. While I was feeling so weak, I had some idea of what I wanted. I have been on a journey to get off these pills for nearly 2 years. I wanted to get my overall health and strength a little better because I knew I was getting to a place I was ready to deal with some more of my “stuff”.
I did know I was having some PTSD triggers There were some encounters with people I cared about where I felt under attack so decided to disengage from those relationships. That is not something I do lightly. Yet, in retrospect it showed I was getting stronger because I was able to say to myself, “this is not healthy for me”.
In late February or early March was one occasions and I handled myself with composure (maybe showing a slight displeasure but that is all) and then returned the next day to discuss the situation and stated what behaviors I could handle. That is a HUGE thing for me.
As time passed and other situations occurred I knew I needed to do some digging to see why I so easily get triggered by certain personalities. To be frank, I believe it’s because of my mother and our relationship and her behaviors. There are certain behaviors in women I just cannot tolerate at all. It gets my ruff up so bad and I have to just clench my teeth. Pointing, especially if someone pokes my chest, intimidation posturing, badgering, and overly aggressive. I have a tolerance and then it just is gone. It was like I was doing okay, handling each situation the best I could while trying to be professional in my role as “property manager”, and then it was over the edge.
I had told a few folks about my encounters and how they were affecting me. I had thought I had stated I was getting very stressed and overwhelmed, but again, I believe others hear it as “whining”. It was in late March that I picked up paperwork to get back into counseling. I didn’t get it turned in until mid-April after recovering from the flu. I didn’t get back in until about the end of June for intake. Back in late March I knew I was over-stressed and had taken on more than I could handle.
In my perception a great deal of the stress came because what I perceived as agreed conversations on what was going on with the property and tenants wasn’t happening. I also had a situation with a friend and it was just the last straw. I was so overwhelmed trying to get this property ready for renters. I had to help pack up a house that was full of many collections. Tapes(VCR and Cassette), books and mountains of electronics. The entire second story was just storage! I also had to get ready for an Estate Sale. I had never done one before and what a TON of work that is. I also had to help Mr. Chicago’s brother find an apartment and then I had to help him figure out how to make a home for himself in his new place. January was exhausting.
Then in February I was still doing okay after taking a little break, but that is when some of the encounters with PTSD triggers really started. After the first one I was shook up and tearful for a couple days. Then I tried to rectify things in an adult manner and carried on. Then there was another encounter in March. Again, I held my tongue, waited a day or two and then tried to rectify it. I also was telling my family and loved ones about the stress this was bringing me. Yet, no one is around me to actually see what those affects looked like. Often when you have PTSD triggers in my mind I feel like I sound like I am “complaining”. But what I’m trying to convey is I am getting over-stressed and I can’t make prudent choices and I need some help.
I had my trip to Chicago in late March and then came home and landed in the hospital for 4 days with the flu and pneumonia and when I came home and got well enough I had to stretch myself again. I was interviewing potential land renters. I had to run ads and make phone calls and then talk with these people at length regarding their needs and what we could provide for them. I am not a good salesperson. It makes me very uncomfortable, so I was stressing about that. More stress. I am feeling like I am falling behind here. There is so much work to be done and I am coming home after a nearly 2 week absence and it’s time to start the gardens and I still have things to haul to the dump and things to sale and continued encounters that were less than comfortable with some people.
Then came May. I did forget to mention that I had a very serious family issue that occurred in January that was an ongoing concern and stressor until early June. Those of you who follow my FB page remember, Mr. Chicago came out for my birthday in May. It was truly the BEST surprise I’ve ever had for my birthday. The BEST. During the time he was here I was able to show him a little of what the issues were but by that point I was definitely at a point that any more encounters with triggers was going to set me off. But to him I’m sure they seemed small, each little instance.
That is not so for someone with PTSD. I’ve only had one occasion where it was a single incident that triggered me. Even at that time, I had been under a LOT of stress. Typically when I go into a meltdown mode (post gambling…completely different scenario) I have had a number of stressors on top of a number of triggers. I can only take so much. Which, is another reason I have been trying to get disability.
