Guest guest Posted June 9, 2006 Report Share Posted June 9, 2006 From what I've > learned here in > the short time I've been here (2-3 months?), Lol Wayne, Aloha, I'm a brand new member ... So it's been slightly over a month, may the Dexadrine be affecting your sense of time ? I'd be interested to know what my GP could prescribe dexedrine for, though. My urologist said ADHD (which seems strange). Cheers, x JanR __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2006 Report Share Posted June 9, 2006 From what I've > learned here in > the short time I've been here (2-3 months?), Lol Wayne, Aloha, I'm a brand new member ... So it's been slightly over a month, may the Dexadrine be affecting your sense of time ? I'd be interested to know what my GP could prescribe dexedrine for, though. My urologist said ADHD (which seems strange). Cheers, x JanR __________________________________________________ Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2006 Report Share Posted June 9, 2006 Wayne, - Can you share briefly what you have learned so I can speed read thru you and I'll also look at old posts to see what it is I can learn to do for myself. What are you doing that is working for you? Ria ======== > I took Celexa for only 18 months and had every ED problem a guy > could have. I could STILL get and erection and and orgasm with a LOT > of work from masturbation, but forget just (just?!?) making-loving. - Yes, it does take _a lot_ of work and by the time I think I am supposed to finished I forget what I was doing in the first place & fall asleep. > Yours is the first I've heard from about Cymbalta and was really > hoping it would NOT be the same as other SSRI anti-d's, however, I > see it's the same. Too bad. - My psych says that ALL patients he has put on that drug has sexual side effects. He does not know of one single drug that is supposed to side step that. > The good news is and it's also good news about this group is 99% of > all my sexual dysfunctions have disappeared! > > > > > > > > Hello. I am new to this group. I too am suffering from the > effects of > > a SNRI called Cymbalta. I no longer have sexual drive OR orgasm. It > > did not happen overnight - it just happened over time. Sneaky > meds... > > > > Is there a list of antidotes to try that you folks have come up > with? > > > > I am willing to _try anything_ at this point. My psych says to take > > drug holidays. He also says that Wellbutrin taken along with the > > Cymbalta can help. Has anyone take Wellbutrin also to bolster drive > > and orgasm? > > > > Any advice you can give is appreciated. I am female but feel free > to > > chat as women also have these problems... > > > > Ria! > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2006 Report Share Posted June 9, 2006 Jr and everyone? Whenever I make a reference to " time " in ANY way, IGNORE IT. In the last 9+ (I'm SURE of THAT at least), 'time' is just another day of waking up in such severe pain that in the first 15 minutes of waking, if a revolver was within arms reach, I'd take myself out. PLEASE LET ME EXPLAIN THAT. Of course as most everyone knows, chronic pain that can no longer be treated in any way except by medications is a COMPLETELY DIFFERENT DISEASE. It changes from " Chronic Pain " to " INTRACTABLE PAIN " . Intractable Pain has FOUR outstanding characteristics: (1) constant, (2) severe, (3) disabling and (4)detectable biologic impacts on the body's blood pressure, pulse rate, hormone levels and neurologic systems. It's a catastrophic conditions that, inadequately treated, leads to PREMATURE DEATH. Some complications include dementia, osteoporosis, muscle wasting, obesity and cardiovascular disease. There is no suffering worse than Intractable pain (IP). If you ever have to define IP to someone, this is it: " Asevere, constant pain that is NOT curable by ANY KNOWN means and which causes a bed or house-bound state and earlky death if not adequately treated. It couses adverse biologic affects on the body's cardiovascular, hormone and neurologic systems. " People with IP in the past would simply be those that you'd see wasting away in a darkened corner in a vegitative state of mind. It's impossible to live with. Thankfully for me, I was born in 1955 and was told by all my surgeons, doctors and my pain management doctor that there was nothing more they could do for me except help control the pain so I don't " waste away and, more than likely, end my life. " That is why at one time I was ingesting over 4 grams of morphine daily along with opiod breakthrough pain meds and needing valium to control my back muscle spasms. Of course, as with most powerful pain medications my libido didn't matter to me anymore let alone orgasm, however, my WIFE could only take so much (or so little. Depending on how you look at it.)So I had my Testosterone level checked and whatever the " normal range " of 290 to ? is (Total " T " or Free " T " ?), my level came out to be 84. You see, in order for your body to 'survive' in such pain, it makes all sorts of chemical changes, including hormonal. I'm positive the pain medications and the other 11 meds I take also make a difference. So, my fellow members, I am a real mess. Of ALL the careers to pick from out there, I chose accounting (actually, IT chose ME, but that's another novel). I no longer can be depended upon to meet deadlines, calculate percentages, fill out simple forms and all the other requirments needed to be