Is Medical Marijuana Really Medicine?

Hello my friends! I was just reading one of the comments, and have decided to address the issue of medical marijuana as actual medicine. I would like to begin by sharing how I found out for myself this could truly be used for pain medication.

When my brother came to live with me two and a half years ago, I was prescribed 520 mg of methadone and 32 mg of dilaudid, each day. I would get an infection in the open wounds on my feet at least every four to six weeks.  During these “pain cycles,” I would take all of the medication that had been prescribed to me. Too often, it was not enough. I would get in so much pain, I would have difficulty breathing. I would feel like I was going to lose my mind if the pain increased any further. Of course, it always got worse! My brother was with me on this particular day. I was crying in my wheel chair. There was nothing else I could think to do. I had gotten my medical marijuana prescription many years ago, and had been smoking for relief since. I would load my pipe and smoke it until I felt a little high in my head. It helped relax me, and helped me cope with the pain. On this day, I had already taken my dose of methadone and dilaudid. I had smoked my pipe, and I am sitting there crying, tears rolling down my face, when my brother hands me a joint. He says, “Smoke the whole thing!” I took a couple of hits, got relaxed and stopped smoking. He tapped me on the shoulder and said, “No, I said smoke the WHOLE thing!!!” When I got a little over two-thirds of the way through, a funny thing happened …… I stopped crying, started breathing. even laughed at a joke my brother made … and by some miracle felt actual pain relief. After years of smoking my pipe and receiving minimal relief, I began to think this might be true pain medicine. It worked when 520 mg of methadone didn’t!

After this experience, I tried smoking a joint instead of taking a dose of my dilaudid. I realized it was possible, I could take a lot less of the opiate medication, if I increased my cannibas intake. The problem I faced was how expensive it is. I believe for those of us in this much pain who use marijuana as our medication, the only feasible way to provide what we need may be to grow it ourselves. This is at least until the insurance companies, and doctors start seeing it as medication.

Frequently when I would go to the dispensary to purchase medication, I would try one of their new edibles. I was very blessed to find a large dispensary in Santa Rosa, CA that had delicious food with cannibas in it. The edibles always helped with my pain, however with their prices, I could not afford, at the time to use the edibles as part of my daily routine.

When I purchased medicine at the dispensary I would keep track of the type of medicine I used and what it helped with. Every time I bought a new strain I would write down the results in a book. I found some strains were really good for nausea, while others were helpful with muscle pain. Some increased my appetite, while others helped me sleep. I found there was almost always one that would help with whatever symptom I was having, not the least of which was help with my anxiety and pain.

On one trip to the dispensary, I purchased a new balm they were selling. I took it home, and when the nerve in my right foot turned on, and would not shut off, I rubbed balm all over the area where the nerve was hurting. I was shocked, and amazed 15 minutes later when the nerve relaxed and stopped hurting completely!! I now knew, for the first time in nearly twelve years, I could actually get nerve pain relief. I had tried other prescription creams, pills and endless procedures prescribed by my doctor. Nothing had ever relieved the nerve pain, when it turned on like this. I was thrilled, and more determined than ever that I would take as little opiate medication as possible.

As I increased my cannibas intake, and began using the balm regularly I was more than pleased with the results. Every drop I made in the opiate medication made me feel like I was coming back to life. I felt like I was becoming smarter. I began to get some of my focus back, which made it possible to actually start managing my pain. I cannot describe what it’s like to be in so much pain, you are willing to do ANYTHING for just a little relief. Even if relief only lasts an hour, that is one hour I can breathe, think and feel something other than my pain. The problem, for me, with using opiates as a tool for my pain, they make it impossible for me to manage and cope with the pain, when the pill wears off … which is almost always before I can safely take more! Once I realized this, I knew I would drop the opiate medication as much as I possibly could. In truth, I was in so much pain, I did not believe it was possible I would ever be able to live without the opiate medication. I just thought I would see how low I could go.

About a year ago, I started baking with the oil and butter, infused with cannibas. I used to bake a lot, before my illness. I love to bake. I had not baked in over seven years. I had some friends who were growing on their own prescriptions, and I began to learn what I could, in order to start growing myself. I got a hold of some leaves, made some butter and began baking. At first, I didn’t like much of the food I cooked with the butter. It just didn’t taste all that great. I found it difficult to eat enough of the sweets to relieve my pain, significantly.

