An Interview With An Aromatherapist

Back in the early 2000’s, I became friends with a great lady who was the owner of a little online business called Mystick Scents. Her name is Becky Long. I started by purchasing products from her for my own use and for my little online business called Scents Essential. We became fast friends and in 2006 she sold her business to me! I merged the two businesses together and kept the Mystick Scents name.

I had learned a great deal about aromatherapy and how to make lotions and creams, body sprays, bath salts, etc., from this woman, my mentor, and friend. Eventually, I started to venture out into creating my own recipes. It was a great experience! But, my physical health was slowly on the decline and I had to close Mystick Scents in 2010.

Becky and I are still friends; besties if you will. She now owns a business called Herbs 4 Health. She writes a blog and has a Facebook page. She has been forever trying to educate the public about essential oils and aromatherapy. I thought an interview would be a fabulous idea! (Links are located at the end of the interview for your convenience.) Enjoy!


Becky, can you start by telling my readers about yourself, your specializations, and where you can be found for more information?

I am certified in both herbal medicine and in aromatherapy. I am also known as Herbmama. The business I own is Herbs 4 Health and I also have a blog called Herbmama’s Words. I can be found on Facebook along with the business and blog.


What is an aromatherapist?

An aromatherapist is one that is educated in and uses essential oils to help improve one’s health whether it be physical, emotional or psychological.


What exactly is aromatherapy? 

Aromatherapy uses plant materials & aromatic plant oils, AKA essential oils and other aroma compounds for improving health, psychological or emotional well-being.


What or who inspired you to go into this field and when did you get started? 

The quest for knowledge in this field happened when I had a bath/body biz called Mystick Scents. Then I became a sponge and just had to know more & more which led to my certification.


How are essential oils used? 

Essential oils can be used via inhalation, topically and internally — the later only by a trained aromatherapist as it can be dangerous.


How are essential oils extracted from plants? 

There are basically 2 methods for extraction: the distillation process where the plant material is heated and then the water/oils are separated. Any by-product from such is sold off. Then there is cold pressed which is exactly what you think it is….peelings from the citrus are pressed to get the oils.


How do people know the best method for using essential oils? 

A lot of people don’t know, which is why they can get into trouble. The best way to find out is to ask, not just assume you already know. You might have an essential oil that can cause more issues than what you started with.


How do they work? 

Essential oils can actually change brain chemistry. They can work on what the body needs at a particular time. They are a type of fat or oil so they can easily get into the body’s cells to do the work. Although we aren’t allowed to say…they can heal. They are anti-viral, anti-microbial, and anti-fungal so they can work on those types of maladies.


Can they be used straight on your skin? 

It’s not advisable to use essential oils straight out of the bottle. Only lavender is gentle enough for some. Always dilute and do a patch test if you are new to essential oils or a particular oil.


What is a carrier oil? 

A carrier oil is an oil one mixes with essential oils to apply topically to the skin. Some examples are sweet almond, jojoba, fractionated coconut oil, grapeseed oil, olive oil.


How do you know you’re buying quality essential oils? 

One has to find a reputable essential oil supplier with learned knowledge so you know what you are looking for and who you can trust. So many are adulterated now which means other chemical components have been added to dilute the healthful benefits of the essential oils and the body can’t synthesize chemicals. Once you find a good company, there is a way to test to see if your essential oil has been adulterated. Place 1 drop on a piece of paper and let it evaporate. If there is no residue and no oily stain then they are pure.


What’s the difference between therapeutic grade and manufacturer’s grade essential oils? 

There really isn’t a thing as manufacturer’s grade as you say. There is food grade which is different than therapeutic grade. Therapeutic grade can be a relative term as ALL non-adulterated essential oils are therapeutic in their own right. A lot of companies say therapeutic as a marketing ploy. Food grade essential oils are diluted with additives to sell to the food or perfume industry.


How should we store our essential oils? 

Essential oils should be stored in air-tight dark colored glass bottles away from heat and direct light. The more you open them, the faster they can go bad and evaporate.


Some people/companies suggest taking essential oils internally. Is that really safe? 

NO! It’s not safe in my opinion. There are essential oils that can be ingested but only with advice and guidance from a qualified aromatherapist. No way should they be taken full strength as the molecules are too strong for the sensitive tissues internally. There have been (reports of) damage done to esophageal tissues, organs and stomach tissues from essential oils.


 Are essential oils safe for kids and pets? 