an accountant. I managed to hang onto my career until March of 2005 when my left knee " went out " on me and I needed to have surgery for a torn meniscus. I DID have a fairly successful addounting business at home for the last three years so I could lay down when needed and work only when I could. But the surgery and the recovery time needed took too long for my clients, so I had to give them to other firms. I've now swallowed all my pride as the " breadwinner " and " man of the house " and have an appointment with Social Security for Disability Insurance next week. OK, now, back to the Dexadrine...what I should be taking is Provigil. In fact, I TOOK Provigil for the last year that my pain management doctor worked before retiring. As you can imagine, I get quite groggy by 2 to 4 in the afternoon from the medications, so I asked about that and was given Provigil, NO PROBLEM. After my Pain doc retired, he had one hell of a time finding another doctor for me. Most of you know how hard it is just to get a vicoden from a doctor, let alone what I was taking. Well, it just so happened that the psychiatrist I'd been seeing was my pain docs " best friend " in the medical field and my 'shrink' was only too happy to take me " off his hands " . Provigil is normally prescribed to Narcoleptics to keep them from falling asleep during the day. The person who prescribes it has to be a Board Cert. Sleep Doctor which my shrink isn't. In order for my shrink to prescribe Provigil, he had to prescribe two other drugs first (this is the insurance company TELLING doctors how to treat their patients, AGAIN! Gggrrrrrr...). the first was Ritalin (yes, my shrink had to mention ADHD or whatever it is for this). Ritalin made me feel as if someone had closed a curtain halfway across my brain and gave me such a unusual stimulant feeling that I would start one project, think of another and start that, think of another and start that until I found all the " started projects " but none of them finished!!!! It didn't agree with me also. Just made me feel 'wierd'. The next drug in line was Dexadrine. I was completely taken aback by that because back in my " partying days " , stimulants were my drug of choice (beside pot, but back then, pot was just a " staple " drug. It was always around and there were days when I'd wake up with a joint in my mouth even before my feet hit the floor! Those were good times and I wouldn't change a thing about those days! Living with five guys and my girlfriend. I don't think the stereo EVER went off!), however, stimulants also got me put in the hospital (self-admitted) because my heart had been beating so fast for so long that the lining around it had swollen, so I was a little leary about them at first. Of course a medical practitioner didn't prescribe them the same way I 'used' to take them. So I gave them a try and lo and behold! Not only do they work fine for " wakefuleness " , but they also seem to raise more than my libido! This just happened to be a pleasant side effect because I was only looking for something to stop me from " taking naps at 2PM through 4PM which would turn out to be all night " naps " instead. I didn't like that nor did my wonderful wife. I was surprised to read a post from Vornan, our moderator, about the chemical effects dexadrine has on our brains that stop/reverse the nasty sexual side effect(s) of SSRI's! But, whatever, for now I'll just stick to the " Dex " and my lowered dose of the SSRI, Celexa (I tapered from 20mgs to 5mgs WITH my doctors blessings and started taking Testosterone Replacement Therapy (TRT). As I've stated probably 25 times already, 99% of all my bad sexual side effects have gone away! I'm one happy man. Not to mention my wife. One LAST thing (you REALLY believe that?), I would like to mention the QUALITY of my erections, QUANTITY AND QUALITY of my semen, the RE-ENERGIZING of the nerves around and on my genitals and lastly but CERTAINLY NOT LEAST the length, force and emotional power of my orgasms now. But I won't. I've written too much the way it is. JanR? I don't know how much all of the above matters to you, but I'd tell the doc to say ANYTHING S/HE WANTS TO just to get something that MAY help you. It very well may NOT work for everyone since it's a 'side effect', I only know it has that added benefit for me. OK? Hawaiian Wayne Aloha, I'm a brand new > member ... > So it's been slightly over a month, may the Dexadrine > be affecting your sense of time ? > > I'd be interested to know what my GP could prescribe > dexedrine for, though. My urologist said ADHD (which > seems strange). > > Cheers, > > x JanR > > > > __________________________________________________ > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted June 9, 2006 Report Share Posted June 9, 2006 Hi Wayne, How much of your sexual recovery do you attribute to: a. reducing your dosage of celexa from 20 to 5 mg b. starting TRT c. starting dexedrine Would be interested to hear your opinion of what helped the most... Thanks, Vornan Aloha, I'm a brand new > > member ... > > So it's been slightly over a month, may the Dexadrine > > be affecting your sense of time ? > > > > I'd be interested to know what my GP could prescribe > > dexedrine for, though. My urologist said ADHD (which > > seems strange). > > > > Cheers, > > > > x JanR > > > > > > > > __________________________________________________ > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted December 2, 