Having a disability like this doesn’t mean I can’t function or that I’m not smart or capable. It means I can’t take the daily struggles like a person who doesn’t have a disability. Over the years I’ve tried to explain so much. I can do a little physical and deal with the pain, but then my stress will get up and so I can’t deal with people or additional stress. Or, I can be medicated and take it gentle on my body and not do a bunch of hard things and my brain works. In fighting chronic pain as well as mental health issues life gets very overwhelming at times.
After Mr. Chicago went home, I thought we kind of had things under control. But that was not the case at all. There were still unresolved issues that came up and a number of incidents that made me uneasy around the 12th of June and that was when I started going over the edge.
After my first blow up, I had a few days where I just was telling everyone “I’m done”. I am not able to make these decisions. I was trying so hard to take care of the area here and do a good job. I went up and down and up and down for a couple weeks and then settled down a bit. But by then, I was really struggling inside with a lot of things.
I didn’t feel safe anymore. Because I had “acted out” I was scared and embarrassed and pushed everyone away more. I didn’t want anyone to see me unhinged. The lonelier I got and the more I tried to figure out what I could have done different I just got more and more distressed.
I tried to “pull it together”, but I had forgotten that back in May I had purposefully come to the point that I wasn’t gong to refill the Oxycodone anymore. That had been my goal and I reached it and was doing okay. I didn’t take into account how that my affect my mental health when I was already under stress. I continued to rage and then cry and then rage and then cry. I’ve said “I’m sorry” so many times in the last 2 months and then gone and done the same exact thing.
That is what happens when you have a PTSD breakdown. You feel okay for a few minutes and think you are okay to be around others and then Every Little Thing bugs the hell out of you. Drivers that are speeding and reckless caused me to be the same…trying to chase them down to tell them what crazy drivers they are. Ha ha ha….and who was the undone woman chasing them? Yes…that was me! Hence the limited driving these days.
So June ended and July rode in and yet another big stressor met me on the 5th. Something that made me think of bad things from long ago. I tried to explain to the other my feelings but was met with resistance. This made me feel even more unworthy and increased my angst.
So on 7/12 I had ran out of Xanax and decided not to go to town to pick up my prescription the next day. I had made a choice. Not wise, with my thinking at the time, but it was just me here and I was going for it. The first night I found out some information that truly just made my head burst. My head has been racing and my heart has been racing and I became obsessed with this information and it was rough that first day or two. I was not only going through Detox and PAWS, but I was in the midst of a mental health breakdown and kept getting news that left me feeling so alone and so WRONG for everything. Lots of thoughts of “why am I here?”.
That’s the mindset of a PTSD person. When I am in a PTSD head, I am in total fight/flight mode. I feel horrible. I think I am the worst person in the world. I want no one to see me. I don’t behave in ways that are typical for me. I get quite mean (to push people away) I’ve been told. I typically am NOT mean! I am a lover and a giver and a smiler. But under duress from a PTSD flare I can dish out some verbal bashing and be quite harsh.
I hate that. Which is a big reason for going back to counseling. I know I still have learning to do. I am hoping by completing my detoxification off the narcotics and benzodiazapines my head will be clearer for doing the work I have in front of me.
I know nothing about my future right now. Neither do you…if truth be told. I remember my counselor telling me that I learned early in life, it can all change overnight. In the meantime I am hunkering down and just trying to take care of myself. I deserve it. So do those who love me. I despise scaring them so. Evidently, as I was recently reminded, it’s been going on for some time. When I get to my lowest I have very pronounced suicidal ideation. I forget about it for the most part when I’m well. I know how that feels as my mother suffered with the same. It is very hard for those around a person feeling like this.
Today has been the clearest my mind has been in a very long time. A very very long time. Even with the fatigue of not sleeping the last two nights (going on being awake for about 58 hours now) my brain is clear. I truly am grateful for being able to finally get off all that.
The cannabis is working. The dosing is not exact, yet. Just like me. I’m working on it. Thanks God for a gentler alternative that comes form the earth!
Up and down and up and down and around the bend and back again. Battling through PAWS (Post Acute Withdrawal Syndrome) is like being on a roller coaster ride, on the mixer, walking around in the funny house and sick with the flu at times. Add to that my PTSD being triggered and it’s been a rough couple of weeks.
