Posted by SuperADDMom on July 5, 2010
So planning things is helping me not have so much anxiety.
becoming more aware of my high anxiety times is helping me avoid total add/aspie meltdowns.
all my life I’ve been a sort of “fly by the seat of my pants and see where I land and deal” kind of person.I think one of the reasons I avoided it like the plague is because I fear needing to be very rigid and have strict planning to function. it’s almost like dealing with the chaos feeds my ADHD need for stimulation, and my aspie side of me is cringing, and having anxiety the whole time.
So planning things, and using a day planner/to do list has not been natural to me, nor has it it been easy to start as a habit.
I’ve finally come to some habits that are making things easier for me, though if I get interrupted/sidetracked in my routines, I forget things lose things etc.
Slowly I’m trying to fix the mess I’ve made of this place since our move and my mental burnout. Your looking at someone who has taken 11 years to remember hubby needs his bread toasted to be able to eat it ( oral sensory issues)
So, I have a day planner I write a week out in, in an overall plan, and then each day of the week after the general plan I write out info that is important as those days come, like who I called, recipes, my master to do list for the week, and next steps in those projects .. really it’s just a composition book, with blank pages, so I have no worries of needing to remain neat, or confined to a certain amount of space. it IS my brain it holds everything.
and I have a calendar I write out meals on for a week or more to have a plan.
On Sundays I plan the weeks meals ( generally, sometimes they change)
This week, my menu plans are
Chicken taco crockpot w/home made Naan bread
Salmon Croquettes w/dill sauce
beef crock pot & gravy w/mashed potato
Veggie Lasagna
Pizza
Crock Pot Pork with orange and Videlia onions & rosemary rice.
Posted by SuperADDMom on May 26, 2010
doing paper work…i hate paper work
the amount of paper work that it takes to get things from our disability support is a full time job in an of itself. they changed the way you file for gas for medical travel.
It’s a TOTAL pain in the ass. they are cutting me short for mileage to my ADHD dr appointments, using google maps and having me travel on back dirt ( bog) pot hole infested unmaintained roads to shorten the distance, that are not even plowed in the winter and are considered snowmobile trails in the winter.
I don’t travel those roads, so they are cutting me short on klm per trip of the crappy 18 cents a klm to travel it… the trip is 137 klm round trip. it minimal, but it’s the point, they try to cut corners every chance they get.
Last year they took away the back to school clothing allowance for children, and the winter clothing allowance for children.
the 18 cents per klm doesn’t even cover the actual gas we use to go there and back. ( lets not even factor in maintenance and wear and tear on our vehicle, and the fact that we are too rural to take a bus, or taxi cab.)
and now for every trip I take BESIDES that appointment for medical travel, I have to fill out a medical cost form, submit gas, parking receipts for THAT day. We live rural, so we don’t buy gas ON THE DAY, we buy gas and fill up for multiple trips, and try to do so when gas prices are lower, since they go up and down more than a cheap hooker on Jarvis Street ( local Toronto ref sorry)
So, I just KNOW that when I submit one gas receipt for two seperate trips, because it was a 40 dollar gas purchase we made knowing we had multipul medical trips coming up, it’s going to confuse the morons that seem to work in our local office.
Once The Mundane One had to step by step, with a calculator, talk the worker for disability through a math calculation, because they were trying to say they over paid us, and were cutting us off for a funding we needed and were entitled to, and they still owed us for for another 5 months.
People seriously lose their brain matter when working for an agency or company that requires them to work from the step by step instructions in a book, they cannot think for themselves. it’s insane really!
He had to finally talk to her supervisor to get it straightened out! this is the level of competence we are dealing with here. We are smarter than them literally, but they treat us like we are retarded because we are disabled.
did I mention I hate paper work?
