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mully2014

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Posts posted by mully2014

  1. I will even have breathing issues while I am passed out and come to. I have O2 readings that are low or not in the normal range during some of these times and even occasionally when doing orthostatic checks at my doctors appointments. More often now do I have problems getting enough O2 and my eyes will even get extremly bloodshot looking when O2 levels are not good.

  2. My sister is on Florinef .1mg she is 13 and is MANAGED very well on it!!!!! She doesn't have any side effects on it either.

    I am also on florinef and have been for a couple of years. I am extremely sensitive to meds but I didn't have any side effects from florinef. I am currently on .3mg but have been on .4mg before. When I started out I was on .1mg.

    I hope this really helps you!!!

  3. I get really bad muscle tension that seems to be related to my conditions. Does anyone else have this problem if so what do you do to help? I have done massage and chiropractor but it adds up especially when it doesn't hold/help for very long (on average only 24hours) and just started up with manipulation and physical therapy. I'm hoping to feel better especially when I will have to sit all day long at school in a wheelchair.

  4. Lauren's Hope is where I ordered mine from it holds up really well and you can have different bands that hold the alert part. All my friends and family comment on it and love it. I like that it looks like jewelry and can get a starting point for anyone that would be around me when I pass out. I put my name, conditions (NCS: syncope : fainting, P.O.T.S.) then allergies, and a contact number for a family member. I had fainting put on the alert so anyone would be able to understand that it was I medical condition and it was a normal thing for me. I didn't include meds because they are constantly changing. For me the medical alert bracelet became even more important after I had mutiple concussions and ended up losing my memory.

  5. I went to Mayo in MN and I had a good experience there and my regular cardiologist still keeps in contact with my doctor there. They didn't have much for me personally to help me but they did reassure us in a lot of our thoughts and treatments. The cardiologist I normally see always goes above and beyond and Mayo said they couldn't believe everything we had already done.

  6. I have lots of relatives that have symptoms of dysautonomia but I definetly have the worst problems with it. On both of my parents sides there is issues with low blood pressure, one person has laughing asthma that cause them to faint, others have orthostaic intolerance, my younger sister has some similiar symptoms and is diagnosed with POTS. My family medical history is a long confusing web of connections to dysautonomia that seems to increase all the time.

  7. I know of a lot of organizations I filled out all of the work and sent it into capable canines but haven't heard back yet. There is also custom canines and the canine partners for life. A problem I found is that some of them want you to travel to their training site for a long period of time and stick to a specific training schedule but with my body I don't think I could make the traveling and be able to go train on a schedule like they say. I normally don't have a schedule that I must follow becasue things do come up so instead I consider it "goals to get done".

  8. I am trying to get a hold of a service dog organization and am wondering what groups people on here have been able to get in contact with them about the dogs and if they are a good canidate for a service dog. I would really like to get one but every group we contact they don't contact us back which is disappointing since I know it would help out with every day.

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