To be honest, there are periods of time I don’t really remember much. I have pieced some things together from those that I’ve talked to on the phone or who saw me during those days as well as various texts and emails. I wasn’t very nice. I lashed out at those I love the most during the worst of it. Including myself. PAWS can be a serious medical condition. There are times I have felt very disconnected and it’s taking all my ability to maintain some semblance of “normal”. I’m sure there are a few of my people that would have liked to see me be hospitalized for a few of those days.
While I did have a long morning in the ER after one of the most rough days/nights, (un)fortunately they let me go home. There had been paperwork filled out to put me on a hold, but I know what the hospital means if you are detoxing and/or going through PAWS. It means being stuck inside, put on benzos and who knows what other meds as well as starving because they don’t have any food I can eat. So I pulled myself together and talked with a little intelligence and very nicely and they literally dumped me out in the waiting room. They know what the PAWS crazies are like. They wanted me out of there!
I don’t want it to sound like I take this lightly. I don’t. I am scared out of my sometimes too smart mind. I just can’t see any way through this other than just doing it on my own using medical marijuana. I can’t go to a treatment facility because they will put me on pharmaceuticals and that is what has been making my life a living hell for the last few years. I can’t go to the hospital because that’s all they have to treat me also. I still am taking my anti-depressant and would be happy to consult with a psychiatrist about my PTSD if I could get a referral. I was supposed to have one over 4 months ago, but that’s how it’s been with my PCP, we talk about it and then a year or two later after me reminding her multiple times it finally gets ordered.. Right now I just am doing my best and trusting that those that love me will still be around when I come out the other side. Cuz this ain’t pretty!
I’ve been through PAWS before with my gambling addiction. I vaguely remember the jitters and the crying jags and the frustration with having my brain not working right. I remember getting upset easily and feeling a little “out of body” at times when I first started trying to live life without my addiction activity. What is different about this is I didn’t realize that I had any emotional attachment to my medications. Also, when I was detoxing off gambling (yes, you detox off gambling just like alcohol or drugs, it is truly miserable) they were giving me pain medication and anti-anxiety medications. I was just doing what the doctor ordered. I was taking medications in order to be comfortable living life. Now that I have been off the opiates for nearly 60 days, I don’t crave the pills…but I wish so much for something to make all the bad feelings go away. I am not feeling comfortable at all.
What am I doing to take care of myself through this you might ask? I admit, I haven’t been that great to myself. One thing is I have absolutely NO appetite and so making food is a challenge. Fortunately my son has been around and so I occasionally feel a motherly calling and will cook for him and then I’ll eat too.
Tonight I was finally able to drive to town to get a few things at the grocery store. I bought some good healthy foods to cook and eat, including a few easy things like soup and cheese and crackers and avocadoes. Things I don’t have to think about to create something to fill the empty spot in my belly. I also found some specialty teas to help me relax and to be positive. Additionally, I am following suit with millions of others around the world and have embraced the idea of coloring for therapy. I bought myself a coloring book and some colored pencils. Combined with a little medicine that should be a great way to be creative and reduce my anxiety at the same time.
I am really proud of myself for driving to town. Driving has not been a good thing during this particular time in life. I either find myself extremely anxious while driving or I get road rage. These are new things for me. So, I have not drove much at all the last couple weeks. But, I needed groceries and food for the plants and animals too!
The other things that are keeping me grounded are my furbabies and the other wildlife around here and my gardening. I have my dog who is the best. I freaked her out a little the night things got so crazy for me, but she came around in no time after she saw I was home and okay. Then there is my partially feral kitty that was indoors but escaped just about the time everything else took a dive for me. I am slowly encouraging her out of her hiding spot under the deck. I also love keeping the hummingbirds happy by having their feeder full and water nearby for them to drink or play in. They are so beautiful and I love to hear them buzzing around. Then there are the butterflies and the snakes and lizards that catch my eye. They are beautiful and I thank them for letting me get so close to take their photo. Watering the gardens and tending my first few medicine plants helps keep me focused outside myself also.
