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Too Many Meds

Dylanc1500
By Dylanc1500
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Anxiety meds that I'm dependent on and my doctor refuses to take me off them even though they cause:

  • Memory loss
  • Blurry vision
  • Shakes
  • Drowsiness
  • Dizzyness
  • Dry mouth
  • Dehydration
  • Head aches

I also can't stop myself on the drug because if I do, I can't see, the dizzyness gets so extreme that I can't walk. I can't focus on anything without getting nauseated. My anxiety comes back in such a force that I can't think of anything but worries. Massive soul draining headaches. Illusions. The constant feeling of spiders crawling on me.

 

Remember kids its okay if a doctor hooks you up to drugs and doesn't let you stop, but if a drug dealer does it, its a big no-no!

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6 hours ago, Teddy07 said:

I throw my prescription note usually in the garbage as long as it not urgent. I don't need medicine cause my body will cure itself. I only take it if it is really urgent but i don't have any problems currently.

I sincerely hope this is "/s", because if not, you're playing lottery with your health.

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2 minutes ago, dalekphalm said:

I sincerely hope this is "/s", because if not, you're playing lottery with your health.

I am serious.

I am totally healthy. Why should I take medicine with just minor things like an influenza or my wisdom teeth when I didn't feel any pain? The immune system will handle most illnesses just fine so need for medication.

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Just now, Teddy07 said:

I am serious.

I am totally healthy. Why should I take medicine with just minor things like an influenza or my wisdom teeth when I didn't feel any pain? The immune system will handle most illnesses just fine so need for medication.

Okay so you're either not understanding my post, or you're conflating "non-serious" medical issues with actual necessary medication.

 

First thing's first: Most people with the flu don't take prescription medicine. It's generally not necessary, and is ONLY to control the symptoms, not to make you healthy faster. There's the Flu vaccine, but because of how quickly the Flu mutates, those vaccines have a pretty low success rate (though, for the average person, the side effects are extremely low or non-existent).

 

As for Wisdom teeth - assuming you were only prescribed pain meds (Tylenol, Codeine, etc), those are... obviously... for pain control. If you don't feel any pain, you don't take them. Simple, yeah?

 

However, if they prescribed antibiotics or something like that, you'd be stupid not to take them. You could get a serious infection and not even know about it until it's too late.

 

So yeah, when you're talking about wisdom teeth removal and the Flu, yes, the immune system will handle that.

 

However, the idea that the immune system will handle "most illnesses" is just flat out wrong, and absurd. Many illnesses will flat out kill you (or give you serious, permanent afflictions for life) without treatment.

 

It's kind of the reason why vaccinations and cures exist.

 

So it sounds like, to me, that you've just never had an actually serious illness.

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On 3/30/2017 at 2:02 PM, Dylanc1500 said:

I was going through my prescriptions today and reordering them all for this month and realized I take 68 pills a day and take 14 inhaled meds. Man I feel like if I was raided by cops I'd be charged for distribution.

 

What meds do you all have to take, if at all?

Blood Pressure and Allergy. 

I just want to sit back and watch the world burn. 

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what kind of medical madness condition are you in man?... 68 pills and 14 inhalers PER DAY??? how are you alive if you need all that... good luck with getting better or something to be able to cut the meds atleast

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16 hours ago, Teddy07 said:

I just watched a BBC documentary about the huge problems the NHS is facing because of the problem with diabetes. It might collapse according to the BBC if changes are not made soon to stop the diabetes epidemic.

nah it's sound

like the BBC is all about fair criticism, it's not going to go any time soon but it's just about making the public aware about the issues in the NHS. There always are issues in the NHS, issues that people in countries with private healthcare would find unacceptable but in the UK it's cool.

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I don't take anything, not even fluoride or vitamins. When I have a migraine or headache I sleep instead of taking pills. 

▓ƆԀ▓ S▓₱▓Ɇ▓c▓s▓: i7 6ʇɥפᴉƎ00K (4.4ghz), Asus DeLuxe X99A II, GT҉X҉1҉0҉8҉0 Zotac Amp ExTrꍟꎭe),Si6F4Gb D???????r PlatinUm, EVGA G2 Sǝʌǝᘉ5ᙣᙍᖇᓎᙎᗅᖶt, Phanteks Enthoo Primo, 3TB WD Black, 500gb 850 Evo, H100iGeeTeeX, Windows 10, K70 R̸̢̡̭͍͕̱̭̟̩̀̀̃́̃͒̈́̈́͑̑́̆͘͜ͅG̶̦̬͊́B̸͈̝̖͗̈́, G502, HyperX Cloud 2s, Asus MX34. פN∩SW∀S 960 EVO

