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Improved Health Outcomes!

Celeste’s autism symptoms and seizures have improved greatly since starting Charlotte’s Web CBD oil and she has been taken off one of her traditional medications since being on the oil.

If we didn’t receive the grant we wouldn’t be able to afford Charlotte’s Web for Celeste. We would be stuck with the traditional medications that were no longer working. I like Charlotte’s Web because it has no negative side effects.

My kids feel that it is really cool that y’all help us so they don’t have to go without some of the extras that the grant has allowed us to have. I am just grateful that people like you exist and are so generous.

Celeste’s story

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She is more active with more verbal communication

Story provided by Grace’s family

Grace is doing so well since she has been on her CBD, I can’t even explain how appreciative we are. We have not seen any seizures, and her skin is looking so much better. She is more active with more verbal communication and seems to be getting her milestones caught up. Her bloodwork is improving, we are feeling so blessed! Sending the RoC team HUGS <3

 

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Fibromyalgia pain is crippling

For years I have dealt with chronic pain, muscle spasms and nerve pain and my doctors couldn’t figure out what was wrong. Along with severe fatigue, I had a hard time managing daily life activities and work.  Brain fog consumed me. I couldn’t concentrate or keep my train of thought. I lost the ability to carry meaningful conversations because I couldn’t grasp my words.  Eventually my doctor diagnosed me with fibromyalgia.  

I started taking cannabis oils and using vape pens a couple of years ago and have seen an incredible difference.  I use a combination of THC and CBD in addition to topical balms for the pain. 

After a few weeks I starting seeing changes and in a few months I could say confidently that I have my life back! 

Jessica’s story

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CBD has improved my child’s life

Bradley is autistic. Health wise he is okay, as far as I know, he can’t tell me. Cannabinoid therapy has helped with his violent meltdowns, eye contact, and his concentration. It has not helped with his language, still non-verbal. I would say his meltdowns have improved by 90%.

This is my theory: autistic children have lots of inflammation. Inflammation causes pain and the pain caused his violent meltdowns. CBD reduces inflammation, which took his pain away. I kept taking Bradley to doctors saying it looks like he’s in pain and all these doctors just ignored me and wanted to put him on psych meds, which I never did. I’m so happy I found CBD, it has improved my child’s life.

CBD is expensive. I’m a single mother of a severely autistic child. I am a nurse but had to quit my job because I couldn’t find daycare for my child. Plus, trying to work full-time and take care of a disabled child all by yourself is extremely physically and mentally exhausting. I want the best for my child and it so hard to do that when you can’t work. I am so grateful for this grant.

Bradley has violent meltdowns and as he gets older he gets stronger. If I didn’t find CBD Bradley could have been seriously injured or dead from his meltdowns. I believe it has saved his life.

Bradley’s story

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She is usually sick all winter long

This winter my daughter has not gotten sick with the flu, cold, or illness.  In other years she was sick all winter long. This is absolutely amazing and I believe it is because of the CBD.  My daughter’s seizures have decreased but the wean off of the pharmaceutical medications has been very difficult.

This RoC grant has made a huge impact on our family.  We are seeing so many better days with my daughter than we have ever seen.  Her brother and sister, who are several years younger, have also noticed that she is talking more clearly and they are able to understand her.

Maricella’s story

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Chloe is now seizure free

Story provided by Chloe’s family

Chloe has been taking cannabinoid therapy for three years and after an EEG to measure seizures, we were told Chloe is now seizure free! To put the icing on the cake, her neurologist admitted to us that she truly believes it was all the oil! She said she has never seen someone with the type of seizures that Chloe has recover so well.  

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Jason knows that he MATTERS!!

Being on CBD has given Jason hope. He hasn’t had that in quite some time and being accepted into this program and starting to take CBD he has found hope. He knows that someone out there cares and is listening. He knows he matters!

The grant money has helped him with everyday needs like food and medication. People with disabilities get pushed aside a lot and don’t get nearly the amount of help they need. The fact that the Realm of Caring exists and that there is someone out there pushing boundaries to help people is a wonderful boost. It reminds him, and me, that if we just have faith, everything is going to be okay.

Story provided by Jason’s family

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Chronic pain has wreaked havoc on Sheila’s life

I have only recently been able to begin experimenting with the CBD tincture but my initial results are incredibly encouraging!  Even if the only benefit derived is an increase in my ability to achieve sleep for longer than an hour or two at a time (which has been the norm for nearly 2 decades, constant waking and poor sleep) it would be more than worthwhile!  However, I am still hopeful and expectant that it may have other benefits, especially in relation to calming my overactive neurological system, with muscle spasm and constrictor. I expect part of the reason for the intensity of my pain is a constant state of muscle tension, caused by both chemical aspects of the disease and my unstable musculature and body alignment. It causes me to spend probably 3 of every 4 weeks bedbound in a state of torture, gripped by pain and unable to move or do anything.  Nothing has been able to touch it and muscle relaxers only make me sick and loopy but don’t ease the muscle tightness, certainly not enough to outweigh the negative side effects.