Many of the things I have growing were started from seeds. I love watching things grow. It gives me hope. Even the flowers that are less than perfect or the cilantro that bolts before I can get any of it…..they all are such a support and source of encouragement to me. They give me some purpose when I am feeling so out of touch with the rest of the world. The living things that rely on me for their care give me so much back. I am so grateful that II have been able to stay here, where I can grow things and be in nature.
It’s the end of the day now. I have much to be grateful for. I know I have a number of people that are praying for me. Thank you. That is another of the challenges with PAWS and the PTSD. It seems to darken the spirituality part of my life. I trust your prayers will be sufficient, for praying is a challenge for me right now. I still have hope and I know that comes from something outside myself.
I thank those who have not been scared away but have said “I love you, how can I help?”. I’m grateful for being able to drive myself to town and for a full fridge and pantry. I will do this!!! If there is one thing I know about me, I perservere! I don’t know what it’s all going to look like on the other side, but I choose to view the future as very lovely and peaceful and full of promise!
I believe the last day I had any opiates was May 10. That means today is day 51. Whew! What a roller-coaster it has been. Physical pain some days, other days tons of energy and low pain, emotional highs and lows, anhedonia, obsessive compulsive behaviors, restless legs, sweating, raging, sleeplessness, tearful, irrational, sensory overload, lonely (this is my own choice to be alone, yet it still is a lonely place). Yet, here I am, upright, breathing and doing my best!
Yesterday was a pretty decent day overall. I started the day opening the blinds in my bathroom. My veggie garden is my view out the back of my fifth wheel. Its coming along nicely for what I’ve had to work with. The best thing was my kitty that had fled the coop a week or so ago is living under the porch now and I got to see her. I took her food and water. I also filled the hummingbird feeder, watered the garden, took some photos, got a shower and went out for pizza with my son after we had a little talk.
I finally asked him about last Friday night. That was a really bad night. In attempting to be social and be out, I over-imbibed in alcohol and it was not a good thing. Alcohol while detoxing off narcotics is a potentially lethal mix. In more calm and rational times having a glass of wine or two is not a big deal for me. What I learned over the last 2 weeks or so is that if you are removing something that has been part of your pain regimen, it is really easy to substitute alcohol. So a glass or two becomes 3 or 4 and then more. I would not make a good alcoholic. I found that out in just a short couple weeks of doing some “substituting”. I was somewhat aware I was doing that, but I thought I could control it. I let it get out of hand. Right now I have to be very very careful of any thing that might be a potential replacement, other than the medical marijuana.
Even tho I’ve been on a taper for over 18 months, my brain knows that those pills are now gone. Those receptors are screaming for something to fill them up so they can relax. That is what causes me so many symptoms. What I am needing is some better guidance on strains of medical marjuana (MMJ) to use.
Since I started using MMJ, I’ve only had strains I received as compensation for work and what I received from the person who grew for me last year. I’ve been give a few names and very basic descriptions of what the strain is good for. What I need is some direction and expert knowledge of what strains will help with the anxiety and some of the other symptoms that I have been recently struggling with. I have decided I need to take a trip to one of the local dispensaries. Most the strains I have are good for getting me up and moving. Right now, I need something a little more calming. I’ve visited a couple with a friend once but have not had the resources to spend on what I considered as “extras”, when I have plenty here. What I have come to realize is that I need some specific components and for my health it isn’t an “extra”. This is my medicine now.
I am coming to truly understand that this is a science. I have much to learn. I know from the great success I’ve already had the last 18 months that it can be done. I want this to work and it is working. Had I been more mindful I may have waited to stop that last pill until I didn’t have so much stress going on around me. Yet, I could have made an excuse to keep that pill for quite some time. It was my medicine. Now it isn’t.
I’m not good at “fake it til you make it”. My brain doesn’t grasp that. What I do have success with is keeping on keeping on. It might not look pretty all the time, but I’m not giving up, even when my head sometimes tells me that sounds like a pretty good idea for everyone’s sake. I have been through so much and I know that there is good on the other side of dark times like this.
My hope for my loved ones is they too remember that no matter what happens, my track record has been good for waking up and making it through the days. And for all of you reading, I wish you the best day possible. If it’s not so great hang on, because tomorrow can be, if you just get through what ever it is you have to get through. Peace.
