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During hard times you'll want a support group that shares the same needs that you do. A reliable support group in which you can contact could be http://www.turnersyndrome.org/ .  There's many others but this one of the many that are out there to help families who seek information about Turner Syndrome patients.

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https://www.turnersyndromefoundation.org/

https://ghr.nlm.nih.gov/condition/turner-syndrome?_u=b897-33f7&utm_expid=.qfbuu21fTGm4jYz6mrmJMw.1&utm_referrer=https%3A%2F%2Fwww.google.com%2F

http://www.mayoclinic.org/diseases-conditions/turner-syndrome/basics/definition/con-20032572

http://www.turnersyndrome.org/

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Kids with Turner Syndrome may be under care of a pediatric endocrinologist during their childhood and adolescence. Turner Syndrome kids benefit from growth hormone injections. The injections begin in their early childhood. The injections may increase final adult weight by a few inches.Estrogen replacement therapy is sometimes started at the time of puberty. Babies that are born with a heart murmur or narrowing of the aorta may need surgery to correct the problem. A cardiologist will follow up any treatment that is necessary. High blood pressure is common between women who have Turner. Blood pressure should be checked routinely and treated with medication if it's necessary. Women with Turner have a slightly higher risk of having an under active thyroid or of developing diabetes. It's important that Turner Syndrome patients get regular health checks. With all the appropriate medical treatment and support a Turner Syndrome patient can lead a normal, healthy and happy life.

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Turner Syndrome is a chromosomal disorder in which a female is born with only one x chromosome. Turner Syndrome can also be called Gonadal Dysgenesis. The exact cause of Turner Syndrome is not known, it appears to occur as a result of a random error during the formation of either the eggs or sperm. This condition alters development in females. Symptoms of Turner Syndrome are that the girls that are diagnosed with this are shorter than average. Diagnosis of this disease can take place later when puberty doesn't occur. Turner Syndrome may also be diagnosed during pregnancy. The child may have a normal height for the first 3 years of their life, but then they begin to have a slow growth rate. These kids don't have a usual growth spurt at  puberty. The females have non-functioning  ovaries. Girls with Turner Syndrome don't produce sex hormones ( estrogen and progesterone).  Girls don't start their period or develop breasts when they hit puberty. They need hormone treatments to develop these things. Females have a totally normal vagina and womb, even though many women with Turner have non-functioning ovaries and are infertile. Pregnancy with a donor embryo may be possible though. During childhood, kids with Turner syndrome can have frequent middle ear infections.Recurrent ear infections can lead to hearing loss in some cases. Kids with Turner usually have normal intelligence with good verbal skills and hearing skills, however they have problems with math memory skills and fine-finger movement. Some additional symptoms of Turner Syndrome are that patients have a wide neck and a low or indistinct hairline. They have a broad chest. Having a child that has Turner Syndrome can affect all of the family members' lives but with the right support it can help the whole family cope with this.