Just keeping this here as a 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̌̅̒̾̈́̆͌̌̾̎̽̐̅̏́̈̔͛̀̋̃͊̒̓͗͒̑͒̃͂̌̄̇̑̇͛̆̾͛̒̇̍̒̓̀̈́̄̐͂̍͊͗̎̔͌͛̂̏̉̊̎͗͊͒̂̈̽̊́̔̊̃͑̈́̑̌̋̓̅̔́́͒̄̈́̈̂͐̈̅̈̓͌̓͊́̆͌̉͐̊̉͛̓̏̓̅̈́͂̉̒̇̉̆̀̍̄̇͆͛̏̉̑̃̓͂́͋̃̆̒͋̓͊̄́̓̕̕̕̚͘͘͘̚̕̚͘̕̕͜͜͝͝͝͠͝͝͝͝͠ͅS̷̢̨̧̢̡̨̢̨̢̨̧̧̨̧͚̱̪͇̱̮̪̮̦̝͖̜͙̘̪̘̟̱͇͎̻̪͚̩͍̠̹̮͚̦̝̤͖̙͔͚̙̺̩̥̻͈̺̦͕͈̹̳̖͓̜͚̜̭͉͇͖̟͔͕̹̯̬͍̱̫̮͓̙͇̗̙̼͚̪͇̦̗̜̼̠͈̩̠͉͉̘̱̯̪̟͕̘͖̝͇̼͕̳̻̜͖̜͇̣̠̹̬̗̝͓̖͚̺̫͛̉̅̐̕͘͜͜͜͜ͅͅͅ.̶̨̢̢̨̢̨̢̛̻͙̜̼̮̝̙̣̘̗̪̜̬̳̫̙̮̣̹̥̲̥͇͈̮̟͉̰̮̪̲̗̳̰̫̙͍̦̘̠̗̥̮̹̤̼̼̩͕͉͕͇͙̯̫̩̦̟̦̹͈͔̱̝͈̤͓̻̟̮̱͖̟̹̝͉̰͊̓̏̇͂̅̀̌͑̿͆̿̿͗̽̌̈́̉̂̀̒̊̿͆̃̄͑͆̃̇͒̀͐̍̅̃̍̈́̃̕͘͜͜͝͠͠z̴̢̢̡̧̢̢̧̢̨̡̨̛̛̛̛̛̛̛̛̲͚̠̜̮̠̜̞̤̺͈̘͍̻̫͖̣̥̗̙̳͓͙̫̫͖͍͇̬̲̳̭̘̮̤̬̖̼͎̬̯̼̮͔̭̠͎͓̼̖̟͈͓̦̩̦̳̙̮̗̮̩͙͓̮̰̜͎̺̞̝̪͎̯̜͈͇̪̙͎̩͖̭̟͎̲̩͔͓͈͌́̿͐̍̓͗͑̒̈́̎͂̋͂̀͂̑͂͊͆̍͛̄̃͌͗̌́̈̊́́̅͗̉͛͌͋̂̋̇̅̔̇͊͑͆̐̇͊͋̄̈́͆̍̋̏͑̓̈́̏̀͒̂̔̄̅̇̌̀̈́̿̽̋͐̾̆͆͆̈̌̿̈́̎͌̊̓̒͐̾̇̈́̍͛̅͌̽́̏͆̉́̉̓̅́͂͛̄̆͌̈́̇͐̒̿̾͌͊͗̀͑̃̊̓̈̈́̊͒̒̏̿́͑̄̑͋̀̽̀̔̀̎̄͑̌̔́̉̐͛̓̐̅́̒̎̈͆̀̍̾̀͂̄̈́̈́̈́̑̏̈́̐̽̐́̏̂̐̔̓̉̈́͂̕̚̕͘͘̚͘̚̕̚̚̚͘̕̕̕͜͜͝͠͠͝͝͝͝͠͝͝͝͠͝͝͝͝͝͝ͅͅͅī̸̧̧̧̡̨̨̢̨̛̛̘͓̼̰̰̮̗̰͚̙̥̣͍̦̺͈̣̻͇̱͔̰͈͓͖͈̻̲̫̪̲͈̜̲̬̖̻̰̦̰͙̤̘̝̦̟͈̭̱̮̠͍̖̲͉̫͔͖͔͈̻̖̝͎̖͕͔̣͈̤̗̱̀̅̃̈́͌̿̏͋̊̇̂̀̀̒̉̄̈́͋͌̽́̈́̓̑̈̀̍͗͜͜͠͠ͅp̴̢̢̧̨̡̡̨̢̨̢̢̢̨̡̛̛͕̩͕̟̫̝͈̖̟̣̲̖̭̙͇̟̗͖͎̹͇̘̰̗̝̹̤̺͉͎̙̝̟͙͚̦͚͖̜̫̰͖̼̤̥̤̹̖͉͚̺̥̮̮̫͖͍̼̰̭̤̲͔̩̯̣͖̻͇̞̳̬͉̣̖̥̣͓̤͔̪̙͎̰̬͚̣̭̞̬͎̼͉͓̮͙͕̗̦̞̥̮̘̻͎̭̼͚͎͈͇̥̗͖̫̮̤̦͙̭͎̝͖̣̰̱̩͎̩͎̘͇̟̠̱̬͈̗͍̦̘̱̰̤̱̘̫̫̮̥͕͉̥̜̯͖̖͍̮̼̲͓̤̮͈̤͓̭̝̟̲̲̳̟̠͉̙̻͕͙̞͔̖͈̱̞͓͔̬̮͎̙̭͎̩̟̖͚̆͐̅͆̿͐̄̓̀̇̂̊̃̂̄̊̀͐̍̌̅͌̆͊̆̓́̄́̃̆͗͊́̓̀͑͐̐̇͐̍́̓̈́̓̑̈̈́̽͂́̑͒͐͋̊͊̇̇̆̑̃̈́̎͛̎̓͊͛̐̾́̀͌̐̈́͛̃̂̈̿̽̇̋̍͒̍͗̈͘̚̚͘̚͘͘͜͜͜͜͜͜͠͠͝͝ͅͅͅ☻♥■∞{╚mYÄÜXτ╕○\╚Θº£¥ΘBM@Q05♠{{↨↨▬§¶‼↕◄►☼1♦  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18 hours ago, Celios said:

Glad to hear you're doing okay!

 

My old hospital was very tiny, only had 2 floors. The ward itself didn't even feel like a hospital to me, I kinda liked going there every once in a while for a stay, it was like a little vacataion, haha. They had WiFi and there was also a Blockbuster 5 minutes down the road so I would rent DVDs (that Blockbuster shutdown 2 years ago though, rest in peace) and never get too bored.

 

It is also a pain if I want to get admitted for IVs to this new hospital, in fact, it's a pain to even get hold of them. I was trying to contact the CF nurse about something rather important the other day and it took 6 hours (no exaggeration) of being hung up on and people telling me I would get a call back shortly. I never got a call back "shortly" I got a call back 2 days later, ridiculous. 

 

And yeah, the Accapellas are a pain, the little metal circle thing inside starts to go rusty after you clean it a few times to as well.

 

Undortunately not, they haven't offered the vest to me so I've never thought to ask, I will try ask at my next appointment. 

 

The doxtors and nurses always nag me to do more exercise but I hate sports and things like that.  It's been like this since I was a kid. I know they are trying to help, I guess I need to push myself to become fitter. My lung function is around 52% right now.

 

The tablet is called "Orkambi" and apparently can do a lot of good but they aren't really giving to anybody due to funding issues. I've always thought why would they make these kind of treatments if they won't bother to help anyone? I guess they just sell them for a lot of money to richer families who can afford t. Not sure if this is an issue only in the UK, do you take it?

 

 

Holy smokes that's small. Children's had a whole floor of 26 rooms dedicated to CF. I liked going in when I was in school but now I get bored and KU gets a little angry that I bring in a entire desktop while I'm in. lol I have to work. Honestly never used Blockbuster, but luckily they had different game systems (Xbox 360, PS3 and Wii) that they would bring you if you wanted.

 

I'm really sorry that you have to deal with that. That is absolutely appalling and there is no excuse for it. Have you or your parents confronted them about it? With KU I had to actually confront them about their mistakes and mix-ups before they would do anything about it.

 

I had a couple do that and afterwards I started cleaning them with only 91% rubbing alcohol, have yet to have the issue since. They really like to get gross quickly.

 

I would certainly try. It can be a little weird at first but man once you get used to the vibrations and pressure it can actually make you fall asleep.

 

Ya I wrestled and played baseball through high school, along with band. My senior year however took a pretty shard downturn I went into the hospital two times and once for 4 weeks and the other for 5 weeks (school was not happy with that). I started with a base line around 85% and by graduation I was at 65%.