Posted by SuperADDMom on May 18, 2010
- 4 yo me saw my third term of SK marked as “behind her peers” and would be held back in SK if I didn’t show significant improvement
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4 year old me did not get along well with the other girls, i didn’t understand “playground soial rules” and the teacher was concerned for me
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4 year old me, was clumsy, and accident prone, and was no longer allowed un covered cups at snacktime…i remember the yelling
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4 yo me, had hearing tests because I appeared to have a hearing deficit, but my physical hearing tests came back fine
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4 yo me had to take speech therapy bcause I could not talk well…speech therapy taught me how to read lips, little did they know..
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4 yo me could not count to 15, i would count, 1,2,3,4,5,6,7,8,9,10,12, 11,13,14,15 EVERYTIME, and was scolded for it ( i remember well)
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4 yo old me, refused to play building blocks with a partner, and wanted to be alone and would have temper tantrums if forced to play blocks
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4 yo me, could not sit still for reading circle, interrupted with questions, being “picky” on the teacher paraphrasing the storys she knew..
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4 yo me…hated chalk and paint on my hands, refused to do those activities. liked to play house with dolls, in the dress up area alone..
so, ya.. looking at this report card.. the signs are SO CLEAR…but not in a public school classroom in 1978
Posted by SuperADDMom on May 12, 2010
I live on the outskirts of a small town. I used to live in the small town, and for the last 5 years attended mommy play groups with other parents. So, when I go to town, I see some people I “know” on a hello basis.
Tonight when taking the girl to her swim class in town at the rec centre, I knew I had to go and pick up milk at the store my kids call “Big Tig” ( the store has a huge tiger painted on the side)
A few weeks ago we ran into the coordinator of a mommy and me evening program called Busy feet, and we had not gone since we moved from town.
Since the programs on Wednesdays overlap by an hour, she invited us to bring the boy while the girl is at her class, and tonight he mentioned to me that he wanted to go to busy feet.
He mentioned this as we were getting back in the van from dropping off the girl, and I happily agreed that we’d stop by to see after I picked up some milk.
And the very second I agreed to go check it out, and see people we have not seen in a while, I got in the van and flipped down the sun visor and noticed something that made me want to get out of going anywhere in public.
big black chin hairs! OHHHHHH crap! As a 35 year old ADD woman, with changing hormones, I no longer worry about pimples, but I’ve started growing stray dark black chairs out of my chin….this would not be so bad, but I forget to do a good check and pluck them out, and then I notice them at really awkward times, like when I’m in town, without tweezers, and needing to go somewhere in public.
I frantically searched my backpack for a pair of tweezers. I own several pair.. and I had THOUGHT i left a pair in my back pack for just this kind of situation…but a 5 minute search resulted in nothing, and found me bargaining with my 5 year old to find a reason to NOT go to busy feet, where I’d have to talk to people, and be totally aware in my own head of the black chin hairs. I rationalized that I’m sure no one will notice, but that it didn’t matter. I’d notice, and that was enough to make me nervous and anxious. I have social anxiety enough as it is with my communication issues due to hearing processing, and also reading people’s body language, so I didn’t need this kind of extra anxiety.
So, I drove to run an errand for The Mundane One, and got stuck in traffic, then went to big tig for milk, and decided to see if they had some cheap tweezers.
Cleaning the car last week while waiting for a dr appointment I’d found a $1 coin ( called a looney in Canada) and thought perhaps it wold save me.
IT DID. they had a pair of tweezers for a dollar!!!! so I bought them, and plucked them suckers out of my chin in the parking lot, and then went off to the play group with my boy for the last 40 minutes of it. And in all of that, I almost forgot to buy the milk!
(me in total “no makeup, hair in ponytail, not brushed today, stained sweater going to town mode”)
Being a sexy SuperADDmom is no simple task!
And I’m gonna yell at the Mundane One for letting me out the door like that!
I’m keeping the tweezers I bought today in the van from now on, for just this kind of situation!
Posted by SuperADDMom on May 3, 2010
Uggg. I can’t find the arm pit spray! Because I have to attend the gym and swim program with the boy, I put my personal hygeine products in a travel bag to take back and forth with me, and now I’ve lost my underarm deoderant! I have b ack ups, but I didn’t want to smell like Vanilla today, I wanted to smell like Cucumbers.
