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Living with #Lyme disease

Since starting the hemp oil, I have had some days when I have been free of pain; not what has been usual for me since having Lyme.  This seems to last until the next change in barometric pressure – not long, this is the midwest, where we say “if you don’t like the weather, wait a few minutes, it’ll change.” I have also noticed that my ability to sleep is improving, and the timing of my hours of sleep is more normal than it has been since I’ve been ill.

The financial assistance is allowing me to make a fair attempt at using cannabinoid therapy for Lyme disease, which I would not have been able to do without it.  The good results so far give me hope. I look forward to seeing what will happen after I have worked up to the full recommended dose.

Sharon’s story

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iROC365

Jayden has meltdowns with her autism

Jayden did really well with the CBD oil when we first started it last year. As we increased the oil, she continued to do well. Then after about 4 months, she seemed to become immune to the oil. We ran out of the oil after 5 months of use and we decided to give it a break. Jayden has autism and has severe meltdowns. The days that the oil seemed to get in her system, she had less severe meltdowns. She has once again increased her speech. We are super excited about starting the CBD oil therapy again!

Jayden’s story

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iROC365

Parkinson’s Disease symptoms are improving!

My health has improved all over. I have Parkinson’s Disease and my illness was very poor; ie: my limbs, feet, hands, and fingers constantly shook, along with the feeling of swelling in my throat, biting my inside cheeks and tongue to where they bleed, eye twitching, mouth opening and closing. All of the above is remarkably improving! It’s amazing! I can NOT take Parkinson’s medicines, because I get horrific side effects, so thank you from the bottom of my heart for this medicine!!

Without this grant from Realm of Caring, I would be mostly bedridden. The 24/7 pain I was enduring, along with all of the above ailments are slowly subsiding. It brings tears to my eyes as to how grateful I am, and my caregiver son is so grateful, too! For example, my son had to help me get up out of chairs, the couch, etc., but now I can do it by myself most of the time.Although he had to help me walk from point A to point B, this is subsiding also!!!

Sonya’s story

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iROC365

Not all stories are success stories

Payton’s health has not improved. She is having complications with her stomach. She has been vomiting and coughing. Her stomach will not digest properly.  She had a G-tube placed and it has helped some. The CBD oil has helped with Payton’s pain and sleeping. I do believe her seizures have slowed down a bit since she has been on CBD.   

Payton’s story

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iROC365

Living with GI issues

I’ve been experiencing abdominal cramping and hot flashes before a bowel movement, waking up at night with hot flashes, cramps, and severe diarrhea. My only relief would come after a bowel movement.

My GI Doctor decided to run some tests to eliminate cancer. I immediately went home started on cannabis oil/hash oil and ordered a high CBD oil.

After using the cannabis oil (high in THC) the next morning the cramping reduced by 80%, stools were firming up, and hot flashes reduced dramatically. On day two my symptoms were gone. I started the CBD oil around day 3 and cut back on the high THC oil until I eliminated the THC oil completely.

I’m only using CBD only now and feeling great, my system is back on track and I take 1/8 tsp twice a day.

The help & info from ROC is fantastic!

John’s story

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iROC365

Quality of Life Matters!!

Overall, Raymond’s health has improved. His appetite has increased and he is starting to have better coordination allowing him to move around more freely. The progress is slow but still steady. He is also beginning to make more sounds and try and talk. He is able to enjoy life so much more than before and we are so thankful!

Raymond’s story

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iROC365

I wasn’t aware of CBD

Jazzlyn’s seizures are pretty much kept to baseline. She’ll have maybe 1 or 2 every 1 – 2 weeks except for when she gets sick. Her immune system is weak so it’s very easy for her to get sick and when she does she can have a seizure every day for however many days she’s sick with multiple seizures some days day.  Maybe increasing the dosing when she is sick will help. I usually give her clonazepam, which her neurologist recommends when this happens, and it doesn’t help but I’m working on it.

This aid really makes a difference given CBD isn’t covered by medical insurance and it’s pricey. AED’s do not work for my daughter to their full potential alone, she’s currently on 4, and CBD does. It’s unfortunate that for a lot of families the difference between seizure free and not is being able to afford CBD products. Of course, the legality part of it plays a part as well depending on where you live but the financial burden is definitely impactful. I mean, for the longest I stuck to just AED’s because I wasn’t aware of CBD and when I became aware, I couldn’t afford it. So thank you to the RoC!

Jazzlyn’s Story

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iROC365

Alternative to antidepressants

The cannabinoid therapy has helped me in many ways such as constipation relief from rare illness (SMAS) and a better sense of well being. My current health prognosis is I will not get better as I have dealt with this rare illness since 11/2010 and struggle daily with severe fatigue, abdominal pain, constipation, lack of normal digestion, etc. Plus cancer, aneurysm, and damaged spinal cord T6. I stopped using the oil and I got back on it as it helps with many things such as increased energy, sense of well-being, and helps a little with severe chronic pain.

