Guest guest Posted February 2, 2004 Report Share Posted February 2, 2004 Dear mom about to give up--- ((((HUGS)))) to you, and please don't give up. I know you don't want to give up just by the fact that you wrote. What kind of symptoms does your daughter exhibit? What medications is she taking? I'm wondering if maybe the meds are starting to poop out or might need adjusting? Has she seen her therapist/psychiatrist recently? I have a now 13-year-old daughter with OCD (dx since Oct 2002) who is on Lexapro now. She has made good progress over the last 16 months, but there are days that I, too, am ready to retire/throw in the towel. Hang in there...so many parents on this list have been or are where you are...I'm sure you'll get lots of support and advise. Blessings- (Ohio) Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 3, 2004 Report Share Posted February 3, 2004 > Dear mom about to give up--- > ((((HUGS)))) to you, and please don't give up. I know you don't > want to give up just by the fact that you wrote. What kind of > symptoms does your daughter exhibit? What medications is she > taking? I'm wondering if maybe the meds are starting to poop out or > might need adjusting? Has she seen her therapist/psychiatrist > recently? > I have a now 13-year-old daughter with OCD (dx since Oct 2002) who > is on Lexapro now. She has made good progress over the last 16 > months, but there are days that I, too, am ready to retire/throw in > the towel. Hang in there...so many parents on this list have been > or are where you are...I'm sure you'll get lots of support and > advise. > Blessings- > (Ohio) thanks for getting back to me. this is the first group I encountered that actually has given me some hope. Yes, she has seen a therapist. she is currently seeing her third one. she has been to two psychiatist who " blew us off " see to look at her one would never know anything is wrong. but at home it is a terrible nightmare. And I seem to be in the brunt of it all. She is on luvox, paxil and risperdal and the wait for a true pediatric psy. is months so in between a family doc. and a nurologist, we are trying to maintain the drugs. Yes, I do think an adjustment is needed. I just cannot believe that with all the millions of people and children suffering from this illness there are not more support groups like aa or cancer. this illness is like living with someone who has ahlzimers. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 4, 2004 Report Share Posted February 4, 2004 Hi and (((hugs))) I'm sorry things are so very rough for you and your daughter right now. What three meds is she taking, and are you confident in the prescribing doctor's skill in balancing these meds? What does this doctor say about the current situation? It may be that one of her meds has stopped working (SSRIs may do this for unknown reasons), the dose may be too low, or that a med is unexpectedly worsening the symptoms of her OCD. You might consider a second assessment and opinion regarding your child's diagnoses, perhaps at a University-based anxiety clinic, which can often offer well-trained clinicians and frequently a sliding fee scale. In any case, given her symptom level, it seems she needs more help from her meds to be able to function at home as well as at school. Does she have a therapist, and do Cognitive Behavior Therapy with Exposure and Response Prevention? This is the one type of therapy that does reduce and eliminate OCD compulsions, other types do not. Expert therapy plus an effective SSRI (may be trial and error to find the right one for your daughter, and the right dose) is perhaps the quickest route to low, stable symptoms. If money is getting tight, then it's especially important to thoroughly vet the doctor and the therapist, to be certain they are capable of providing the medication expertise and therapy that your daughter needs. Then monitor results, while it can take months to get meds sorted out, you should see improvement in symptom level from therapy within a few visits. Three years, even off and on, is far too long to be seeing a therapist with no better results than what your daughter has experienced. Many on this list saw several doctors and therapists before finding the ones who could actually help and get results, you want to be sure you don't fall into this trap. It's pretty common for kids to do all they can to hold it together at school and then come home and let all the accumulated stress of the day go--blow ups, meltdowns, ugly tirades and behavior. Very often it's Mom (safe person) who sees the OCD and etc. in all its " glory " . It's also pretty common for school personnel to think a parent is being overdramatic or making up that their child suffers from OCD, especially if the child is not a behavior problem or struggling with grades. I and so many of us here have been through this or are going through it currently. One thing that has worked well for us is to have my daughter's psychiatrist speak with the teacher, guidance counselor, principal or whoever at the school most needs to hear from a professional, the ways in which OCD affects a young person. He has usually said basically what I had told the teacher, but it was more creditable coming from a doctor. Ineffectively treated, waxing OCD can drive anyone to their wits' end and beyond. I'm sorry to read that things are so very difficult right now but the right treatment can turn things around fairly quickly. In the meantime you must do all you can to take care of yourself, find time for yourself even if it's just to walk around the block, take 20 minutes to read the paper, or other things you enjoy. Your daughter may not act appreciative at this point, but no doubt she is relying heavily on you and you can't help her if you don't take care of yourself first. Kathy R. in Indiana p.s. Symptoms of other diagnoses can fade away once OCD is adequately treated. Raging OCD can look like all kinds of other problems, but it can be really hard to get a good idea about this until the OCD is under control ----- Original Message ----- > Hi. I am almost at my wits end. my 14 year old has ocd and I also > think ocpd. she has seen a therapist off and on for the last three > years but recently, she has become worse with her ocd and attitude > towards us (her family). she is on three different kinds of meds and > I am doing every research piece I can about this. Our family is being > ripped apart because of this illness. she is an honor student and a > very quite young lady in school. the school officials all think we > are somewhat making this up. but they don't live with her. we are > running out of $resources to help her and not sure what else we can > do. any advise would be helpful. > mom about to give up Quote Link to comment Share on other sites More sharing options...
Guest guest Posted February 5, 2004 Report Share Posted February 5, 2004 Hi: Many of us can relate all too easily to what you wrote about home being a terrible nightmare compared to outside the home. That is part of the cruelty of OCD that it attacks sufferers all the more stongly when they are most relaxed and in a safe place. As the daughter of someone with Alzheimers and the mother of a son with OCD, I do notice some similarities in living with these disorders. However OCD has a very different prognosis and responds to good treatment so you can get your life back. Please have lots of hope that things will get better for your daughter and the whole family. Good luck, take car, aloha, Kathy (h) kathy.hi@... > > thanks for getting back to me. this is the first group I encountered > that actually has given me some hope. Yes, she has seen a therapist. > she is currently seeing her third one. she has been to two > psychiatist who " blew us off " see to look at her one would never know > anything is wrong. but at home it is a terrible nightmare. And I seem > to be in the brunt of it all. She is on luvox, paxil and risperdal > and the wait for a true pediatric psy. is months so in between a > family doc. and a nurologist, we are trying to maintain the drugs. > Yes, I do think an adjustment is needed. I just cannot believe that > with all the millions of people and children suffering from this > illness there are not more support groups like aa or cancer. this > illness is like living with someone who has ahlzimers. Quote Link to comment Share on other sites More sharing options...
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