There are some essential oils safe for pets but that should be done through research and usually on a case by case basis. One e.o. for a dog or cat may not be ok for another breed for example. Kids…generally, yes but further dilution should be done before and of course the child’s weight/age have to be factored in. There are aromatherapists out there that only treat animals though.


Are essential oils really better/more effective than conventional treatments? 

Essential oils are better than conventional, in my opinion. They are powerful and natural. But that question is really hard to answer so I don’t get myself into hot water with certain government agencies if you know what I mean. 


Can you boost your immunity with essential oils? 

Oh yes, the body’s immune system can be greatly enhanced and boosted with essential oils!


What’s the biggest mistake you see people making concerning essential oils? 

Ingesting them and applying them without proper dilution. Thinking they know it all with like 5 minutes of experience.


Which 5 essential oils are the best to get started with, to always have on hand?

One’s basic ‘medicine cabinet’ should include lavender, peppermint, tea tree, rosemary, and lemon.


What is an essential oil ‘blend’?

A blend is more than one essential oil together with a carrier oil that helps a specific problem whether it be physical or emotional.


Is there a blend or blends that we should always have on hand? 

Oh I think so, yes. Blends for colds, flu, pain issues, things like that.


What’s the most common way people are using essential oils? 

Topically, diffusers and in the bath.


What do you enjoy the most about working with essential oils? 

Mostly I enjoy developing the blends I guess!! Sniffing them as I put them together, figuring out which oil would be best to use, knowing it can possibly help the next person who uses that blend.


How do you use essential oils in your own life? 

I use them for health prevention, to help boost my immune system, as a perfume, in bathing, at times in cleaning too.


What are your favorite essential oils/blends? 

My favorites are the Krud Kicker, my Taurus ‘perfume’ blend, the memory oil. I like them all pretty much. If the blends don’t smell ‘attractive’ people won’t use them.


What do you think scares people the most about essential oils? 

That they know little to nothing about them and that is THE greatest obstacle…educating the public!


What advice would you give someone considering a career in aromatherapy? 

Don’t try to learn or memorize ALL the essential oils, there are far too many. pick a few you want to start with and learn all you can about those. When you are ready, add slowly to your repertoire.


And my last question…. Is there ONE tip you would like to give my readers?

Don’t judge essential oils without learning just a little about them. Try them. They come from plants, trees, barks, roots, flowers, so how bad can they be for our health??!!


I hope you’ve enjoyed my interview with Becky (Herbmama) and that you feel you’ve learned a little about essential oils. For more information, please check out the following links on Facebook:

Herbs 4 Health 

Herbmama’s Words 

Or go to her blog directly at:

Herbmama’s Words  



What I Have Learned About Dieting

Many of you who know me or have been following my blog, know that I have weight issues and furthermore, issues with doctors and their fat shaming. I’ve been having weight issues since my first child was born, due to under-active thyroid. I think the biggest issue with that under-active thyroid was that for 5 years it went undiagnosed because doctors passed my weight gain off as “still eating for two” or “finishing what’s on the kids’ plates” or “sitting on my ass all day.” Those were just the nicer things they said to me. Once I was diagnosed and put on medication, I was able to lose some weight but then I hit a plateau….and stayed on that plateau for many years. Then I started having pain issues and my activity level decreased. That’s when my weight increased. At my heaviest, I was 275 lbs.!

Fast forward, to March 2016, when I was so fat shamed and humiliated that I left a doctor’s office in tears. I had no choice but to purchase a diet program — because up until then I had tried every diet known to man, except for the ones you have to pay for. I learned a lot about losing weight since then. I lost 10, then 20….and more. It was coming off! I lost 60 lbs. total! I hit a couple plateaus along the way. I even gained a little back, but I’m back on track now. I won’t give up!

Keep in mind, I am not a nutritionist. I am not a dietician. I am not a diet or weight loss counselor. I am writing from my own experience and the things I have learned are things that have worked for me. I hope this might help someone who is in the same boat as I am…..because we all know how much help doctors can be sometimes.


Eat. Eat. Eat. Don’t starve yourself! You have to keep your metabolism going throughout the day but you will slow it down to a snail’s crawl if you skip meals or starve yourself. Also, be prepared to eat every 2-3 hours. That’s 3 meals, and 3 snacks per day. No, it’s not a lot! Eating this often keeps your blood sugar stable and you won’t get those sudden urges to pig out!

