Many readers are interested in the right subject: the Ehlers-Danlos syndrome and its new treatment with Cannabis. Our manufacturer is pleased to report that we have already done modern research studies on your fascinating subject. We will give you a wide range of answers based on the latest medical reports, advanced research papers and sample surveys. Keep repeating to find out more.
Annabelle Griffin, a six-year-old girl, likes to go to interesting fairs, play at attractions, and rock like other women her age. But doctors have told her caregivers that her life could be in jeopardy if she just goes out and plays like any other kid. This 6 year old cannot play with She will not have the opportunity to attend high school or participate in sporting events. This is because she suffers from a serious but rather rare disease commonly referred to as Ehlers-Danlos syndrome. This disease is also known as vascular ED. In this condition, a small punch or the smallest touch can lead to serious internal bleeding and can actually result in death. This disease runs in families and is passed from caregivers to offspring.
What is Ehlers-Danlos syndrome?
Edition or ehlers-danlos syndrome is a rare genetic disorder in which there is a deficiency in the metabolism of the connective tissue that anchors and supports our large bones. There are all kinds of biochemical types of connective tissue that play an important role in the synthesis or stiffness of all kinds of body structures, including auxiliary blood vessels, bones, and skin. Connective tissue is made of a special type of protein called collagen and fibrous material. there are six important forms of Eleur-Danlos syndrome :
- Arthrochalasis eds
- Classical eds
- Hypermobility eds
- Vascular eds
- Kyfoscoliosis eds
- Dermatosparaxis eds
What are the symptoms of Ehlers-Danlos syndrome?
Characteristic signs and symptoms of this condition include
- Muscle soreness and muscle fatigue are considered the most common signs. You may still suffer from acquired pains, uncanny bruising, early osteoarthritis, etc.
- Very flexible joints: the joints are still considered loose or kinetic because the connective tissue is loose (unstable) and the range of motion is increased. The tongue can also be used to touch the tip of the nose.
- Skin elasticity: Due to lack of collagen and weak connective tissue, the skin is more extensive than normal. And your peel will be velvety smooth.
- Fragile skin: because the connective tissue has weakened, the skin is fragile, sensitive to touch, and healed wounds are not easy to treat. For example, if there are stitches, they will likely leave a gnarly wound, leaving a fissure and a graceful, awkward scar.
- Fatty ridges: Small fatty ridges have a great chance to sit around the knees and elbows. These fatty ridges are easily identified with x-rays. The severity of symptoms may vary from patient to patient. Some can develop all of these symptoms, while others show no symptoms except for inflexible joints.
Symptoms of Vascular Eler-Danlos Syndrome
Vascular Eler-Danlos syndrome A subtype, and a much more extensive one at that. EDS with It is distinguished by small ears, an elegant beak, upper lip, and striking eyes. The patient’s skin may be narrow or colorless. In fact, you can sometimes see blood vessels through the skin, which may just contract.
In addition, the blood vessels elerae danlos can syndrome weaken the arteries of the spleen and soul, as well as the very large arteries of the heart. If it leads to lacerations of these blood vessels, your life is at risk. More than that, this condition prepares the tract or uterine wall over the colon for weakening or tearing.
What are the causes of Ehlers-Danlos syndrome?
As previously discussed, Ehlers-Danlos is so syndrome A rare genetic disorder is that it is inherited from the affected caregiver of the offspring. However, very small cases of ED are not inherited and may produce spontaneous genetic mutations.
The genetic defect usually involves an inability to regulate collagen synthesis, resulting in a free set of collagen. Collagen is necessary for the formation of healthy blood vessels and skin covering. After the formation of these free collagen fibers, the vascular lining becomes fragile and may bleed. If someone has vascular ED, the chance of this disease being transferred to later life is almost 50%.
What about the use of cannabis to treat Ehlers-Danlos syndrome?
There are no medications for EDS. Opiates and other intoxicants are usually used to treat this condition, but they are addictive and carry a higher risk of side effects such as drowsiness, loss of appetite, and constipation.
- In recent years, it was medically cannabis used as an intolerable candidate for classic anesthetics such as opiates. Cannabis has numerous narcotic drugs and potent anti-inflammatory qualities that are very helpful in relieving the nerve, joint, and muscle pain suffered by ED patients.
- Cannabis acts as a mild muscle relaxant and can significantly reduce the risk of bruising and bruising in people with ED.
- Persistent insomnia is considered an annoying sign of Ehlers-Danlos syndrome. and cannabis It helps to get a good night’s sleep.
- Other effects of cannabis Healing of EDS, arthritis, myalgia, migraine headaches, rib bone subluxations, etc. enlightenment.
How to use cannabis for Ehlers-Danlos syndrome?
For healing of EDS, it is recommended to swallow the medicinal cannabis orally via tincture or use another concentrated form of cannabis . Smoking cannabis Usually discouraged due to the fact that it may destroy non-nostalgic tissues. Vaporization is considered legal in Illinois and the nation and is considered the second best option for intake. cannabis It allows SED patients to control their intake without damaging non-tissues.
Treatment Options for Ehlers-Danlos Syndrome
Special support is needed to cure this condition. This can be easily accomplished with the right steps.
1. ed
- If a person has a positive Ehlers-Danlos home situation syndrome and considering establishing a family, genetic advice during this period is considered an important option to prevent disease transfer. A trained genetic consultant can help determine disease patterns and associated risks of with inheritance in different scenarios.
- Skin is touchy and vulnerable and should be protected primarily with pleather soap and sunscreen.
- Avoid activities that could lead to unintended injury, such as weightlifting and contact sports. Do not place excessive or itchy mats, rugs, or electronic cords on the floor. This increases the potential for falls and injuries. Ensure that doors are free of malfunction or excitement.
2. model a support system
Build rapport. with People who applaud and give support have a positive impact on someone’s attitude. Get online and join a variety of assistance groups that are likely to share illness skills and corresponding conclusions. Creating a support system can help counsel and minimize the risk of depression/emotional challenges.
3. take medications
Painkillers: physicians prescribe painkillers to relieve muscle pain. Recipe – not usually used. Can prescribe stronger medications for severe pain.
Blood pressure reducing agents: due to the fragility of the blood vessels, the physician may prescribe blood pressure lowering factors to reduce pressure on the blood vessels.
4. remember physical therapy
Physical therapy is recommended to strengthen muscles. since the muscles are simply hanging on ehlers-danlos. syndrome Physical therapy is considered the first option to improve mobility. Special types of braces are still recommended to prevent joint disease place.
5. recovery surgery
If the joint is out of the bowl and there is no opportunity to move, surgery is recommended with Physical therapy. However, it should be considered that healing is cancelled by weakened collagen fibers.