This treatment gives me a better mood without taking antidepressants. I notice a huge difference when I take it daily and when I stop for a week so I can tell the difference. It does help once I load in my system (endocannabinoid) and I have also tried taking more such as 1 mL three times a day but it affected my liver so I dropped back down to .5 mL twice a day.

Zane’s Story

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iROC365

Less aches and pains

The cannabinoid therapy has helped me a great deal. Although I have not been able to determine my therapeutic dosage because I cannot afford to take more at this point. However, taking it consistently I have noticed a difference as far as the aches and pains I used to feel.

Adele’s story

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iROC365

Her Crohn’s disease and arthritis are in remission

Provided by Michelle’s family

Michelle is our only child. She became sick at 15 months old following an encephalopathy that destroyed her health. Michelle is now 23. She’s been diagnosed with severe autism (non-verbal), intractable grand mal epilepsy, Crohn’s disease, spondyloarthritis, uveitis, legal blindness, osteoporosis, severe deformity bilateral (feet bones), stage III steatohepatitis (liver disease) and severe static encephalopathy.

When Michelle was 10 years old she had her first grand mal seizure. It was so strong that it caused her to drop straight down twisting her legs beneath her, causing a compound open fracture (bone busting right through her shin). She was in the hospital for 6 weeks following this seizure and surgery. She was put on anti-seizure medication during that time. This point was really the beginning of a worsening overall in Michelle’s health. She had trouble healing from the bone break. She continued to have severe Crohn’s, painful arthritis, painful foot deformities, insomnia, and increasing grand mal seizures. Of everything that she had going on, the seizures were the most terrifying to us. We took her to five different neurologists to try to get her help for the seizures. All they could offer was more anti-seizure medications and brain surgery. We were told that she was at a high risk to die from SUDEP.

A few years ago I began researching medical marijuana, with an emphasis on CBD. I saw the CNN specials with Dr. Gupta and felt this was something that may be able to help. Michelle’s health was not good and continued to decline. She was on several strong anti-inflammatory drugs including Humira and Remicade, as well as very high doses of anti-seizure medications. She was feeding tube dependent yet severely overweight (steroids beginning at 8 years). She had horrific pain just to walk. She was in a wheelchair when outside of the home. It took two people to help her walk because she had to hold on. She continued to have grand mal seizures, clustering while she was sleeping to as many as nine at a time. She was repeatedly hospitalized for abdominal wall abscesses at the feeding tube sight. Her body couldn’t fight the infections because her immune system had been suppressed for so long. She continued to have seizures. She didn’t feel good. She was having horrible self-injurious behaviors because of pain. Michelle was completely debilitated at this point. None of her specialists could offer anything more for her. I had only one hope and that was to try medical marijuana. I had already been researching it off and on for several years. But I wasn’t sure where to start. I saw a presentation online from a doctor in California who was treating children with CBD, Dr. Goldstein, and we made an appointment to see her.

From the beginning of taking CBD we could see a difference. The first thing we saw was Michelle began to smile. We titrated weekly for a few months to reach a therapeutic level. The seizures began to decrease with seizure-free periods. Two months after starting CBD, Michelle began to taste food by mouth. Previously, she was feeding tube dependent with only rice crackers and water by mouth. Now she was tasting cooked food, pot roast with vegetables. Within a few months, we had her GI’s permission to discontinue tube feedings and feed only by mouth! So now Michelle was eating meat, chicken and a variety of vegetables!

Because of the constant infections, we had to consider discontinuing Humira. We stopped Humira but Michelle continued to improve with the Crohn’s disease symptoms. Although she was eating by mouth, she no longer was having chronic diarrhea. She began having regular bowel movements and still does! By the end of the first year, she was no longer showing signs of active arthritis. She began to walk more, lose weight and become very alert. She continued to have good seizure control with only occasional breakthroughs. I was able to get her into adaptive exercise classes. She lost more weight and began to improve overall. Today, she is no longer taking any anti-inflammatory medication. She is slowly weaning off of her seizure medications. Her seizures are well controlled. She had her feeding tube removed after 13 years!! Her doctors say her Crohn’s disease and arthritis are in remission. She has imaging and lab results showing her liver to be improving. She is able to sit through speech and OT therapy because her autism symptoms are lessening and she is able to participate now. She has begun using an AAC iPad device. She is happy and laughs with us. Her quality of life has improved by 1000%, and she is healing. This treatment has been a real life changer for Michelle.