A new Beta Blocker for those with Dyautonomia
Hello everyone! It has been a few weeks since I have not written. I been dealing with different doctor's for my son and getting new information all the time. Seems like this time we are finding doctor's who have been very helpful. I like to thank the Children Hospital Cardiologist in Boston for being very supportive and a great help. Recently my son was put on a Beta Blocker. It is called Betaxolol. (Betaxolol relieves anxiety and panic symptoms much faster than antidepressants. It works within 1-3 days while antidepressants take up to 12 weeks.) He takes a .5mg a day. To remind you, people with Dysautonomia are sensitive to medications. If they take normal dosages they will get most of the side effects. It is important to take small dosages because your body is 80 to 85 percent low on fluids. What this Beta Blocker is doing for him is controlling his hard throbbing palpitations that never go away. It is with him 24/7. The palpitations is another main symptom most complained about who have Dysautonomia. Well, so far he has been on it for 2 weeks and he does not have that hard pounding palpitation he's had since he hit his teenage adolescent life. One symptom relieved from his body so far. More to conquer.
I was skeptical at first because he has low blood pressure and very nervous thinking his blood pressure would drop more. Well, it did not. Thank god! : ) There is hope yet and there are doctor's out there that are willing to help. The more we get the word out the more they will take this more seriously. With everyone writing there blogs about it, the word is getting out. Great job all!!!
I will speak in my other blogs about teenage children with Dysautonomia. It is harder for them since they are going through the hormonal changes. Also, I still will talk about nutrition and exercise in the other blogs as well. There is allot to talk about and allot to express to help those in need and who are suffering with this disease.
Until my next blog, blessed be. : )
I was skeptical at first because he has low blood pressure and very nervous thinking his blood pressure would drop more. Well, it did not. Thank god! : ) There is hope yet and there are doctor's out there that are willing to help. The more we get the word out the more they will take this more seriously. With everyone writing there blogs about it, the word is getting out. Great job all!!!
I will speak in my other blogs about teenage children with Dysautonomia. It is harder for them since they are going through the hormonal changes. Also, I still will talk about nutrition and exercise in the other blogs as well. There is allot to talk about and allot to express to help those in need and who are suffering with this disease.
Until my next blog, blessed be. : )
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