COPD :: Inhalers / Meds May Work For You But Not For Me


Sep 15, 2015

Including, inhalers, ingested, etc....  To say it again, what works for one may or may not work for another person.  I don't understand why people ask this or that inhaler or whatever med. worked for them?  It, to repeat myself, may work for you but not for me.  What I have realized in this whole journey of copd and other chronic diseases that I'm dealing with is that it is up to me to do everything I can to find out about the disease; ie. research, talking to people and pulmonary care.  That's about it really. 

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Mucus In Chest - Inhalers Only Solution?

I have never used an inhaler before and I don't have Asthma, but I think it's allergies, nonetheless, inhalers scare me I had seizures when. I was younger in fact last one was 20 some yrs ago.

Don't like what is on directions (precautions)...my main concern is the mucus in chest, I cough and a lot of time bring up phlegm, my Dr said the inhaler would stop the rattling.........she is good, but not an allergist.

Now question........what is good (besides inhaler) to loosen mucus. Right now drinking tea and honey.

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Asthma :: Inhalers Causing Chest Pains

I have been diagnosed with Bronchial asthma all my life (22 years), My inhalers have not been a bother with me worked perfect helped me so much expect the Blue one which made my Asthma worse. As of lately, I am on a Brown inhaler and all of a sudden when I take it I get really severe chest pains on my lungs and ribs, (Inflamed lungs) which has been caused by taking my inhaler, I have been to the doctors and she just says it's because it's "opening my airways" I have stopped taking them and the pain has gone, but I have to take them because change of weather makes me breathless. I am struggling on what to do. It gets so bad that I have to hold my chest and rub the area to calm the pain.

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ADHD / ADD :: Genetic Testing For Meds?

I have a 10 year old son who is diagnosed with ADHD, Anxiety, SPD/IPD and rule out of Asperger's/PDD in 2013. Currently, we have him on Methylphenidate ER 30mg per day, but lately we have been noticing issues. Mind you, the school hasn't been very helpful this year with information on how he is doing so I can only go by the vague messages received... the first 6 months, they say he was great! Though I have documents to prove otherwise - lately though, the teacher keeps saying he lacks focus, needs to pay attention and all that jazz. (I say it so flippantly because this teacher has been a pain to work with.

I spoke with the doctor and she wants us to come in next week to discuss his meds, but we have had issues with additives in the past and it's not a route I want to go... to sit and wait. His diet is modified already, we also work with a behavioral therapist and a chiropractic neurologist and he takes Taekwondo.

With all this, I'm wondering if anyone has tried the genetic testing (IE: HarmonyX or Genesight) to see what meds would work best with his specific genetic makeup?

I read all these stories of parents having all these issues and suddenly their kids are on Vyvanse or something else and it's a miracle.  I wouldn't mind that... him being able to function better at school (academically and socially) ... he gets bullied (though he can start it up too) - I just wonder, what next?

Here is his medication history:

August 2011 – Vyvanse ??mg (very small amount)
September 2011 – Vyvanse 30mg (adjusted to 30 mg)
May 2012 – Trial samples of Intuniv w/ Vyvanse for two weeks. After two weeks he was out of         school and parents decided not to continue the Intuniv.

September 2013 – Intuniv 2mg w/ Vyvanse
September 2013 – Concerta 36mg (removed from Vyvanse and Intuniv because he became over-emotional and violent/aggressive)

December 2013 -  Concerta 54mg (Dr. Snyder prescribed)

March 2014 – Methylphenidate 10mg (3 times a day) (March 7th thru March 14th)
Methylphenidate 15mg (3 times a day) (started March 15th)
April 2014 – Methylphenidate 20mg (3 times a day) (started April 14th)
May 2015 – Adderall (adderall) 10mg (3 times a day) (started May 14th)
June 2015 – Adderall (adderall) 15mg (3 times a day) (started June 3rd)
August 2015 – Guanfacine 1/2mg (3 times a day) (started August 21st)

September 2015 – Methylphenidate ER 30mg (once a day) (started September 6th)

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Gabapentin :: Stopping The Meds Can Cause Seizures?

Went to see new neurosurgeon on Monday and she has prescribed Gabapentin to add to the mix of my daily cocktail of drugs. Having looked it up though, it seems to have some pretty worrying side effects. For me, as I work full time, I am concerned about being drowsy, sleepy and generally spaced out at work. Apparently it is all magnified if you are also on opiate based painkillers too. I am also concerned that I may pile on the weight!