2006 Report Share Posted December 2, 2006 30 year old male, 1 1/2 years approx. Lexapro usage. Right now I am having many troubles socially and I continuously meet the WRONG girls.That is actually an advantage because though I can " perform " i have almost no libido.If i for instance , go to a place where there are girls I can't get enough of it, but because I am very depressed and shy and have had my throat cut one too many times, I keep my distance and can only suffer. I hate myself for it all and don't know what to do.It's been 5 years since i have been in a meaningfull(though very disfuctional) relationship and am very lonely.I cannot stop taking lexapro though because i just get worse, i also am on a 2 other meds which disinhibit the whole black and white issue of whether your penis works or not more later Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2009 Report Share Posted March 31, 2009 Hi, Chris! Thanks for your encouraging words. " With the language delay you mentioned, what exactly is the delay? Is it his being able to speak/talk or his articulation or...? With the high IQ but problems learning, have they identified a learning disability? " -------------------- My son has an expressive/receptive language delay - he started talking very late - so it's taken him a while to catch up. He also has an articulation problem with certain sounds. The school psychologist also mentioned that he might have a learning disability due to the IQ/ Achievement discrepancy. " Have you talked to him yet about OCD? " ---------------------- I haven't really talked to him about OCD yet. With his language delay, he probably wouldn't understand it yet. But, someone in this group suggested a good children's book. I think it would help him to see that other kids sometimes feel like he does. " Do you think he understands the game? Is he excited about playing it? " ---------------------- I think he understands some aspects of the game, but not everything. I personally think he gets " overwhelmed " when he's out there with all those kids " fighting " for the ball.but my husband insists on having him play.You may be right, he might just feel " stressed " after having a full day at school!! What are some of the things he wants " just so " ? ---------------------- He gets stuck easily on certain things; for instance, there's a certain process when he's taking a bath (there's a certain order to the way he does things) and if you mess with that " order " he gets mad. Another example - when he's getting dressed for school, his socks have to fit a certain way and if they don't, he takes them off and says that they don't fit - it's SOOOO annoying!! Another example - if daddy is not home by the time we arrive, he'll say, " Oh, Daddy is at work, " and I'll say, " No, Daddy went out with his friends " , he'll get very upset and say, " NO, Daddy is at work. " So, I just HAVE to AGREE with him, or he won't stop, and start crying and throw a fit. One time we went out to lunch with the family, and he wanted to go to the bathroom - well, while he was peeing, a drop fell on his underpants (literally, a drop). He cried during the whole entire time we were there and demanded we take him back home to get changed. I kept telling him it was nothing and that I had already dried it off. He wouldn't let it go. It's the little things that upset him - and most people don't understand why.not even my husband!! _____ From: [mailto: ] On Behalf Of Sent: Monday, March 30, 2009 10:22 PM To: Subject: Re: New to the group Hi Carolina, welcome! So sorry you're having to deal with OCD on top of everything else. With the language delay you mentiones, what exactly is the delay? Is it his being able to speak/talk or his articulation or...? With the high IQ but problems learning, have they identified a learning disability? Glad he's doing better in that EELP setting. He has lots of years of school ahead, best to get all the basics down well before putting more learning & work on him. Sounds like he's very frustrated too, not wanting to work on it at home. What are some of the things he wants " just so " ? Have you talked to him yet about OCD? There are some good books out for young kids about OCD. Once he learns what is OCD and that he needs to boss it back, he & you could do things like choose something he wants " just so " and mess it up in some way; see how long he can stand it that way before getting it " just so. " Or if he has routines he just HAS to do, mess up the routine maybe. Of course you don't tackle all the stuff at once, choose 1 or 2 easier things to work on. With soccer - well he is just 5. Having had 3 sons who played soccer (sons now ages 24 and twins are 20; a twin has OCD), I remember that age! Do you think he understands the game? Is he excited about playing it? Also am wondering - with the mention of his struggle with learning letters & numbers, could some of that difficulty (whatever is causing it) carry over to the soccer or other things? Sorry for all the questions! But glad you found our group. My son's OCD began in 6th grade, though he had his quirks before that. He also has Aspergers Syndrome, mild I guess. Also a dysgraphia diagnosis that he got when his handwriting changed after OCD began, became illegible. But then he already had some fine motor skills difficulties too. single mom, 3 sons , 20, with OCD, dysgraphia and Aspergers Quote Link to comment Share on other sites More sharing options...