Make sure you buy double,”travel” items, and leave your home stuff home.
also, when you are trying to establish a new “home” for things so you never lose them…maybe write down on a card for the fridge where you made the new home cause last night I searched for my day planner for an hour.
I finally remembered I had put in in my nap sack in one of my “i’m gonna get all organized moments”, and promptly forgot it was there. Where I intended it to always be, but have not put it there in over a year.
IT took me over 3 years to establish a “hang your keys up right away when you walk in the door” routine.. and some days I still don’t because i have to run in fast to pee…and on top of that, the kids like to steal my keys to open the workshop, or turn on the radio in the van when they are waiting for me.
Posted by SuperADDMom on April 29, 2010
ohhhh my… i just witnessed in myself a near meltdown from sensory overload.
This naming it to claim it stuff is draining.
Now that we’ve made the correlation of the Aspergers traits I have, I’ve been working on becoming more aware of when i’m having what I call “An Aspie Moment”
Sensory overload is a thing.. too much noise, to much light, to many colors. I am a very visual person, I see things very vivid and i notice EVERYTHING…unless I’m really hyper focused on something, I see and take in everything around me.
In the last few weeks, it has been interesting basically evaluating myself to see what is bothersome, when do things get too overwhelming, and how I deal with them, so I can deal with them better.
Being tired. Being in pain…they make it harder for me to filter, and process everything I take in. It then makes my ADHD traits worse, and I’m essentially a bumblling idiot who can’t remember what you call that thing you put things in to stay cold in the kitchen.
When I get that way, I get flustered, anxious. I have a hard time finding words to speak and I go inward. I get clumsy and trip over my own feet. I make mistakes, I get scatterbrained more. My depth perception is off, i break glasses, burn dinner, etc..the list goes on and on.
I recognize that in the past…I’ve dealt with these things, and have been avoiding actual panic attacks, or temper tantrums I guess by becoming actually moody, bitchy, cranky, sometimes even reach a boiling over point to near, if not total rage.
When I’m moody, bitchy, cranky, no one wants to be around me, and it was I guess a backward, sub conscious thing that allowed me some alone time. It gave me the time I needed to recuperate and stop the panic inside, calm down, and find a way to regroup and move on, and handle the sensory overload better.
So, with this awareness, i’ve been trying not to be cranky and be a bitch when I notice these overwhelming feelings coning on, and I’ve been trying to find a way to cope better that is healthier for the relationships with the other people in my life.
Diverting the kids to go somewhere else away from me, using my ear phones, but still being physically present etc.
But today was too much…..I’ve been this overloaded before…many times… but by now I’d always have been bitchy, cranky at people’s needs, yelled at the kids for the smallest things like how they are chewing their cookie near me ( the sound is SOOO ANNOYING and LOUD i can hardly stand it). I’d been cranky with hubby, and then this would cause strife for a while. There would be bad feelings between everyone, and then I’d need to recoup, AND get over the bad feelings, and apologize for my behaviour.
Today I fought the urge to be bitchy…It is very hard to fight the tendancy to revert to a coping stragedy I’ve used for 35 years. I managed to not flip out, but it was replaced by the urge to physically run away…I’ usually run away to the computer, and that in an of itself causes issues, because I retreat to the computer as a way to shut out the stuff that is overloading me, and then I get less done, and hubby gets mad at me for “being addicted” to the computer.
I’ve been trying not to run to the computer for a mental escape as much lately, and have been using a timer to force myself to do things that need to be done, for a certain period of time, before I go take a break.
So I didn’t run to the computer….but I got a feeling of being out of control and stuck in a situation I could not get out of, and I started to have a panic attack. Of course I put myself in the situation with my limits I’m trying to pose on myself in small ways.
But I could not run away from what I was doing to retreat to the computer, or even run away outside, because I was cooking food for people, baking cookies, and listening to hubby talk about stuff he wanted to tell me.
I had a loud self talk in my head saying. “pay attention, pay attention, listen….don’t panic, just finish the cookies and then you can leave. hang on ok!? Don’t get mad at everyone.”