Watch your portions. Read the labels. Don’t take just a little extra; stick to one portion.

Find what your calorie intake should be and try to aim for that number. And yes, you have to count your calories. If you have had doctors tell you, “You just need to count calories,” they are only partially right. Counting calories is just a small part of losing weight, which is why I failed for so many years. I’m sure there are others who have had the same problem.

Drink 64 oz. of water each day. Tea and coffee can be part of that 64 oz. if it’s not doctored up with fats and sugars. (Use artificial sweeteners or honey, and fat-free, sugar-free creamers.) Other drinks like Crystal Light and the like are also acceptable – but drink mostly water.

Make sure to eat at least 4 servings of vegetables each day! Seems like a lot, I know. It’s really not. Half a cup cooked or 1 cup raw is one serving. Make sure they are non-starchy vegetables. Oh, and the best part (to me, because I love my veggies!) is that you can eat as many as you want and you really don’t have to count those calories!! If you get hungry during the day at any time, break out the veggies! (Just don’t drench your veggies with oils, dips, and dressings! Those calories will count.)

Limit salt, alcohol, sugar, fat, and calories. Limit the extras as well; things like salad dressing, ketchup, mayo, syrup, olives, chocolate, etc. It’s ok to have a serving (look on the bottle) of ketchup on your turkey burger but let’s not go nuts and consume too many extras. Salt and alcohol will cause a little weight gain so limit those and drink a lot of water. Water will flush it out.


BREAKFAST: Eat within an hour of getting out of bed. This gets your metabolism going. Eat a protein and a carb. Not just any protein or carb. Eat LEAN protein and carbs that are low on the glycemic index. Look them up. Make a list of the items you like and can afford to purchase for your diet. Try low-fat, low-calorie yogurt and 1/2 of a whole wheat bagel or a serving of granola cereal and 1/2 cup of low-fat milk. There are many possibilities.

AM SNACK: 2-3 hours after breakfast have a snack. Your snack should be a LEAN protein at this time. Try a boiled egg, yogurt, or a palmful of nuts. It’s a great time to have a glass of water too!

LUNCH: 2-3 hours after your snack, have lunch. Have 1 LEAN protein and 1 carb, again low on the glycemic index. This is a great time to add 2 servings of veggies! If you love salads like I do, be sure to limit your salad dressings to 1 tablespoon. You could have tuna salad with wheat crackers or a turkey burger with a small wheat bun.

PM SNACK: 2-3 hours after lunch, have another snack. This time, have a LEAN protein and a carb. Could be an apple and a tablespoon of peanut butter, or wheat crackers and a tablespoon of cream cheese. Don’t forget the water!

DINNER: 2-3 hours after your snack have dinner. Here’s where you get 2 LEAN proteins and a carb. You could have a chicken enchilada with cheese, or salmon and 1/2 baked sweet potato. Don’t forget to add 2 servings of veggies!

AFTER DINNER SNACK: 2-3 hours after dinner, choose a cookie, popcorn, pretzels, peanuts, fruit or a brownie. Be sure to stick to one portion! You have to treat yourself or you will go nuts! Trust me, every single time I have tried to cut out my favorite snacks I have felt deprived and it just doesn’t work! Have your sweet or salty snack and then STOP!


Just a few last things:

If you mess up, don’t beat yourself up! Just do better next time. You’re worth it!

Don’t forget to exercise a little. Every little bit counts.

Don’t weigh yourself every day. Weigh yourself once a week, in the morning.

Make yourself accountable. Write down everything you eat and drink, including calories. Don’t cheat. Don’t lie. Be honest with yourself. Reward yourself but not with food. When you lose 10 pounds, buy a new dress or new purse. Be kind to yourself. You didn’t gain the extra 10/20/30 pounds overnight. You’re not going to lose it overnight.

Create an inspiration board. I put post-it notes all over one wall where I can see it from my desk. My granddaughter even added one for me.

                        Image Copyright Being Aunt Debbie


                             Image Copyright Being Aunt Debbie


I hope this will help someone. I know how it feels to not get any help from doctors. I know what it’s like to lose a little weight and then gain it back. I know how hopeless a person feels after trying so hard to lose, only to gain. It’s frustrating. It makes you feel like a failure. You’re NOT a failure. You just haven’t found what works for you. Just keep trying. NEVER give up! I’m here for moral support if anyone is in need.

Seriously, I’m here.