In January, of this year, I was given a considerable amount of olive oil, infused with cannibas. I started baking with the oil. I found a recipe for seven layer bars in my grandmother’s cook book. To my surprise they were absolutely delicious! I started trying other recipes. I began using the edibles every day. Honestly, at the time, I had no clue how much they were helping.

In April just after I cut my opiate medication in half, I went on vacation to visit my sister. I had been using the edibles regularly for four months. I ran out of what I had a couple of days after I got to my sister’s. An unusual cold spell, for this time of year, hit hard when I arrived. I realized I had met my pain, once again. The pain in my legs had been mostly manageable since the wounds had closed.

When my feet and legs get cold … things can get bad, if I do not find a way to warm my legs. At first, it feels like I am walking in ice buckets. As time goes on, the nerves in my feet turn on. If I don’t find a way to get warm, they will eventually go numb. But the nerve pain will continue. So … I run out of edibles. I knew they were helping, just didn’t know how much. My pain began to grow … and I knew I had to find a way to address it, or end up in a terrible pain cycle. I was blessed beyond measure when a dear friend, gave me a bag of leaves, so I could make oil to cook with. As soon as I began using the edibles again, my pain became bearable, once again. I was amazed … I knew part of the trick for managing my pain on little or no opiates would be using the edibles on a regular basis.

As I returned home, from this vacation, I entered another pain cycle. I did not know at the time my disease had progressed to my upper body. I believed the pain in my abdomen, which felt like impending death, to be caused by withdrawal. I had been aggressively tapering for about five months. I became convinced the only way to stop the pain was to detox completely.

If I am completely honest with you, and myself, I am not sure what I would have chosen if I had known the new pain was the disease, not withdrawal. Which is one reason I am glad I did not know. When I made the decision to completely eliminate my opiate medication, I was deep in a pain cycle. I was depressed. I was afraid I would die if I continued to taper. I was on 30 mg of oxycodone a day, at the time. I tried to find a treatment or detox center that would help me. No one would treat me without putting me on another opiate. As in the day when methadone was found to help heroin addicts, they have found a new drug to help those addicted to the average opiate. The latest craze in drug treatment programs is a subutex/suboxone regiment. They take you off the drug you are addicted to, as they put you on the new one. I did some research. What I found scared me. It turns out many patients described the withdrawal and detox from this new medication as being much worse than the drug they were originally addicted to. Today methadone addiction is a serious problem for many. I was concerned this might eventually be the case for this new treatment. I did not believe this new drug regiment would work for me. My big problem was my dependency on the opiates, as well as the consequence to my body for taking them so regularly.

I then tried to get help from my pain specialist. I was shocked at his unwillingness to help me rid myself of the drug he so freely prescribed, that I believed was causing my pain. Out of desperation, I turned to my family. I cannot begin to tell you what great pride and appreciation I have for them, and their willingness to help me through this.

Detoxing from the opiates was a difficult process. I was convinced the new pain in my abdomen, chest and organs was a result of withdrawal. This drove me to detox completely, after nearly twelve years of using opiates as my main tool for pain control. What a journey this was! During my detox, I experienced the highest high, and the lowest low. I got a few medications from my primary care to help with the worst of the withdrawal symptoms. I got several herbs to boost my energy, and help with the pain. I drank tea, and ate scrambled eggs, and chocolate protein shakes with cannibas oil in them. Most helpful, were the baths. I would put three tablespoons of oil in a very warm bath. I would soak my entire body for at least twenty minutes, two or three times a day, if necessary. I was amazed at my ability to deal with the pain this way. I knew without a doubt. during my detox … marijuana IS medicine.

Many who are trying to use medical marijuana for pain relief, do not know how to use it effectively as medicine. It was only through trial and error I came to the following conclusion: Ingesting the cannibas in my food is like taking an extended release medication such as methadone, ms contin or oxycontin. Smoking it, for me, is like taking an instant release medication such as vicodin, dilaudid, or oxycodone. The balms, tinctures and baths are part of my pain management regiment. I believe with further study we will find even more helpful ways to use this medication effectively.