Can I ask what adverse reactions others have had to this? Also it says on the box that stopping the meds can cause seizures, but is this only in people that have epilepsy (the main reason the drug is prescribed) or can it cause that in people that have never had a history of epilepsy?

By the way, my meds had not changed since May 2007. Nobody has had the slightest interest in monitoring me, either in terms of if they are still suitable, dosage levels, if I am now addicted, if they are working well or even if they are harming my body. Some of the boxes state that you should have regular blood tests but I have never been offered any. Considering I have had two lumbar operations since last May and numerous problems since, it seems quite odd that this has been allowed to go on for so long with not one of the numerous doctors/surgeons giving a damn. I just order the meds from my GP surgery online and then pick up the prescription. That gives a review date, usually 6 monthly intervals, but nobody actually reviews me, they just put a new review date down on the records.

Apart from back pain my main problem these days is the burning/numbness the whole length of my leg and my locked up toes. Apparently the Gabapentin will help with this. But the worse of the problem is at night, hence the fact that I can function reasonably well during the day. But now if these new tablets are going to knock me out and render me incapable during the day, then I'm tempted just not to bother.

All in all the meeting with the new neurosurgeon went quite well. I will be having another MRI shortly (my 6th in 16 months) and hopefully I'll know more then about what is going to happen going forward. The bad news is that she thinks that a lot of the problems are from the internal scarring from the two operations and nothing can be done about that. Hey, ho, I guess I'll find out in time.

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Substance Abuse :: Detox Meds?

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Thyroid Meds To Treat Fibromyalgia?

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He called in a script for synthroid name brand for me, I haven't picked it up yet I guess I am nervous to try it.

He did do my bloodwork, TSh was in guidelines, free T 4 and T3 were in range but at 50% of the range.

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I'm starting to feel tired and colder (as I am now under replaced), but I am still feeling a pounding in my chest.

has anyone else experienced this side effect of liothyronine and does it get better?

i'm desperate to stay on the T3 as it helps a lot with the tiredness and brain fog and Levo alone just doesn't work for me.

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Now, my question. lisinopril used to be a very effective drug for me, but I couldn't tolerate it. 10 mg would tank my BP by 30 points. So, when I started having the spikes, I figured, I'll tough out the side effects to keep my BP down, and go ahead and take the lisinopril However, now even 40 mg. of lisinopril doesn't do anything for me, and neither, it seems, does the cozaar. I am currently on 240 mg of diltiazem and that seems to at least keep the pressure around 140/80, most of the time.

I am hypercalciuric, which means my kidneys are excreting the excess calcium caused by the HPT that I supposedly have. I was wondering if anyone here has heard of any medical situation in which lisinopril or cozaar might actually exacerbate BP issues? It seems really odd to me that a formerly very (almost too) effective a drug, now does nothing, and even seems to make it worse. Any thoughts?

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Hypothyroidism :: Muscle Weakness With Thyoid Meds

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Alcohol :: Can I Drink With Vulvar Vestibulitis And Treatment Meds?

I was diagnosed with vulvar vestibulitis, a condition where the nerves in my vulval area are hypersensitive and cause swelling and itching upon the slightest disturbance (i.e. tight clothing, vibration from car rides, etc.). This was about 8 months ago, and my OBGYN prescribed me amitriptyline (25 mg)/ night and lexapro (10 mg)/day to calm these nerves over time. Can I have a drink or 2 with this condition? I really want to but am afraid that it will make my vestibulitis worse. Anyone else out there with vestibulitis who is facing or has faced this problem?

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Chronic Fatigue Syndrome :: Favourite Meds And Supplements?

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Anxiety :: Zoloft Stopped Working - Switching Meds?

Say my Zoloft pooped out and I increased to 75 with no help in 4 weeks, what should I switch to that will help GAD, panic and possibly some agoraphobia?

One dr. says to try Luvox and just switch out the dosage with no weening.

Then I am thinking switching to Lexapro is there a ween process here?

Or, I am thinking of adding in BuSpar to the Zoloft since it has minimal side effects. 

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Parkinson :: Meds A Poison Chalice Or A Life Saver?

My mother died in June and was in final stage parkinsons. 

reflecting on her illness and treatment I feel that not enough information is given about the long term side effects and the progression of the disease. 