An Insight Into Autism

My “other daughter” has become a very invested, loving parent not only to her own biological children but to 2 step-sons as well. This is her wonderful opinion piece and I hope you will give it a read. I dare you to walk away without getting it in the ‘feels.’ Please do share, and share again…..

Autism: 4 Reasons Why I will Never Accept the Statement “I hope they don’t find a cure for autism” by Alyssa Anderson


   I was sitting in Phase I training soaking in all of the knowledge I could in order to help my step-son who has autism advance in learning. I understood that his autism was something that made it hard for us to communicate. Sometimes we speak the same language, and sometimes we don’t. Sometimes he would understand what I meant when I said, “I’m going to get some milk.” He knew I meant “Alyssa is going to get some milk.” Other times, I could say that exact same sentence, “I am going to get some milk”, and this time his response is “Ah! I don’t want any milk!” Yes, those pronouns are sometimes tricky. He processed it as “Colton is going to get some milk.”

   Yes, I was there sitting in training hoping I was determined as Temple Grandin’s mom. I wanted to learn his specific language. I wanted to break that language barrier. I wanted to break that barrier so we could talk and learn things from one another about things way bigger than who wants milk. I wanted to help him count money. I wanted him to understand what rent was. I was soaking in this information like a sponge, and then I heard something that made me angry. Instantly I realized that I didn’t understand why this person said what she did and what she said made me so mad.

   This “autism specialist”, our team leader, was explaining that her son had aspurgers. It was wonderful hearing her talk about his quarks and about how much she loved him. Then she said something that had me seeing red (a metaphor Colton wouldn’t quite understand). She said, “I hope they never find a cure for Autism. Actually, the world would be a lot better place if everyone had Autism.” That statement was made to me about 8 months ago.

   I understand very well that my thinking and opinion is often in the minority, therefore I said nothing. Often, I have to research the opposing opinion and sometimes I realize I’m in the wrong. So, over the next few months, I combed through the comments on news blogs and social media posts with titles like, “Mother of Child With Autism determined to ‘Kick Autisms Butt”‘. Once again, I found that I was holding the minority opinion. Comments similar to “how dare you try to change your child, he is who he is and you not accepting that means you don’t love him” riddled the comments. Out of hundreds of comments, maybe ten said “good job, momma”. Out of thousands of reactions, there were few “likes” or “loves” and plenty of “angry” and “wow”. Yes, wow can be on the fence, I understand. Moving forward, I had to ask myself as I often do when my opinion differs: Why? Why do I still feel like I would want a cure? Why am I not convinced? I agreed with their statements like “My son isn’t any less of a person because of his autism”, but I didn’t agree with people ridiculing other parents dealing with autism as trying to “beat it” or advancing their children’s learning to hopefully one day function in society like Temple Grandin. She is an amazing person whose mother never gave up on her. In fact, just like stated earlier, I wanted to have her mother’s determination. Temple’s mom is a hero! That was one determined momma. (If you don’t know the story, look it up. It’s not fiction. If you don’t want to read about it, there is a movie. Watch the movie and the bonus features. You will see Temple herself, and you will most likely cry.)

   I thought long and hard, trying to understand the popular opinion. After a considerable amount of time thinking about my opinion and why I felt that way, at 3 am this morning (yes this thought has been plaguing me enough to keep me awake sometimes) I zeroed in on 4 main reasons why I can not accept the statement, “I hope they don’t find a cure for Autism.”


   Before I start my list of reasons, I want you, as the reader, to understand a little about Colton. He is somewhere between “low functioning” and “aspurgers”. He babbles, but he can speak English. Forming complete sentences in normal conversation isn’t always something he does IF you can get him to hold a conversation in the first place. His favorite word is “no”, and he’s doing this new thing, “Shush! I am the great shusher” when you say something he disagrees with like “eat your vegetables”. He flaps his hands, gets frustrated easily, jumps around, and he does this high-pitched, loud squealing thing and squawking thing when he’s excited watching his movies or playing games like “you’re a dirty old man” with his dad. He is a joker, a prankster, has a wonderful love for his brother, he is exemplary at art, he loves animals, and he draws funny cartoons. One time, he drew me with wings flying in the air, and my arms were open wide, welcoming the children floating around me that were all in the fetal position. He kept saying about the picture “She’s going to love us. That Alyssa is going to love us!” Oh, he is one sweet boy. Do not doubt my love for him because he certainly doesn’t. So here are the reasons why I couldn’t agree with our “team leader”.