Guest guest Posted March 31, 2009 Report Share Posted March 31, 2009 Hi again Carolina! My twins were delayed with their talking also. More around age 3. They just " jibber-jabbered " before that. Also had the articulation problems. But then my oldest son also needed speech for that. Figured they all inherited that from me, I also needed speech therapy for it. Oldest son wasn't as affected though. I also wondered a bit with one twin about the expressive/receptive possibility. Well, more the receptive part. just didn't seem to know exactly what I was asking/telling sometimes. Oh, soccer! Well - just didn't get it either. I'd be yelling " move, move! " and he wasn't quite sure what to do. It's hard if the kids are all bunched up chasing the ball too, not yet playing their positions, all trying to kick it, sort of moving as one huge group, LOL. was also distracted easily, might be more concerned with a cut on his finger or something. Once we got him to understand " defense " he was determined to stand there in position ( " move, move! " ) and then later you could sort of see the bulldog determination to block the ball (not that he was the best at that either). The other 2 sons picked up on it more easily. My oldest probably began to hit his prime around 4th or 5th grade maybe; whereas some of the other players were just " great " from age 5 on, the skill! Anyway, oldest played about year-round later, on county teams, etc. But I think I may have yelled " move " at him too when younger, LOL. And with and baseball/T-ball - well, too many things to remember, know to do once it got past T-ball. But was surprised how often he did hit the balls pitched, good eye. Just too other much stuff to remember, multi-task, etc. The OCD stuff you mentioned - not unusual. Some kids just have to get that " right " answer or will keep asking you for it. When things have to be in a certain routine or " just so " , reasons can vary with OCD. Might be just a feeling of anxiety if not done that way, might be a feeling that something bad will happen, or they have to feel a " just right " feeling...can possibly be any reason. Some younger kids do like things " their way " though, can be difficult at times to decide if it's a phase or OCD. But either way, I think you can work on the problem using the same methods. The underwear incident - we've had here some children who change their's frequently during the day, worried or say it feels wet or " might be " , just want a clean, dry pair.... With the socks, could it be the seams?? Lots of kids have problems with the seams. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2009 Report Share Posted July 20, 2009 It's so hard to watch them talk themselves out of something that could be so fun and good for them. For me, it's like watching myself all over again, since I have OCD too. I was hoping she wouldn't have to go through what I went through. <sigh> Hang in there! Laurie > > Things need to done right and if she's not sure she can do them right the first time then she may opt out of trying them at all. This is heartbreaking for a parent to see as I'm sure everyone on this site already knows. But this is new for her daddy and I (and her 2yr old brother). It's hard to watch her miss out on something because of these thoughts. It's also tough to try to get through one her episodes without taking time from her brother. She's a bright, beautiful, sweet and loving little girl. I wish I could fix this for her but realize I can't. I can only help her try to come to the decision herself that she wants to control the ocd and not let it control her. For a 5 year old, that is a tough thing to do. > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2009 Report Share Posted July 20, 2009 Thanks Missy. It's amazing for us to realize we're not alone in this. I try to talk to her about whether its her or the ocd (in her case she has named them swirly's because that is what it feels like in her mind when she goes through this. I'm encouraged that a 5 yr old can name and describe it. When she has an episode or is feeling anxious she describes it as her " tummy getting dizzy " . Being 5 yrs old is hard for her to really understand what she has. At 5 yrs they are very literal. But we're working on it. We've started with the smaller / easier things for her to take control of (hand washing) and will move from there. Today she went to the doctor's and we were told she has fifth's disease which I suspected earlier this week. I asked them randomly to perform a strep test on her (although all she had was a cold and cough) .... our therapist suggested it a couple weeks ago in passing and just said " if you go to the dr's for anything have them run a quick strep " . Surprisingly the doctor said her strep test came back positive VERY quickly. I've heard that strep can increase the symptoms of ocd in children of this age. I'm hoping the antibiotics for the strep will help some of the symptoms subside but if not ... we are in this for the long haul ... with her and for her .... no matter what. Thank you for your note and your welcome to the group. It's nice to have others around that are going through or have gone through what we're going through now. > > > Welcome to the group.? I have a 7 year old daughter who was recently diagnosed but whom I've suspected of having OCD since she was 