For anyone reading this who is on a considerable amount of opiate medication, it is likely way too much to consider eliminating them at this time. For me, when I truly started using marijuana for my medication, I just added it to my tool chest. Most of us suffering with this extreme level of chronic pain need every tool we can find, as our pain is chronic. Our pain is persistent, and finds its way through every blockade we build against it. It is resilient, and seemingly so very strong. For me … my resolve to manage it is stronger!

I highly recommend anyone considering this path get themselves a prescription. The law is changing, as are the attitudes towards cannibas. As more of us use this tool, and educate those who love us, and don’t wish to see us suffer, I believe the law and the attitude of society will continue to change for the better. I met a woman on the train, while on vacation. We were chatting, and I shared a little of my story with her. She looked at me and told me she had never met anyone who actually used marijuana for medicine. She had only known those who used it to get “high.” She for the first time believed it was medicine, and offered to vote for its legalization when it hit the ballot. I believe if we will share our stories, people will learn, and have compassion. I believe most of what people are afraid of with marijuana is a result of bad information, and a lack of education. Because it is such a taboo subject, and mostly practiced in hiding, we have not learned the true nature and ability of this medicine. Also … part of the “attitude” of society, in my opinion, comes from the fact that most people smoke marijuana when using it for their pain. Many just cannot get past the fact that it has been used in this way as a “recreational” drug by so many, for so long. I can tell you without a doubt, you do not have to smoke it to get relief from it. Use it in your food, rub the balm anywhere you have pain.Take a bath in the oil. There are also tinctures and pills made from cannibas concentrate, that are very helpful. All of these are effective pain management tools. It is not a requirement to smoke it. That is a personal preference for some.

For a few, even after hearing my story, it will be difficult to see marijuana as medicine. We have been told for quite some time it is no different from any other street drug. If that is the case for you … I would challenge you to ask yourself why you still believe it is not medicine? If you would be willing to take a pain pill prescribed by your primary care doctor, what is the actual difference between taking that pill and eating some food with cannibas in it?? For starters, the pill likely takes your ability to think straight from you. If you take too many pills, it will kill you. If you have been taking the pills for a long time, and just stop taking them, it could kill you. The pills likely cause other problems in your body … such as constipation, itching, mental cloudiness, fatigue, nausea, vomiting, and so much more. The pill might give you some relief, but mostly it will numb the brain so you don’t care that it still hurts. At least, this was my experience. When the pill wears off, you will likely have to wait a bit, while suffering in pain, before it is safe to take more.

Now let’s examine what happens if you use medical marijuana instead of a pain pill. If you eat something with cannibas in it, you could get tired or hungry, depending on your tolerance and the type of medication you used to make the oil or butter. If you take too much of it, you will pass out, get some sleep and likely feel much better when you wake up. There is not one case documented where someone has died from an overdose of marijuana. If you don’t take enough of it, or skip a dose, or even stop taking it cold turkey … you will likely get a headache, and probably be irritable. If the effect wears off, you can take more, without deadly consequences. I challenge you to consider … could it be … medical marijuana is actually medicine? Can we learn to be use in effective ways to treat our pain?

I am not a doctor, and I do not have statistics to back up what I am saying, yet. That is one reason for the non-profit charity I am starting. I do intend to do the research and provide the statistics. For now … these are my opinions. Take what works for you, and leave the rest. While I do not have an MD behind my name, I have my experience … which is great. I ask you to open your heart, and your mind. Consider what you would be willing to do for your parent, spouse or child was suffering every day with debilitating pain? Would you consider it medicine then? Would you not hand your sister a joint and say, “Smoke the whole thing?”