   It is hard watching this wonderful, beautiful child cope with his condition. He is frustrated. He may not fully understand autism. He may not fully understand why he feels like he’s different than the majority of people, but he does understand that he IS different. He sees people communicating with one another with ease. He will watch (while looking away. He watches with his ears by putting one close to the conversation with his head slightly turned toward you) in bewilderment as I have a conversation with his dad. It’s so easy for us. I imagine it’s like sitting in a room full of people speaking Spanish while I only speak a little and can’t keep up with deciphering the words. He knows he can’t do that, and it frustrates him. How do I know? Well, no one talks to him here saying he’s different. We try to assimilate and treat him just like we would the other kids in our family. We don’t tell him, “you have autism”. Despite that, he makes statements like “My brain is sick” and “I don’t want friends” (obviously just trying to avoid having to confront his frustration at communication). He has even asked me, “Why do I have to be a human anyway? Why can’t I be a dinosaur? Being a human is stupid. Humans are stupid.” No, I’m not projecting. Sometimes he hurts because of his autism. He doesn’t speak everything on his mind. In fact most of his speaking is trivial and impossible like asking dad to make him a time machine so he can go back in time or asking me to make a DNA splicer since he knows I like Science. Him saying these deeper things are real to him. To him, they are not a joke or a fantasy. He sees the difference, and he doesn’t like it. No one pointed it out to him. Why wouldn’t a parent want for their child exactly what the child wants for his/her own self, especially regarding the struggle with mental health? Could you imagine him asking me to take it away and instead of helping if I could, I tell him “Sorry, I’d rather you have autism”? It would be wrong. I cried thinking about him being upset that “his brain is sick”, those were his words! So for Colton, that dear, loving, wonderful human being, I can not agree with the statement, “I hope they don’t find a cure for Autism.”


   Autism is a significantly broad spectrum. In no way am I downplaying aspurgers, I grew up with someone who had aspurgers. It’s very hard. However, I found it very insensitive for this mother of a child who has aspurgers to say, “I hope they don’t find a cure for autism” to the mother in the back whose child bangs her head up against the wall in a fit, bites bloody chunks of flesh out of her own arms and legs (most likely out of the mother’s arms too), who is incontinent, has sleepless nights, seizures, and people, the list goes on and on! It’s hard for parents to watch that, and I assure you, this poor child doesn’t want this for herself. It is very insensitive to simply say to this mother and child, who go through this daily, “Actually, the world would be a better place if everyone had autism.” My son does none of these self-harming things, but for the sake of these parents and children who experience it daily, weekly, or even once a year, I refuse to agree with the statement, “I hope they don’t find a cure for autism.”


   Oh boy, this is a conundrum. Not the first definition. No, it isn’t a hard question that has a hard-to-find answer. No, the answer is simple. In fact, it was the first thing we went over during this Phase I training. My son HAS autism. Everyone who has a child with autism can well agree with that. Autism is a mental disorder. Look up “mental disorder”, and you will see autism on the list. Just like a smart woman said at the beginning of Phase I training, we would not say a person IS ADHD, we would say they HAVE ADHD. The main and most important point of it: AUTISM DOESN’T DEFINE A PERSON. They are who they are and autism is a series of symptoms. It is so important, not just politically correct, to say this correctly as we talk about this condition. So then, why is this conundrum amusing? Put frankly, you can’t say “my child has autism” in one breath and “You don’t love your child because you want to “beat autism”. You should love them just the way they are” in another breath because the two sentiments are exactly the opposite. This is a heavy burden and a huge controversy for people with children who have autism, and people with children who don’t have autism cannot understand. Therefore, any person not directly caring for a child with autism has no right to an opinion for no cure (which I’m sure on these comment boards there were many), and their comments are null and void. Sorry. I love you all the same, but you cannot understand. So, now only thinking about the parents who have a right to an opinion and agree that they don’t want a cure, I tried to understand. Every comment section had hundreds of parents saying to other parents who would want to eradicate autism sentiments to the effect of, “how dare you want to change your child. My child is perfect, and I wouldn’t change them for anything. It’s who they are, and you need to accept that.” Ah ha. There it was. They were essentially saying, “My child IS autistic.” In their eyes, if their child didn’t have autism, their child would not be the same person. These same people, who would have another person’s head chopped off if they didn’t say “has autism” instead of “is autistic”, weren’t playing by their own rules. This is identifying autism as the person, not the disease. So I asked myself and pondered on it for a while, “Do I think Colton would be Colton if he didn’t have autism?” Yes, I do. He would still love art. He would still be hilarious and a joker. He would still do “Colton things”. Yes, he still be “Colton”, but he wouldn’t feel the frustration that comes with autism. That child mentioned earlier would still be the same child, but wouldn’t be hanging her head against the wall. It can be said of all mental disorders, “(insert any disorder here) doesn’t define who a person is.” If this is true, then how could my child possibly be a different person if there was a cure? If autism is truly a mental disorder like ADHD (once again: it is defined that way, don’t shoot the messenger), then how would you feel if a parent said, “I hope they don’t find a cure for ADHD” or “I hope they don’t find a cure for tourettes syndrome, depression, anxiety, seizures, OCD, PTSD, schizophrenia..” Ok people, once again, the list goes on. I understand autism is different for each child and it is almost impossible to “cure” because no two children with autism are the same. Even the cause varies from person to person. Getting back on track, if it’s true that the disease doesn’t define the person, then how would they be a different person if somehow someone found a “cure all”? The cure would be for the symptoms. It would not result in some new person who is nothing like your old child being born into a more-grown-than-an-infant body. A person can not say their child has autism if their thinking doesn’t line up with that sentiment. Either their child HAS autism, and it doesn’t define the child, or the child IS autistic and would not be your “real” child should there be a cure. My child HAS autism, and I want to help him in any way that he wants to be helped. This is another reason why I can not accept the statement, “I hope they don’t find a cure for autism”.