3.? We've been through the apologizing and also watched her not participate in activities (usually because she's afraid she will throw up).? It's heartbreaking.? Now that we're all learning how to respond (or in some cases, not respond) she's doing much better.? It's all still new to us and I never feel like I'm the right person to give advice but one thing that usually helps when she keeps apologizing is to ask her if she thinks it's OCD or her who wants her to apologize.? Usually she's able to recognize it as OCD and stop.? Good luck to you and your family. > > Missy in OH > > > > > > > > New to the group > > > > > > > > > > > > > > > > > > > > > > > > > > Hello All, > > My 5yr old daughter was recently diagnosed with OCD. We always noticed some quirky behaviors of hers since she was little and they would subside here and there. This past May, my husband and I were getting ready to put our home on the market and also start our girl in summer camp. All these changes at once caused a sudden checking and rechecking behavior that was nonstop. Things have slowed a little bit in this area but she still is dealing with a lot. We've moved through the basic ritual of hers which was hand washing. This was easier than what the future ones will entail. She apologizes all the time, for everything. She doesn't want to do something wrong and it actually will prevent her from participating in games and fun activities with her group at camp. Things need to done right and if she's not sure she can do them right the first time then she may opt out of trying them at all. This is heartbreaking for a parent to see as I'm sure everyone on this site already knows. But this is new for her daddy and I (and her 2yr old brother). It's hard to watch her miss out on something because of these thoughts. It's also tough to try to get through one her episodes without taking time from her brother. She's a bright, beautiful, sweet and loving little girl. I wish I could fix this for her but realize I can't. I can only help her try to come to the decision herself that she wants to control the ocd and not let it control her. For a 5 year old, that is a tough thing to do. I'm happy that I've found this site. Our therapist and Dr Wagner's book encouraged us to look for support here. Any feedback or advice you can give us (knowing what it was like to first start dealing with this illness yourselves) is greatly appreciated. Thank you. > > > > > > > > > > > > > > > > > > > > > > > > > ________________________________________________________________________ > Email message sent from CompuServe - visit us today at http://www.cs.com > > > Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 20, 2009 Report Share Posted July 20, 2009 Hello and welcome! My daughter is 6 now, but she was diagnosed when she was 5. She does the checking and the hand-washing. She also had a touching ritual last year that has subsided a little this year. Now she constantly checks the bottoms of her feet every time she walks on our stairs inside our home to make sure there are no bugs on her feet. There was a dead bug on the stairs a few weeks ago and she still skips that step that the bug was on AND she checks her feet too. She also has been diagnosed with Asperger's, ADHD, and Nonverbal Learning Disorder. I also suspect an auditory processing issue. Welcome to the group and please know you're not alone. Misty mom to 3 Aspie girls & a nearly 3yo boy ________________________________ To: Sent: Monday, July 20, 2009 1:18:39 PM Subject: New to the group  Hello All, My 5yr old daughter was recently diagnosed with OCD. We always noticed some quirky behaviors of hers since she was little and they would subside here and there. This past May, my husband and I were getting ready to put our home on the market and also start our girl in summer camp. All these changes at once caused a sudden checking and rechecking behavior that was nonstop. Things have slowed a little bit in this area but she still is dealing with a lot. We've moved through the basic ritual of hers which was hand washing. This was easier than what the future ones will entail. She apologizes all the time, for everything. She doesn't want to do something wrong and it actually will prevent her from participating in games and fun activities with her group at camp. Things need to done right and if she's not sure she can do them right the first time then she may opt out of trying them at all. This is heartbreaking for a parent to see as I'm sure everyone on this site already knows. But this is new for her daddy and I (and her 2yr old brother). It's hard to watch her miss out on something because of these thoughts. It's also tough to try to get through one her episodes without taking time from her brother. She's a bright, beautiful, sweet and loving little girl. I wish I could fix this for her but realize I can't. I can only help her try to come to the decision herself that she wants to control the ocd and not let it control her. For a 5 year old, that is a tough thing to do. I'm happy that I've found this site. Our therapist and Dr Wagner's book encouraged us to look for support here. Any feedback or advice you can give us (knowing what it was like to first start dealing with this illness yourselves) is greatly appreciated. Thank you. Quote Link to comment Share on other sites More sharing options...