I am working closely with others who are researching the medicinal benefits of medicinal marijuana on chronic pain. I believe we continue to find ways to use this to treat our pain. I believe those who wish to can live a life without opiates, and still get relief from their pain. I would invite others to begin a dialogue

About Kimberly

I am a 46 year old woman, diagnosed in 1998 with Reflex Sympathetic Dystrophy Syndrome (RSDS), more recently renamed Complex Regional Pain Syndrome (CRPS). I moved to Colorado a few years ago. I am living here in Longmont, with my beautiful sister, and niece ... who bring so much joy to my heart! Life is short ... too short to waste on hate and frustration! Love is the only reality I seek!!
This entry was posted in Chronic Pain, CRPS/RSDS, Medical Marijuana. Bookmark the permalink.

6 Responses to Is Medical Marijuana Really Medicine?

  1. Sue B. says:

    Thank you for your comments about marijuana as medicine.

    I have Fibromyalgia, a chronic pain syndrome with symptoms of overall nerve and muscle pain which is always present. I have been using Methadone for 10 years ranging from 200 mg. to 20 mg. each day. I wake up every morning with back and leg pain and if I do not medicate, by mid-morning, I feel like I have a severe case of the flu with muscle cramps and depression and totally unable to function.

    In my 49th year, I began suffering from unexplanable leg pain: it felt like my legs had turned to concrete. The doctors could not help. After hearing of so many people suffering from Fibromyalgia, I started a support group. All of the group members reported that they could not find effective relief. Many of their doctors did not understand their symptoms and thought them to be hypochondriacs. We shared our stories but did not find a way to manage the pain. Now 10 years later, doctors are prescribing major opiates which reduce the quality of life because of their severe side effects.

    I recently tried the marijuana balm in a bath as well as edibles. The relief is amazing!
    Because of my profession, I will not smoke but want to use the oils.

    It is time for our laws to allow us to grow and use methadone medicinally. It is far superior to many prescribed medicines. What a concept, that those of us who need pain relief could grow a few plants and use this healing herb. Let us speak up for this right.

    Kim, thank you for sharing your experience and having the courage to pursue your own healing when all seems lost. Those of us who suffer need you!

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    • Kimberly says:

      Dear Sue …

      First let me say, I am so sorry for your pain. Your journey has been a most difficult one. Chronic pain is a difficult path for those of us challenged with this imbalance. I believe your imbalance and mine are the same … our hearts are sick. We live in such a chaotic time We live in a time where trauma is a daily occurrence, for many of us. There is not enough food, money, clothes or shelter to meet our needs today, much less tomorrow. The worst result I believe comes from the stress of this life we live, is we believe there is not enough love. It’s not true … it’s just so hard to see the beauty and feel the joy in the midst of such severe pain. I would encourage us to come together … to share love … to share hope. I encourage us to remind each other of the beauty on this earth, and in the universe. I encourage us to remind each other of the beauty within! Tell your friends, family and loved ones how special they are, how beautiful they are. During the time when your pain is so great that you do not feel capable of sharing on that level, come here and talk to us. We can share our pain, with those who understand it. We can be seen … and encouraged to choose love anyway. We can heal ourselves, choose love … choose life!

      I want you to know … I see your pain … it is not invisible to me. That is for many of us the most difficult part … to feel invisible. Worst, to have our pain be invisible, to those who are in a position to help us, is a most humiliating experience.

      About a year and half ago, I was laying in my doctor’s office. He was the specialist who had been treating me for CRPS. I was at my regular monthly appointment, in terrible distress. I had been vomiting, with constant nausea since the intra-spinal pain pump was installed. The pain in my feet had improved considerably, and my wounds were healing. However, the vomiting and nausea had now become a serious problem. I would wake up vomiting, and be unable to take my oral opiate medication. I would go into horrible withdrawal and begin to dehydrate. They had already changed the medication in the pump two or three times. I told the doctor I was convinced this was somehow tied to the pump. I had taken the same oral medications I was taking before the pump surgery. Nothing else made sense, it had to be related to the pump. He looked at me … very confused. He then said the words so many of us have heard … “I have never heard of the pump causing vomiting and nausea like this. I’m confused at how it could possibly cause these symptoms. I think maybe it’s in your head.” I would, over one year later, have a conversation with him about this. He doesn’t remember saying it. He didn’t mean to. He would never! His words … his tone … his doubt … still ring in my ears, today. After completely detoxing, and finding a very compassionate ER doctor, and a new pain specialist … I now know the cause of the vomiting to be the progression of my CRPS brought on by the pump surgery, and worsened by the subsequent surgeries. This doctor, believe it or not, is a very compassionate man. He was confused. He didn’t have the latest research which shows CRPS can progress to areas other than the extremities. He said out loud, without meaning to, what was in his head. Since he didn’t have an explanation, it must have been in my head. I believe this response from our doctor’s may come from their feeling of helplessness and confusion. Although, occasionally, it’s a result of ego. If they don’t know the cause, there must not be one?? I believe the doctor just shared his feelings with me inappropriately. In the end, perhaps it is my job … or my purpose to educate him? However, for those of us suffering from such severe and debilitating pain, to hear those words can strip of us of the little hope we have left.