As I look back over the years, so many hopes and dreams, always feeling like I was working hard, trying my best. Right now, it’s actually pretty amazing what I’ve done with the deal I got dealt. My life has handed me circumstances that not everyone goes through. The multiplicity of the stress of various circumstances have created changes in my brain. I do not see things the way you do. Add to that, the medical arena not knowing how to deal with my various symptoms and handing out prescriptions of mood stabilizers, SSRI’s, pain medications, sleep medications, Neurontin for foot pain, anti-inflammatories, anti-diarrheals, anti-constipation, anti-anxiety medications….among the top 10! It’s truly amazing that I am sitting here able to even be partially present in my day.
I have learned over the years what some of my triggers are. Certain smells like old medicine bottles, slamming of a cupboard door, yelling of any type. I can not tolerate perfumes. I notice them right away. The same can be said to the feel of clothing against my skin. It has to be soft cotton and loose and not too hot and able to be layered because I can’t regulate my temperature when my adrenal glands are on overdrive.
So I’ve been trucking along working my recovery from gambling, slowly tapering off all those medications and got down to where I was hardly taking any oxycodone anymore. For instance, I might even have a day or two that I took none.Unfortunately, in late March on my trip to Chicago, I got really sick with pneumonia and bronchitis, the flu and pleurisy. I was miserable. So, since I had them, of course I took the pain meds. I was in pain. Right?
Then, just a couple weeks after healing up from that and back down to just one dose a day or less, I have this incredible ride on a 1939 Ford F9 tractor down a hill with no brakes and out of gear which caused me to dislocate a rib, and so I had to take them again. I actually had a rib poking out (still under the skin), and shoved it back in. I awoke the next morning to the bruise from doing it. That was late April.
In the interim period of time that I am kind of subconsciously getting myself off the meds (this has been a slow steady progression since 11/14) while huge amounts of stress get added. Big stuff in January, then some big triggers in February. Based on my journaling and emails from February through March, I was trying to share that I was not feeling safe, or in a place of peace. Then after I got well from all my ailments, there were more triggers. I tried telling people. I wrote letters and tried to have conversations about how it felt to be triggered and how someone could help me. But if someone has not had to really feel what having a PTSD flare-up feels like, they can’t understand my language. In my mind, I think it must sound like “WAW WAH WAW WAH WAW: and they think I am just being a complainer.
So here is where I am going to say I gave everyone the best I could and I am really proud I hung on as long as I did without exploding in someone’s face. Well….that is, until I did. But I held on for a couple months under what felt like incredible stress with no one speaking the same language as me. I’m sure over the last couple of weeks not much of my language has made sense. I know my brain feels pretty fried.
You see, without really thinking about it, I stopped taking the pain pills. I was feeling better. I was using medical marijuana with good success. I had stopped the muscle relaxers and the anti-anxiety medications quite some time ago….except for that night time dose of Xanax which is what the NP prescribes for my severe insomnia. Oregon Health Plan won’t pay for anything less addictive for chronic insomnia, so this was my option for a long time. I still have to wean myself off of it.
Unbeknownst to me, combining ongoing PTSD triggers and withdrawal from opioid’s is a horrible situation. Had I thought about it, I would not have done it, but now I’m 6 weeks or more into it and don’t want to have to go through all this again.
So….things you need to know if you have PTSD and you also are considering detoxing off opiates with medical marijuana!
Be good to yourself. Be kind. Remember it took years to get here. Keep in contact with a medical care provider if you can’t be certain you or others are safe while withdrawing. Realize it takes time.
I am not having a good time with this and it isn’t looking ladylike when I rage and roar…but I am determined to find peace without handfuls of medications that do nothing in the long run. While all of this is not so great of a time and at times quite embarrassing, if one person reads this with chronic pain or PTSD and keeps from getting themselves from being addicted to prescription pain and anxiety meds then I have done a good thing.
I am sharing this because I want to help others. There are other options to all the pills our doctors so freely hand out. I hope if you are reading this…it’s before you have a 20 year habit that you don’t even recognize it is a bad habit. I was just following doctors orders.