   If I could get Colton to understand why bad things happen to good people (yes there is a satisfying answer to that question), this would help him. However, I can’t at this point. I can’t explain to him that someday all of his loving parents who love him greatly will probably die before he does. He will have to go on to live somewhere else. Most likely in a group home. Sure, he will most likely be older, but that doesn’t make it any less unnerving that this innocent person will be at the world’s mercy. I know we all want to give ourselves reassurance that at OUR group home, everyone loves my child. At OUR group home, there are no sexual predators, and no one takes advantage of MY child. Reality: I’ve worked in homes and have seen first hand the neglect and two-faced actions of many caregivers. Not all caregivers are that way, but I assure you, every child and/or adult living in these homes will be exposed to one or more people like that. Oh, and that nice caregiver, the one who genuinely cares, (speaking from experience) will turn in abuse and neglect to the administrator and they will say something exactly like this: we have investigated your claim, and we have determined that this situation met at least MINIMAL care requirements. Yes. Minimal is just fine in their book. After all, the worker to resident ratio is way overwhelming, so how could they possibly be taken care of properly. Too many residents, not enough workers. I will not kid myself. Sure the staff will be wonderful when you’re there visiting, and the abuse and neglect will be on a smaller scale for those whose family visits often. That girl who was abused in the care facility I worked at had no one. No visitors. No family (who did exist) came to see her. She got the brunt of it the abuse, and no one helped her. I will never send Colton to a residential place, and I can only hope and pray that one of our other children steps up to the plate and takes on that large responsibility. Yes, it scares me on a deep level. What is going to happen to this wonderful child of mine who has a problem counting money and may never be able to live on his own? He’s 14 now and for the future safety and well-being of this growing human (yes he is a human, not a dinosaur as he longs to be), I cannot agree with the Statement, “I hope they don’t find a cure for autism.”

   Yes, four reasons why I can not find it in myself to agree with this heart-wrenching statement. Yes, I realize I’m in the minority. Yes, I’m sure there will be more “how dare you” comments or thoughts from anyone able to read this. Yes, I understand that the world we live in isn’t able to solve his problems fully. Yes, I know his only real hope for his safety and cure for this disease that does not define him doesn’t rest in the hands of this world’s system and maybe not even Science. Perhaps someday someone will find a cure, but I’m not counting on it. I just can’t bring myself to agree with the statement, “I hope they don’t find a cure for autism”. We have to be there for those who want to help their children beat autism. So next time you see someone trying to defeat it for their child and if the thought to ridicule them crosses your mind, don’t.. Try to understand their opinion like I tried to understand theirs. I wrote this for people to try to understand. Don’t claim superior parenting by degrading their hopes for their children because “THEIR child has autism”, not “their child IS autistic”. Paraphrasing a loving mother of a child with autism, “Leave them alone. We all have a journey with autism, and this is hers.”