      I celebrate with you the moment you realized the cannibas balm, and edibles could provide you with relief. If you haven’t already, I recommend you get yourself a medical marijuana recommendation. Then visit your local dispensary, and try different products that are available. I encourage you to try putting the balm on the areas where you have pain, and then take a warm bath, for at least 20 minutes. I believe your experience will be a good one! You may find relief in your entire body. I believe the cannibas tincture may work similarly to smoking it, as an instant release medication, if you are in need of that. If you do and are able, I recommend you try it. Check with a local dispensary, and they should be able to assist you.

      Thank you for taking the time to share your story, and your heart with us. If we can share our stories, more of our neighbors, friends and family they may begin to see this IS medicine. They will begin to notice the consequence, of using cannibas for pain medication, is much less than most of the drugs the doctor will offer you, without hesitation! I believe they will see the need for legalizing this completely for the use of medicine. Keep sharing your story … we need each other!!!

      You too have much courage. Few can know how much effort, drive and determination it takes for some of us to get out of bed in the morning. I tip my hat to you for your willingness to travel this path. I believe more than ever, this life is a worthwhile one. I encourage you to find every moment of joy … to focus on them until they grow into the most wonderful feelings of love. I encourage you to heal your heart, and watch your mind, body and spirit follow! It’s an experiment … let’s see if it works!

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  2. Catherine says:

    I really thank you for sharing your experience. I had been too afraid to share my experience because my doctors act like they don’t even consider my use of this medicine, which I find so strange since the hospital where I am seen has its own experiment in the use of MM for CPRS. In fact, when I was first injured, a friend suggested it since the Vicodin was making me sleep all the time and I have someone I am responsible to care for too. As my experience developed, and I read more, I realized that because there is no ‘cure’ for CPRS, doctors could only offer pain ‘management’ – for a variety of reasons, I have been dealing with the CPRS pain only with MM, rubs (which do exactly what you say, and are a huge part of pain management for my legs) and edibles. There are times, like when its cold, when there is break-through pain, and in those moments, yes, I think I better get myself to a hospital because this pain is beyond what I can manage as a human being. I know that they can only offer me drugs and another blank stare. I use breathing techniques, baths, and sleep.

    I feel so amazed to hear your experience is similar, thank gosh to hear your story.

    Early on, baths became my healing ‘medium’ as I realized first that warm water helped calm the worst pain, having to sometimes sit various times a day. Its taken these two years to start making my daily bath a prayer session, and exercise arena. I’ve been writing a bit on my blog Letters of Courage, about the different herbs and other healing aromas I combine in my bath.

    Also, I believe that water carries and magnifies our thoughts, that magnetic energy strip is super charged. So, its where I go to pray, to ask for guidance, to speak to my body, cells, healing capacity inside, its where I cry on those days the pain goes high, or when I think how will i ever survive financially like this, its where I give thanks during warm weather when I am doing so well.

    I have an added complication of having medical access issues. It has made me turn to other techniques because I believe there was healing before there were ‘doctors’ and hospitals. Since I can not access the care, I have to care for myself.

    I had a sore recently on my foot, opened between my toes. I was alarmed at first, I become so when I feel or see the disease manifesting as it reminds me I don’t have a doctor I can turn to ask for help. I used aloe vera juice, soaking my foot several times a day. This has cleared the sore and its slowly dying up.