At some point, I had three people trying to tell me something all at once over each other, and I could feel the need to get mad and yell “go away from me now, you’re driving me nuts!” I answered in a snappy tone and had to take a breathe and appologize right away to not let the responses to my snapping, roll over into the same old song and dance we always end up doing when I get to feeling this way.
I don’t know how I got through finishing the things I was doing in the kitchen, but the second I was done, I HAD to go away.
I had a tight chest, heavy breathing, and a headache behind my eyes coming on from the stress, because I wasn’t reverting to just coping by getting mad.
I’m upstairs now, in the office where I usually gazelle. it’s quiet, it’s good.I txt messaged hubby to tell him where i was and why.
I started writing this to try and get it out as it is pouring out of my brain, and I’m trying to relax.
I’m still buzzing in my brain and my body feels like how it feels when you drink too much caffine in a short amount of time…jittery and jumpy. But as that slowly starts to die off, and the adrenaline from my little Aspie moment is spent, I can feel how spent of energy I am…
My brain is fried right now, and I feel like I just need to sleep for a little while. I feel guilty about that, and I’m not sure anyone here would let me sleep for a little while to get some equilibrium back.
I hate this feeling.. these are the times, when I would get mad and bitchy at everyone and say “maybe I just need to live alone on a mountain in a yurt with no one around me, cause I can’t take this crap anymore”
sigh…..
A blog of a woman with aspergers has been really insightful in allowing me to go, hey…there’s a name for that!?
It’s a good thing to be making the connections… but also…. it processing, and dealing with stuff, and THAT is tiring to.
I never made the connections before but this is why I have what I call “recoup days” after we’ve had a day out shopping, or driving far to the city etc.
I’m discovering the reasons behind elements of who I am, I never really gave a second thought to.
if you’re interested in reading it…
http://www.aspieteacher.com/2009/07/be-an-aspie/
thanks for letting me spill that
Posted by SuperADDMom on
Aaaaaaaaaaaaaaaaaaaaaaaaaaakkkkkkkk
I’m going to lose my shit! Seriously… the noise is nuts! POLLUTION to my brain.
I’m having a bad auditory day….every noise is grating on my nerves, and is amplified and making me jumpy.
I’ve been up since 8 am, with 4 hours of poor sleep due to pain. I go up today and took the boy to his dash and splash program which I have to paricipate in too. So I’ve trampolined, and swam today and coached the boy in his classes.
He loves the water, but is freaky about water on his face and ears, and that was today’s class…WOOHOO.
So he practically drowned me in the pool clinging to me, and near ripping off my bathing suit.
Anyway….I’ve somehow hurt my right rotator cuff and am in pain It feels like someone slammed my shoulder joint area with a sledge hammer. it feels bruised…i’ve never felt this kind of thing before. Anyway, physical pain always lowers my ability to filter things, and makes me more scatterbrained, and I’m a low hormone level in my monthly cycle anyway, so I am just less able to cope right now with too much sensory input. Even lights are too bright today, and the shades are drawn, and the lights are off.
I ran errands, drove home ( which always takes extra concentration effort when I’m having “bad brain” day.) and I’m exhausted mentally.
These are the current noises going on around me at seemingly IMAX theater surround sound levels:
Hubby playing a first person shooter game on the wii in the living room in surround sound sterio.
The kids arguing in the kitchen over a train set we borrowed from the toy lending library, the CAPD boy has the tendancy to talk too loud, and especially when he’s frustrated, and due to his sensory issues and exercising for 2 hours this morning, he is cranky and tired from working his gross muscles and practising his balance, and getting lots od vestibular stimulation.
the bread machine churning dough for pizza later. The Aspie girl is dressed up to be pretty today and wearing high heeled shoes she loves and they are clicking on the floor like riverdance.
Hubby yelling at the kids to not step in the wayof his game.
The dog barking in the bag porch.
And the timer beeping to warn that the cookies can come out of the oven.
I am gonna seriously freak out! I’m physically tired, I need a nap to rejuvinate my brain power to cope with this stuff, but at 2 pm, there are too many things going on and too many things I’m needed for.