I was diagnosed with PTSD when I was in treatment for my Gambling addiction over 6 years ago. As well as generalized anxiety disorder. I have been to counselors off and on since I was 17 years old and it took nearly 30 years for someone to see what was then obvious. I do remember one or two people that knew some of my life story commenting that I probably had PTSD but I thought then it was for people who had experienced war or something like 9/11.
Additionally, I have learned over the years that there is a subdivision of PTSD called Complex PTSD. This form of PTSD is more common for combat vets, those who have been victims of being held prisoner, or anyone with multiple traumas over a lifetime. Children that had been abused physically or mentally or left without their basic needs being meet. Those that were abandoned or left in vulnerable places with no protection over and over can develop C-PTSD. Or a person who has had multiple traumas throughout their life. While I do have the diagnosis of PTSD, it is my own conclusion that I most likely have C-PTSD.
Most the times the symptoms are much better than they used to be and I do have tools that I’ve used to keep my levels of stress tolerable. I have been on Effexor XR for over 6 years and it’s been the best medication (and only one I take anymore) for these conditions. So in addition to stress from outside my body I was having additional stressors internally as my body experienced some withdrawls, as after 18 months I had completely weaned myself off all pain and fibromyalgia related medications. I have been off all narcotics and muscle relaxers for nearly 2 months. So having some symptoms of Post Acute Withdrawl Syndrome (PAWS). The combination of stressors where I live and what my body has been going through with pain and PAWS was ripe for a significant event.
Last week week I had a complete PTSD meltdown. I had one trigger too many and I had no control of myself anymore. It was so scary and so terrifying and it completely turned my life upside down. I frightened my family and loved ones with ridiculous threats of harming others and disappearing and never to be seen and all types of crazy stuff. I remember some of it, but there were some times it was like an out of body experience. That’s called disassociation. It’s a really weird feeling. I know it’s me having the feeling, but it’s like I’m watching someone else going through it…or something like that. Very hard to describe..but very scary.
This was the first ever that I can recall that in my mind I was so angry and so hurt and so scared that I had truly violent thoughts against others. Typically I just shut down after the meltdown as a crying puddle of emotions for a week or so. I wasn’t going to act on them…but stating it out loud and letting my mind go to those places was somewhat cathartic. In all honesty, I would never hurt a person. But dang, I sure could day dream about it and verbalize it in the moment. It wasn’t because I really wanted to hurt someone. It was because my cortisol levels had become so elevated my brain wasn’t functioning property.
I’m not going to go into all the physiological components of what happens to a brain when PTSD is triggered in this writing, but maybe another time I will explain how the reptilian part of the brain is what is affected.
So, yesterday I went in for an intake appointment for counseling…again. I’ve been in counseling off and on since I was 17. I’ve worked on so many of my issues and I’m so much better. In fact, I’m feeling strong enough I am ready to dig deep to get to some of the core issues that have caused so much angst through my life. I know that sounds ridiculous to someone who just said they had a PTSD meltdown, but sometimes that’s how this crazy stuff works. It takes a catalyst to get you prodded to do more work.
Lastly, one of my biggest components of having a PTSD meltdown is that I push everyone away. I am embarrassed, I am frightened, I am feeling out of control, and I feel so unworthy of any love or caring of any kind. I know that is ridiculous now…but in the moment that is how I behave. The truth of the matter is… that is when I need love and support and caring more than ever. I need to know I’m worth loving. I need to be reminded it will pass and I’ll be okay. I need reassurance that I’m worth having around. Because at that moment….anywhere would be better than being in my body and my mind.
I apologize to family and friends for the fear and concerns and the challenges loving me brings. I can only hope that my star shines more often than the occasional storm cloud that blocks the light.
I share this as a public service announcement because I am wanting the general public to have a better understanding of mental health issues. People don’t hold it against a diabetic for having a crisis or a seizure patient for having a seizure. Please have understanding with mental health. No one asks for these conditions. It’s not a sign of weakness or bad morals or anything like that. It’s an illness in our body. I’m trying to treat my illness. Please don’t think I am my illness…I’m still me. I still love to garden and take photos and love people…well…some of them. I still laugh and cry over things you do. I’m not that different, I just have my moments.
Share your story. Educate. Speak up. Challenge perceptions. Be brave. You are not alone! End the stigma of mental health.
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