Scleroderma's signs and symptoms vary, depending on which parts of the body are involved:
- Skin. Nearly everyone who has scleroderma experiences a hardening and tightening of patches of skin. These patches may be shaped like ovals or straight lines, or cover wide areas of the trunk and limbs. The number, location and size of the patches vary by type of scleroderma. Skin can appear shiny because it's so tight, and movement of the affected area may be restricted.
- Fingers or toes. One of the earliest signs of scleroderma is an exaggerated response to cold temperatures or emotional distress, which can cause numbness, pain or color changes in the fingers or toes. Called Raynaud's disease, this condition also occurs in people who don't have scleroderma. (During high school, i always brag about how my hand cold when the weather is scorching hot. I thought it was a cool thing since I'm different from others 😌😮)
- Digestive system. In addition to acid reflux, which can damage the section of esophagus nearest the stomach, some people with scleroderma may also have problems absorbing nutrients if their intestinal muscles aren't moving food properly through the intestines.
- Heart, lungs or kidneys. Scleroderma can affect the function of the heart, lungs or kidneys to varying degrees. These problems, if left untreated, can become life-threatening
Since scleroderma can take many forms and affects so many different areas of the body, it might be difficult to be diagnosed. Myself had been misdiagnosed for about a year and half. During that time, I was diagnosed with various problems like muscle spasm, gout, AVN (avascular necrosis), frozen shoulder and vitiligo. Luckily, I get to be diagnosed correctly after that or else it might get worse than now.
Doctors will always ask for blood test and urine test on every appointment. It is actually quite troublesome to drew blood from my body since the skin is hardening with minimum twice injection to collect the blood. I also had undergone chest x-ray, MRI, kidney ultrasound and echocardiogram (as I can remember since I've done a lot of things). Alhamdulillah praise to Allah. So far so good. All I need to do is maintaining this from not getting any worse. It will be better if it progressed towards a better condition.
Having illnesses can give direct impact on mental health. Denial, anger and frustration are common in someone with chronic illness. Having support and understand from family members and friends are very important. Joining support group also can help by sharing experiences and feelings with each other. Currently, I still didn't found any support group in Malaysia, so i joined the USA support group. There are also doctors in the support group that always give us new information about new founding on recent research. I wonder how many Malaysian have scleroderma because I never heard any. Even at the hospital, I didn't found anyone that have the symptoms. Maybe they went on different day (if there were any).
So, I am very thankful for those who were with me during ups and downs till this day. Love You All.
~End of Sclerowhat?~