It is moments like this that I think my father’s ability to turn off his hearing with his cochlear implant must be a great blessing.
Where can I sign me up for one of those..like right now….PLEASE!?
Anyone have an auger? Can I borrow it? Left ear first please.
Posted by SuperADDMom on April 22, 2010
SOURCE LINK: http://www.publicnewsarchive.com/rewards-work-like-drugs-in-adhd/
The brains of children with attention-deficit disorders respond to on-the-spot rewards in the same way as they do to medication, say scientists.
A Nottingham University team measured brain activity as children played a computer game, offering extra points for less impulsive behaviour.
Their findings, published in Biological Psychiatry, could mean lower doses of drugs such as Ritalin in severe cases.
But they warn teachers and parents may often struggle to give instant rewards.
Estimates vary, but it is believed that up to 5% of children in the UK have some form of attention-deficit hyperactivity disorder (ADHD).
This can lead to behavioural problems including impulsive actions, fidgeting and poor attention span, and can affect a child’s academic and social progress.
In severe cases, stimulant drugs such as Ritalin, which act on parts of the brain associated with attention and behaviour, can be given.
In addition, parents are often asked to try to influence the child’s actions directly by rewarding positive behaviour and making sure that there are negative consequences if a child behaves badly.
Research has suggested that, unlike in non-ADHD children, these incentives and disincentives only work well if delivered on the spot, as opposed to later in the day or week.
The Nottingham team wanted to look at the effects of this “behaviour therapy” in the brain of the child.
They devised a computer game in which children had to “catch” aliens of a certain colour, while avoiding aliens of a different colour.
The game was designed to test the children’s ability to resist the impulse to grab the wrong sort of alien.
To test whether incentives made a difference, in one variant of the game the reward for catching the right alien was increased fivefold, as was the penalty for catching the wrong one.
Lower doses
Activity in different parts of the brain was monitored using an electroencephalogram (EEG).
They found that the incentives helped the children perform better at the game, although not to the same extent as the child’s normal dose of Ritalin.
However, the EEG revealed that both were “normalising” brain activity in the same regions.
Professor Chris Hollis, who led the research, said that the combination of drugs and incentives produced the best results, and might mean children with ADHD could take lower doses of drugs while maintaining control of their behaviour.
He said: “Although medication and behaviour therapy appear to be two very different approaches of treating ADHD, our study suggests that both types of intervention may have much in common in terms of their effect on the brain.
“Both help normalise similar components of brain function and improve performance.”
However, he conceded that it might not always be practical to use behavioural therapy.
“We know that children with ADHD respond disproportionately less well to delayed rewards – this could mean that in the ‘real world’ of the classroom or home, the neural effects of behavioural approaches using reinforcement and rewards may be less effective.”
Andrea Bilbow, from the National Attention Deficit Disorder Information and Support Service (Addiss), echoed this: “It means you have to be in front of that child 24/7, and you just can’t do that – teachers and schools would have to totally change the way they deal with this.”
This article is from the BBC News website. © British Broadcasting Corporation, The BBC is not responsible for the content of external internet sites.
Published by BBC on April 19th, 2010.
Posted by SuperADDMom on April 19, 2010
The stigma of living with ADHD is pretty negative at times. The negative impact it has on our day to day lives, and the people we live with can get pretty stressful. So stressful in fact that without help from medications to regulate brain chemistry, and being on top of RIGID routines to make life easier, we can end up being sucked down the big black ADHD holes of depression and inability to cope.
I grew up not knowing I had ADHD. I was just told I was lazy, and stupid, and bad, a daydreamer, etc. I didn’t learn to cope with my ADHD well, and now in my 30′s I’m basically teaching myself stuff i should have learned when i was younger. Kids today have advantages in the life skills with ADHD arena.But it is still not easy.
Some people think living with ADHD is a walk in the park because we get prescription drugs that are basically cousins in chemical make up to drugs that people take to get high, like Meth. ( drugs that have been around since 1955 BTW)
People see celebrities like Richard Branson, or Robin Williams ( with suspected ADHD) and think it must be a blast to have ADHD.