This treatment is my only hope for relief in this area, and so far it seems it will help. My concern is how much I’ll have to continually increase the dosage in order to outpace the adaptation to it. The dispensary told me that will be a factor. I have been tested genetically to have resistance to opioid medications, which partially explains why even with large doses of Oxycontin, etc, I have very limited relief. Hopefully, the tincture will be a way to get around the lack of efficacy of opioids, and also help me avoid their terrible side effects, including constant opioid-induced constipation and many other problems.  This would be a more natural, less harmful solution; the only inhibitor is cost, which is why this aid is so important and appreciated!

This financial aid of $150 per month has been the difference between being locked into the old methods of treatment that have been ineffective or under effective and trying new solutions.  It allows me to purchase CBD tincture to explore other ways to alleviate symptoms that cause such tremendous pain and disability. I am only able to get out of bed a couple of days per week around the house, and if I’m lucky, to get out of the house for errands approximately one day a week for 2 or 3 hours.  This is not enough window to accomplish even the basic tasks to sustain life, even one as sedentary as mine. I am always behind, always struggling and letting things fall between the cracks. It’s stressful and devastating. If the tincture can give me even hours of function, it’s well worth it. Anything more is gravy!!

When you have as little functional time available to you as I do, and have for 2 decades now, it takes a huge toll on yourself but also, and more so, family members.   My beautiful daughter, Allegra, was only four years old when I was injured and has gone through so much with having a mother who was around but not really around and able to do things. She had become my caretaker, and that’s a role she cannot handle any longer, it’s taken a terrible and devastating toll on her.   She is the second victim of my injuries and subsequent illness. My mother, 85 years of age, having lived through bombings in England during WWII, even having her school bombed into oblivion at age 10, has been more affected by my prolonged, extreme state of illness than anything in her long, not always easy life! It means everything to us, and others, friends and community, who are affected, inconvenienced, saddened by my suffering.  It takes a village to raise a child, but also to care for a sick person. The more that burden can be reduced the better for everyone!

Sheila’s story

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I was contemplating suicide because of the pain and feeling hopeless

Now my worst days are better than my best days before CBD. My fibromyalgia symptoms have decreased by 80% with some days not having any symptoms. That hasn’t happened in over 25 years! My headaches and the pressure in my head are gone. I no longer suffer from interstitial cystitis or any painful bladder symptoms or the regular UTIs I was having. My blood pressure has returned to normal and I sleep like a baby. Arthritis and other joint pain has gone from a 7-10 on the pain scale to 2-4.  

I think the biggest miracle is that I’ve been able to stop all pain and sleep medications and had no withdrawal symptoms. I had been taking 4 Norcos a day for over 25 years and stopped them within a couple of months. I had tried stopping them in the past but the withdrawal symptoms were too much. I NO LONGER HAVE TO TAKE OPIATES OR AMBIEN!!

Before taking CBD I was contemplating suicide because of the pain and feeling hopeless. I’ve been able to start a Facebook group for seniors helping seniors and encourage members to look into using CBD. Most are low-income and feeling desperate so I referred them to RoC for help. Your kindness and generosity have made me feel hopeful again and I look forward to helping others.  

Story from Alice

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Did I mention she can see again?

Born happy and healthy, Jaqie was stricken by the first of what would be thousands of seizures just days after a normal well check which included scheduled vaccines. Up to that point, Jaqie had progressed normally according to the doctor’s growth charts. After that first seizure, Jaqie was only four months old and would never be the same. She would actually regress.

Over the years, through pharmaceutical trial and error, Jaqie would lose her fine motor functions, unable to hold her own head up. She couldn’t scratch her own butt if it itched, nor vocalize it to someone who could. She never learned to sit, scoot, crawl or walk. The medicines, forced as the only option for relief, proved to make her worse. By the time she was two years old, she was pronounced legally blind.

The doctors threw their hands in the air and said there was nothing more to be done.  In April of 2014, unwilling to believe she was a lost hope, we put cannabis oil in our toddler’s mouth.

Today, Jaqie not only scratches her own butt when it itches, but she also rolls over, cries, laughs, babbles, kisses, hugs, stands with help (that’s huge for a child that previously had zero muscle tone) and she takes no pharmaceutical drugs. Cannabis only.

Did I mention she can see again?

Story provided by Jaqie’s parents