The drugs do reverse symptoms which does give quality of life and prolong life. In early stage parkinson's the sufferer is able to think clearly and make decisions and yet no care plan is set out asking the patient what choices they wish to make re their care. I went to every appointment with my mother . And found the doctors to treat Parkinson's like they did cancer in the past. We can't say how you will progress , everyone's different and not setting out the long term side effects of the drugs.

as a carer to prepare yourself for what you will face and for a patient to decide whether they want a long drawn out illness in which you end up with parkinsons dementia caused by the drugs you have taken or a shorter intense illness . Just as you can choose chemotherapy or not. I believe most people would choose the drugs . But the family could sit and plan their care with them. Making decisions if I can't live alone anymore I will live in a granny flat etc if I get dementia find a nursing home .... 

By the time my mother moved in with us she was beginning to suffer with dementia and severe weight loss due to constant dysphasia movement of arms and legs side effect of drugs . She made decisions on her drugs all the way through and wanted more and more but she wasn't in a right state of mind .... If she had made these decisions in the beginning she wouldn't I know of chosen to be over medicated ... She ended up 4 stone 7llb with severe movement of tongue arms and legs due to drugs , suffering from memory loss and personality change brain scan showed wasn't Alzheimer's but was side effect of meds. 

Action is needed to spell out the end of an illness when u r at the beginning so that you can choose your path through it. 

Before she died they took all her medication away except ne .palliative care . She was peaceful calm couldn't move much it's true but she responded smiling , crying and nodding  and gesturing . She was unmedicated  and I thought what if ? 

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Substance Abuse :: Still Depressed AFTER Quitting Drugs/drink/meds

I finally quit abusing various substances 7 weeks ago. My addiction started with alcohol, went onto street drugs and then ended 7 weeks ago with prescription drug abuse. I saw an addiction specialist before i got clean and she told me i had 'polysubstance' addiction and wanted £40k from me to get clean so i decided to do it myself and i finally detoxed  7 weeks ago.  I have to say i don't miss the drugs and i have absolutely no desire to return to any kind of substance but i'm really struggling on a daily basis right now. I'm so depressed, lacking in motivation, low on energy, suffering memory loss, bored.... the list goes on. Every negative emotion you can think of i am experiencing it everyday. SURELY this can't be right?? I mean its been 7 bloody weeks and i'm still a scruff-bag. I can't apply myself to do anything meaningful other than a bit of light daily exercise and showering. Those 2 small things take me forever to do because i just put them off as long as possible. I feel like i'm not getting better. I really really hope someone reads this and has experienced something similar and can tell me i'm going to eventually feel happy again?!? The thought of my life continuing on like this just ***** and i have no idea what to do. I thought about maybe i need to be put on some anti depressants but due to my medication abuse in the past i'm very dubious. I just want to know what's wrong with me and why i cant get better. why am i a nervous wreck and unrecognisable even 7 weeks on. :o(

Has anyone any clue or ideas about how long this torture is going to last? Its actually worse than the initially detox because its not improving. I'm stuck in a living hell. This discussion is related to Depression after quitting heroin and crack.

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Heart Disease :: Treatment Options Stent With Meds Or CABG?

70 year old male in good shape been exercising 6 days a week cardio and weights for the past 5 years or so.Last couple of weeks or started to feel discomfort in my neck and jaw while exercising, it would go away when I stopped. Went to to non interventional cardiologist who ordered up an angiogram which I had 4 days ago. Results were Right artery 99%  blocked, LAD 70 % and two other arteries on the left also 70% blocked. Interventional Cardiologist recommended CABG surgery because of multiple artery involvement and that the left arteries were not good candidates for stenting due to the position of the blockage.

My non interventional cardio after conferring with the interventional cardio said that I had options other than CABG. Both doctors agreed that my angina was most likely coming from the 99% right block.

Option is stenting the 99% blocked right and the OMT for the rest. A surgeon was also called in for consultation and neither he  or the two other Cardios would predict outcomes or give an opinion as to which course of treatment I should follow. Regardless something had to be done sooner rather than later for the  right artery. I sent the pics to  another interventional Cardio  who validated the position of my non interventional cardio that I do have choices other than CABG and that the which ever decision I would make I would probably have a good outcome. So next week I'm going to have the right artery stented and then medically treat the rest of my disease and see where it goes from there.

I also plan to make major changes in my diet to hopefully control the progression of the disease or even possible improve my condition

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