Guest guest Posted July 21, 2009 Report Share Posted July 21, 2009 Hi there and Welcome, Our son is almost 18yrs old and is doing well now, after three years from onset of OCD. For us it came in overnight and took over our lives for a good two years. I do still remember the horror of it, feeling helpless while I watched our son suffer so much. For us it was around the clock, even in his dreams. We spent two years sorting out medication, but it really was needed to reduce the level of anxiety, so he could eventually take on the ERP. In our case, with a teen, the biggest challenge, beyond the medication, was waiting it out until he was willing to really take on the ERP. We found that really hard. You wonder if they ever will take it on. I know many others here have dealt with the same thing, and for longer. Hopefully with a younger child you can more easily pursuade? I'm sure it depends. It is heartbreaking as you say, to see your child missing out on " normal " life and experiences. Eventually though, this can be one of the things that finally gets them on board to do the ERP. They want their life back, or to be able to play a game, or whatever. Often when the incentive is great enough they will push themselves through their fear/anxiety. Again, it depends how severe it is though. Dr.Pinto-Wagner's book is very good, as are her books for children. She is very encouraging too. You can always post a question to her on this site, she is generally very responsive, and I have found her responses very helpful, personally. She seems to be able to cut through the confusion and make clearer the issue or next step. This is a great bunch with good ideas for dealing with the day to day challenges that come with living with a child with OCD. Keep posting, both the good and the bad of it - nice to share the victories too! Hang in there. They can get better with time and persistence with the ERP, ours did. Warmly, Barb Ontario, Canada > > Hello All, > > > > > > My 5yr old daughter was recently diagnosed with OCD. We always noticed some quirky behaviors of hers since she was little and they would subside here and there. This past May, my husband and I were getting ready to put our home on the market and also start our girl in summer camp. All these changes at once caused a sudden checking and rechecking behavior that was nonstop. Things have slowed a little bit in this area but she still is dealing with a lot. We've moved through the basic ritual of hers which was hand washing. This was easier than what the future ones will entail. She apologizes all the time, for everything. She doesn't want to do something wrong and it actually will prevent her from participating in games and fun activities with her group at camp. Things need to done right and if she's not sure she can do them right the first time then she may opt out of trying them at all. This is heartbreaking for a parent to see as I'm sure everyone on this site already knows. But this is new for her daddy and I (and her 2yr old brother). It's hard to watch her miss out on something because of these thoughts. It's also tough to try to get through one her episodes without taking time from her brother. She's a bright, beautiful, sweet and loving little girl. I wish I could fix this for her but realize I can't. I can only help her try to come to the decision herself that she wants to control the ocd and not let it control her. For a 5 year old, that is a tough thing to do. I'm happy that I've found this site. Our therapist and Dr Wagner's book encouraged us to look for support here. Any feedback or advice you can give us (knowing what it was like to first start dealing with this illness yourselves) is greatly appreciated. Thank you. > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > > __________________________________________________________ > > > Email message sent from CompuServe - visit us today at http://www.cs.com > > > > > > > > > Quote Link to comment Share on other sites More sharing options...
Recommended Posts
Join the conversation
You are posting as a guest. If you have an account, sign in now to post with your account.
Note: Your post will require moderator approval before it will be visible.