People make comments about being on medications for it, like we’ve somehow cheated a system to be granted legal narcotics, so we can get high.
As representatives of ADHD, you see these celebs as jovial, and friendly, and chatty. They are daredevils in racecars, or actors or comediens, business people, teachers, even doctors.
But you don’t see us ADDers among you scramble to keep a house clean, make dinner on time,get our kids out the door in a presentable fashion, With everything they need. You don’t see us struggle to make appointments on time, and the stress it causes us internally.You don’t see us struggle to keep a job, struggle to pay for these medications that are far more expensive then any street drug.
You don’t see us search for the 10th time this week for our missing car keys because we got side tracked or interrupted in the middle of putting them away, and we laid them down someplace, and we only realize it when we are already 5 minutes late to an appointment, or lunch with you. You don’t see that we are late because we also didn’t have any clean socks.
ADDers live a life of secret embarrassment for these kinds of things. We blame the traffic, or roll our eyes and say “kids! what are ya gonna do?” or we say ” hey I thought you said <insert what ever time is cloest to us not being late but just on time>, I’m sorry about that.”
We have to do things like set our clocks a half hour earlier and get everywhere a half hour before, just to ensure a “saftey zone” in our schedules to allow for ADHD blunders and mixups.
People with ADHD make mistakes, A LOT. Daily. hourly. We struggle to keep up in a world with standards and time tables set by people who don’t have ADHD.
So, as a person with ADHD it really pisses me off when people make jokes about my medication, or imply that I must be a “happy mommy” because I take amamphetamines to “get through the day”. Or they joke and ask me how I pulled off an ADHD diagnoasis just to “score”. They say things like ” nice deal if you can get it”
So…
Just to clarify…
An Amphetamine is a psychostimulant drug that is known to produce increased wakefulness and focus in association with decreased fatigue and appetite. Amphetamine is related to drugs such as methamphetamine and dextroamphetamine, which are a group of potent drugs that act by increasing levels of norepinephrine, serotonin and dopamine in the brain. All chemicals, if you bothered to look into it further,that you’d know ADDers have lower levels of.
We chose to put these chemicals in our systems, because it alters our brain chemistry to try and put us on a par level with people who don’t struggle through life with a sleepy brain, and so we can live better among a society who sees us as “broken, annoying, and beneath the rest” that need to be fixed.
FYI the hyper activity of ADHD is CAUSED by LACK of the chemicals those drugs help our bodies produce at more “normal” levels in order to STOP the hyperactivity. To bring us UP to a level of “normal” functioning like you have the ability to do just by breathing. We don’t take them to make us high. Bt they’d likely make YOU high.
I personally struggle in the morning to wake up because those chemicals are so low in my system. I could just sleep all the time without my ADHD medication. Did you know there are scientifically proven links between ADHD and narcolepsy
In order to be able to just walk to the bathroom upright in the morning, due to the morning haze my ADHD brain has, I have to set two alarms, one to take my meds and snooze back asleep until they start to wake me up more due to the chemicals in my brain rising from the help of the meds, and then I wake up to the second alarm, and even then STILL, it takes my brain at least an hour to feel functional. When my meds wear off toward the end of their effectivenes in the day, as a mother and wife I still have a lot of “work ” to do to keep a family with special needs functioning, and prepared for tomorrow.
If I don’t remember my meds one day, we fall out of routines and things get way out of sync, and we all must struggle to get back on track, because I go around in a scatterbrained haze unable to accomplish much of anything.
If I take my meds too late in the day, my brain is wide awake, and I can’t get to sleep and I’ll find myself awake at 4 am, planning a menu for the month, or tweeting, or watching movie, because my brain then won’t shut down until the chemicals dwindle down to a lower level to bring on sleep.
And, just so you understand the cycle… once my brain is FINALLY sleepy from the lack of chemicals again needed to stay awake… my brain will just want to stay sleepy, and we start the cycle the next morning all over again.