 

I take Orkambi. It was a godsend for me. If you have at least one copy of the ΔF508 gene then it will help. I lucked out have two copies of the gene. It has a slightly weird symptom for the first week or so were it can kind of make your chest feel tight at times but only a small amount of people really notice it. My mucus in my chest has gone from being almost impossible to get out to being thin and almost water like. It makes treatment a thousand times easier. My vitamin levels and weight have increased. I even had my lung function jump by almost 15% when I started it. I see absolutely no reason whatsoever for them to not offer it. It has shown major increases in quality of life for people with that gene, hell some people have been able to stop almost all meds. Yes its expensive, my insurance is charged $32,000 a month just for it. Every single private insurance I know covers it. The only people that have had issues in the U.S. with obtaining it are people with Medicaid because it isn't covered, even though it is approve by the FDA. I see no reason not to when the prevalence of CF in Europe is close to the same as the U.S. in relation to the population. I hope they change that.

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18 hours ago, Teddy07 said:

I throw my prescription note usually in the garbage as long as it not urgent. I don't need medicine cause my body will cure itself. I only take it if it is really urgent but i don't have any problems currently.

Good to hear you're happy and healthy. I wish my body would decide to heal itself, seems like its trying to self destruct if I don't take meds lol.

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11 hours ago, Bananasplit_00 said:

what kind of medical madness condition are you in man?... 68 pills and 14 inhalers PER DAY??? how are you alive if you need all that... good luck with getting better or something to be able to cut the meds atleast

One word, Cystic Fibrosis. Wait that's two words, oops. None of my pills are narcotics of any sort. They are a make-up of antibiotics, NSAIDs, antihistamines, antacids, enzyme replacements, and a combination drug that acts as a protein binder and a migrator inside of cells. Two of my Inhaled meds are typical "puffer" inhalers. They are albuterol and Advair. The rest are nebulized meds.

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I remember back in high school that someone that had just recently graduated from my school received a double lung transplant due to his Cystic Fibrosis. He was originally told that he wouldn't live past his late 20s, early 30s but the operation gave him approximately another 20 years. Hopefully gene therapy research will help tremendously with this disease and other genetic disorders in future.

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14 minutes ago, DeadEyePsycho said:

I remember back in high school that someone that had just recently graduated from my school received a double lung transplant due to his Cystic Fibrosis. He was originally told that he wouldn't live past late 20s, early 30s but the operation gave him approximately another 20 years. Hopefully gene therapy research will help tremendously with this disease and other genetic disorders in future.

I loathe the day they tell me I need a transplant. I don't know what makes it so much more difficult for lung transplants but, the success rate is a lot lower than with most other transplants. They have actually done a lot of research into gene therapy for CF, the big problem is that the mutation falls in the CFTR gene. There are thousands of different sections that can be mutated that cause the same issue and trying to correct the CFTR as a whole has been found to not be permanent. For some reason the gene will continue to revert the mutation. They theorize that it's due to having a mutation in both copies of the gene and not being able to correct both copies at once. I hope they figure it out soon, I mean seriously, I'm starting to look like Joan Rivers without the plastic and Botox (and I'm only 23).

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5 hours ago, Dylanc1500 said:

One word, Cystic Fibrosis. Wait that's two words, oops. None of my pills are narcotics of any sort. They are a make-up of antibiotics, NSAIDs, antihistamines, antacids, enzyme replacements, and a combination drug that acts as a protein binder and a migrator inside of cells. Two of my Inhaled meds are typical "puffer" inhalers. They are albuterol and Advair. The rest are nebulized meds.

wow, well thats pretty bad. hope you can get better or something, cant be fun to take all that :/ 

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I take about 1mg of Melatonin every evening, but that's it.

Quote me to see my reply!

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On April 2, 2017 at 7:50 AM, Bananasplit_00 said:

wow, well thats pretty bad. hope you can get better or something, cant be fun to take all that :/ 

Eh, it's not too bad. I learn to make the best of it. Like for example I will purposely go to mcdonalds some mornings and take my cup of pills with me and set them on my table while eating. Then I'll wait for someone to give me a dirty look and when they do I'll start really erratically scratching my neck and chest and take my pills really fast. Peoples reactions to it are hilarious. I actually had one guy who kept staring at me so I did that, and next thing I know I hear "oh hell naw!" He jumped up and ran out. I started laughing so hard I almost shot Dr. Pepper through my nose.

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