    I pray by April to have Medicare and hopefully, now, can get to a doctor. In the meantime, I like your exercise on the money issue. I am going to try it. In those moments of high pain, I remember how the hospital has treated me to protect itself, and I cry. I am young, and never planned in midlife to be so unable to work, and some days, I wonder what the heck I am going to do. I also have to consider growing MM at some point because its too expensive. I also wish there was coverage for Medical Marijuana. I also make note of the strains and what it helps with and I wish we could find a grower who would be willing to work with patients with CPRS to grow strains that might address our specific symptoms.

    The Legalization effort in California, I felt, went the wrong direction. Instead of creating a cottage industry of medicine growers, they were going for the industrial farm idea and in that, I could see the medicine being drained out. Its very important the intention of growing to produce medicine. I really wish this issue could be taken off the political burner, its just crazy that there are thousands of years of evidence of its medical use, and we are stuck with some policy that is so deeply harmful and ignorant to the point of not developing what could be such a valuable contribution to society.

    Enough of the soapbox but honestly when one feels the medicine work, its pretty hard not to be in favor.

    Thank you so much for sharing.

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  3. steve brown says:

    I suffer from the severe non-stop burning and intense soreness of CRPS. My RSD 1 – AKA CRPS developed after having 2 total knee replacement in my right knee. My right leg from my hip socket down to right foot is hot and even the skin is sensitive to the touch of my cloths. It seems like when the pain flares up in my right leg that my left lower legs feels hot too. My wife and I are hoping to relocate to California in a couple of years if I last that long because the CRPS PAIN is so bad that it seems to making my heart cramp up and beat funny. Here in NJ you cannot get a medical prescription for medical cannabis for the severe pain of CRPS. I could easily get prescriptions for powerful opioid drugs, but opioids are highly addictive and cause severe constipation which fills your insides with rock hard poisonous fecal matter. The thing about severe physical pain is that unless you are the person that is suffering from it you cannot understand how it feels or the misery that it (Pain) inflicts upon every moment of your life. Having CRPS AKA RSD 1& 2 is a life sentence of having to suffer non stop moderate to severe to wicked burning and soreness. Also CRPS is considered the worst type of pain according to the MCGILL PAIN SCALEhttps://www.google.com/search?q=The+fiercest+viking+warriors&biw=1440&bih=725&source=lnms&tbm=isch&sa=X&ved=0CAYQ_AUoAWoVChMIutyWhe2NyAIVAlA-Ch1gQADA

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    • Kimberly says:

      Thank you so much for your comment! It is true that unless you’ve experienced something similar, few people could possibly comprehend the intensity of pain that comes with this illness! I’ve been dealing with this condition for more than 17 years and I’ve found a tool box full of tools is a wonderful thing! There are so many things that can help calm the nervous system down and for me Cannibas is one of the most consist and efficient tools I use.

      I recently found out you can use it very effectively for pain without any “high” or side effects at all for those who prefer that experience. It turns out it is highly effective just ground to powder and placed in gel caps for consumption. (Be sure to strain it and remove any stems before placing in the gel caps. This technique is called a cold cure. The thc doesn’t get activated because it’s not heated. Therefore no “high” effect. Due to the canniboids it is extremely effective for pain this way. It also has an incredible anti-inflammatory result and taken over time it can be very helpful for so many issues!! You can use trim or bud, both will work. Although in my experience I did find the better the quality the better the relief.

      I have noticed over the last several years the climate is changing. More and more people are becoming aware of the wonderful healing properties of this herb. Even the government appears to be shifting its stand against it, at least for medical use. There are so many states already allowing it for medical patients, as well as several even allowing it for recreational use. I hope you’re able to land somewhere where you can use it or even grow it for yourself!!

      Meanwhile I hope you’re able to find some other ways to gentle up the experience! It is a challenging condition and anyone dealing with this is so courageous and strong just to get through each day!! As much as you can be gentle with yourself, it can help. Please feel free to contact me if you have any questions or feel I can help in any way. I wish you so much joy, love and peace on your journey!!

      Kimberly

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  4. Olga says:

    My son has Complex Regional Pain syndrome, and CBD is also one of the few things that’s actually helping him. I give him water soluble BioCBDplus for his pain. – Olga

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