ADHD medication make us not want to eat as much and people struggle to get in the proper daily intake to remain healthy. This is especially a concern with children who are still growing.
I’m not sure what the Non ADHD world thinks, but having ADHD is not all fun and games. People with ADHD come from higher rates of divorced homes due to the chaos and stress ADHD traits cause in everyday living. Adults with ADHD, struggle in relationships to find a balance that works, and also have a higher rate of divorce.
People with ADHD have increased risk of drug and alcohol abuse ( trying to self medicate a constant sleepy brain), have higher rates of severe low self esteem and depression than the general population, as well as debilitating anxiety problems, and higher suicide rates.
Ya! pretending to have ADHD when I was 6 months pregnant and depressed to get a diagnosis finally, just to not be able to get any help with my brain chemistry for over a year, due to breastfeeding my son was a SURE sign I was looking for a quick cheap legal high.
HAHA YOU R FUNNY!
Oh? it is just a joke? oh. my bad…I’m such a stiff!
People with ADHD have higher rates of being in lower income levels due to struggling through school with learning difficulties, keeping jobs due to ADHD interrupting their ability to do their job to expected standards ( late for work, poor performance on bad days, forgetting projects due etc)
People with ADHD try to be upbeat and positive because we have SO MUCH negative stuff in our lives to deal with. Prescription drugs for ADHD is not a COPING thing. We are not getting high. Shit, smoking pot in highschool didn’t make me high, it made me normal! YA that was fun! Everyone else was giddy and high as a kite, and I was able to finally focus enough to go home and do my homework for the first time in my highschool career.
Our meds are helpers to the chemicals our brain cannot produce well enough on their own.PLAIN AND SIMPLE.
You’re stigma, prejudice and “jokes” are offensive. PLAIN AND SIMPLE.
So if you are gonna look in my face and say to me that my drugs make me hyper, or happy, or that ADHD can just be “cured or solved” with some basketball… well, sorry to be so blunt, but I’m gonna have to say…
FUCK YOU!
Plain and Simple.

YMCA Vancouver Paid Ad in a local paper. Charlene Giovannetti-King, the YMCA Vice President of Funds Development directly linked to the Advertisement said “We don’t see this really as a mistake” on a CBC radio interview with Rick Cluff.
Posted by SuperADDMom on July 1, 2009
sigh…..where do I even begin with THIS one… ugggg… my poor husband….he is such an amazing man to put up with everything that ADD has a part in for the chaos that is often our life caused by me.
IT’s been a rather interesting week or so, you see…I’m hitting menopause…yes, at 34 years old. I’m on the way out of the childbearing years. I knew it was likely to come earlier then typical for most, because all the women in my family have started their journey to “mature womanhood” around this age.
As such I’ve been having a lot of issues related to hormones…typical ones like heavier periods, longer ones, then shorter ones, hormones and mood fluctuations. Not to mention hitting a sexual peak for being REALLY interested and easily aroused, and being REALLY REALLY scatterbrained!
So today the BIG ADD moment and screw up was I drove to the city for about 20 KLM with the parking brake on.. yes folks… totally in a daze… mostly a sexual one, being all hot and bothered for my hubby sitting beside me smelling so damn hot, while we flirted obscurely without the kids aware of what we were saying from the back seat. I drove with the parking brake on. You see I have a check list I do for a lot of stuff I do, to make sure I do them…habits that I’ve come to incorporating to make sure I don;t make scatterbrained mistakes. IF I get side tracked from them,,, my world starts to unravel and I make a LOT of mistakes. So I forgot to do my checklist hen I got in the car before I put the car in drive.
It was NOT a nice moment when hubby realized it… I had to pull over the van and he got out and walked off the steam coming from his head from the anger at THAT one… the brakes are not good at best right now, and then I go an do that
THAT was a crappy moment
We managed to make it through the rest of our trip relatively unscathed from my lack of ability to concentrate well, and are home now.. kids are fed and in bed. and I’m heading there now too. To take advantage of this new shift in sexual interest I have to THOROUGHLY make it up to hubby for the day we had !